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Research 391–420 of 1000+
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Table 2_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Ocular manifestation in progeria: A case report
- Hairy tale of signaling in hair follicle development and cycling
- Endocrinology of Hirsutism: From Androgens to Androgen Excess Disorders
- Table 1_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- Etiopathogenesis of acne
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Trichothiodystrophy: Current Concepts
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Androgenetic alopecia, hirsutism and hypertrichosis
- Molecular basis of congenital atrichia in humans and mice.
- Alopecia totalis in an infant