Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 250

1.

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. doi: 10.1111/bjd.13477. Epub 2015 Jan 6.

PMID:
25314673
2.

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. doi: 10.1111/cod.12097. Epub 2013 Jun 28.

PMID:
23808934
3.

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. doi: 10.1111/bjd.12083.

4.

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. doi: 10.1111/j.1365-2133.2008.08730.x. Epub 2008 Jul 10.

PMID:
18637008
5.

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. doi: 10.1111/cod.12021. Epub 2013 Jan 24.

PMID:
23343419
6.

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. doi: 10.1111/j.1468-3083.2009.03469.x. Epub 2009 Oct 23.

PMID:
19874431
7.

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. doi: 10.1111/j.1365-2133.2011.10475.x. Epub 2011 Oct 17.

PMID:
21692775
8.

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. doi: 10.1111/j.1744-313X.2009.00859.x.

PMID:
19602001
9.

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. doi: 10.1111/ijd.13401. Epub 2016 Sep 22.

PMID:
27653621
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;124(3):507-13, 513.e1-7. doi: 10.1016/j.jaci.2009.07.034.

11.

Low frequency of filaggrin null mutations in Croatia and their relation with allergic diseases.

Sabolić Pipinić I, Varnai VM, Turk R, Breljak D, Kezić S, Macan J.

Int J Immunogenet. 2013 Jun;40(3):192-8. doi: 10.1111/iji.12006. Epub 2012 Oct 18.

PMID:
23078034
12.

Clinical course of occupational irritant contact dermatitis of the hands in relation to filaggrin genotype status and atopy.

Landeck L, Visser M, Skudlik C, Brans R, Kezic S, John SM.

Br J Dermatol. 2012 Dec;167(6):1302-9. doi: 10.1111/bjd.12035.

PMID:
22962861
13.

Filaggrin mutations in a Western siberian population and their association with atopic dermatitis in children.

Komova EG, Shintyapina AB, Makarova SI, Ivanov MK, Chekryga EA, Kaznacheeva LF, Vavilin VA.

Genet Test Mol Biomarkers. 2014 Dec;18(12):791-6. doi: 10.1089/gtmb.2014.0247.

PMID:
25390410
14.

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. doi: 10.1111/cod.12731. Epub 2016 Dec 20.

PMID:
27995642
15.

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;163(1):20-4. doi: 10.1159/000355965. Epub 2013 Nov 16.

PMID:
24247645
16.

Filaggrin mutations may confer susceptibility to chronic hand eczema characterized by combined allergic and irritant contact dermatitis.

Molin S, Vollmer S, Weiss EH, Ruzicka T, Prinz JC.

Br J Dermatol. 2009 Oct;161(4):801-7. doi: 10.1111/j.1365-2133.2009.09245.x. Epub 2009 Apr 22.

PMID:
19538184
17.

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. doi: 10.1111/cod.12109. Epub 2013 Jul 15.

PMID:
23848345
18.

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;122(19-20):551-7. doi: 10.1007/s00508-010-1449-3. Epub 2010 Sep 27.

PMID:
20865458
19.

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.

PMID:
18073125
20.

The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohort.

Margolis DJ, Apter AJ, Gupta J, Hoffstad O, Papadopoulos M, Campbell LE, Sandilands A, McLean WH, Rebbeck TR, Mitra N.

J Allergy Clin Immunol. 2012 Oct;130(4):912-7. doi: 10.1016/j.jaci.2012.07.008. Epub 2012 Aug 27.

Supplemental Content

Support Center