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Research 301–330 of 591
- Epidemiology and Disease Burden of Androgenetic Alopecia in Chinese Adolescents: a Population-based Study (Preprint)
- Don't miss this blue toe: Hair tourniquet syndrome
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Diagnosis of common, benign neonatal dermatoses
- Aesthetic Strategies for the Aging Asian Face
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Gender-Affirming Hormone Therapy for Transgender Men
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Formulation And Evaluation Of Emulgel Of An Antifungal Drug For Topical Drug Delivery
- Dermatology for the elderly: An Indian perspective
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- The prevalence of hair loss and its association with iron deficiency among adolescents in northern Sudan: a school-based cross-sectional study
- 46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
- Hot topics in research and patient care in Dermatology and Venereology, 2019
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Woolly Hair in Two Siblings
- Uji Aktivitas dan Keamanan Kombinasi Ekstrak Bawang Putih (Alium sativum.l) dan Ekstrak Kemiri (Aleurites molucanna) sebagai Penyubur Bulu Kelinci
- <i>Hoxc13</i> mutant mice lack external hair
- Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- 9 Role of 5α-reductase in health and disease
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Nutrition and Hair
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Epidemiology, Diagnosis, and Treatment of Atopic Dermatitis in the Developing Countries of Asia, Africa, Latin America, and the Middle East: A Review
- Androgens and Female Sexual Function and Dysfunction—Findings From the Fourth International Consultation of Sexual Medicine
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase