Kuhlisch E - Search Results

1

Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.

Fitze G, Schreiber M, Kuhlisch E, Schackert HK, Roesner D. Fitze G, et al. Am J Hum Genet. 1999 Nov;65(5):1469-73. doi: 10.1086/302618. Am J Hum Genet. 1999. PMID: 10521317 Free PMC article. No abstract available.

2

Association of germline mutations and polymorphisms of the RET proto-oncogene with idiopathic congenital central hypoventilation syndrome in 33 patients.

Fitze G, Paditz E, Schläfke M, Kuhlisch E, Roesner D, Schackert HK. Fitze G, et al. J Med Genet. 2003 Feb;40(2):E10. doi: 10.1136/jmg.40.2.e10. J Med Genet. 2003. PMID: 12566528 Free PMC article. No abstract available.

3

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.

Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E, Roesner D, Schackert HK. Fitze G, et al. Lancet. 2002 Apr 6;359(9313):1200-5. doi: 10.1016/S0140-6736(02)08218-1. Lancet. 2002. PMID: 11955539

4

Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease.

Fitze G, Schierz M, Kuhlisch E, Schreiber M, Ziegler A, Roesner D, Schackert HK. Fitze G, et al. Hum Mutat. 2003 Aug;22(2):177. doi: 10.1002/humu.9161. Hum Mutat. 2003. PMID: 12872262

5

RET-protooncogene variants in patients with sporadic neoplasms of the digestive tract and the central nervous system.

Rückert F, Görgens H, Richter I, Krex D, Schackert G, Kuhlisch E, Fitze G, Saeger HD, Pilarsky C, Grützmann R, Schackert HK. Rückert F, et al. Int J Colorectal Dis. 2011 Jul;26(7):835-40. doi: 10.1007/s00384-011-1150-7. Epub 2011 Feb 11. Int J Colorectal Dis. 2011. PMID: 21311890

6

The impact of single nucleotide polymorphisms of the thrombin activatable fibrinolysis inhibitor (TAFI) gene on TAFI antigen levels in healthy children and pediatric oncology patients.

Knoefler R, Ludwig K, Kostka H, Kuhlisch E, Siegert G, Suttorp M. Knoefler R, et al. Semin Thromb Hemost. 2003 Dec;29(6):575-83. doi: 10.1055/s-2004-815625. Semin Thromb Hemost. 2003. PMID: 14719174

7

Association of chondromodulin-II Val58Ile polymorphism with radiographic joint destruction in rheumatoid arthritis.

Graessler J, Verlohren M, Graessler A, Zeissig A, Kuhlisch E, Kopprasch S, Schroeder HE. Graessler J, et al. J Rheumatol. 2005 Sep;32(9):1654-61. J Rheumatol. 2005. PMID: 16142856

8

Development of the X-linked tetrameric microsatellite marker HumDXS6789 for forensic purposes.

Hering S, Kuhlisch E, Szibor R. Hering S, et al. Forensic Sci Int. 2001 Jun 1;119(1):42-6. doi: 10.1016/s0379-0738(00)00396-0. Forensic Sci Int. 2001. PMID: 11348792

9

Matrix metalloproteinase 2 polymorphisms in a caucasian population with abdominal aortic aneurysm.

Hinterseher I, Bergert H, Kuhlisch E, Bloomenthal A, Pilarsky Ch, Ockert D, Schellong S, Saeger HD, Krex D. Hinterseher I, et al. J Surg Res. 2006 Jun 15;133(2):121-8. doi: 10.1016/j.jss.2005.12.001. Epub 2006 Feb 3. J Surg Res. 2006. PMID: 16458924

10

Prevalence of HLA-DRB1 genotype and altered Fas/Fas ligand expression in adrenocortical carcinoma.

Wolkersdörfer GW, Marx C, Brown J, Schröder S, Füssel M, Rieber EP, Kuhlisch E, Ehninger G, Bornstein SR. Wolkersdörfer GW, et al. J Clin Endocrinol Metab. 2005 Mar;90(3):1768-74. doi: 10.1210/jc.2004-1406. Epub 2004 Dec 7. J Clin Endocrinol Metab. 2005. PMID: 15585555

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