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Journal Abstract Search

180 related items for PubMed ID: 9427080

  • 21. Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3.
    Kariminejad A, Barzegar M, Abdollahimajd F, Pramanik R, McGrath JA.
    Clin Exp Dermatol; 2014 Jun; 39(4):492-5. PubMed ID: 24758389
    [Abstract] [Full Text] [Related]

  • 22. [Acral melanoma in a patient with hereditary keratoderma of the palms and soles (mal de Meleda): A chance association?].
    Korbi M, Hickman G, Routier E, Bagot M, Bourrat E.
    Ann Dermatol Venereol; 2019 Nov; 146(11):730-736. PubMed ID: 31582262
    [Abstract] [Full Text] [Related]

  • 23. Aberrant expression of aquaporin-3 in hereditary papulotranslucent acrokeratoderma and aquagenic palmoplantar keratoderma.
    Gironi LC, Colombo E, Zottarelli F, Guala A, Arduino C, Leutner M, Camillo L, Valente G, Boldorini RL, Savoia P.
    Eur J Dermatol; 2018 Apr 01; 28(2):262-263. PubMed ID: 29724688
    [No Abstract] [Full Text] [Related]

  • 24. 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 01; 57(1):e11-3. PubMed ID: 25557416
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  • 25. Progressive symmetric erythrokeratodermia: report of a Chinese family and evidence for genetic heterogeneity.
    Cui Y, Yang S, He PP, Zhou WM, Li M, Gao M, Chen JJ, Yan KL, Xiao FL, Xu SJ, Huang W, Zhang XJ.
    J Dermatol Sci; 2004 Sep 01; 35(3):233-5. PubMed ID: 15381248
    [No Abstract] [Full Text] [Related]

  • 26. Mal de Meleda.
    Lestringant GG, Halawani NA, Zagzouk F.
    Int J Dermatol; 1989 May 01; 28(4):277-8. PubMed ID: 2524451
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  • 29. Hidrotic ectodermal dysplasia: study of a large Chinese pedigree.
    Rajagopalan K, Tay CH.
    Arch Dermatol; 1977 Apr 01; 113(4):481-5. PubMed ID: 139851
    [Abstract] [Full Text] [Related]

  • 30. Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda.
    Radiono S, Pramono ZAD, Oh GGK, Surana U, Widiyani S, Danarti R.
    Int J Dermatol; 2017 Nov 01; 56(11):1161-1168. PubMed ID: 29023701
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  • 32. What syndrome is this? Greither syndrome.
    Tay YK.
    Pediatr Dermatol; 2003 Nov 01; 20(3):272-5. PubMed ID: 12787282
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  • 34. Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates.
    Eckl KM, Stevens HP, Lestringant GG, Westenberger-Treumann M, Traupe H, Hinz B, Frossard PM, Stadler R, Leigh IM, Nürnberg P, Reis A, Hennies HC.
    Hum Genet; 2003 Jan 01; 112(1):50-6. PubMed ID: 12483299
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  • 36. Verrucous pits on the palms.
    Fernández-Crehuet P, Ruiz-Villaverde R.
    J Paediatr Child Health; 2016 Mar 01; 52(3):352. PubMed ID: 27124850
    [No Abstract] [Full Text] [Related]

  • 37. Hereditary palmoplantar keratoderma and dermatophytosis.
    Nielsen PG.
    Int J Dermatol; 1988 May 01; 27(4):223-31. PubMed ID: 2968959
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  • 40. Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM interval at 21q11.2-21q21.2.
    Cui Y, Yang S, Gao M, Zhou WM, Li M, Wang Y, Chen JJ, Yan KL, Niu ZM, Wang PG, Xiao FL, Liang YH, Sun LD, Fan X, Huang W, Zhang XJ.
    J Invest Dermatol; 2006 Sep 01; 126(9):2136-9. PubMed ID: 16691195
    [No Abstract] [Full Text] [Related]

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