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Research 31–60 of 1000+
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Focal and Generalized Alopecia
- Disorders of hair in children
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- TRICHOPATHOPHOBIA.
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Diseases of Periocular Hair
- Hair and scalp disorders
- Hair Disorders
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Alopezien und Hypotrichosen im Kindesalter
- Bimatoprost in the treatment of eyelash hypotrichosis
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Molecular Genetics of Alopecias
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Genetic Hair Disorders: A Review
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- From Eye Care to Hair Growth: Bimatoprost
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- 14 Rhytidectomy
- Atlas of Geriatric Dermatology
- Value of dermoscopy for the diagnosis of monilethrix