Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Cholangitis and NOD2[original query] |
---|
[NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study]. Orvosi hetilap 2004 Jul 145 (27): 1403-11. Lakatos László, Lakatos Péter László, Willheim-Polli Claudia, Reinisch Walter, Ferenci Péter, Tulassay Zsolt, Molnár Tamás, Kovács Agota, Papp János, Szalay Ferenc, |
Lack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients. BMC medical genetics 2008 9 (1): 81. Gaj Pawel, Habior Andrzej, Mikula Michal, Ostrowski Jer |
NOD2 gene variants confer risk for secondary sclerosing cholangitis in critically ill patients. Scientific reports 2017 08 7 (1): 7026. Jüngst Christoph, Stadlbauer Vanessa, Reichert Matthias C, Zimmer Vincent, Weber Susanne N, Ofner-Ziegenfuß Lisa, Voigtländer Torsten, Spindelböck Walter, Fickert Peter, Kirchner Gabriele I, Lammert Frank, Lankisch Tim O, Krawczyk Marc |
Genetic Sequencing of Pediatric Patients Identifies Mutations in Monogenic Inflammatory Bowel Disease Genes that Translate to Distinct Clinical Phenotypes. Clinical and translational gastroenterology 2020 Feb 11 (2): e00129. Ashton James J, Mossotto Enrico, Stafford Imogen S, Haggarty Rachel, Coelho Tracy A F, Batra Akshay, Afzal Nadeem A, Mort Matthew, Bunyan David, Beattie Robert Mark, Ennis Sar |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: