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Research 61–90 of 555
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Hair Loss in Children
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- 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
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Hair That Is Difficult to Manage in a Hispanic Girl
- Biotin
- Keratin disorders: from gene to therapy
- Hair and Nail Manifestations of Systemic Disease
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Hypotrichosis in a child with olmsted syndrome
- Anagen effluvium
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The Genetics of Human Skin Disease
- Uveodermatological syndrome associated with alopecia areata in a one‐year‐old female spayed Cavalier King Charles Spaniel dog
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- [Frizzy hair pathology].
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Enanthem in Patients With COVID-19 and Skin Rash
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Genetic Hair Disorders: A Review
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair shaft disorders in children – An update
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle