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Research 211–240 of 1000+
- Ophthalmologic Comorbidities in Alopecia Areata
- Bachmann–Bupp syndrome and treatment
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Immune therapies for alopecia areata: evidence and new perspectives
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Painful thickened skin on the soles of the feet
- Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Eyebrow and Eyelash Alopecia: A Clinical Review
- FOXN1 deficient nude severe combined immunodeficiency
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- British Society for Dermatopathology: Summaries of Papers
- Inherited Epidermolysis Bullosa: A Clinical Case
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The Spectrum of Skin Disease Among Indian Children
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- LITERATURE REVIEW
- Dermatologic manifestations of endocrine disorders
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Cases Report the Cronkhite-Canada Syndrome
- Ernährungsstörungen des Haares und deren Management
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Alopecia in Children
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- TONGUE, RED
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome