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Research 31–60 of 1000+
- Hair Loss in Children
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Dermatopathology and molecular genetics
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hairless is a nuclear receptor corepressor essential for skin function
- Le gène<i>hairless</i>de la souris
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Hair Loss in Children
- Disorders of hair in children
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hair and Nail Relationship
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Hair loss and its management in children
- Hair loss in children.
- Hair and scalp disorders
- Biotinidase deficiency characterized by skin and hair findings
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Current Genetics in Hair Diseases
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Congenital atrichia associated with situs inversus and mesocardia
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Focal and Generalized Alopecia
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Alopecia Areata