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Research 241–270 of 1000+
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Analogs of human genetic skin disease in domesticated animals
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Enhancing the Growth of Natural Eyelashes: The Mechanism of Bimatoprost-Induced Eyelash Growth
- Hair disorders in patients with cancer
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Principles of Hair Cycle Control
- Safety of low-dose oral minoxidil for hair loss: A multicenter study of 1404 patients
- Female Adolescent Hair Disorders
- Minoxidil tópico o minoxidil oral en la alopecia. ¿Cuál es su elección?
- Cutaneous Side Effects of Chemotherapy and Radiotherapy
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- Evaluación de la seguridad de minoxidil oral a dosis bajas en el tratamiento de la alopecia
- General Characteristics of Hair in Eating Disorders
- Calcineurin-based immunosuppression in renal transplantation : focus on efficacy, the role of steroids, and the cardiovascular risk
- Hormone und Haarwachstum
- TERAPIA ORAL OU TÓPICA? REVISÃO INTEGRATIVA SOBRE O USO DE MINOXIDIL NA ALOPECIA ANDROGENÉTICA
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- New clinico‐genetic classification of trichothiodystrophy
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Ichthyosis with confetti: clinics, molecular genetics and management
- MiR‐200c‐3p as a novel genetic marker and therapeutic tool for alopecia areata
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.