Fitze G - 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. Hum Mutat. 2003 Aug;22(2):177. doi: 10.1002/humu.9161. Hum Mutat. 2003. PMID: 12872262

2

[Popliteal artery entrapment syndrome. Case report of an 11-year-old boy].

Fitze G, Taut H, Rupprecht E, Roesner D. Fitze G, et al. Langenbecks Arch Chir. 1997;382(6):393-7. Langenbecks Arch Chir. 1997. PMID: 9498213 German.

3

Evidence that TSG101 aberrant transcripts are PCR artifacts.

Hampl M, Hampl J, Plaschke J, Fitze G, Schackert G, Saeger HD, Schackert HK. Hampl M, et al. Among authors: fitze g. Biochem Biophys Res Commun. 1998 Jul 30;248(3):753-60. doi: 10.1006/bbrc.1998.9038. Biochem Biophys Res Commun. 1998. PMID: 9704000

4

Multiple endocrine neoplasia type 2-associated RET proto-oncogene mutations do not contribute to the pathogenesis of sporadic parathyroid tumors.

Willeke F, Hauer MP, Buchcik R, Gebert JF, Hahn M, Fitze G, Mechtersheimer G, Möller P, Saeger HD, Herfarth C, Schackert HK. Willeke F, et al. Among authors: fitze g. Surgery. 1998 Sep;124(3):484-90. Surgery. 1998. PMID: 9736899

5

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.

6

Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain.

Sobottka SB, Haase M, Fitze G, Hahn M, Schackert HK, Schackert G. Sobottka SB, et al. Among authors: fitze g. J Neurooncol. 2000 Sep;49(3):187-95. doi: 10.1023/a:1006442024874. J Neurooncol. 2000. PMID: 11212897

7

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

8

Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.

Fitze G, Schierz M, Bredow J, Saeger HD, Roesner D, Schackert HK. Fitze G, et al. Ann Surg. 2002 Nov;236(5):570-5. doi: 10.1097/00000658-200211000-00006. Ann Surg. 2002. PMID: 12409662 Free PMC article.

9

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.

10

Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.

Fitze G, Cramer J, Serra A, Schreiber M, Roesner D, Schackert HK. Fitze G, et al. Eur J Pediatr Surg. 2003 Jun;13(3):152-7. doi: 10.1055/s-2003-41270. Eur J Pediatr Surg. 2003. PMID: 12939698

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