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Research 91–120 of 1000+
- Open questions in hidradenitis suppurativa research: a hair biologist's perspective
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- A review of the etiologies, clinical characteristics, and treatment of canities
- HAIR AND SYSTEMATIC DISEASE
- AN UPDATE OF HAIR SHAFT DISORDERS
- ABC of Dermatology: Diseases of the hair and scalp
- 329 Mechanisms of Cutaneous Adverse Events during Targeted Cancer Therapy
- Uncombable hair syndrome and beyond
- 308 Epidermal keratinocytes regulate bacterial immune responses and host defense through EGFR
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- Low prevalence of twisted hair in anorexia nervosa
- Monilethrix, a rare inherited hair shaft disorder in siblings
- КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2)
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.
- Enhancing diagnostic yield of monogenic diabetes through phenotypic and molecular reanalysis of 128 individuals with young onset hyperglycemia: highlighting the significance of accurate case characterization
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Inborn Errors of Biotin Metabolism
- Inherited Hair Disorders
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Generalized atrophic benign epidermolysis bullosa.
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Melanocytes: The new Black
- Pigmentary mosaicism: An update
- PA33 When bones speak through nails: insights from a paediatric case series
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Human skin color: Origin, variation and significance
- Alopecia totalis in an infant