Ziegler A - Search Results

1

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. Among authors: ziegler a. Hum Mutat. 2003 Aug;22(2):177. doi: 10.1002/humu.9161. Hum Mutat. 2003. PMID: 12872262

2

Lack of association between endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population: evidence of racial/ethnic differences.

Krex D, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: ziegler a. Stroke. 2001 Nov;32(11):2689-94. doi: 10.1161/hs1101.098660. Stroke. 2001. PMID: 11692035

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. Among authors: ziegler a. Lancet. 2002 Apr 6;359(9313):1200-5. doi: 10.1016/S0140-6736(02)08218-1. Lancet. 2002. PMID: 11955539

4

Polymorphisms of the NADPH oxidase P22PHOX gene in a Caucasian population with intracranial aneurysms.

Krex D, Ziegler A, König IR, Schackert HK, Schackert G. Krex D, et al. Among authors: ziegler a. Cerebrovasc Dis. 2003;16(4):363-8. doi: 10.1159/000072558. Cerebrovasc Dis. 2003. PMID: 13130177

5

Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).

Fitze G, Appelt H, König IR, Görgens H, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK. Fitze G, et al. Among authors: ziegler a. Hum Mol Genet. 2003 Dec 15;12(24):3207-14. doi: 10.1093/hmg/ddg354. Epub 2003 Nov 4. Hum Mol Genet. 2003. PMID: 14600022

6

Tissue inhibitor of metalloproteinases-1, -2, and -3 polymorphisms in a white population with intracranial aneurysms.

Krex D, Röhl H, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: ziegler a. Stroke. 2003 Dec;34(12):2817-21. doi: 10.1161/01.STR.0000099966.51485.5F. Epub 2003 Nov 6. Stroke. 2003. PMID: 14605322

7

Matrix metalloproteinase-9 coding sequence single-nucleotide polymorphisms in caucasians with intracranial aneurysms.

Krex D, Kotteck K, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: ziegler a. Neurosurgery. 2004 Jul;55(1):207-12; discussion 212-3. doi: 10.1227/01.neu.0000126882.17878.6d. Neurosurgery. 2004. PMID: 15214991

8

Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences.

Krex D, König IR, Ziegler A, Schackert HK, Schackert G. Krex D, et al. Among authors: ziegler a. Cerebrovasc Dis. 2004;18(2):104-10. doi: 10.1159/000079257. Epub 2004 Jun 22. Cerebrovasc Dis. 2004. PMID: 15218274

9

Analysis of the base excision repair genes MTH1, OGG1 and MUTYH in patients with squamous oral carcinomas.

Görgens H, Müller A, Krüger S, Kuhlisch E, König IR, Ziegler A, Schackert HK, Eckelt U. Görgens H, et al. Among authors: ziegler a. Oral Oncol. 2007 Sep;43(8):791-5. doi: 10.1016/j.oraloncology.2006.10.004. Epub 2007 Jan 4. Oral Oncol. 2007. PMID: 17207658

10

Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease.

Fitze G, König IR, Paditz E, Serra A, Schläfke M, Roesner D, Ziegler A, Schackert HK. Fitze G, et al. Among authors: ziegler a. Am J Med Genet A. 2008 Jun 1;146A(11):1486-9. doi: 10.1002/ajmg.a.32300. Am J Med Genet A. 2008. PMID: 18438890 No abstract available.

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