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Research 61–90 of 1000+
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Biotin
- Hair Shafts in Trichoscopy
- Anagen effluvium
- Keratin disorders: from gene to therapy
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Hair and Nail Manifestations of Systemic Disease
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Effectiveness of Autologous Platelet-Rich Plasma for Androgenetic Alopecia: A Double-Center, Non-Controlled, Randomized Clinical Study in Vietnam
- Acquired progressive kinking of the hair in a prepubertal boy
- Canine alopecia X-Like disorder
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Genetic Hair Disorders: A Review
- Diagnostic challenges in determining alopecia areata
- Hyperadrenocorticism in Ferrets
- Clinical markers of androgenicity in acne vulgaris
- Topical Treatment for Scarring and Non-Scarring Alopecia: An Overview of the Current Evidence
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Temporal Triangular Alopecia—Clinical and Dermoscopic Features of a Rare Entity
- Two females with hair loss
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Hair loss in children.