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Research 91–120 of 1000+
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Regional Dermatology
- holistic view of management of polycystic ovarian syndrome
- Commentary
- Cyberspace Chat: When finasteride suddenly stops working—is it counterfeit?
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables
- Apoptosis May Explain the Pharmacological Mode of Action and Adverse Effects of Isotretinoin, Including Teratogenicity
- Drug repositioning: current approaches and their implications in the precision medicine era
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Management of CAH during pregnancy
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Aetiology and Pathophysiology of Hair Loss
- Síndrome do nevo de Becker
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Congenital Adrenal Hyperplasia
- Intralesional betamethasone as a therapeutic option for alopecia areata
- Inherited Disorders of Corneocyte Proteins
- Hair Care and Dyeing
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- Follicular Unit Transplantation
- Premature graying of hair: Risk factors, co‐morbid conditions, pharmacotherapy and reversal—A systematic review and meta‐analysis
- Clinical and epidemiological characteristics and associated factors of hair graying: a population-based, cross-sectional study in Turkey
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy