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Research 241–270 of 1000+
- Mixing the Old with the New: Drug Repurposing for Immune Deficiency in the Era of Precision Medicine and Pediatric Genomics
- Therapeutic approach and management of Marz-e-Shayb (Premature greying of hair) in the perspective of Unani medicine: A case study
- Do you know this syndrome? * Você conhece esta síndrome? *
- Oral Presentations
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Physiology and Medical Treatments for Alopecia
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- The involvement of androgens in human hair growth
- The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders
- Normal Hair Growth in Children
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Folliculin: A surprising molecular brake in the human hair follicle
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Genetic Basis of Male Pattern Baldness
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Ulerythema Ophryogenes in a Saudi Male: A Case Report
- Hypotrichosis in a child with olmsted syndrome
- A Signature of Genes Featuring FGF11 Revealed Aberrant Fibroblast Activation and Immune Infiltration Properties in Keloid Tissue
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines