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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

251 related items for PubMed ID: 18396323

  • 21. 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; 69(6):355-62. PubMed ID: 23808934
    [Abstract] [Full Text] [Related]

  • 22. Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease.
    Van Limbergen J, Russell RK, Nimmo ER, Zhao Y, Liao H, Drummond HE, Davies G, Gillett PM, McGrogan P, Bisset WM, Mahdi G, Wilson DC, Brown SJ, McLean WH, Satsangi J.
    Inflamm Bowel Dis; 2009 Oct; 15(10):1492-8. PubMed ID: 19408338
    [Abstract] [Full Text] [Related]

  • 23. Eczema severity in preadolescent children and its relation to sex, filaggrin mutations, asthma, rhinitis, aggravating factors and topical treatment: a report from the BAMSE birth cohort.
    Ballardini N, Kull I, Söderhäll C, Lilja G, Wickman M, Wahlgren CF.
    Br J Dermatol; 2013 Mar; 168(3):588-94. PubMed ID: 23445315
    [Abstract] [Full Text] [Related]

  • 24. Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march.
    Marenholz I, Nickel R, Rüschendorf F, Schulz F, Esparza-Gordillo J, Kerscher T, Grüber C, Lau S, Worm M, Keil T, Kurek M, Zaluga E, Wahn U, Lee YA.
    J Allergy Clin Immunol; 2006 Oct; 118(4):866-71. PubMed ID: 17030239
    [Abstract] [Full Text] [Related]

  • 25. Filaggrin gene loss-of-function mutations explain discordance of atopic dermatitis within dizygotic twin pairs.
    Thomsen SF, Elmose C, Szecsi PB, Stender S, Kyvik KO, Backer V, Thyssen JP.
    Int J Dermatol; 2016 Dec; 55(12):1341-1344. PubMed ID: 27653621
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. Meta-analysis of filaggrin polymorphisms in eczema and asthma: robust risk factors in atopic disease.
    Rodríguez E, Baurecht H, Herberich E, Wagenpfeil S, Brown SJ, Cordell HJ, Irvine AD, Weidinger S.
    J Allergy Clin Immunol; 2009 Jun; 123(6):1361-70.e7. PubMed ID: 19501237
    [Abstract] [Full Text] [Related]

  • 28. Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis.
    Winge MC, Bilcha KD, Liedén A, Shibeshi D, Sandilands A, Wahlgren CF, McLean WH, Nordenskjöld M, Bradley M.
    Br J Dermatol; 2011 Nov; 165(5):1074-80. PubMed ID: 21692775
    [Abstract] [Full Text] [Related]

  • 29. 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; 124(3):507-13, 513.e1-7. PubMed ID: 19733298
    [Abstract] [Full Text] [Related]

  • 30. Health-related quality of life in adult dermatitis patients stratified by filaggrin genotype.
    Heede NG, Thyssen JP, Thuesen BH, Linneberg A, Szecsi PB, Stender S, Johansen JD.
    Contact Dermatitis; 2017 Mar; 76(3):167-177. PubMed ID: 27995642
    [Abstract] [Full Text] [Related]

  • 31. Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance.
    Esparza-Gordillo J, Matanovic A, Marenholz I, Bauerfeind A, Rohde K, Nemat K, Lee-Kirsch MA, Nordenskjöld M, Winge MC, Keil T, Krüger R, Lau S, Beyer K, Kalb B, Niggemann B, Hübner N, Cordell HJ, Bradley M, Lee YA.
    PLoS Genet; 2015 Mar; 11(3):e1005076. PubMed ID: 25757221
    [Abstract] [Full Text] [Related]

  • 32. Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis.
    Visser MJ, Landeck L, Campbell LE, McLean WHI, Weidinger S, Calkoen F, John SM, Kezic S.
    Br J Dermatol; 2013 Feb; 168(2):326-332. PubMed ID: 23039796
    [Abstract] [Full Text] [Related]

  • 33. Filaggrin loss-of-function mutations as risk factors for ischemic stroke in the general population.
    Varbo A, Nordestgaard BG, Benn M.
    J Thromb Haemost; 2017 Apr; 15(4):624-635. PubMed ID: 28164424
    [Abstract] [Full Text] [Related]

  • 34. Elder siblings enhance the effect of filaggrin mutations on childhood eczema: results from the 2 birth cohort studies LISAplus and GINIplus.
    Cramer C, Link E, Horster M, Koletzko S, Bauer CP, Berdel D, von Berg A, Lehmann I, Herbarth O, Borte M, Schaaf B, Behrendt H, Chen CM, Sausenthaler S, Illig T, Wichmann HE, Heinrich J, Krämer U, LISAplus Study Group and the GINIplus Study Group.
    J Allergy Clin Immunol; 2010 Jun; 125(6):1254-1260.e5. PubMed ID: 20513523
    [Abstract] [Full Text] [Related]

  • 35. The eczema risk variant on chromosome 11q13 (rs7927894) in the population-based ALSPAC cohort: a novel susceptibility factor for asthma and hay fever.
    Marenholz I, Bauerfeind A, Esparza-Gordillo J, Kerscher T, Granell R, Nickel R, Lau S, Henderson J, Lee YA.
    Hum Mol Genet; 2011 Jun 15; 20(12):2443-9. PubMed ID: 21429916
    [Abstract] [Full Text] [Related]

  • 36. 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 15; 24(5):607-10. PubMed ID: 19874431
    [Abstract] [Full Text] [Related]

  • 37. Hand eczema, atopic dermatitis and filaggrin mutations in adult Danes: a registry-based study assessing risk of disability pension.
    Heede NG, Thuesen BH, Thyssen JP, Linneberg A, Szecsi PB, Stender S, Menné T, Johansen JD.
    Contact Dermatitis; 2017 Aug 15; 77(2):95-105. PubMed ID: 28425595
    [Abstract] [Full Text] [Related]

  • 38. Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age.
    Flohr C, England K, Radulovic S, McLean WH, Campbel LE, Barker J, Perkin M, Lack G.
    Br J Dermatol; 2010 Dec 15; 163(6):1333-6. PubMed ID: 21137118
    [Abstract] [Full Text] [Related]

  • 39. FLG mutations in ichthyosis vulgaris and atopic eczema: spectrum of mutations and population genetics.
    Akiyama M.
    Br J Dermatol; 2010 Mar 15; 162(3):472-7. PubMed ID: 19958351
    [Abstract] [Full Text] [Related]

  • 40. Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations.
    O'Regan GM, Campbell LE, Cordell HJ, Irvine AD, McLean WH, Brown SJ.
    J Allergy Clin Immunol; 2010 Jan 15; 125(1):170-4.e1-2. PubMed ID: 20109745
    [Abstract] [Full Text] [Related]

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