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Research 61–90 of 1000+
- Trichoscopy in Hair Shaft Disorders
- Genetics of Structural Hair Disorders
- Dermatoscopy of hair shaft disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Hair loss in infancy and childhood
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Hair Shaft Dysplasias
- Congenital hair loss disorders: Rare, but not too rare
- Unruly hair
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- WOOLY HAIR PALMOPLANTAR KERATODERMA : A CASE REPORT
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A rare case of woolly hair with unusual associations
- Marie-unna hereditary hypotrichosis
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Keratin disorders: from gene to therapy
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Trichoscopy in genetic hair shaft abnormalities
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Keratins: the hair shaft's backbone revealed
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Hair growth promoting effects of adipose tissue-derived stem cells
- Hair shaft disorders
- Hair loss in children.
- Hair Loss: A Harbinger of the Morbidities to Come!
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome