Witt H - Search Results

1

Evaluation of complement factor 5 variants as genetic risk factors for the development of advanced fibrosis in chronic hepatitis C infection.

Halangk J, Sarrazin C, Neumann K, Puhl G, Mueller T, Teuber G, Klinker H, Hinrichsen H, Buggisch P, Landt O, Weich V, Bergk A, Wiedenmann B, Neuhaus P, Berg T, Witt H. Halangk J, et al. Among authors: witt h. J Hepatol. 2008 Sep;49(3):339-45. doi: 10.1016/j.jhep.2008.05.021. Epub 2008 Jun 23. J Hepatol. 2008. PMID: 18644651

2

Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.

Witt H, Luck W, Hennies HC, Classen M, Kage A, Lass U, Landt O, Becker M. Witt H, et al. Nat Genet. 2000 Jun;25(2):213-6. doi: 10.1038/76088. Nat Genet. 2000. PMID: 10835640

3

Rapid detection of the Wilson's disease H1069Q mutation by melting curve analysis with the LightCycler.

Witt H, Landt O. Witt H, et al. Clin Chem Lab Med. 2001 Oct;39(10):953-5. doi: 10.1515/CCLM.2001.153. Clin Chem Lab Med. 2001. PMID: 11758609

4

Analysis of tumour necrosis factor alpha and interleukin 10 promotor variants in patients with chronic pancreatitis.

Beranek H, Teich N, Witt H, Schulz HU, Mössner J, Keim V. Beranek H, et al. Among authors: witt h. Eur J Gastroenterol Hepatol. 2003 Nov;15(11):1223-7. doi: 10.1097/00042737-200311000-00012. Eur J Gastroenterol Hepatol. 2003. PMID: 14560157

5

Apolipoprotein E4 allele is associated with poor treatment response in hepatitis C virus (HCV) genotype 1.

Mueller T, Gessner R, Sarrazin C, Graf C, Halangk J, Witt H, Köttgen E, Wiedenmann B, Berg T. Mueller T, et al. Among authors: witt h. Hepatology. 2003 Dec;38(6):1592; author reply 1592-3. doi: 10.1016/j.hep.2003.09.042. Hepatology. 2003. PMID: 14647071 No abstract available.

6

Keratin 8 Y54H and G62C mutations are not associated with liver disease.

Halangk J, Berg T, Puhl G, Mueller T, Nickel R, Kage A, Landt O, Luck W, Wiedenmann B, Neuhaus P, Witt H. Halangk J, et al. Among authors: witt h. J Med Genet. 2004 Jul;41(7):e92. doi: 10.1136/jmg.2003.011650. J Med Genet. 2004. PMID: 15235035 Free PMC article. No abstract available.

7

Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel disease.

Büning C, Halangk J, Dignass A, Ockenga J, Deindl P, Nickel R, Genschel J, Landt O, Lochs H, Schmidt H, Witt H. Büning C, et al. Among authors: witt h. Dig Liver Dis. 2004 Jun;36(6):388-91. doi: 10.1016/j.dld.2004.01.020. Dig Liver Dis. 2004. PMID: 15248378

8

Influence of interleukin 12B (IL12B) polymorphisms on spontaneous and treatment-induced recovery from hepatitis C virus infection.

Mueller T, Mas-Marques A, Sarrazin C, Wiese M, Halangk J, Witt H, Ahlenstiel G, Spengler U, Goebel U, Wiedenmann B, Schreier E, Berg T. Mueller T, et al. Among authors: witt h. J Hepatol. 2004 Oct;41(4):652-8. doi: 10.1016/j.jhep.2004.06.021. J Hepatol. 2004. PMID: 15464247

9

Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.

Verlaan M, Drenth JP, Truninger K, Koudova M, Schulz HU, Bargetzi M, Künzli B, Friess H, Cerny M, Kage A, Landt O, te Morsche RH, Rosendahl J, Luck W, Nickel R, Halangk J, Becker M, Macek M Jr, Jansen JB, Witt H. Verlaan M, et al. Among authors: witt h. J Med Genet. 2005 Oct;42(10):e62. doi: 10.1136/jmg.2005.032599. J Med Genet. 2005. PMID: 16199544 Free PMC article.

10

Evaluation of the -26G>A CC16 polymorphism in acute respiratory distress syndrome.

Frerking I, Sengler C, Günther A, Walmrath HD, Stevens P, Witt H, Landt O, Pison U, Nickel R. Frerking I, et al. Among authors: witt h. Crit Care Med. 2005 Oct;33(10):2404-6. doi: 10.1097/01.ccm.0000181526.24809.3e. Crit Care Med. 2005. PMID: 16215398

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