Search Results - "Török, H.P"

The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease by Radlmayr, M., Török, H.P., Martin, K., Folwaczny, C.

“…GASTROENTEROLOGY 2002;122:2091-2092…”
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The −295T-to-C promoter polymorphism of the IL-16 gene is associated with crohn’s disease by Glas, J, Török, H.P, Unterhuber, H, Radlmayr, M, Folwaczny, C

“…Recently, a T-to-C polymorphism at position −295 in the promoter region of the human interleukin-16 (IL-16) gene was reported. The expression of IL-16 is…”
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The Δ32 mutation of the chemokine-receptor 5 gene neither is correlated with chronic hepatitis C nor does it predict response to therapy with interferon-α and ribavirin by Glas, J, Török, H.P, Simperl, C, König, A, Martin, K, Schmidt, F, Schaefer, M, Schiemann, U, Folwaczny, C

“…Unlike in HIV, homozygosity for a 32-bp deletion (Δ32) of the chemokine receptor 5 (CCR5) gene was recently described in increased frequency in patients with…”
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Serum antibodies in first-degree relatives of patients with IBD: a marker of disease susceptibility? A follow-up pilot-study after 7 years by Török, H P, Glas, J, Hollay, H C, Gruber, R, Osthoff, M, Tonenchi, L, Brückl, C, Mussack, T, Folwaczny, M, Folwaczny, C

“…Various disease-specific serum antibodies were described in patients with inflammatory bowel disease and their yet healthy first-degree relatives. In the…”
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Adoptive transfer of genetic susceptibility to Crohn’s disease by Folwaczny, C, Glas, J, Mussack, T, Török, H P

“…[...]at best only an extremely weak genetic predisposition can be extracted from the extensive genotyping and thus the postulated transfer of genetic…”
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