All Stories

  1. Crinecerfont: emerging role in the management of congenital adrenal hyperplasia
  2. Histopathological stratification of primary aldosteronism using the CYP11B2 size ratio: first evaluation in clinical routine
  3. Survival without treatment of patients with classic and nonclassic 21-hydroxylase deficiency: a multicenter retrospective cohort study
  4. Psychosocial retrospective follow-up of young adults with congenital adrenal hyperplasia
  5. Psychiatric morbidity following liothyronine exposure in autoimmune hypothyroidism: a Swedish nationwide cohort study
  6. The association of antidepressants with hyponatremia - preventable side-effect?
  7. Mild Autonomous Cortisol Secretion and Psychiatric Morbidity in Patients with Adrenal Tumours: A Population-Based Retrospective Cohort Study
  8. Emerging methods for subtype differentiation in primary aldosteronism
  9. Letter to the Editor from Hedberg et al: Treatment of Hypothyroidism That Contains Liothyronine Is Associated with Reduced Risk of Dementia and Mortality
  10. Neurologic and psychiatric disorders following correction of profound hyponatremia - A cohort study
  11. Psychiatric and Sleep Disorders in Patients With Nonfunctional Adrenal Tumors
  12. Hyponatremia and mortality: Marker of disease or modifiable risk? Rethinking causality in large-scale observational research. Authors’ reply
  13. Mortality and causes of death in patients hospitalized with hyponatremia – a propensity matched cohort study
  14. Improving diagnosis in primary aldosteronism using HISTALDO and nodule size metrics
  15. Dysmagnesemia in the ICU: A Comparative Analysis of Ionized and Total Magnesium Levels and Their Clinical Associations
  16. Differences in Clinical Presentation Between Pheochromocytomas and Paragangliomas
  17. Drug-induced hyponatremia in clinical care
  18. The association of selective serotonin reuptake inhibitors and venlafaxine with profound hyponatremia
  19. The Role of Cortisol Secretion in Pheochromocytomas and Paragangliomas: Clinical and Perioperative Implications
  20. Influence of Preexisting Psychiatric Morbidity on Liothyronine Use in Hypothyroidism: A Swedish Nationwide Cohort Study
  21. Survival probabilities in patients with ectopic Cushing's syndrome—a systematic review and a single-arm meta-analysis
  22. Cytological Assessment of Adrenal Tumours: Insights From 22‐Years Single Centre Experience
  23. Risk of Dementia in Non‐Overtly Functional Adrenal Tumours (NOFAT)—Reply
  24. Adrenal Tumors in Children and Adolescents in Sweden: A Register-Based Study Covering 15 Years
  25. Validation of ICD-10 codes used to identify the main reason for hospitalization due to hyponatremia in Sweden
  26. Recent advances in treatments for congenital adrenal hyperplasia
  27. Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications
  28. Challenges in Adolescent and Adult Males With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
  29. Offloading Interventions for the Management of Charcot Neuroarthropathy in Diabetes
  30. Prevalence and Incidence of Dementia in Patients With Non‐Overtly Functional Adrenal Tumours
  31. Renal pseudohypoaldosteronism type 1—an adult case series including a novel gene variant
  32. Adrenocortical tumors and hereditary syndromes
  33. Adrenal Crisis and Adrenal Insufficiency Admissions in Patients 30–59 Years: Contribution of Psychosocial Factors
  34. 17α-Hydroxylase/17,20-lyase Deficiency (17-OHD): A Meta-analysis of Reported Cases
  35. Women’s response regarding timing of genital surgery in congenital adrenal hyperplasia
  36. The Association of Outdoor Temperature with Severe Hyponatremia
  37. Cardiometabolic Aspects of Congenital Adrenal Hyperplasia
  38. The Incidence of Cancers in Patients With Nonfunctional Adrenal Tumors: A Swedish Population-Based National Cohort Study
  39. Prevalence of Dysmagnesemia among Patients with Diabetes Mellitus and the Associated Health Outcomes: A Cross-Sectional Study
  40. Memory in female adolescents with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  41. Population data evidence of interdependence of the limbs of hormonal feedback loops
  42. Adrenal tumors in patients with neuroendocrine neoplasms
  43. A clinical perspective on ectopic Cushing’s syndrome
  44. Surgical outcome after thyroidectomy due to Graves’ disease and Lugol iodine treatment: a retrospective register-based cohort study
  45. Re: “Thyroid Stimulating Hormone and Thyroid Hormones (Triiodothyronine and Thyroxine): An American Thyroid Association-Commissioned Review of Current Clinical and Laboratory Status” by Van Uytfanghe et al.
  46. Lung Carcinoids: A Comprehensive Review for Clinicians
  47. Increased Prevalence of Accidents and Injuries in Congenital Adrenal Hyperplasia: A Population-based Cohort Study
  48. Incidence of Dysmagnesemia among Medically Hospitalized Patients and Associated Clinical Characteristics: A Prospective Cohort Study
  49. The Stability of Analytes of Ionized Magnesium Concentration and Its Reference Range in Healthy Volunteers
  50. Approach to the Patient: Reninoma
  51. Hypermagnesemia in Clinical Practice
  52. Congenital adrenal hyperplasia in the Nordic countries – a potential base for long-term outcome studies
  53. Adrenal cysts: an emerging condition
  54. Response to Letter to the Editor From Yu: “Adrenal Medullary Hyperplasia: A Systematic Review and Meta-analysis”
  55. Transition Readiness in Adolescents and Young Adults Living With Congenital Adrenal Hyperplasia
  56. Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease Management
  57. Adrenal Medullary Hyperplasia: A Systematic Review and Meta-analysis
  58. Tuberculosis of Adrenal Glands—A Population-based Case-control Study
  59. Corticosteroid-binding globulin (CBG): spatiotemporal distribution of cortisol in sepsis
  60. Hypoglycemia after exposure of diclofenac medication
  61. Congenital adrenal hyperplasia in patients with adrenal tumors: a population-based case–control study
  62. Physiological linkage of thyroid and pituitary sensitivities
  63. Long-Term Outcomes of Congenital Adrenal Hyperplasia
  64. Long-Term Results of Surgical Treatment and Patient-Reported Outcomes in Congenital Adrenal Hyperplasia—A Multicenter European Registry Study
  65. Ambulatory fludrocortisone suppression test in the diagnosis of primary aldosteronism: Safety, accuracy and cost‐effectiveness
  66. Adrenal crises in adolescents and young adults
  67. Prevalence and incidence of diabetes among Aboriginal people in remote communities of the Northern Territory, Australia: a retrospective, longitudinal data-linkage study
  68. Adrenal trauma experience at a major tertiary centre in Sweden: Clinical and radiological findings
  69. Current and Future Burdens of Heat-Related Hyponatremia: A Nationwide Register–Based Study
  70. Pheochromocytomas and Abdominal Paragangliomas: A Practical Guidance
  71. Current and Novel Treatment Strategies in Children with Congenital Adrenal Hyperplasia
  72. The impact of adherence and therapy regimens on quality of life in patients with congenital adrenal hyperplasia
  73. Institutional characterisation of water clear cell parathyroid adenoma: a rare entity often unrecognised by TC-99m-sestamibi scintigraphy
  74. Increased Prevalence of Fractures in Congenital Adrenal Hyperplasia: A Swedish Population-based National Cohort Study
  75. Thyroid testing paradigm switch from thyrotropin to thyroid hormones—Future directions and opportunities in clinical medicine and research
  76. Metastasis to the thyroid gland: Characterization and survival of an institutional series spanning 28 years
  77. Non‐thiazide diuretics and hospitalization due to hyponatraemia: A population‐based case‐control study
  78. Corrigendum to “Protective Effect of the HIF-1A Pro582Ser Polymorphism on Severe Diabetic Retinopathy”
  79. Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
  80. Time-dependent association between selective serotonin reuptake inhibitors and hospitalization due to hyponatremia
  81. Top End Pulmonary Hypertension Study: Understanding Epidemiology, Therapeutic Gaps and Prognosis in Remote Australian Setting
  82. First insights into the genetics of 21‐hydroxylase deficiency in the Roma population
  83. Metastatic Pheochromocytomas and Abdominal Paragangliomas
  84. Assessment of medication adherence in children and adults with congenital adrenal hyperplasia and the impact of knowledge and self‐management
  85. Bone Mass in Young Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  86. Authors' Response to Hennessey re: DOI: 10.1089/thy.2019.0535
  87. Clinical Parameters Are More Likely to Be Associated with Thyroid Hormone Levels than with Thyrotropin Levels: A Systematic Review and Meta-Analysis
  88. 11C-Metomidate PET/CT Detected Multiple Ectopic Adrenal Rest Tumors in a Woman With Congenital Adrenal Hyperplasia
  89. Correction to: Inverse association between glucose-lowering medications and severe hyponatremia: a Swedish population-based case-control study
  90. Reproductive and Perinatal Outcomes in Women with Congenital Adrenal Hyperplasia: A Population-based Cohort Study
  91. Prevalence and Characteristics of Adrenal Tumors and Myelolipomas in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis
  92. Increased Plasma Soluble Interleukin-2 Receptor Alpha Levels in Patients With Long-Term Type 1 Diabetes With Vascular Complications Associated With IL2RA and PTPN2 Gene Polymorphisms
  93. Obstructive sleep apnoea and adherence to continuous positive airway therapy among Australian women
  94. Top End Pulmonary Hypertension Study: Understanding Epidemiology, Therapeutic Gaps and Prognosis in Remote Australian Setting
  95. Predictors of normalized HbA1c after gastric bypass surgery in subjects with abnormal glucose levels, a 2-year follow-up study
  96. Lower extremity amputations and long-term outcomes in diabetic foot ulcers: A systematic review
  97. Update on the Swedish Newborn Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
  98. Highly proliferative anal neuroendocrine carcinoma: molecular and clinical features of a rare, recurrent case in complete remission
  99. The Success of a Screening Program Is Largely Dependent on Close Collaboration between the Laboratory and the Clinical Follow-Up of the Patients
  100. Trends in the incidence of adrenal incidentaloma diagnosed by CT abdomen in 2002 and 2015: Preliminary data from a retrospective study in regional sweden
  101. Diabetes during pregnancy and birthweight trends among Aboriginal and non-Aboriginal people in the Northern Territory of Australia over 30 years
  102. Bone Mineral Density in Adults With Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis
  103. Cardiovascular Manifestations and Complications of Pheochromocytomas and Paragangliomas
  104. Ectopic ACTH- and/or CRH-Producing Pheochromocytomas
  105. Reduced risk for hospitalization due to hyponatraemia in lithium treated patients: A Swedish population-based case–control study
  106. Riedel Thyroiditis
  107. Liver nucleotide biosynthesis is linked to protection from vascular complications in individuals with long-term type 1 diabetes
  108. Adrenal crises in older patients
  109. Lactation Ketoacidosis: A Systematic Review of Case Reports
  110. Genetic and Biological Effects of ICAM-1 E469K Polymorphism in Diabetic Kidney Disease
  111. The effect of patient‐managed stress dosing on electrolytes and blood pressure in acute illness in children with adrenal insufficiency
  112. Multiple cutaneous lesions and pulmonary cysts
  113. Current Management and Outcome of Pregnancies in Women With Adrenal Insufficiency: Experience from a Multicenter Survey
  114. Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  115. Mucormycosis in a 40-year-old woman with diabetic ketoacidosis
  116. Associations Between Antihypertensive Medications and Severe Hyponatremia: A Swedish Population–Based Case–Control Study
  117. MON-183 Adrenal Androgen Control and Steroidal Side Effects in Adolescents and Adults with Congenital Adrenal Hyperplasia Treated with Glucocorticoids
  118. OR25-05 Increased Overall Mortality and Cardiovascular Morbidity in Patients with Adrenal Incidentalomas and Autonomous Cortisol Secretion: Results of the ENS@T NAPACA-Outcome Study
  119. Lipoadenoma of the Parathyroid Gland: Characterization of an Institutional Series Spanning 28 Years
  120. Sexual Orientation in Individuals With Congenital Adrenal Hyperplasia: A Systematic Review
  121. Clinical features, complications, and outcomes of exogenous and endogenous catecholamine‐triggered Takotsubo syndrome: A systematic review and meta‐analysis of 156 published cases
  122. Bone mineral density and fractures in congenital adrenal hyperplasia: Findings from the dsd‐LIFE study
  123. To Treat or Not to Treat Subclinical Hypothyroidism, What Is the Evidence?
  124. All-cause mortality following low-dose aspirin treatment for patients with high cardiovascular risk in remote Australian Aboriginal communities: an observational study
  125. Stumbling broke the spleen and unveiled pheochromocytoma, which in turn broke the heart
  126. Inverse association between glucose-lowering medications and severe hyponatremia: a Swedish population-based case-control study
  127. Lactation Ketoacidosis: A case series
  128. P450 Oxidoreductase Deficiency: A Systematic Review and Meta-analysis of Genotypes, Phenotypes, and Their Relationships
  129. Acute suppurative thyroiditis with thyroid abscess in adults: clinical presentation, treatment and outcomes
  130. Acute suppurative thyroiditis with thyroid abscess in adults: clinical presentation, treatment and outcomes
  131. Factors of importance for discontinuation of thiazides associated with hyponatremia in Sweden: A population‐based register study
  132. Tramadol- and codeine-induced severe hyponatremia: A Swedish population-based case-control study
  133. Pyogenic hepatic abscess secondary to gastric perforation caused by an ingested fish bone
  134. Acute suppurative thyroiditis with thyroid abscess in adults: clinical presentation, treatment and outcomes
  135. Acceptance and tolerability of 75 g Pregnancy Oral Glucose Tolerance Test in Pregnancy
  136. Sex-specific risks of death in patients hospitalized for hyponatremia: a population-based study
  137. Adrenal Crisis
  138. Pheochromocytoma- and paraganglioma-triggered Takotsubo syndrome
  139. Carriers of a Classic CYP21A2 Mutation Have Reduced Mortality: A Population-Based National Cohort Study
  140. Amputations in patients with diabetic foot ulcer: a retrospective study from a single centre in the Northern Territory of Australia
  141. Presentation, Treatment, Histology, and Outcomes in Adrenal Medullary Hyperplasia Compared With Pheochromocytoma
  142. Population data provide evidence against the presence of a set point for hemoglobin levels or tissue oxygen delivery
  143. Protective Effect of the HIF-1A Pro582Ser Polymorphism on Severe Diabetic Retinopathy
  144. Management and outcome of pregnancies in women with adrenal insufficiency: experience from a retrospective European study
  145. Prevalence of autonomous cortisol secretion as defined in ESE guidelines in a Swedish cohort of patients diagnosed with adrenal incidentaloma: A prospective study in regional Sweden
  146. Adrenal insufficiency due to bilateral adrenal metastases – A systematic review and meta-analysis
  147. Glucocorticoid Regimens in the Treatment of Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis
  148. New cost-effective pleural procedure training: manikin-based model to increase the confidence and competency in trainee medical officers
  149. Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
  150. MANAGEMENT OF ENDOCRINE DISEASE: Diagnosis and management of the patient with non-classic CAH due to 21-hydroxylase deficiency
  151. Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency
  152. Antipsychotics and severe hyponatremia: A Swedish population–based case–control study
  153. Mortality in patients with diabetic foot ulcer: a retrospective study of 513 cases from a single Centre in the Northern Territory of Australia
  154. Associations of proton pump inhibitors and hospitalization due to hyponatremia: A population–based case–control study
  155. 11β-Hydroxylase Deficiency
  156. Epidemiology of Pulmonary Hypertension at the Top End of Australia
  157. Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitals
  158. Treatment and outcomes in pheochromocytomas and paragangliomas: a study of 110 cases from a single center
  159. Psychological adjustment, quality of life, and self-perceptions of reproductive health in males with congenital adrenal hyperplasia: a systematic review
  160. A Sickening Tale
  161. Differences in associations of antiepileptic drugs and hospitalization due to hyponatremia: A population–based case–control study
  162. Lactation ketoacidosis: case presentation and literature review
  163. Extensive Bilateral Adrenal Rest Testicular Tumors in a Patient With 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
  164. Bilateral Adrenalectomy in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis
  165. Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations
  166. Health status in 1040 adults with disorders of sex development (DSD): a European multicenter study
  167. Successful fertility outcome in a woman with 17ɑ-hydroxylase deficiency
  168. Riedel’s thyroiditis: clinical presentation, treatment and outcomes
  169. Gonadal function in adult male patients with congenital adrenal hyperplasia
  170. Differences in Associations of Antidepressants and Hospitalization Due to Hyponatremia
  171. Magnesium and Human Health: Perspectives and Research Directions
  172. Adrenal Crises in Children: Perspectives and Research Directions
  173. Skeletal fragility induced by overtreatment of adrenal insufficiency
  174. Initial clinical presentation and spectrum of pheochromocytoma: a study of 94 cases from a single center
  175. Trends in surgery, hospital admissions and imaging for pituitary adenomas in Australia
  176. Lugol’s solution and other iodide preparations: perspectives and research directions in Graves’ disease
  177. Pleural Lipomatosis Masquerading as Pleural Mass With Effusion
  178. Cost-effectiveness of stroke care in Aboriginal and non-Aboriginal patients: an observational cohort study in the Northern Territory of Australia
  179. Reduced Frequency of Biological and Increased Frequency of Adopted Children in Males With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
  180. Increased mortality in patients with adrenal incidentalomas and autonomous cortisol secretion: a 13-year retrospective study from one center
  181. Swyer-James-MacLeod syndrome-a rare diagnosis presented through two adult patients
  182. Rescue pre-operative treatment with Lugol’s solution in uncontrolled Graves’ disease
  183. Hospitalisation in Children with Adrenal Insufficiency and Hypopituitarism: Is There a Differential Burden between Boys and Girls and between Age Groups?
  184. Adrenal crises: perspectives and research directions
  185. Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
  186. Are carriers ofCYP21A2mutations less vulnerable to psychological stress? A population-based national cohort study
  187. Frequency of Cushing’s syndrome due to ACTH-secreting adrenal medullary lesions: a retrospective study over 10 years from a single center
  188. Dopa-testotoxicosis: disruptive hypersexuality in hypogonadal men with prolactinomas treated with dopamine agonists
  189. A 42-year-old man presented with adrenal incidentaloma due to non-classic congenital adrenal hyperplasia with a novelCYP21A2mutation
  190. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Presenting as Adrenal Incidentaloma: A Systematic Review and Meta-Analysis
  191. Adrenocortical cancer: mortality, hormone secretion, proliferation and urine steroids – experience from a single centre spanning three decades
  192. Relationship between depression and diabetes in pregnancy: A systematic review
  193. Hospital Admission Patterns in Children with CAH: Admission Rates and Adrenal Crises Decline with Age
  194. Congenital Adrenal Hyperplasia, Polycystic Ovary Syndrome and criminal behavior: A Swedish population based study
  195. Congenital adrenal hyperplasia and risk for psychiatric disorders in girls and women born between 1915 and 2010: A total population study
  196. Biochemical and genetic diagnosis of 21-hydroxylase deficiency
  197. Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
  198. Clinical Outcomes in Adrenal Incidentaloma: Experience From one Center
  199. Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome
  200. Limited value of long-term biochemical follow-up in patients with adrenal incidentalomas-a retrospective cohort study
  201. Genetic studies of body mass index yield new insights for obesity biology
  202. New genetic loci link adipose and insulin biology to body fat distribution
  203. Pregnancy and neonatal outcomes in Indigenous Australians with diabetes in pregnancy
  204. Increased Mortality in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
  205. Ileal neuroendocrine tumors and heart: not only valvular consequences
  206. GP4-3: Epigenetic analyses of the insulin-like growth factor binding protein 1 gene in diabetes and diabetic nephropathy
  207. Epigenetic analyses of the insulin-like growth factor binding protein 1 gene in type 1 diabetes and diabetic nephropathy
  208. Suboptimal Psychosocial Outcomes in Patients With Congenital Adrenal Hyperplasia: Epidemiological Studies in a Nonbiased National Cohort in Sweden
  209. Increased Psychiatric Morbidity in Men With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  210. Non-functioning adrenal incidentalomas caused by 21-hydroxylase deficiency or carrier status?
  211. Quality of life, social situation, and sexual satisfaction, in adult males with congenital adrenal hyperplasia
  212. 68Ga-DOTA-TOC-PET/CT detects heart metastases from ileal neuroendocrine tumors
  213. One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study
  214. Voice problems due to virilization in adult women with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency
  215. A threefold increase in gestational diabetes over two years: Review of screening practices and pregnancy outcomes in Indigenous women of Cape York, Australia
  216. Bone mineral density, bone markers, and fractures in adult males with congenital adrenal hyperplasia
  217. Pattern of Dyslipidaemia in Subjects with Coronary Artery Disease: A Study Comparing Indigenous and non-Indigenous Australians
  218. New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes
  219. IGF2BP2 and IGF2 genetic effects in diabetes and diabetic nephropathy
  220. Thyrotoxic periodic paralysis: clinical and molecular aspects
  221. Clinical outcomes in the management of congenital adrenal hyperplasia
  222. Anthropometry in Congenital Adrenal Hyperplasia
  223. Fertility, sexuality and testicular adrenal rest tumors in adult males with congenital adrenal hyperplasia
  224. Cardiovascular risk, metabolic profile, and body composition in adult males with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  225. Pattern of Dyslipidaemia in Subjects with Coronary Artery Disease: A Study Comparing Indigenous and non-Indigenous Australians
  226. Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due toCYP21A2Deficiency: Clinical Perspective and the Patients’ Perception
  227. Maternal and neonatal outcomes in the Torres Strait Islands with a sixfold increase in type 2 diabetes in pregnancy over six years
  228. Gender Role Behaviour, Sexuality and Sexual Function in Women With Congenital Adrenal Hyperplasia
  229. Adult case of partial trisomy 9q
  230. Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due toCYP21A2Deficiency
  231. Maternal and neonatal outcomes following diabetes in pregnancy in Far North Queensland, Australia
  232. Pathological gambling and hypersexuality in cabergoline‐treated prolactinoma
  233. Increased Liver Enzymes in Adult Women with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
  234. Transient cardiac arrhythmias related to lopinavir/ritonavir in two patients with HIV infection
  235. Voice characteristics in women with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency
  236. Hyperpigmentation, nail dystrophy and alopecia with generalised intestinal polyposis: Cronkhite–Canada syndrome
  237. Physician on call: Sweden compared with Australia
  238. Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  239. Voice Characteristics Related to Increased Levels of Androgens in Women with Congenital Adrenal Hyperplasia (CAH)
  240. Type of Mutation and Surgical Procedure Affect Long-Term Quality of Life for Women with Congenital Adrenal Hyperplasia
  241. A 31-year-old woman with infertility and polycystic ovaries diagnosed with non-classic congenital adrenal hyperplasia due to a novel CYP21 mutation
  242. HD3-2 Screening and follow-up for gestational diabetes in the Torres strait Islands
  243. Fractures and Bone Mineral Density in Adult Women with 21-Hydroxylase Deficiency
  244. Distribution of neuropeptide Y Leu7Pro polymorphism in patients with type 1 diabetes and diabetic nephropathy among Swedish and American populations
  245. Metabolic Profile and Body Composition in Adult Women with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  246. Genetic association analysis of the adiponectin polymorphisms in type 1 diabetes with and without diabetic nephropathy
  247. Genetic influences of the intercellular adhesion molecule 1 (ICAM‐1) gene polymorphisms in development of Type 1 diabetes and diabetic nephropathy
  248. An 88-year-old woman diagnosed with adrenal tumor and congenital adrenal hyperplasia: Connection or coincidence?