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Research 61–90 of 1000+
- Hair Loss in Children
- Clinical relevance of hair microscopy in alopecia
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Biology and Genetics of Hair
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Congenital atrichia associated with nevus flammeus: A rare association
- Congenital atrichia associated with situs inversus and mesocardia
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Congenital atrichia with papular lesions
- Claves diagnósticas en displasias pilosas II
- Congenital atrichia with papular lesions
- Current Genetics in Hair Diseases
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Secondary cicatricial and other permanent alopecias
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Amino Acid Content of Damaged Human Hair
- Genetic Hair Disorders: A Review
- Dermatopathology and molecular genetics
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2