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Research 631–660 of 1000+
- Knowledge, Beliefs, and Perceptions among Alopecia Areata Patients: A Cross-Sectional Study in CMH Kharian
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Secondary Cicatricial and other Permanent Alopecias
- Androgenetic alopecia – is contact dermatitis an accelerating factor?
- New Publications
- Relation between dermal papilla cells and androgenetic alopecia
- TREATMENT OF HAIR LOSS
- Monilethrix: A rare hereditary condition
- Hair loss
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- ABC of Dermatology: Diseases of the hair and scalp
- Biology and Genetics of Hair
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
- Multiple, hereditary dome-shaped papules and acrochordons. Birt-Hogg-Dube syndrome
- Gene-knockout mice with abnormal epidermal and hair follicular development
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Current Genetics in Hair Diseases
- Androgenic alopecia and differential diagnoses of alopecia
- Current advances in stem cell-based therapies for hair regeneration
- Androgenic alopecia
- Androgenetic alopecia: Quality-of-life and associated lifestyle patterns
- Molecular Genetics of Alopecias
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- News in brief
- A rare hair loss in children: Monilethrix