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Research 661–690 of 1000+
- Clinical Snippets
- Clinical Snippets
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Alopecia in a 19-Month-Old Boy
- Monilethrix: A rare hereditary condition
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Frontal Alopecia after Repeated Botulinum Toxin Type A Injections for Forehead Wrinkles: An Underestimated Entity?
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Microneedling plus topical dutasteride solution for androgenetic alopecia: a randomized placebo‐controlled study
- A study of the Geheimratsacken angle as predictor for early diagnosis of androgenetic alopecia in adolescent population
- Nutrition and hair
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- The Hair Shedding Visual Scale: A Quick Tool to Assess Hair Loss in Women
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Nonclassic adrenal hyperplasia
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Hair Anomalies in a 6-Year-Old Girl
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Targeting integrin pathways: mechanisms and advances in therapy
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Role of caffeine in the management of androgenetic alopecia