Lacher M - Search Results

1

Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children.

Lacher M, Schroepf S, Ballauff A, Lohse P, von Schweinitz D, Kappler R, Koletzko S. Lacher M, et al. Acta Paediatr. 2009 Nov;98(11):1835-40. doi: 10.1111/j.1651-2227.2009.01438.x. Epub 2009 Jul 29. Acta Paediatr. 2009. PMID: 19659808

2

Association of a CXCL9 polymorphism with pediatric Crohn's disease.

Lacher M, Kappler R, Berkholz S, Baurecht H, von Schweinitz D, Koletzko S. Lacher M, et al. Biochem Biophys Res Commun. 2007 Nov 23;363(3):701-7. doi: 10.1016/j.bbrc.2007.09.020. Epub 2007 Sep 18. Biochem Biophys Res Commun. 2007. PMID: 17892861

3

Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.

Glas J, Stallhofer J, Ripke S, Wetzke M, Pfennig S, Klein W, Epplen JT, Griga T, Schiemann U, Lacher M, Koletzko S, Folwaczny M, Lohse P, Göke B, Ochsenkühn T, Müller-Myhsok B, Brand S. Glas J, et al. Among authors: lacher m. Am J Gastroenterol. 2009 Jul;104(7):1737-44. doi: 10.1038/ajg.2009.163. Epub 2009 May 19. Am J Gastroenterol. 2009. PMID: 19455118

4

Nuclear pregnane X receptor single nucleotide polymorphism (-25385C/T) is not associated with inflammatory bowel disease in pediatric patients.

Lacher M, Kappler R, Schroepf S, Berkholz S, Ballauff A, Bufler P, Baurecht H, von Schweinitz D, Koletzko S. Lacher M, et al. J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):147-50. doi: 10.1097/MPG.0b013e31818de1a8. J Pediatr Gastroenterol Nutr. 2009. PMID: 19516190

5

Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children.

Lacher M, Schroepf S, Helmbrecht J, Von Schweinitz D, Ballauff A, Koch I, Lohse P, Osterrieder S, Kappler R, Koletzko S. Lacher M, et al. Acta Paediatr. 2010 May;99(5):727-733. doi: 10.1111/j.1651-2227.2009.01680.x. Epub 2010 Feb 26. Acta Paediatr. 2010. PMID: 20192940

6

Early and long term outcome in children with esophageal atresia treated over the last 22 years.

Lacher M, Froehlich S, von Schweinitz D, Dietz HG. Lacher M, et al. Klin Padiatr. 2010 Sep;222(5):296-301. doi: 10.1055/s-0030-1249610. Epub 2010 May 12. Klin Padiatr. 2010. PMID: 20464650

7

NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Lacher M, Helmbrecht J, Schroepf S, Koletzko S, Ballauff A, Classen M, Uhlig H, Hubertus J, Hartl D, Lohse P, von Schweinitz D, Kappler R. Lacher M, et al. J Pediatr Surg. 2010 Aug;45(8):1591-7. doi: 10.1016/j.jpedsurg.2009.10.046. J Pediatr Surg. 2010. PMID: 20713205

8

Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease.

Schroepf S, Kappler R, Brand S, Prell C, Lohse P, Glas J, Hoster E, Helmbrecht J, Ballauff A, Berger M, von Schweinitz D, Koletzko S, Lacher M. Schroepf S, et al. Among authors: lacher m. Inflamm Bowel Dis. 2010 Nov;16(11):1882-90. doi: 10.1002/ibd.21312. Inflamm Bowel Dis. 2010. PMID: 20848514

9

Hirschsprung-associated enterocolitis develops independently of NOD2 variants.

Lacher M, Fitze G, Helmbrecht J, Schroepf S, Berger M, Lohse P, Koletzko S, Ballauff A, Grote V, Goedeke J, von Schweinitz D, Kappler R. Lacher M, et al. J Pediatr Surg. 2010 Sep;45(9):1826-31. doi: 10.1016/j.jpedsurg.2010.02.039. J Pediatr Surg. 2010. PMID: 20850627

10

Postoperative bladder and rectal function in children with sacrococcygeal teratoma.

Berger M, Heinrich M, Lacher M, Hubertus J, Stehr M, von Schweinitz D. Berger M, et al. Among authors: lacher m. Pediatr Blood Cancer. 2011 Mar;56(3):397-402. doi: 10.1002/pbc.22887. Pediatr Blood Cancer. 2011. PMID: 21061314

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