All Stories

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