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319 related items for PubMed ID: 17973888

  • 1. Bullous congenital ichthyosiform erythroderma of Brocq.
    Kucharekova M, Mosterd K, Winnepenninckx V, van Geel M, Sommer A, van Steensel MA.
    Int J Dermatol; 2007 Nov; 46 Suppl 3():36-8. PubMed ID: 17973888
    [Abstract] [Full Text] [Related]

  • 2. Epidermolytic hyperkeratosis type NPS-3: a case report.
    Prohić A, Selmanagić A, Bilalović N.
    Acta Dermatovenerol Croat; 2007 Nov; 15(1):20-3. PubMed ID: 17433175
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  • 4. Epidermolytic hyperkeratosis.
    Kwak J, Maverakis E.
    Dermatol Online J; 2006 Sep 08; 12(5):6. PubMed ID: 16962021
    [Abstract] [Full Text] [Related]

  • 5. Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.
    Betlloch I, Lucas Costa A, Mataix J, Pérez-Crespo M, Ballester I.
    Pediatr Dermatol; 2009 Sep 08; 26(4):489-91. PubMed ID: 19689541
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  • 6. A case of bullous congenital ichthyosiform erythroderma (BCIE) caused by a mutation in the 1A helix initiation motif of keratin 1.
    Uezato H, Yamamoto Y, Kuwae C, Nonaka K, Oshiro M, Kariya K, Nonaka S.
    J Dermatol; 2005 Oct 08; 32(10):801-8. PubMed ID: 16361731
    [Abstract] [Full Text] [Related]

  • 7. Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.
    Covaciu C, Castori M, De Luca N, Ghirri P, Nannipieri A, Ragone G, Zambruno G, Castiglia D.
    Br J Dermatol; 2010 Jun 08; 162(6):1384-7. PubMed ID: 20302579
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  • 9. Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.
    Nomura K, Umeki K, Hatayama I, Kuronuma T.
    Arch Dermatol; 2001 Sep 08; 137(9):1192-5. PubMed ID: 11559215
    [Abstract] [Full Text] [Related]

  • 10. [Bullous congenital ichthyosiform erythroderma of Brocq; 2 patients with different phenotype and genotype].
    Lavrijsen AP, Bergman W, Steijlen PM.
    Ned Tijdschr Geneeskd; 2001 Aug 04; 145(31):1527-8. PubMed ID: 11569466
    [No Abstract] [Full Text] [Related]

  • 11. Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement.
    Math A, Frank J, Handisurya A, Poblete-Gutiérrez P, Slupetzky K, Födinger D, Winter D, Stingl G, Kirnbauer R.
    Eur J Dermatol; 2006 Aug 04; 16(5):507-10. PubMed ID: 17101470
    [Abstract] [Full Text] [Related]

  • 12. A keratin 10 gene mutation (Arg156Cys) in a Japanese patient with bullous congenital ichthyosiform erythroderma.
    Saeki H, Hattori N, Mitsui H, Adachi M, Imakado S, Ishibashi Y, Tamaki K.
    J Dermatol; 2002 Mar 04; 29(3):168-71. PubMed ID: 11990254
    [Abstract] [Full Text] [Related]

  • 13. Epidermolytic hyperkeratosis.
    Bale SJ, Compton JG, DiGiovanna JJ.
    Semin Dermatol; 1993 Sep 04; 12(3):202-9. PubMed ID: 7692917
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  • 14. [Mutation analysis of KRT10 gene in a patient with bullous congenital ichthyosiform erythroderma].
    Zhang SD, Liu JJ, Tian W, Zhao ZJ, Zhao JJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 04; 28(4):421-3. PubMed ID: 21811984
    [Abstract] [Full Text] [Related]

  • 15. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
    Sybert VP, Francis JS, Corden LD, Smith LT, Weaver M, Stephens K, McLean WH.
    Am J Hum Genet; 1999 Mar 04; 64(3):732-8. PubMed ID: 10053007
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  • 16. Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation.
    Morais P, Mota A, Baudrier T, Lopes JM, Cerqueira R, Tavares P, Azevedo F.
    Eur J Dermatol; 2009 Mar 04; 19(4):333-6. PubMed ID: 19443303
    [Abstract] [Full Text] [Related]

  • 17. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
    Terron-Kwiatkowski A, Terrinoni A, Didona B, Melino G, Atherton DJ, Irvine AD, McLean WH.
    Br J Dermatol; 2004 Jun 04; 150(6):1096-103. PubMed ID: 15214894
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  • 18. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene.
    Cserhalmi-Friedman PB, Squeo R, Gordon D, Garzon M, Schneiderman P, Grossman ME, Christiano AM.
    Clin Exp Dermatol; 2000 May 04; 25(3):241-3. PubMed ID: 10844506
    [Abstract] [Full Text] [Related]

  • 19. Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation.
    Tsubota A, Akiyama M, Kanitakis J, Sakai K, Nomura T, Claudy A, Shimizu H.
    J Invest Dermatol; 2008 Jul 04; 128(7):1648-52. PubMed ID: 18219278
    [Abstract] [Full Text] [Related]

  • 20. Bullous ichthyosiform erythroderma in a child born to a parent with systematized linear epidermolytic hyperkeratosis.
    Akhyani M, Kiavash K, Kamyab K.
    Int J Dermatol; 2009 Feb 04; 48(2):215-7. PubMed ID: 19200214
    [No Abstract] [Full Text] [Related]

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