Török HP - Search Results

1

Folwaczny C, Glas J, Török HP. Folwaczny C, et al. Among authors: torok hp. Eur J Gastroenterol Hepatol. 2003 Jun;15(6):621-6. doi: 10.1097/00042737-200306000-00007. Eur J Gastroenterol Hepatol. 2003. PMID: 12840672 Review.

2

Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patients.

Török HP, Glas J, Lohse P, Folwaczny C. Török HP, et al. Dig Dis. 2003;21(4):339-45. doi: 10.1159/000075357. Dig Dis. 2003. PMID: 14752224 Review.

3

Crohn's disease is associated with a toll-like receptor-9 polymorphism.

Török HP, Glas J, Tonenchi L, Bruennler G, Folwaczny M, Folwaczny C. Török HP, et al. Gastroenterology. 2004 Jul;127(1):365-6. doi: 10.1053/j.gastro.2004.05.051. Gastroenterology. 2004. PMID: 15236225 No abstract available.

4

Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype.

Glas J, Török HP, Tonenchi L, Kapser J, Schiemann U, Müller-Myhsok B, Folwaczny M, Folwaczny C. Glas J, et al. Among authors: torok hp. Inflamm Bowel Dis. 2005 Dec;11(12):1031-7. doi: 10.1097/01.mib.0000187574.41290.b1. Inflamm Bowel Dis. 2005. PMID: 16306764

5

Genetic variants and the risk of Crohn's disease: what does it mean for future disease management?

Török HP, Glas J, Lohse P, Folwaczny C. Török HP, et al. Expert Opin Pharmacother. 2006 Aug;7(12):1591-602. doi: 10.1517/14656566.7.12.1591. Expert Opin Pharmacother. 2006. PMID: 16872262 Review.

6

The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.

Glas J, Konrad A, Schmechel S, Dambacher J, Seiderer J, Schroff F, Wetzke M, Roeske D, Török HP, Tonenchi L, Pfennig S, Haller D, Griga T, Klein W, Epplen JT, Folwaczny C, Lohse P, Göke B, Ochsenkühn T, Mussack T, Folwaczny M, Müller-Myhsok B, Brand S. Glas J, et al. Among authors: torok hp. Am J Gastroenterol. 2008 Mar;103(3):682-91. doi: 10.1111/j.1572-0241.2007.01694.x. Epub 2007 Dec 20. Am J Gastroenterol. 2008. PMID: 18162085

7

rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.

Glas J, Seiderer J, Pasciuto G, Tillack C, Diegelmann J, Pfennig S, Konrad A, Schmechel S, Wetzke M, Török HP, Stallhofer J, Jürgens M, Griga T, Klein W, Epplen JT, Schiemann U, Mussack T, Lohse P, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Brand S. Glas J, et al. Among authors: torok hp. Am J Gastroenterol. 2009 Mar;104(3):665-72. doi: 10.1038/ajg.2008.65. Epub 2009 Feb 3. Am J Gastroenterol. 2009. PMID: 19262523

8

The -295T-to-C promoter polymorphism of the IL-16 gene is associated with Crohn's disease.

Glas J, Török HP, Unterhuber H, Radlmayr M, Folwaczny C. Glas J, et al. Among authors: torok hp. Clin Immunol. 2003 Mar;106(3):197-200. doi: 10.1016/s1521-6616(03)00021-4. Clin Immunol. 2003. PMID: 12706406

9

Prevalence of the chemokine receptor CCR5-Delta32 gene mutation in periodontal disease.

Folwaczny M, Glas J, Török HP, Fricke K, Folwaczny C. Folwaczny M, et al. Among authors: torok hp. Clin Immunol. 2003 Dec;109(3):325-9. doi: 10.1016/j.clim.2003.08.001. Clin Immunol. 2003. PMID: 14697747

10

Lack of association between the TNF alpha G -308 A promoter polymorphism and periodontal disease.

Folwaczny M, Glas J, Török HP, Mende M, Folwaczny C. Folwaczny M, et al. Among authors: torok hp. J Clin Periodontol. 2004 Jun;31(6):449-53. doi: 10.1111/j.1600-051x.2004.00499.x. J Clin Periodontol. 2004. PMID: 15142214

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