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Research 91–120 of 1000+
- Manifestaciones dermatológicas por Covid-19 y su aporte en la comprensión de la enfermedad
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Long-term treatment within a maximum of 96 weeks of tinea unguium with long-pulsed neodymium-doped yttrium aluminum garnet laser
- Dermatological drugs, topical agents, and cosmetics
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Dermatological Illnesses of Immigrant Poultry-Processing Workers in North Carolina
- Intramuscular Corticosteroid Therapy in the Treatment of Alopecia Areata: A Time-to-Event Analysis
- Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations
- Prognostic factors that affect the response to topical treatment in patchy alopecia areata
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Risks of Skin, Hair, and Nail Supplements
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Trichothiodystrophy
- Metabolic syndrome
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- P095 The Very Interesting Small Bowel Lesions of Cronkhite-Canada Syndrome
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa