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Research 901–930 of 1000+
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Erosive pustular dermatosis of the scalp: challenges and solutions
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Disease progression of dermatophytic pseudomycetoma in a Persian cat
- Satoyoshi Syndrome
- Global research trends in non-muscle invasive bladder cancer: Bibliometric and visualized analysis
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- Warty Dyskeratoma Involving Two Adjoining Follicles
- Efficacy of Longdan Xiegan Decoction on the Treatment of Eczema: A Systematic Review and Meta-Analysis
- Cutaneous Crohn's disease treated with infliximab and 4 years of follow up
- Inborn errors of biotin metabolism
- Desmoplastic melanoma presenting as primary alopecia neoplastica: a report of two cases
- Erosive pustular dermatosis of the scalp - is it really a rare condition?
- Case Report: A Virilizing Adrenal Oncocytoma
- Recent Advances in the Medical and Surgical Treatment of Priapism
- Acral lymphomatoid papulosis
- Pruritic urticarial papules and plaques of pregnancy
- Rituximab for Bone Lymphoma
- Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata
- Ophthalmic manifestations of Demodex spp. infection – what should a dermatologist know?
- Scalp basal cell carcinoma: A different entity?
- Perspectives in Head and Neck Medical Oncology
- The effect of COVID‐19 on development of hair and nail disorders: a Turkish multicenter, controlled study
- Omeprazole-induced hypertrichosis in two children
- Psoriatic Alopecia in a Patient with Systemic Lupus Erythematosus
- Alopecia Areata in an Adolescent With Inflammatory Bowel Disease
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix