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Research 721–750 of 1000+
- Trichothiodystrophy
- Cutaneous toxicities of cancer therapy
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Acquired Zinc Deficiency Dermatosis in Man
- JAK inhibition in the treatment of alopecia areata – a promising new dawn?
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Case of Cronkhite-Canada Syndrome Involving the Entire Gastrointestinal Tract
- Olmsted syndrome
- The Coexistence of Trachyonychia and Mucocutaneous Lichen Planus: A Case Report
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Polyglandular Syndrome Type 1 Complicated with Dilated Cardiomyopathy: A Case Report
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Zinc: an undervalued microelement in research and treatment
- Clouston’s Syndrome-A Case Report
- Clouston’s syndrome: a rare case report
- The relevance of collagen XVII expression in epidermal differentiation and proliferation
- リリース：Microsoft RSAT for Windows 7 SP1（20110412-1）
- Alopecia Universalis
- The incidence and management of cutaneous adverse events of the epidermal growth factor receptor inhibitors
- PA05 A rare case of cardiocutaneous syndrome in a young child
- 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
- Generalized atrophic benign epidermolysis bullosa.
- FOXN1 deficient nude severe combined immunodeficiency