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Research 991–1000 of 1000+
- Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases
- A Case of Kerion Celsi Caused by Microsporum gypseum (Arthroderma gypseum ) in a Child
- Alopecia Areata of the Beard: A Review of the Literature
- Case 21-2012
- Congenital adrenal hyperplasia
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- A Comprehensive Approach to Hair Pathology of Horizontal Sections
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Biotinidase deficiency characterized by skin and hair findings