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Journal Abstract Search

167 related items for PubMed ID: 11030771

  • 21. Olmsted syndrome: mutilating palmoplantar keratoderma with periorificial keratotic plaques.
    Mevorah B, Goldberg I, Sprecher E, Bergman R, Metzker A, Luria R, Gat A, Brenner S.
    J Am Acad Dermatol; 2005 Nov; 53(5 Suppl 1):S266-72. PubMed ID: 16227106
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  • 24. Keratoderma with scleroatrophy of the extremities or sclerotylosis (Huriez syndrome): a reappraisal.
    Delaporte E, N'guyen-Mailfer C, Janin A, Savary JB, Vasseur F, Feingold N, Piette F, Bergoend H.
    Br J Dermatol; 1995 Sep; 133(3):409-16. PubMed ID: 8546996
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  • 32. [Recessive keratosis palmoplantaris progrediens (Meleda's disease)].
    Camarasa JG, García Flores A.
    Med Cutan Ibero Lat Am; 1987 Sep; 15(1):24-8. PubMed ID: 2955177
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  • 33. Mal de meleda with lip involvement: a report of two cases.
    Nath AK, Chaudhuri S, Thappa DM.
    Indian J Dermatol; 2012 Sep; 57(5):390-3. PubMed ID: 23112362
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  • 34. A novel mutation in the ARS (component B) gene encoding SLURP-1 in a family with Mal de Meleda.
    Yerebakan O, Hu G, Yilmaz E, Celebi JT.
    Clin Exp Dermatol; 2003 Sep; 28(5):542-4. PubMed ID: 12950349
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  • 36. Mal de Meleda.
    Urbina F, Cristóbal MC, Sandoval R.
    Cutis; 1995 Oct; 56(4):235-8. PubMed ID: 8575224
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  • 39. Type I hereditary punctate keratoderma associated with widespread lentigo simplex and successfully treated with low-dose oral acitretin.
    Erkek E, Erdogan S, Tuncez F, Kurtipek GS, Bagci Y, Ozoguz P, Ozdemir S.
    Arch Dermatol; 2006 Aug; 142(8):1076-7. PubMed ID: 16924070
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  • 40. Patient with Mal de Meleda in whom a Novel Gene Mutation was Identified.
    Gurel G, Cilingir O, Kutluay O, Arslan S, Sahin S, Colgecen E.
    Eurasian J Med; 2019 Jun; 51(2):206-208. PubMed ID: 31258365
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