All Stories

  1. Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies

    Article • Journal of the Endocrine Society, September 2017, Endocrine Society

    Berenice Mendonca, Vinicius Brito, Professor Berenice B Mendonca

  2. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty

    Article • The Journal of Clinical Endocrinology & Metabolism, January 2017, Endocrine Society

    Andrew Dauber, Berenice Mendonca, Ana Claudia Latronico, Ursula Kaiser, Professor Berenice B Mendonca

  3. Expression of LIN28 and its regulatory microRNAs in adult adrenocortical cancer

    Article • Clinical Endocrinology, November 2014, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  4. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort

    Article • Growth Hormone & IGF Research, October 2014, Elsevier

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  5. Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay

    Article • Fertility and Sterility, September 2014, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  6. Quality of life in a large cohort of adult Brazilian patients with 46,XX and 46,XY disorders of sex development from a single tertiary centre

    Article • Clinical Endocrinology, September 2014, Wiley

    Berenice Mendonca, Dr Rita Cassia Amaral, Professor Berenice B Mendonca

  7. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: The Influence of a SOCS2 Polymorphism

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2014, Endocrine Society

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  8. Quality of life of patients with 46,XX and 46,XY disorders of sex development

    Article • Clinical Endocrinology, August 2014, Wiley

    Berenice Mendonca, Dr Rita Cassia Amaral, Professor Berenice B Mendonca

  9. ARMC5Mutations Are a Frequent Cause of Primary Macronodular Adrenal Hyperplasia

    Article • The Journal of Clinical Endocrinology & Metabolism, August 2014, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  10. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

    Article • The Journal of Clinical Endocrinology & Metabolism, June 2014, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  11. Increased expression of ACTH (MC2R) and androgen (AR) receptors in giant bilateral myelolipomas from patients with congenital adrenal hyperplasia

    Article • BMC Endocrine Disorders, May 2014, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  12. Long-Term Followup of a Large Cohort of Patients with Ovotesticular Disorder of Sex Development

    Article • The Journal of Urology, May 2014, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  13. Análise de um radioimunoensaio iodado para determinação de 11-deoxicortisol

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, April 2014, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  14. Clinical management of transsexual subjects

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, March 2014, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  15. Avanços na etiologia, no diagnóstico e no tratamento da puberdade precoce central

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, March 2014, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  16. Atividades Musicais Interativas como Instrumento Humanizador para Redução do Estresse de Crianças Submetidas a Cirurgias Urológicas.

    Article • March 2014, Editora Edgard Blucher, Ltda.

    Berenice Mendonca

  17. 46,XY DSD due to 17β-Hydroxysteroid Dehydrogenase 3 Deficiency

    Article • January 2014, Elsevier

    Berenice Mendonca

  18. Amplification of theInsulin-Like Growth Factor 1 ReceptorGene Is a Rare Event in Adrenocortical Adenocarcinomas: Searching for Potential Mechanisms of Overexpression

    Article • BioMed Research International, January 2014, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  19. Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia

    Article • International Journal of Endocrinology, January 2014, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  20. Homozygous Inactivating Mutation inNANOS3in Two Sisters with Primary Ovarian Insufficiency

    Article • BioMed Research International, January 2014, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  21. Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

    Article • Fertility and Sterility, September 2013, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  22. 103 TRANSSEXUAL GENITAL SURGERY: COMPLICATIONS AND FUNCTIONAL RESULTS AFTER 13 YEARS OF EXPERIENCE

    Article • The Journal of Urology, April 2013, Wolters Kluwer Health

    Berenice Mendonca

  23. Relatively high frequency of non‐synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly

    Article • Clinical Endocrinology, March 2013, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  24. Analysis of the insulin‐like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p.Arg511Trp)

    Article • Clinical Endocrinology, March 2013, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  25. Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, March 2013, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  26. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia

    Article • Hormone Research in Paediatrics, January 2013, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  27. The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty

    Article • Seizure, January 2013, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  28. Molecular and Gene Network Analysis of Thyroid Transcription Factor 1 <b><i>(TTF1)</i></b> and Enhanced at Puberty <b><i>(EAP1)</i></b> Genes in Patients with GnRH-Dependent Pubertal Disorders

    Article • Hormone Research in Paediatrics, January 2013, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  29. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for <b><i>SHOX</i></b> Analysis

    Article • Hormone Research in Paediatrics, January 2013, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  30. Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, December 2012, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  31. Analysis of anti-Müllerian hormone (AMH) and its receptor (AMHR2) genes in patients with persistent Müllerian duct syndrome

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2012, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  32. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2012, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  33. Disorders of Sex Development

    Article • Seminars in Reproductive Medicine, October 2012, Thieme Publishing Group

    Berenice Mendonca, Professor Berenice B Mendonca

  34. DSD Due to 5α-Reductase 2 Deficiency - from Diagnosis to Long Term Outcome

    Article • Seminars in Reproductive Medicine, October 2012, Thieme Publishing Group

    Berenice Mendonca, Professor Berenice B Mendonca

  35. Advice on the Management of Ambiguous Genitalia to a Young Endocrinologist from Experienced Clinicians

    Article • Seminars in Reproductive Medicine, October 2012, Thieme Publishing Group

    Berenice Mendonca, Professor Berenice B Mendonca

  36. Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency

    Article • PLoS ONE, September 2012, PLOS

    Berenice Mendonca, Professor Berenice B Mendonca

  37. Growth standards of patients with Noonan and Noonan‐like syndromes with mutations in the RAS/MAPK pathway

    Article • American Journal of Medical Genetics Part A, August 2012, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  38. Laparoscopic adrenalectomy in children

    Article • Journal of Pediatric Urology, August 2012, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  39. 1527 GONADAL TUMOR DETECTION AND TREATMENT IN PATIENTS WITH DISORDER OF SEX DEVELOPMENT (DSD) LONG-TERM ONCOLOGICAL OUTCOMES

    Article • The Journal of Urology, April 2012, Wolters Kluwer Health

    Berenice Mendonca

  40. Potential Effects of Alendronate on Fibroblast Growth Factor 23 Levels and Effective Control of Hypercalciuria in an Adult with Jansen's Metaphyseal Chondrodysplasia

    Article • The Journal of Clinical Endocrinology & Metabolism, April 2012, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  41. The Interactive Effect ofGHR-Exon 3and −202 A/C IGFBP3Polymorphisms on rhGH Responsiveness and Treatment Outcomes in Patients with Turner Syndrome

    Article • The Journal of Clinical Endocrinology & Metabolism, April 2012, Endocrine Society

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  42. GH-Releasing Hormone Receptor Gene: A Novel Splice-Disrupting Mutation and Study of Founder Effects

    Article • Hormone Research in Paediatrics, January 2012, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  43. Absence of Functional <b><i>LIN28B</i></b> Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty

    Article • Hormone Research in Paediatrics, January 2012, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  44. Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2011, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  45. 18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased18F-FDG Uptake

    Article • The Journal of Clinical Endocrinology & Metabolism, November 2011, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  46. Catch-Up Growth in Patients with Congenital or Acquired Growth Hormone Deficiency After GH Replacement: Clinical Features and Hypothalamic–Pituitary Imaging

    Article • October 2011, Springer Science + Business Media

    Berenice Mendonca

  47. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2011, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  48. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys–Drash syndrome

    Article • Pediatric Nephrology, August 2011, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  49. Clinical and molecular aspects of a pediatric metachronous adrenocortical tumor

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2011, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  50. Frequency of genetic polymorphisms of PXR gene in the Brazilian population

    Article • Clinics, January 2011, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  51. Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    Article • Clinics, January 2011, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  52. 46,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity Syndrome

    Article • January 2011, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  53. 46,XY DSD due to 17β-HSD3 Deficiency and 5α-Reductase Type 2 Deficiency

    Article • January 2011, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  54. MAMLD1 (Mastermind-Like Domain Containing 1) Homozygous Gain-of-Function Missense Mutation Causing 46,XX Disorder of Sex Development in a Virilized Female

    Article • January 2011, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  55. A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2010, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  56. Novel Heterozygous NonsenseGLI2Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly

    Article • The Journal of Clinical Endocrinology & Metabolism, November 2010, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  57. Male hypogonadism: childhood diagnosis and future therapies

    Article • Pediatric Health, October 2010, Future Medicine

    Berenice Mendonca, Professor Berenice B Mendonca

  58. Influence of the Fibroblast Growth Factor Receptor 4 Expression and the G388R Functional Polymorphism on Cushing’s Disease Outcome

    Article • The Journal of Clinical Endocrinology & Metabolism, October 2010, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  59. Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells

    Article • Pediatric and Developmental Pathology, September 2010, Society for Pediatric Pathology (SPP)

    Berenice Mendonca, Professor Berenice B Mendonca

  60. Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development

    Article • The Journal of Urology, September 2010, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  61. Usefulness of MLPA in the detection of SHOX deletions

    Article • European Journal of Medical Genetics, September 2010, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  62. The Role of <i>SRY</i> Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants

    Article • Hormone Research in Paediatrics, August 2010, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  63. Nonsense Mutations inFGF8Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, July 2010, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  64. TAC3/TACR3Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

    Article • The Journal of Clinical Endocrinology & Metabolism, June 2010, Endocrine Society

    Richard Quinton, Berenice Mendonca, Dr Andrew A Dwyer, Professor Berenice B Mendonca

  65. Nonsense Mutations inFGF8Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

    Article • Endocrinology, June 2010, Endocrine Society

    Berenice Mendonca

  66. Nonsense Mutations inFGF8Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

    Article • Endocrine Reviews, June 2010, Endocrine Society

    Berenice Mendonca, Ana Claudia Latronico

  67. TAC3/TACR3Mutations Reveal Preferential Activation of GnRH Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

    Article • Endocrinology, April 2010, Endocrine Society

    Richard Quinton, Berenice Mendonca

  68. TAC3/TACR3Mutations Reveal Preferential Activation of GnRH Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

    Article • Endocrine Reviews, April 2010, Endocrine Society

    Richard Quinton, Berenice Mendonca

  69. 46,XY DSD due to impaired androgen production

    Article • Best Practice & Research Clinical Endocrinology & Metabolism, April 2010, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  70. Long-Term Surgical Outcome of Masculinizing Genitoplasty in a Large Cohort of Patients With Disorders of Sex Development (DSD)

    Article • Journal of Pediatric Urology, April 2010, Elsevier

    Berenice Mendonca

  71. Fatigue Life Curves of NiTi Alloys – The Z Effect

    Article • Materials Science Forum, March 2010, Trans Tech Publications

    Dr Vicente T L Buono, Berenice Mendonca

  72. Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults

    Article • The Journal of Clinical Endocrinology & Metabolism, March 2010, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  73. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation‐dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1

    Article • Clinical Endocrinology, February 2010, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  74. ACTH-Independent Cushing’s Syndrome: Adrenocortical Tumors

    Article • January 2010, Springer Science + Business Media

    Berenice Mendonca

  75. Kinetics of Strain Aging in Cold Rolled Low Strength Multiphase Steel

    Article • ISIJ International, January 2010, Iron and Steel Institute of Japan

    Berenice Mendonca

  76. Could the Leukocyte X Chromosome Inactivation Pattern Be Extrapolated to Hair Bulbs?

    Article • Hormone Research in Paediatrics, January 2010, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  77. Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis

    Article • Clinics, January 2010, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  78. Effectiveness of the Combined Recombinant Human Growth Hormone and Gonadotropin-Releasing Hormone Analog Therapy in Pubertal Patients with Short Stature due toSHOXDeficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, January 2010, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  79. Novel Mutations inCYP11B1Gene Leading to 11β-Hydroxylase Deficiency in Brazilian Patients

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2009, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  80. Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome

    Article • Pituitary, August 2009, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  81. MALIGNANT PHEOCHROMOCYTOMA: A STUDY OF 18 CASES

    Article • The Journal of Urology, April 2009, Wolters Kluwer Health

    Berenice Mendonca

  82. Analysis of glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) expression in human adrenocortical hyperplasia

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, April 2009, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  83. SHORT AND LONG-TERM SURGICAL OUTCOME OF MASCULINIZING GENITOPLASTY IN A LARGE COHORT OF PATIENTS WITH DISORDERS OF SEX DEVELOPMENT (DSD)

    Article • The Journal of Urology, April 2009, Wolters Kluwer Health

    Berenice Mendonca

  84. ANATOMICAL AND FUNCTIONAL OUTCOME OF FEMINIZING GENITOPLASTY FOR AMBIGUOUS GENITALIA IN PATIENTS WITH VIRILIZING CONGENITAL ADRENAL HYPERPLASIA

    Article • The Journal of Urology, April 2009, Wolters Kluwer Health

    Berenice Mendonca

  85. ADRENOCORTICAL CARCINOMA: A 30-YEAR EXPERIENCE AT A SINGLE INSTITUTION

    Article • The Journal of Urology, April 2009, Wolters Kluwer Health

    Berenice Mendonca

  86. Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant

    Article • Growth Hormone & IGF Research, April 2009, Elsevier

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  87. 46,XY disorders of sex development (DSD)

    Article • Clinical Endocrinology, February 2009, Wiley

    Berenice Mendonca

  88. The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, February 2009, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  89. 46,XY disorders of sex development (DSD)

    Article • Clinical Endocrinology, January 2009, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  90. Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway

    Article • Hormone Research in Paediatrics, January 2009, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  91. Analysis of Craniofacial and Extremity Growth in Patients with Growth Hormone Deficiency during Growth Hormone Therapy

    Article • Hormone Research in Paediatrics, January 2009, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  92. Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, January 2009, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  93. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2008, FapUNIFESP (SciELO)

    Berenice Mendonca

  94. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA)

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  95. Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  96. Tall stature and poor breast development after estrogen replacement in a hypergonadotrophic hypogonadic patient with a 45,X/46,X,der(X) karyotype with SHOX gene overdosage

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  97. Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome

    Article • The Journal of Clinical Endocrinology & Metabolism, October 2008, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  98. Effect of finishing rolling temperature on fire resistance and dynamic strain aging behavior of a structural steel

    Article • Journal of Materials Science, September 2008, Springer Science + Business Media

    Berenice Mendonca

  99. Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical Tumors

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2008, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  100. Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients

    Article • Clinical Endocrinology, August 2008, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  101. Y-chromosomal STR haplotypes in a sample from São Paulo (Brazil)

    Article • Forensic Science International Genetics Supplement Series, August 2008, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  102. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, July 2008, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  103. Factors Determining Normal Adult Height in Girls with Gonadotropin-Dependent Precocious Puberty Treated with Depot Gonadotropin-Releasing Hormone Analogs

    Article • The Journal of Clinical Endocrinology & Metabolism, July 2008, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  104. Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamento

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, July 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  105. Síndrome de Noonan: do fenótipo à terapêutica com hormônio de crescimento

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, July 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  106. Long‐term treatment of familial male‐limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole

    Article • Clinical Endocrinology, June 2008, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  107. Role for postoperative cortisol response to desmopressin in predicting the risk for recurrent Cushing's disease

    Article • Clinical Endocrinology, June 2008, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  108. Laparoscopic Adrenalectomy for Pheocromocytoma in Children: Is It Safe?

    Article • Journal of Pediatric Urology, April 2008, Elsevier

    Berenice Mendonca

  109. A GPR54 -Activating Mutation in a Patient with Central Precocious Puberty

    Article • New England Journal of Medicine, February 2008, New England Journal of Medicine (NEJM/MMS)

    Berenice Mendonca, Professor Berenice B Mendonca

  110. Update on the etiology, diagnosis and therapeutic management of sexual precocity

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  111. Uma rara causa de dispnéia com apresentação singular na tomografia computadorizada de tórax: síndrome de ativação macrofágica

    Article • Jornal Brasileiro de Pneumologia, February 2008, FapUNIFESP (SciELO)

    Berenice Mendonca

  112. Population and mutation analysis of Y-STR loci in a sample from the city of São Paulo (Brazil)

    Article • Genetics and Molecular Biology, January 2008, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  113. Polymorphisms Identified in the Upstream Core Polyadenylation Signal ofIGF1Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment

    Article • The Journal of Clinical Endocrinology & Metabolism, December 2007, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  114. Microconversion betweenCYP21A2andCYP21A1PPromoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, October 2007, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  115. The degree of external genitalia virilization in girls with 21‐hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

    Article • Clinical Endocrinology, July 2007, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  116. Exon 3‐deleted genotype of growth hormone receptor (GHRd3) positively influences IGF‐1 increase at generation test in children with idiopathic short stature

    Article • Clinical Endocrinology, May 2007, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  117. Y‐STRs in Forensic Medicine: DNA Analysis in Semen Samples of Azoospermic Individuals

    Article • Journal of Forensic Sciences, April 2007, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  118. Variabilidade do fenótipo de pacientes com síndrome de Noonan com e sem mutações no gene PTPN11

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, April 2007, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  119. Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism

    Article • Fertility and Sterility, March 2007, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  120. Classical osteoblastoma, atypical osteoblastoma, and osteosarcoma: a comparative study based on clinical, histological, and biological parameters

    Article • Clinics, January 2007, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  121. The role of desmopressin in bilateral and simultaneous inferior petrosal sinus sampling for differential diagnosis of ACTH‐dependent Cushing's syndrome

    Article • Clinical Endocrinology, November 2006, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  122. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe

    Article • Clinical Endocrinology, November 2006, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  123. Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia

    Article • The Journal of Clinical Endocrinology & Metabolism, October 2006, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  124. Effectiveness of treating ovarian hyperstimulation syndrome with cabergoline in two patients with gonadotropin-producing pituitary adenomas

    Article • Fertility and Sterility, September 2006, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  125. A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin‐independent precocious puberty

    Article • Clinical Endocrinology, July 2006, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  126. Some aspects of the behavior of the hypothalamus–pituitary–adrenal axis in patients with uncomplicated Plasmodium falciparum malaria: Cortisol and dehydroepiandrosterone levels

    Article • Acta Tropica, July 2006, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  127. Anatomical and functional outcomes of feminizing genitoplasty for ambiguous genitalia in patients with virilizing congenital adrenal hyperplasia

    Article • Clinics, June 2006, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  128. Allelic Variants of the γ-Aminobutyric Acid-A Receptor α1-Subunit Gene (GABRA1) Are Not Associated with Idiopathic Gonadotropin-Dependent Precocious Puberty in Girls with and without Electroencephalographic Abnormalities

    Article • The Journal of Clinical Endocrinology & Metabolism, June 2006, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  129. Report of a del22q11 in a patient with Mayer‐Rokitansky‐Küster‐Hauser (MRKH) anomaly and exclusion of WNT‐4, RAR‐gamma, and RXR‐alpha as major genes determining MRKH anomaly in a study of 25 affected women

    Article • American Journal of Medical Genetics Part A, May 2006, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  130. Growth Hormone (GH) Pharmacogenetics: Influence of GH Receptor Exon 3 Retention or Deletion on First-Year Growth Response and Final Height in Patients with Severe GH Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, March 2006, Endocrine Society

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  131. Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism

    Article • Clinics, December 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  132. Padronização da técnica de extração de DNA de células de mucosa oral com NaCl: aplicação no estudo do gene PROP1

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, December 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  133. High Degree of Discordance Between Three-Dimensional and Two-Dimensional Lumbar Spine Bone Mineral Density in Turner's Syndrome

    Article • Journal of Clinical Densitometry, December 2005, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  134. Avanços recentes no conhecimento dos mecanismos moleculares envolvidos na tumorigênese adrenocortical

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  135. PTPN11(Protein Tyrosine Phosphatase, Nonreceptor Type 11) Mutations and Response to Growth Hormone Therapy in Children with Noonan Syndrome

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2005, Endocrine Society

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  136. Letter re: FSH Receptor Polymorphisms and Iatrogenic Ovarian Hyperstimulation

    Article • The Journal of Clinical Endocrinology & Metabolism, August 2005, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  137. Efeito fundador da mutação E180splice no gene do receptor de hormônio de crescimento identificada em pacientes brasileiros com insensibilidade ao GH

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, June 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  138. Absence of follicle-stimulating hormone receptor activating mutations in women with iatrogenic ovarian hyperstimulation syndrome

    Article • Fertility and Sterility, June 2005, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  139. Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein

    Article • The Journal of Clinical Endocrinology & Metabolism, May 2005, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  140. The laparoscopic management of intersex patients: the preferred approach

    Article • BJU International, March 2005, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  141. Refining Hormonal Diagnosis of Type II 3β-Hydroxysteroid Dehydrogenase Deficiency in Patients with Premature Pubarche and Hirsutism Based on HSD3B2 Genotyping

    Article • The Journal of Clinical Endocrinology & Metabolism, March 2005, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  142. Hipoplasia das células de Leydig

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  143. Craniofacial features with growth hormone treatment

    Article • The Journal of Pediatrics, February 2005, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  144. Síndrome de insensibilidade aos andrógenos: análise clínica, hormonal e molecular de 33 casos

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  145. Insensibilidade completa aos andrógenos em pacientes brasileiras causada pela mutação P766A no gene do receptor androgênico

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2005, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  146. Clinical and hormonal features of selective follicle-stimulating hormone (FSH) deficiency due to FSH beta-subunit gene mutations in both sexes

    Article • Fertility and Sterility, February 2005, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  147. Substitutions in the CYP21A2 promoter explain the simple‐virilizing form of 21‐hydroxylase deficiency in patients harbouring a P30L mutation

    Article • Clinical Endocrinology, January 2005, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  148. Adrenal, supra-renal

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  149. Tumores adrenocorticais: novas perspectivas

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  150. Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  151. Estudo multicêntrico de pacientes brasileiros com deficiência da 21-hidroxilase: correlação do genótipo com o fenótipo

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  152. A Single Luteinizing Hormone Determination 2 Hours after Depot Leuprolide Is Useful for Therapy Monitoring of Gonadotropin-Dependent Precocious Puberty in Girls

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2004, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  153. Complexo de Carney: relato de um caso e revisão da literatura

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, August 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  154. Pituitary Apoplexy During Therapy with Cabergoline in an Adolescent Male with Prolactin-Secreting Macroadenoma

    Article • Pituitary, April 2004, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  155. A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, April 2004, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  156. Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

    Article • Nature Genetics, February 2004, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  157. Use of nonradioactive labeling to detect large gene rearrangements in 21-hydroxylase deficiency

    Article • Revista do Hospital das Clínicas, January 2004, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  158. The first homozygous mutation (S226I) in the highly‐conserved WSXWS‐like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration

    Article • Clinical Endocrinology, December 2003, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  159. P450c17 Deficiency in Brazilian Patients: Biochemical Diagnosis through Progesterone Levels Confirmed byCYP17Genotyping

    Article • The Journal of Clinical Endocrinology & Metabolism, December 2003, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  160. Acromegalic features in growth hormore (GH)‐deficient patients after long‐term GH therapy

    Article • Clinical Endocrinology, November 2003, Wiley

    Berenice Mendonca, Professor Alexander A L Jorge, Professor Berenice B Mendonca

  161. A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

    Article • Journal of Clinical Investigation, October 2003, American Society for Clinical Investigation

    Berenice Mendonca, Professor Joshua M Brickman

  162. A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

    Article • Journal of Clinical Investigation, October 2003, American Society for Clinical Investigation

    Berenice Mendonca, Professor Joshua M Brickman, Professor Berenice B Mendonca

  163. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male‐limited precocious puberty

    Article • Clinical Endocrinology, September 2003, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  164. Genética molecular do eixo hipotálamo-hipófise-gonadal

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, August 2003, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  165. Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings

    Article • The Journal of Clinical Endocrinology & Metabolism, July 2003, Endocrine Society

    Berenice Mendonca, Ana Claudia Latronico, Professor Berenice B Mendonca

  166. Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene

    Article • The Journal of Clinical Endocrinology & Metabolism, July 2003, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  167. Cushing’s Syndrome Secondary to Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia due to Activating Mutations ofGNAS1Gene

    Article • The Journal of Clinical Endocrinology & Metabolism, May 2003, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  168. Male Pseudohermaphroditism Due to 5α-Reductase 2 Deficiency: Outcome of a Brazilian Cohort

    Article • The Endocrinologist, May 2003, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  169. Measurement of Dynamic Strain Aging in Pearlitic Steels by Tensile Test.

    Article • ISIJ International, January 2003, Iron and Steel Institute of Japan

    Dr Vicente T L Buono, Berenice Mendonca

  170. GH Values after Clonidine Stimulation Measured by Immunofluorometric Assay in Normal Prepubertal Children and GH-Deficient Patients

    Article • Hormone Research in Paediatrics, January 2003, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  171. Pituitary Magnetic Resonance Imaging and Function in Patients with Growth Hormone Deficiency with and without Mutations inGHRH-R,GH-1, orPROP-1Genes

    Article • The Journal of Clinical Endocrinology & Metabolism, November 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  172. Reply to correspondence from Hall—“Detection of Y‐specific sequences in patients with Turner syndrome”

    Article • American Journal of Medical Genetics, October 2002, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  173. Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  174. Aspectos Moleculares da Determinação e Diferenciação Sexual

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, August 2002, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  175. Bases Genéticas dos Distúrbios de Crescimento

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, August 2002, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  176. Population Genetics of Nine Short Tandem Repeat Loci

    Article • American Journal of Forensic Medicine & Pathology, June 2002, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  177. An Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis

    Article • The Journal of Clinical Endocrinology & Metabolism, June 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  178. Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene

    Article • The Journal of Clinical Endocrinology & Metabolism, April 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  179. Poor Reproducibility of IGF-I and IGF Binding Protein-3 Generation Test in Children with Short Stature and Normal Coding Region of the GH Receptor Gene

    Article • The Journal of Clinical Endocrinology & Metabolism, February 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  180. Variable ACTH-Stimulated 17-Hydroxyprogesterone Values in 21-Hydroxylase Deficiency Carriers Are Not Related to the Different CYP21 Gene Mutations

    Article • The Journal of Clinical Endocrinology & Metabolism, February 2002, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  181. Detection of Y‐specific sequences in 122 patients with Turner syndrome: Nested PCR is not a reliable method

    Article • American Journal of Medical Genetics, January 2002, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  182. Severe and Mild Neonatal Hypothyroidism Mediate Opposite Effects on Leydig Cells of Rats

    Article • Thyroid, January 2002, Mary Ann Liebert Inc

    Berenice Mendonca, Professor Berenice B Mendonca

  183. Zinc supplementation does not inhibit basal and metoclopramide-stimulated prolactinemia secretion in healthy men

    Article • Journal of Trace Elements in Medicine and Biology, January 2002, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  184. Adrenocortical tumors: results of treatment and study of Weiss's score as a prognostic factor

    Article • Revista do Hospital das Clínicas, January 2002, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  185. Telarca reversível espontaneamente em meninas pré-púberes durante o tratamento com hormônio de crescimento recombinante humano

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, December 2001, FapUNIFESP (SciELO)

    Berenice Mendonca

  186. Nongenetic Male Pseudohermaphroditism and Reduced Prenatal Growth

    Article • New England Journal of Medicine, October 2001, New England Journal of Medicine (NEJM/MMS)

    Berenice Mendonca, Professor Berenice B Mendonca

  187. Normal bone density in male pseudohermaphroditism due to 5alpha- reductase 2 deficiency

    Article • Revista do Hospital das Clínicas, October 2001, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  188. An Inherited Mutation Outside the Highly Conserved DNA-Binding Domain of the p53 Tumor Suppressor Protein in Children and Adults with Sporadic Adrenocortical Tumors

    Article • The Journal of Clinical Endocrinology & Metabolism, October 2001, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  189. Adrenocorticotropin-Dependent Precocious Puberty of Testicular Origin in a Boy with X-Linked Adrenal Hypoplasia Congenita Due to a Novel Mutation in theDAX1Gene

    Article • The Journal of Clinical Endocrinology & Metabolism, September 2001, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  190. Absence of Mutations Involving the Lim Homeobox Domain GeneLHX9in 46,XY Gonadal Agenesis and Dysgenesis

    Article • The Journal of Clinical Endocrinology & Metabolism, June 2001, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  191. Premature thelarche in girls after growth hormone therapy

    Article • The Journal of Pediatrics, March 2001, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  192. Laparoscopic management of intersexual states

    Article • Urologic Clinics of North America, February 2001, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  193. Tratamento da hiperplasia supra-renal congênita por deficiência da 21-hidroxilase

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, February 2001, FapUNIFESP (SciELO)

    Berenice Mendonca

  194. 21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

    Article • American Journal of Obstetrics and Gynecology, December 2000, Elsevier

    Berenice Mendonca, Dr Phyllis W Speiser, Professor Berenice B Mendonca

  195. Gonadotropin-Independent Precocious Puberty Due to Luteinizing Hormone Receptor Mutations in Brazilian Boys: A Novel Constitutively Activating Mutation in the First Transmembrane Helix1

    Article • The Journal of Clinical Endocrinology & Metabolism, December 2000, Endocrine Society

    Berenice Mendonca

  196. The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary–gonadal axis in both sexes

    Article • Clinical Endocrinology, November 2000, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  197. No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumors

    Article • Fertility and Sterility, November 2000, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  198. Pubarca precoce: estudo retrospectivo clínico e laboratorial

    Article • Arquivos Brasileiros de Endocrinologia & Metabologia, October 2000, FapUNIFESP (SciELO)

    Berenice Mendonca

  199. Male Pseudohermaphroditism due to 17β-Hydroxysteroid Dehydrogenase 3 Deficiency: Diagnosis, Psychological Evaluation, and Management

    Article • Medicine, September 2000, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  200. Genotyping of the type II 3β-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated δ5-steroids

    Article • Fertility and Sterility, September 2000, Elsevier

    Berenice Mendonca, MD; PhD Francisco de Paula, Professor Berenice B Mendonca

  201. Combined Pituitary Hormone Deficiency Caused by a Novel Mutation of a Highly Conserved Residue (F88S) in the Homeodomain of PROP-11

    Article • The Journal of Clinical Endocrinology & Metabolism, August 2000, Endocrine Society

    Berenice Mendonca

  202. Influence of different genotypes on 17‐hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

    Article • Clinical Endocrinology, May 2000, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  203. Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor

    Article • The Journal of Clinical Endocrinology & Metabolism, March 2000, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  204. Mutation analysis of the follicle-stimulating hormone receptor gene in girls with gonadotropin-independent precocious puberty resulting from autonomous cystic ovaries

    Article • Fertility and Sterility, February 2000, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  205. Clinical features of women with resistance to luteinizing hormone

    Article • Clinical Endocrinology, December 1999, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  206. 17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient andde NovoMutations1

    Article • The Journal of Clinical Endocrinology & Metabolism, December 1999, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  207. A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome

    Article • Human Mutation, October 1999, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  208. A Novel Missense Mutation, GLY424SER, in Brazilian Patients with 21-Hydroxylase Deficiency1

    Article • The Journal of Clinical Endocrinology & Metabolism, August 1999, Endocrine Society

    Berenice Mendonca

  209. Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene

    Article • Fertility and Sterility, April 1999, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  210. Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 Gene1

    Article • The Journal of Clinical Endocrinology & Metabolism, March 1999, Endocrine Society

    Berenice Mendonca

  211. 17β-Hydroxysteroid Dehydrogenase 3 Deficiency in Women1

    Article • The Journal of Clinical Endocrinology & Metabolism, February 1999, Endocrine Society

    Berenice Mendonca

  212. Effect of Acute and Chronic Oral Zinc Administration in Hyperprolactinemic Patients

    Article • Metal-Based Drugs, January 1999, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  213. Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

    Article • Human Heredity, January 1999, Karger Publishers

    Berenice Mendonca, Professor Berenice B Mendonca

  214. Molecular Genotyping in Brazilian Patients with the Classical and Nonclassical Forms of 21-Hydroxylase Deficiency1

    Article • The Journal of Clinical Endocrinology & Metabolism, December 1998, Endocrine Society

    Berenice Mendonca

  215. Effects of acute and chronic zinc administration on growth velocity in patients with hypopituitarism

    Article • Nutrition Research, November 1998, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  216. A study of patients with Nelson's syndrome

    Article • Clinical Endocrinology, October 1998, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  217. The PROP1 2-Base Pair Deletion Is a Common Cause of Combined Pituitary Hormone Deficiency1

    Article • The Journal of Clinical Endocrinology & Metabolism, September 1998, Endocrine Society

    Berenice Mendonca

  218. No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure

    Article • Fertility and Sterility, September 1998, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  219. Activating Mutation of the Stimulatory G Protein (gsp) as a Putative Cause of Ovarian and Testicular Human Stromal Leydig Cell Tumors1

    Article • The Journal of Clinical Endocrinology & Metabolism, June 1998, Endocrine Society

    Berenice Mendonca

  220. A Homozygous Microdeletion in Helix 7 of the Luteinizing Hormone Receptor Associated with Familial Testicular and Ovarian Resistance Is Due to Both Decreased Cell Surface Expression and Impaired Effector Activation by the Cell Surface Receptor

    Article • Molecular Endocrinology, March 1998, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  221. Diagnostic Value of Basal and Stimulated Levels of Gonadotropins Measured By An Immunofluorometric Assay (Ifma) in the Differential Diagnosis of Precocious Puberty. 20

    Article • Pediatric Research, February 1998, Springer Science + Business Media

    Berenice Mendonca

  222. Isosexual Pseudoprecocious Puberty By Ovarian Steroid Cell Tumor 24

    Article • Pediatric Research, February 1998, Springer Science + Business Media

    Berenice Mendonca

  223. A Novel Homozygous Nonsense Mutation E135X in the Type II 3β-Hydroxysteroid Dehydrogenase Gene (3β-Hsd) of A Female Child With Salt-Losing Congenital Adrenal Hyperplasia (Cah). 32

    Article • Pediatric Research, February 1998, Springer Science + Business Media

    Berenice Mendonca

  224. A novel homozygous nonsense mutation E135* in the type II 3β‐hydroxysteroid dehydrogenase gene in a girl with salt‐losing congenital adrenal hyperplasia

    Article • Human Mutation, January 1998, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  225. A novel homozygous nonsense mutation E135* in the type II 3β-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia

    Article • Human Mutation, January 1998, Hindawi Publishing Corporation

    Berenice Mendonca

  226. Apparent mineralocorticoid excess in a Brazilian kindred

    Article • Journal of Hypertension, December 1997, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  227. A Novel Nonsense Mutation in the First Zinc Finger of the Vitamin D Receptor Causing Hereditary 1,25-Dihydroxyvitamin D3-Resistant Rickets

    Article • The Journal of Clinical Endocrinology & Metabolism, November 1997, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  228. The genetic and functional basis of isolated 17,20–lyase deficiency

    Article • Nature Genetics, October 1997, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  229. Growth Hormone Receptor Messenger Ribonucleic Acid in Normal and Pathologic Human Adrenocortical Tissues—An Analysis by Quantitative Polymerase Chain Reaction Technique1

    Article • The Journal of Clinical Endocrinology & Metabolism, August 1997, Endocrine Society

    Berenice Mendonca

  230. Pheochromocytoma: Study of 50 Cases

    Article • The Journal of Urology, April 1997, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  231. Pheochromocytoma

    Article • The Journal of Urology, April 1997, Wolters Kluwer Health

    Berenice Mendonca

  232. Ovarian resistance to luteinizing hormone: A novel cause of amenorrhea and infertility

    Article • Fertility and Sterility, February 1997, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  233. Management of ambiguous genitalia in pseudohermaphrodites: New perspectives on vaginal dilation

    Article • Fertility and Sterility, February 1997, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  234. NORMAL hGH VALUES AFTER CLONIDINE STIMULATION MEASURED BY AN IMMUNOFLUOROMETRIC METHOD

    Article • Pediatric Research, February 1997, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  235. Brief Report

    Article • Obstetrical & Gynecological Survey, July 1996, Wolters Kluwer Health

    Berenice Mendonca

  236. THE MOLECULAR BASIS OF ISOLATED 17,20 LYASE DEFICIENCY. • 519

    Article • Pediatric Research, April 1996, Springer Science + Business Media

    Berenice Mendonca

  237. Male Pseudohermaphroditism Due to Steroid 5α-Reductase 2 Deficiency Diagnosis, Psychological Evaluation, and Management

    Article • Medicine, March 1996, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  238. Testicular and Ovarian Resistance to Luteinizing Hormone Caused by Inactivating Mutations of the Luteinizing Hormone–Receptor Gene

    Article • New England Journal of Medicine, February 1996, New England Journal of Medicine (NEJM/MMS)

    Berenice Mendonca, Professor Berenice B Mendonca

  239. Clinical, Hormonal and Pathological Findings in a Comparative Study of Adrenocortical Neoplasms in Childhood and Adulthood

    Article • The Journal of Urology, December 1995, Wolters Kluwer Health

    Berenice Mendonca

  240. Clinical, Hormonal and Pathological Findings in a Comparative Study of Adrenocortical Neoplasms in Childhood and Adulthood

    Article • The Journal of Urology, December 1995, Wolters Kluwer Health

    Berenice Mendonca, Professor Berenice B Mendonca

  241. Ectopic ACTH syndrome

    Article • The Journal of Steroid Biochemistry and Molecular Biology, June 1995, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  242. The essential role of zinc in growth

    Article • Nutrition Research, March 1995, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  243. Failure of partial hypophysectomy as definitive treatment in cushing’s disease owing to nodular corticotrope hyperpiasia; report of four cases

    Article • Endocrine Pathology, February 1995, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  244. Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain

    Article • Human Mutation, January 1995, Hindawi Publishing Corporation

    Berenice Mendonca, Professor Berenice B Mendonca

  245. Selection of adrenal tumor cells in culture demonstrated by interphase cytogenetics

    Article • Cancer Genetics and Cytogenetics, January 1995, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  246. Ectopic Adrenocorticotropic Hormone Syndrome

    Article • Endocrine Reviews, December 1994, Endocrine Society

    Berenice Mendonca, Professor Berenice B Mendonca

  247. Gonadal agenesis in XX and XY sisters: Evidence for the involvement of an autosomal gene

    Article • American Journal of Medical Genetics, August 1994, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  248. Male pseudohermaphroditism caused by mutations of testicular 17β–hydroxysteroid dehydrogenase 3

    Article • Nature Genetics, May 1994, Springer Science + Business Media

    Berenice Mendonca, Professor Berenice B Mendonca

  249. Natural Mutagenesis Study of the Human Steroid 5.alpha.-Reductase 2 Isoenzyme

    Article • Biochemistry, February 1994, American Chemical Society (ACS)

    Berenice Mendonca, Professor Berenice B Mendonca

  250. The desmopressin stimulation test in the differential diagnosis of Cushing's syndrome

    Article • Clinical Endocrinology, May 1993, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  251. Macrossomia, macrocrania e incoordenação motora da infância síndrome de sotos (Mckusick 11755) estudo de 7 casos e revisão de aspectos clínicos de 198 casos publicados

    Article • Arquivos de Neuro-Psiquiatria, June 1991, FapUNIFESP (SciELO)

    Berenice Mendonca, Professor Berenice B Mendonca

  252. GAPO syndrome (McKusick 23074)—A connective tissue disorder: Report on two affected sibs and on the pathologic findings in the older

    Article • American Journal of Medical Genetics, October 1990, Wiley

    Berenice Mendonca, Professor Berenice B Mendonca

  253. Male pseudohermaphroditism due to nonsalt-losing 3β-hydroxysteroid dehydrogenase deficiency: Gender role change and absence of gynecomastia at puberty

    Article • Journal of Steroid Biochemistry, December 1987, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  254. Low-dose oral clonidine: Effective growth hormone releasing agent in children but not in adolescents

    Article • The Journal of Pediatrics, October 1987, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  255. Spironolactone-reversible rickets associated with 11β-hydroxysteroid dehydrogenase deficiency syndrome

    Article • The Journal of Pediatrics, December 1986, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca

  256. Male pseudohermaphroditism resulting from Leydig cell hypoplasia

    Article • The Journal of Pediatrics, June 1985, Elsevier

    Berenice Mendonca, Professor Berenice B Mendonca