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Research 91–120 of 1000+
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Cutaneous toxicities of cancer therapy
- Cutaneous Drug Eruptions Associated with the Use of New Oncological Drugs
- A patient with diffuse hair loss
- Disorders of the Hair and Nails
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- リリース：Microsoft RSAT for Windows 7 SP1（20110412-1）
- Dermatological drugs, topical agents, and cosmetics
- Epidermolysis bullosa in animals: a review
- Clinical and histological challenge in the differential diagnosis of diffuse alopecia: female androgenetic alopecia, telogen effluvium and alopecia areata – part I
- Efficacy of modern methods for assessing the severity of alopecia areata
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Keratin disorders: from gene to therapy
- Remarkable Improvement of Nail Changes in Alopecia Areata Universalis with 10 Months of Treatment with Tofacitinib: A Case Report
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- “Nail loss after teriflunomide treatment: A new potential adverse event”
- Primary hypothyroidism with exuberant dermatological manifestations
- Alopecia Areata and Habit Tic Deformities
- Koilonychia in a Patient with Alopecia Areata.
- Successful treatment of alopecia areata‐associated trachyonychia with baricitinib
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Painful thickened skin on the soles of the feet
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- TRACHYONYCHIA ASSOCIATED WITH ALOPECIA AREATA AND SECONDARY ONYCHOMYCOSIS
- S127 Regulation of hair growth
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Generalized atrophic benign epidermolysis bullosa.
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- FOXN1 deficient nude severe combined immunodeficiency