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Journal Abstract Search

390 related items for PubMed ID: 19602001

  • 1. Filaggrin null mutations in childhood atopic dermatitis among the Chinese.
    Ching GK, Hon KL, Ng PC, Leung TF.
    Int J Immunogenet; 2009 Aug; 36(4):251-4. PubMed ID: 19602001
    [Abstract] [Full Text] [Related]

  • 2. Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis.
    Greisenegger E, Novak N, Maintz L, Bieber T, Zimprich F, Haubenberger D, Gleiss A, Stingl G, Kopp T, Zimprich A.
    J Eur Acad Dermatol Venereol; 2010 May; 24(5):607-10. PubMed ID: 19874431
    [Abstract] [Full Text] [Related]

  • 3. Association of Filaggrin loss-of-function-mutations with atopic dermatitis and asthma in the Early Treatment of the Atopic Child (ETAC) population.
    Müller S, Marenholz I, Lee YA, Sengler C, Zitnik SE, Griffioen RW, Meglio P, Wahn U, Nickel R.
    Pediatr Allergy Immunol; 2009 Jun; 20(4):358-61. PubMed ID: 19538357
    [Abstract] [Full Text] [Related]

  • 4. Mutations in the filaggrin gene in Han Chinese patients with atopic dermatitis.
    Zhang H, Guo Y, Wang W, Shi M, Chen X, Yao Z.
    Allergy; 2011 Mar; 66(3):420-7. PubMed ID: 21039602
    [Abstract] [Full Text] [Related]

  • 5. Filaggrin mutations confer susceptibility to atopic dermatitis but not to asthma.
    Rogers AJ, Celedón JC, Lasky-Su JA, Weiss ST, Raby BA.
    J Allergy Clin Immunol; 2007 Dec; 120(6):1332-7. PubMed ID: 18073125
    [Abstract] [Full Text] [Related]

  • 6. A prospective study of filaggrin null mutations in keratoconus patients with or without atopic disorders.
    Droitcourt C, Touboul D, Ged C, Ezzedine K, Cario-André M, de Verneuil H, Colin J, Taïeb A.
    Dermatology; 2011 Dec; 222(4):336-41. PubMed ID: 21701148
    [Abstract] [Full Text] [Related]

  • 7. Loss-of-function polymorphisms in the filaggrin gene are associated with an increased susceptibility to chronic irritant contact dermatitis: a case-control study.
    de Jongh CM, Khrenova L, Verberk MM, Calkoen F, van Dijk FJ, Voss H, John SM, Kezic S.
    Br J Dermatol; 2008 Sep; 159(3):621-7. PubMed ID: 18637008
    [Abstract] [Full Text] [Related]

  • 8. Filaggrin loss-of-function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood.
    Rupnik H, Rijavec M, Korošec P.
    Br J Dermatol; 2015 Feb; 172(2):455-61. PubMed ID: 25314673
    [Abstract] [Full Text] [Related]

  • 9. Rare occurrence of common filaggrin mutations in Turkish children with food allergy and atopic dermatitis.
    Vardar Acar N, Cavkaytar Ö, Arik Yilmaz E, Büyüktiryaki AB, Uysal Soyer Ö, Şahiner ÜM, Şekerel BE, Karaaslan IÇ, Saçkesen C.
    Turk J Med Sci; 2020 Dec 17; 50(8):1865-1871. PubMed ID: 32536107
    [Abstract] [Full Text] [Related]

  • 10. Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum.
    Gao PS, Rafaels NM, Hand T, Murray T, Boguniewicz M, Hata T, Schneider L, Hanifin JM, Gallo RL, Gao L, Beaty TH, Beck LA, Barnes KC, Leung DY.
    J Allergy Clin Immunol; 2009 Sep 17; 124(3):507-13, 513.e1-7. PubMed ID: 19733298
    [Abstract] [Full Text] [Related]

  • 11. Lower prevalence of common filaggrin mutations in a community sample of atopic eczema: is disease severity important?
    Gruber R, Janecke AR, Grabher D, Horak E, Schmuth M, Lercher P.
    Wien Klin Wochenschr; 2010 Oct 17; 122(19-20):551-7. PubMed ID: 20865458
    [Abstract] [Full Text] [Related]

  • 12. Carriers of filaggrin gene (FLG) mutations avoid professional exposure to irritants in adulthood.
    Bandier J, Ross-Hansen K, Carlsen BC, Menné T, Linneberg A, Stender S, Szecsi PB, Meldgaard M, Thyssen JP, Johansen JD.
    Contact Dermatitis; 2013 Dec 17; 69(6):355-62. PubMed ID: 23808934
    [Abstract] [Full Text] [Related]

  • 13. Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.
    Stemmler S, Nothnagel M, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.
    Int J Immunogenet; 2009 Aug 17; 36(4):217-22. PubMed ID: 19601998
    [Abstract] [Full Text] [Related]

  • 14. Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis.
    Li M, Liu Q, Liu J, Cheng R, Zhang H, Xue H, Bao Y, Yao Z.
    J Eur Acad Dermatol Venereol; 2013 Feb 17; 27(2):169-74. PubMed ID: 22220561
    [Abstract] [Full Text] [Related]

  • 15. [Association of filaggrin gene polymorphism with atopic dermatitis in southern Chinese Han population].
    Li CX, Li XM, Zhang XB, Han CL, Ma ZL, Lin DZ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct 17; 28(5):572-4. PubMed ID: 21983738
    [Abstract] [Full Text] [Related]

  • 16. Individuals who are homozygous for the 2282del4 and R501X filaggrin null mutations do not always develop dermatitis and complete long-term remission is possible.
    Thyssen JP, Carlsen BC, Bisgaard H, Giwercman C, Johansen JD, Linneberg A, Meldgaard M, Szecsi PB, Stender S, Menné T.
    J Eur Acad Dermatol Venereol; 2012 Mar 17; 26(3):386-9. PubMed ID: 21501248
    [Abstract] [Full Text] [Related]

  • 17. R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients.
    Giardina E, Paolillo N, Sinibaldi C, Novelli G.
    Dermatology; 2008 Mar 17; 216(1):83-4. PubMed ID: 18032906
    [No Abstract] [Full Text] [Related]

  • 18. Filaggrin loss-of-function mutation R501X and 2282del4 carrier status is associated with fissured skin on the hands: results from a cross-sectional population study.
    Thyssen JP, Ross-Hansen K, Johansen JD, Zachariae C, Carlsen BC, Linneberg A, Bisgaard H, Carson CG, Nielsen NH, Meldgaard M, Szecsi PB, Stender S, Menné T.
    Br J Dermatol; 2012 Jan 17; 166(1):46-53. PubMed ID: 21777221
    [Abstract] [Full Text] [Related]

  • 19. Analysis of filaggrin mutations and expression in corneal specimens from patients with or without atopic dermatitis.
    Lapp T, Auw-Haedrich C, Reinhard T, Evans R, Rodríguez E, Weidinger S, Jakob T.
    Int Arch Allergy Immunol; 2014 Jan 17; 163(1):20-4. PubMed ID: 24247645
    [Abstract] [Full Text] [Related]

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