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Research 241–270 of 1000+
- Spectrum of mucocutaneous manifestations in human immunodeficiency virus-infected patients and its correlation with CD4 lymphocyte count
- Dermoscopic evaluation of therapeutic response to an intralesional corticosteroid in the treatment of alopecia areata
- Cronkhite-Canada Syndrome: A Case Report
- Long‐Term Follow‐Up of Pediatric Trachyonychia
- Clinical Presentations and Comorbidities of Pediatric Alopecia Areata
- Management of Alopecia and Onychomycosis in a Lupus Patient
- Cutaneous Drug Reaction Case Reports
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Assessment and Validity of Trichoscopy for Eyebrow Involvement in Lichen Planopilaris: A Case-Control Study
- Frizzled Receptors in Development and Disease
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Spotlight commentary: Navigating the cutaneous side effects of chemotherapy
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Top applications of dermatologic ultrasonography that can modify management
- Cutaneous manifestations of endocrine diseases in children
- Chancres in Syphilis-Reply
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hair Shaft Dysplasias
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Pediatric Psychocutaneous Disorders
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Women's Dermatologic Diseases, Health Care Delivery, and Socioeconomic Barriers
- Alopecia in Cronkhite-Canada syndrome
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia