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Research 91–120 of 1000+
- Congenital hair loss disorders: Rare, but not too rare
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- Enanthem in Patients With COVID-19 and Skin Rash
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Woolly Antics between the Sheaths
- A guide to diagnosis and management of hypertrichosis
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Androgenetic alopecia, hirsutism and hypertrichosis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Hypotrichosis in a child with olmsted syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hairy Pinnae after Orchiectomy and Chemotherapy for Testicular Cancer: Acquired Localized Hypertrichosis of the Ears
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Diseases of Periocular Hair
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