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Research 511–540 of 1000+
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Polycystic ovary syndrome (PCOS) and COVID-19: an overlooked female patient population at potentially higher risk during the COVID-19 pandemic
- Skin Manifestations in Primary Immunodeficient Children
- The Role of Oral Contraceptives in the Treatment of Hyperandrogenic Disorders
- Endocrine-skin interactions
- Toward a Diagnostic Score in Cushing's Syndrome
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Diagnostic approach to low‐renin hypertension
- Ovarian SAHA syndrome is associated with a more insulin-resistant profile and represents an independent risk factor for glucose abnormalities in women with polycystic ovary syndrome: A prospective controlled study
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Clinical relevance of hair microscopy in alopecia
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Differential diagnosis of alopetia in children and adolescents
- Acne-Associated Syndromes
- Diagnosis and management of hair loss in children
- Hair shaft disorders
- Minoxidil ameliorates myelodysplastic syndrome by targeting Wnt4 while sparing normal hematopoiesis
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Multiple congenital smooth muscle hamartoma: A case report
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Definition criteria and diagnostic assessments
- Ischemic onycholysis of the hands