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Research 211–240 of 1000+
- Prevention of chemotherapy drug-mediated human hair follicle damage: combined use of cooling with antioxidant suppresses oxidative stress and prevents matrix keratinocyte cytotoxicity
- Late presentation of myotonic dystrophy
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Clouston’s Syndrome-A Case Report
- Psoriatic Alopecia
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- The hair shaft: normality, abnormality, and genetics
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- EP-2270: Novel protective effect of prostaglandin for timely hair follicle regeneration from radiation injury
- Cellular Senescence and Aging in Myotonic Dystrophy
- Hypotrichosis with juvenile macular dystrophy
- Butyrophilin-like 2 (BTNL2) to the Rescue: controlling autoaggressive dermal gamma delta (GD) T lymphocytes in human hair follicles (HFs) 3747
- Hair Mesotherapy
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- The ProScope HR: A promising diagnostic tool
- S127 Regulation of hair growth
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Generalized atrophic benign epidermolysis bullosa.
- Primary hypothyroidism with exuberant dermatological manifestations
- Koilonychia in a Patient with Alopecia Areata.
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Therapeutic Response of Alopecia Areata‐Associated Nail Changes to Baricitinib
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- [Hirsutism].
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Disease Prevention and Alleviation by Human Myoblast Transplantation