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Research 721–750 of 1000+
- Acne in Dark Skin
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Hirsutism in Children: A Comprehensive Review of Etiology, Clinical Evaluation and Contemporary Management
- Endo&Art why Diana is depicted with mild androgenic alopecia?
- Hair loss in infancy and childhood
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 7745 Hirsutism in young girls, Beyond PCOS
- 7452 A Diagnostically Challenging Case of Hyperandrogenism in Postmenopausal Woman
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Fifteen-minute consultation: Approach to the adolescent presenting with hirsutism
- Clinical, Laboratory, and Radiological Diagnosis of Hyperandrogenism
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- P131 Menstrual irregularity in hirsute women
- Halo Scalp Ring: An Annular Alopecia Associated with Birth Injury
- Hair Disorders
- Committee on database of hair restoration results on patients with cicatricial alopecia and hair diseases other than androgenetic alopecia
- Dermatologic Disorders
- Corticotropin releasing factor-1 receptor antagonism associated with favorable outcomes of male reproductive health biochemical parameters
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Adult Patients with Aphallia: Were they Fertile?
- CECHY ZASTOSOWANIA FIZJOTERAPII WRODZONEGO KRĘCZU SZYI
- Hair Shaft Disorders
- Alopecia Triangular Temporal. Revisión de las manifestaciones clínicas y Dermatoscópicas.
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Persistent Hypoglycemia and Macrosomia in a Newborn
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants