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Research 61–90 of 951
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Keratins and disease at a glance
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Diseases of the Hair and Nails
- Nails and hair
- Nails and hair
- Adverse cutaneous reactions to chemotherapeutic agents and cytokine therapy
- Diseases of Periocular Hair
- Corrective and Restorative Dermatology in Cancer Survivors: An Urgent Unmet Need!
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Biology and Genetics of Hair
- Dermatological history and examination
- TONGUE, RED
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Amino Acids Oral Treatment for the Amelioration of Skin, Hair, and Nails Conditions: An Open-Label Study
- Genetic Hair Disorders: A Review
- Dysfunction of keratinocyte adhesion
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Poster Presentations
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Nutrition and Hair
- Skin ageing
- Congenital hypotrichosis due to short anagen
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