Found: 18
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Verrucous Psoriasis Successfully Treated with Ixekizumab: A Case Report with Review Literature.
- Published in:
- Journal of the Medical Association of Thailand, 2020, v. 103, n. 9, p. 948, doi. 10.35755/jmedassocthai.2020.09.11241
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- Publication type:
- Article
Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities.
- Published in:
- Journal of Investigative Dermatology, 2006, v. 126, n. 9, p. 2039, doi. 10.1038/sj.jid.5700348
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- Publication type:
- Article
Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene.
- Published in:
- Journal of Investigative Dermatology, 2006, v. 126, n. 8, p. 1776, doi. 10.1038/sj.jid.5700339
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- Publication type:
- Article
Genotype–Phenotype Correlation in Recessive Dystrophic Epidermolysis Bullosa: When Missense Doesn't Make Sense.
- Published in:
- 2005
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- Publication type:
- Letter
Reduced Expression of Insulin-Like Growth Factor-Binding Protein-3 (IGFBP-3) in Squamous Cell Carcinoma Complicating Recessive Dystrophic Epidermolysis Bullosa.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 5, p. 1302, doi. 10.1111/j.0022-202X.2004.22525.x
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- Publication type:
- Article
Extracellular Matrix Protein 1 Gene (ECM1 ) Mutations in Lipoid Proteinosis and Genotype-Phenotype Correlation.
- Published in:
- Journal of Investigative Dermatology, 2003, v. 120, n. 3, p. 345, doi. 10.1046/j.1523-1747.2003.12073.x
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- Publication type:
- Article
Clinical and molecular characteristics of autosomal recessive congenital ichthyosis in Thailand.
- Published in:
- Pediatric Dermatology, 2023, v. 40, n. 1, p. 107, doi. 10.1111/pde.15156
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- Publication type:
- Article
Clinical and Molecular Significance of Splice Site Mutations in the Plakophilin 1 Gene in Patients with Ectodermal Dysplasia–Skin Fragility Syndrome.
- Published in:
- 2005
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- Publication type:
- Editorial
Eccrine Angiomatous Hamartoma in an Adolescent.
- Published in:
- Case Reports in Dermatology, 2015, v. 7, n. 3, p. 233, doi. 10.1159/000439399
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- Publication type:
- Article
Clinical practice guideline for diagnosis and management of urticaria.
- Published in:
- Asian Pacific Journal of Allergy & Immunology, 2016, v. 34, n. 3, p. 190
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- Publication type:
- Article
Five New Homozygous Mutations in the KIND1 Gene in Kindler Syndrome.
- Published in:
- 2007
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- Publication type:
- Letter
The South African “Bathing Suit Ichthyosis” Is a Form of Lamellar Ichthyosis Caused by a Homozygous Missense Mutation, p.R315L, in Transglutaminase 1.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Case Report: Disseminated Autochthonous Dermal Leishmaniasis Caused by Leishmania siamensis (PCM2 Trang) in a Patient from Central Thailand Infected with Human Immunodeficiency Virus.
- Published in:
- American Journal of Tropical Medicine & Hygiene, 2017, v. 96, n. 5, p. 1160, doi. 10.4269/ajtmh.16-0472
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- Publication type:
- Article
Rare indolent zygomycosis caused by subcutaneous Saksenaea vasiformis infection.
- Published in:
- Australasian Journal of Dermatology, 2020, v. 61, n. 1, p. e94, doi. 10.1111/ajd.13160
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- Publication type:
- Article
Treatment of male androgenetic alopecia with topical products containing S erenoa repens extract.
- Published in:
- Australasian Journal of Dermatology, 2016, v. 57, n. 3, p. e76, doi. 10.1111/ajd.12352
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- Publication type:
- Article
The efficacy of topical 0.025% capsaicin gel for the treatment of lichen amyloidosis: A pilot study.
- Published in:
- Australasian Journal of Dermatology, 2024, v. 65, n. 1, p. 77, doi. 10.1111/ajd.14198
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- Publication type:
- Article
Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 7, p. 833, doi. 10.1093/hmg/11.7.833
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- Publication type:
- Article
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 3, p. 221, doi. 10.1093/hmg/10.3.221
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- Publication type:
- Article