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Research 31–60 of 1000+
- SUN-364 Panhypopituitarism Induced Ventricular Tachycardia: Hormonal Relationship All Should Keep in Mind
- 6516 A Curious Case of Cushing Syndrome
- 8800 A Case of Hypopituitarism Due to Sheehan Syndrome
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- Efficacy and Safety of Topical Corticosteroid Treatment under Occlusion for Severe Alopecia Areata in Children. A single-center retrospective analysis
- Current and future perspectives on clinical management of classic 21-hydroxylase deficiency
- ODP342 Panhypopituitarism Induced by CTLA-4 and PD-1/PD-L1 Inhibitor Immunotherapy
- Faculty Opinions recommendation of Clinical applications of cortisol measurements in hair.
- DHEA : why, when, and how much ? D’après la conférence de Bruno Allolio (Wuerzburg), 50e Journées internationales d’endocrinologie clinique Henri-Pierre KLOTZ, septembre 2007
- Testosterone Therapy in Women: A Literature Review of Clinical Indications, Dosing, Routes of Administration, and Safety
- Addisonian crisis in a young man with atypical anorexia nervosa
- Attenuation of Autoimmune Phenomena in a Patient with Autoimmune Polyglandular Syndrome Type 1
- An unusual presentation of X-linked adrenoleukodystrophy
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- Autoimmune Polyglandular Syndrome Type 2 Presentation with Alopecia Universalis, Hashimoto’s Disease, and Addison’s Disease
- 46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
- ADRENAL FAILURE: WHEN ANTIPHOSPHOLIPID SYNDROME LEAVES SCARS
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Rapid Intravenous Administration of Corticotropin as a Test of Adrenocortical Insufficiency
- Androgen Treatment in Women
- Autoimmune polyglandular syndrome type 2, alopecia universalis and Crohn's disease
- Scalp hair 17‐hydroxyprogesterone and androstenedione as a long‐term therapy monitoring tool in congenital adrenal hyperplasia
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Toward a Diagnostic Score in Cushing's Syndrome
- Helpful diagnostic markers of steroidogenesis for defining hyperandrogenemia in hirsute women
- Functional medical approach and management for long COVID
- Androgens and Female Sexual Function and Dysfunction—Findings From the Fourth International Consultation of Sexual Medicine
- Diagnosis, Manifestations, Laboratory Investigations, and Prognosis in Pediatric and Adult Cushing’s Disease in a Large Center in China
- Androgenic disorders
- An implication for post-transcriptional control: Reciprocal changes of melanocortin receptor type 2 mRNA and protein expression in alopecia areata