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2. Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda. Zhao L, Vahlquist A, Virtanen M, Wennerstrand L, Lind LK, Lundström A, Hellström Pigg M. Acta Derm Venereol; 2014 Nov; 94(6):707-10. PubMed ID: 24604124 [Abstract] [Full Text] [Related]
3. Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous. Taylor JA, Bondavalli D, Monif M, Yap LM, Winship I. Australas J Dermatol; 2016 Feb; 57(1):e11-3. PubMed ID: 25557416 [Abstract] [Full Text] [Related]
8. A Japanese case of Mal de Meleda with SLURP1 mutation. Sakabe J, Kabashima-Kubo R, Kubo A, Sasaki T, Tokura Y. J Dermatol; 2014 Aug; 41(8):764-5. PubMed ID: 24985918 [No Abstract] [Full Text] [Related]
9. Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene. Nellen RG, Steijlen PM, Hennies HC, Fischer J, Munro CS, Jonkman MF, van Steensel MA, van Geel M. Br J Dermatol; 2013 Jun; 168(6):1372-4. PubMed ID: 23290002 [No Abstract] [Full Text] [Related]
15. SLURP1 is a late marker of epidermal differentiation and is absent in Mal de Meleda. Favre B, Plantard L, Aeschbach L, Brakch N, Christen-Zaech S, de Viragh PA, Sergeant A, Huber M, Hohl D. J Invest Dermatol; 2007 Feb; 127(2):301-8. PubMed ID: 17008884 [Abstract] [Full Text] [Related]
16. Heterogeneity in the properties of mutant secreted lymphocyte antigen 6/urokinase receptor-related protein 1 (SLURP1) in Mal de Meleda. Adeyo O, Oberer M, Ploug M, Fong LG, Young SG, Beigneux AP. Br J Dermatol; 2015 Oct; 173(4):1066-9. PubMed ID: 25919322 [No Abstract] [Full Text] [Related]
17. Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda. Nellen RG, van Geel M, Steijlen PM, van Steensel MA. Br J Dermatol; 2009 Apr; 160(4):878-80. PubMed ID: 19120323 [No Abstract] [Full Text] [Related]
19. A hypomorphic Egfr allele does not ameliorate the palmoplantar keratoderma caused by SLURP1 deficiency. Allan CM, Tran D, Tu Y, Heizer PJ, Young LC, Fong LG, Beigneux AP, Young SG. Exp Dermatol; 2017 Nov; 26(11):1134-1136. PubMed ID: 28418591 [Abstract] [Full Text] [Related]
20. A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family. Shah K, Nasir A, Irfanullah, Shahzad S, Khan S, Ahmad W. Clin Exp Dermatol; 2016 Aug; 41(6):675-679. PubMed ID: 29226984 [Abstract] [Full Text] [Related] Page: [Next] [New Search]