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Research 301–330 of 1000+
- Hair follicles and their role in skin health
- Hirsutism in the Adolescent Female
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- The Spectrum of Skin Disease Among Indian Children
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Skin manifestations of chronic kidney disease
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Causes and Management of Hypertrichosis
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Keratins: the hair shaft's backbone revealed
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Molecular Mechanisms Regulating Hair Follicle Development
- Trichoscopy in genetic hair shaft abnormalities
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Steatocystoma Multiplex
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Molecular Genetics of Human Hair Diseases
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project