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PUBMED FOR HANDHELDS

Journal Abstract Search


164 related items for PubMed ID: 19538184

  • 1.
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  • 2. Filaggrin null mutations and association with contact allergy and allergic contact dermatitis: results from a tertiary dermatology clinic.
    Carlsen BC, Johansen JD, Menné T, Meldgaard M, Szecsi PB, Stender S, Thyssen JP.
    Contact Dermatitis; 2010 Aug; 63(2):89-95. PubMed ID: 20629673
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Deletion of the late cornified envelope genes LCE3B and LCE3C may promote chronic hand eczema with allergic contact dermatitis.
    Molin S, Vollmer S, Weiss EH, Weisenseel P, Ruzicka T, Prinz JC.
    J Investig Allergol Clin Immunol; 2011 Sep; 21(6):472-9. PubMed ID: 21995181
    [Abstract] [Full Text] [Related]

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  • 6. Filaggrin gene mutations in hand eczema patients in the Indian subcontinent: A prospective case-control study.
    Handa S, Khullar G, Pal A, Kamboj P, De D.
    Contact Dermatitis; 2019 Jun; 80(6):359-364. PubMed ID: 30681730
    [Abstract] [Full Text] [Related]

  • 7. Filaggrin mutations are strongly associated with contact sensitization in individuals with dermatitis.
    Thyssen JP, Linneberg A, Ross-Hansen K, Carlsen BC, Meldgaard M, Szecsi PB, Stender S, Menné T, Johansen JD.
    Contact Dermatitis; 2013 May; 68(5):273-6. PubMed ID: 23343419
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  • 9. Genotype-phenotype associations in filaggrin loss-of-function mutation carriers.
    Landeck L, Visser M, Kezic S, John SM.
    Contact Dermatitis; 2013 Mar; 68(3):149-55. PubMed ID: 23421459
    [Abstract] [Full Text] [Related]

  • 10. Filaggrin null alleles are not associated with hand eczema or contact allergy.
    Lerbaek A, Bisgaard H, Agner T, Ohm Kyvik K, Palmer CN, Menné T.
    Br J Dermatol; 2007 Dec; 157(6):1199-204. PubMed ID: 17970802
    [Abstract] [Full Text] [Related]

  • 11. 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; 166(1):46-53. PubMed ID: 21777221
    [Abstract] [Full Text] [Related]

  • 12. Loss-of-function mutations in the filaggrin gene: no contribution to disease susceptibility, but to autoantibody formation against citrullinated peptides in early rheumatoid arthritis.
    Hüffmeier U, Böiers U, Lascorz J, Reis A, Burkhardt H.
    Ann Rheum Dis; 2008 Jan; 67(1):131-3. PubMed ID: 17704064
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Cytokine gene polymorphisms and susceptibility to chronic irritant contact dermatitis.
    de Jongh CM, John SM, Bruynzeel DP, Calkoen F, van Dijk FJ, Khrenova L, Rustemeyer T, Verberk MM, Kezic S.
    Contact Dermatitis; 2008 May; 58(5):269-77. PubMed ID: 18416756
    [Abstract] [Full Text] [Related]

  • 15. Filaggrin mutations and the skin.
    De D, Handa S.
    Indian J Dermatol Venereol Leprol; 2012 May; 78(5):545-51. PubMed ID: 22960809
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Classification of atopic hand eczema and the filaggrin mutations.
    Giwercman C, Lerbaek A, Bisgaard H, Menné T.
    Contact Dermatitis; 2008 Nov; 59(5):257-60. PubMed ID: 18976374
    [Abstract] [Full Text] [Related]

  • 18. Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.
    Ekelund E, Liedén A, Link J, Lee SP, D'Amato M, Palmer CN, Kockum I, Bradley M.
    Acta Derm Venereol; 2008 Nov; 88(1):15-9. PubMed ID: 18176743
    [Abstract] [Full Text] [Related]

  • 19. Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study.
    Thyssen JP, Carlsen BC, Menné T, Linneberg A, Nielsen NH, Meldgaard M, Szecsi PB, Stender S, Johansen JD.
    Br J Dermatol; 2010 Jul; 163(1):115-20. PubMed ID: 20426775
    [Abstract] [Full Text] [Related]

  • 20. No remarkable differences in rates of sensitization to common type I and IV allergens between FLG loss-of-function mutation carriers and wild-type subjects.
    Landeck L, Visser M, Skudlik C, Brans R, Kezic S, John SM.
    Contact Dermatitis; 2014 Jan; 70(1):27-34. PubMed ID: 23848345
    [Abstract] [Full Text] [Related]


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