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Research 841–870 of 1000+
- A “hair‐raising” history of alopecia areata
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Dermoscopy: A rapid bedside tool to assess monilethrix
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Generation of bioengineered feather buds on a reconstructed chick skin from dissociated epithelial and mesenchymal cells
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- Organizational principles of integumentary organs: Maximizing variations for effective adaptation
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues
- Congenital atrichia with papular lesions
- Atrichia with papular lesions
- Transcriptome analyses of reprogrammed feather / scale chimeric explants revealed co-expressed epithelial gene networks during organ specification
- Development and evaluation of formulations of microbial biotransformed extract of tobacco leaves for hair growth potential
- Ocular and Mucocutaneous Sequelae among Survivors of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Togo
- Parry-Romberg Syndrome Augmented by Hyaluronic Acid Filler
- Hair Follicle Regeneration by Transplantation of a Bioengineered Hair Follicle Germ
- Virilising ovarian tumour in a woman with an adrenal nodule
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
- Hypotrichosis with juvenile macular dystrophy
- Substance P in keratosis follicularis spinulosa decalvans
- Marie-unna hereditary hypotrichosis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Monilethrix