All Stories

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