All Stories

  1. Selenium: A Trace Element for a Healthy Skeleton - A Narrative Review
  2. DIAGNOSIS OF ENDOCRINE DISEASE: Evaluation of bone fragility in endocrine disorders
  3. Cortisol secretion, sensitivity, and activity are associated with hypertension in postmenopausal eucortisolemic women
  4. Hypovitaminosis D: Is It Time to Consider the Use of Calcifediol?
  5. Efficacy and safety of abaloparatide for the treatment of post-menopausal osteoporosis
  6. Paget’s Disease of Bone
  7. A rare syndrome of bone fibrous dysplasia associated with intramuscular myxomas.
  8. Multiple Endocrine Neoplasia type 1 Syndrome and GEP-tumors. Gentoype-phenotype correlation
  9. vitamin C roles in osteoporosis and fracture prevention.
  10. Italian Association of Clinical Endocrinologists (AME) and Italian Chapter of the American Association of Clinical Endocrinologists (AACE) Position Statement: Clinical Management of Vitamin D Deficiency in Adults
  11. Evaluation of the effect of denosumab, , in primary hyperparathyroidism-related osteoporosis.
  12. Mitochondriopathies and bone health
  13. New approaches in genetic diagnosis of cancer prone syndromes
  14. Faculty of 1000 evaluation for Complementary activities of DOT1L and Menin inhibitors in MLL-rearranged leukemia.
  15. Faculty of 1000 evaluation for Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4).
  16. Faculty of 1000 evaluation for Next generation sequencing in endocrine practice.
  17. Faculty of 1000 evaluation for Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations.
  18. Faculty of 1000 evaluation for De novo mutation in MEN1 is not associated with parental somatic mosaicism.
  19. Faculty of 1000 evaluation for DIAGNOSIS OF ENDOCRINE DISEASE: High-yield thyroid fine-needle aspiration cytology: an update focused on ancillary techniques improving its accuracy.
  20. Faculty of 1000 evaluation for Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1.
  21. Faculty of 1000 evaluation for Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story.
  22. Faculty of 1000 evaluation for Next-Generation Sequencing Approaches in Cancer: Where Have They Brought Us and Where Will They Take Us?
  23. Faculty of 1000 evaluation for New insights into the generation and role of de novo mutations in health and disease.
  24. vitamin K and bone health
  25. vitamin D metabolites, bone health, bone cells, bone pathophysiology and fracture risk
  26. The Regulatory Network Menin-MicroRNA 26a As a Possible Target for RNA-Based Therapy of Bone Diseases
  27. A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia
  28. Genetic Aspects of Hereditary Hyperparathyroidism
  29. Molecular diagnosis of parathyroid carcinoma: a reality in the near future
  30. Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
  31. Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes
  32. Corrigendum
  33. Ribozyme-mediated compensatory induction of menin-oncosuppressor function in primary fibroblasts from MEN1 patients
  34. LRP5 gene polymorphism and cortical bone
  35. Pagetʼs disease of bone: thereʼs more than the affected skeletal – a clinical review and suggestions for the clinical practice
  36. Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes
  37. Genetic aspects of the Paget’s disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its application
  38. Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and how
  39. Thyroid Cancer: Current Molecular Perspectives
  40. Multiple endocrine neoplasia type 1 (MEN1): Not only inherited endocrine tumors
  41. Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report
  42. Infiltrating giant cell tumor in a case of Paget’s disease of bone
  43. DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes
  44. A Novel Recessive Mutation of Fibroblast Growth Factor-23 in Tumoral Calcinosis
  45. Multiple Endocrine Neoplasia Type I Variants and Phenocopies: More than a Nosological Issue?
  46. Characterization of a Non-UBA Domain Missense Mutation of Sequestosome 1 (SQSTM1) in Paget's Disease of Bone
  47. Faculty of 1000 evaluation for Menin interacts with IQGAP1 to enhance intercellular adhesion of beta-cells.
  48. Surgical Approach in Hereditary Hyperparathyroidism
  49. Genetica dell’osteoporosi, dell’osteopetrosi e dell’osteogenesi imperfetta
  50. Genetic Epidemiology of Paget’s Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases of Paget’s Disease of Bone
  51. Erratum to “ Multiple endocrine neoplasms” [Best Practice & Research Clinical Rheumatology 2008; 22: 149–163]
  52. The genetic ascertainment of multiple endocrine neoplasia type 1 syndrome by ancient DNA analysis
  53. Modulatory effect of farnesyl pyrophosphate synthase (FDPS)rs2297480polymorphism on the response to long-term amino-bisphosphonate treatment in postmenopausal osteoporosis
  54. A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet
  55. Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study
  56. A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet
  57. Silent Familial Isolated Pituitary Adenomas: Histopathological and Clinical Case Report
  58. Multiple endocrine neoplasms
  59. Multiple Endocrine Neoplasia Type 1
  60. Is Total Parathyroidectomy the Treatment of Choice for Hyperparathyroidism in Multiple Endocrine Neoplasia Type 1?
  61. Relationship of Volumetric Bone Mineral Density and Structural Parameters with ERα Gene Polymorphisms
  62. Gastrinoma (Duodenal and Pancreatic)
  63. Poorly Differentiated Carcinomas of the Foregut (Gastric, Duodenal and Pancreatic)
  64. Rare Functioning Pancreatic Endocrine Tumors
  65. Well-Differentiated Duodenal Tumor/Carcinoma (Excluding Gastrinomas)
  66. Well-Differentiated Gastric Tumors/Carcinomas
  67. Well-Differentiated Pancreatic Tumor/Carcinoma: Insulinoma
  68. FokI Polymorphism of the Vitamin D Receptor Gene Correlates with Parameters of Bone Mass and Turnover in a Female Population of the Italian Island of Lampedusa
  69. What Is the Relationship Between Paget's Disease of Bone and Hyperparathyroidism?
  70. TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system
  71. Pancreatectomy in Multiple Endocrine Neoplasia Type 1-Related Gastrinomas and Pancreatic Endocrine Neoplasias
  72. Correction: Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study
  73. MEN1 family with a novel frameshift mutation
  74. Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study
  75. Well-Differentiated Pancreatic Nonfunctioning Tumors/Carcinoma
  76. ER  is a potent inhibitor of cell proliferation in the HCT8 human colon cancer cell line through regulation of cell cycle components
  77. Lessons from genes mutated in multiple endocrine neoplasia (MEN) syndromes
  78. Thymic Neuroendocrine Carcinoma (Carcinoid) in Multiple Endocrine Neoplasia Type 1 Syndrome: The Italian Series
  79. Surgery for gastroenteropancreatic tumours in multiple endocrine neoplasia type 1: review and personal experience
  80. Multiple Endocrine Neoplasias: Types 1 and 2
  81. Azidothymidine Induces Apoptosis and Inhibits Cell Growth and Telomerase Activity of Human Parathyroid Cancer Cells in Culture
  82. Calcium Bioavailability From a Calcium-Rich Mineral Water, With Some Observations on Method
  83. A PolymorphicCYP19TTTA Repeat Influences Aromatase Activity and Estrogen Levels in Elderly Men: Effects on Bone Metabolism
  84. Calcium agonists in hyperparathyroidism
  85. Two Novel Mutations at Exon 8 of the Sequestosome 1 (SQSTM1) Gene in an Italian Series of Patients Affected by Paget's Disease of Bone (PDB)
  86. Genetics of Primary Hyperparathyroidism
  87. Calcium agonists in hyperparathyroidism
  88. Calcium disorders and bone diseases
  89. Influence of Calcium-Sensing Receptor Gene on Urinary Calcium Excretion in Stone-Forming Patients
  90. Genetics of osteoporosis: role of steroid hormone receptor gene polymorphisms
  91. Multiple Endocrine Neoplasia Type 1
  92. Genetics of Osteoporosis
  93. Multiple Endocrine Neoplasia Type 1
  94. CONSENSUS: Guidelines for Diagnosis and Therapy of MEN Type 1 and Type 2
  95. Polymorphism of the Aromatase Gene in Postmenopausal Italian Women: Distribution and Correlation with Bone Mass and Fracture Risk1
  96. Polymorphism of the Aromatase Gene in Postmenopausal Italian Women: Distribution and Correlation with Bone Mass and Fracture Risk
  97. Microencapsulation of Human Parathyroid Cells: An “in Vitro” Study
  98. Somatic Mutation Analysis of the MEN1 Gene in Adrenocortical Tumors Using Denaturing Gradient Gel Electrophoresis (DGGE)
  99. MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1
  100. Telomerase Repeat Amplification Protocol (TRAP): A New Molecular Marker for Parathyroid Carcinoma
  101. FokI Polymorphism at Translation Initiation Site of the Vitamin D Receptor Gene Predicts Bone Mineral Density and Vertebral Fractures in Postmenopausal Italian Women
  102. Polymorphisms of the Calcitonin Receptor Gene Are Associated with Bone Mineral Density in Postmenopausal Italian Women
  103. Allelic Variants of Human Calcitonin Receptor: Distribution and Association with Bone Mass in Postmenopausal Italian Women
  104. Genetic testing for multiple endocrine neoplasias
  105. Aggressive Forms of Gastric Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type I
  106. Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 11
  107. Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 1
  108. HPE Cells: A Clonal Endothelial Cell Line Established From Human Parathyroid Tissue (Human Parathyroid Cell Line)
  109. Clonal Analysis by Chromosome 11 Microsatellite-PCR of Microdissected Parathyroid Tumors from MEN 1 Patients
  110. Are allelic losses at 11q13 universal in MEN 1 tumors?
  111. Steroid 5α-reductase 2 deficiency: virilization in early infancy may be due to partial function of mutant enzyme
  112. Characterization and function of the receptor for IGF-I in human preosteoclastic cells
  113. Evidence for Bioeffects of LY 139478 on the Human Preosteoclastic Cell Line FLG 29.1
  114. Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome
  115. Lack of allelic loss at the multiple endocrine neoplasia type 1(MEN-1) gene locus in a pancreatic ductal (non-endocrine) adenocarcinoma of a patient with the MEN-1 syndrome
  116. RFLP Analysis of Human Chromosome 11 Region q13 in Multiple Symmetrical Lipomatosis and Multiple Endocrine Neoplasia Type 1-Associated Lipomas
  117. Relaxin influences growth, differentiation and cell-cell adhesion of human breast-cancer cells in culture
  118. Production of basic fibroblast growth factor by gastric carcinoid tumors and their putative cells of origin
  119. Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11
  120. Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11.
  121. Clonality of Parathyroid Tumors in Familial Multiple Endocrine Neoplasia Type 1
  122. Genetics of Osteoporosis
  123. Faculty of 1000 evaluation for Menin controls growth of pancreatic beta-cells in pregnant mice and promotes gestational diabetes mellitus.
  124. Faculty of 1000 evaluation for Global expression profiling of murine MEN1-associated tumors reveals a regulatory role for menin in transcription, cell cycle and chromatin remodelling.
  125. Faculty of 1000 evaluation for Care for patients with multiple endocrine neoplasia type 1: the current evidence base.
  126. Faculty of 1000 evaluation for Screening of patients with multiple endocrine neoplasia type 1 (MEN-1): a critical analysis of its value.
  127. Faculty of 1000 evaluation for A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.
  128. Faculty of 1000 evaluation for Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.
  129. Faculty of 1000 evaluation for Age-related penetrance of endocrine tumours in multiple endocrine neoplasia type 1 (MEN1): a multicentre study of 258 gene carriers.
  130. Faculty of 1000 evaluation for Primary lymph node gastrinoma or occult duodenal microgastrinoma with lymph node metastases in a MEN1 patient: the need for a systematic search for the primary tumor.
  131. Faculty of 1000 evaluation for Thymic neuroendocrine tumors in multiple endocrine neoplasia type 1: a comparative study on 21 cases among a series of 761 MEN1 from the GTE (Groupe des Tumeurs Endocrines).
  132. Faculty of 1000 evaluation for Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patients.