Trojan J - Search Results

1

Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis.

Hinrichsen I, Schäfer D, Langer D, Köger N, Wittmann M, Aretz S, Steinke V, Holzapfel S, Trojan J, König R, Zeuzem S, Brieger A, Plotz G. Hinrichsen I, et al. Among authors: trojan j. Carcinogenesis. 2015 Feb;36(2):202-11. doi: 10.1093/carcin/bgu239. Epub 2014 Dec 4. Carcinogenesis. 2015. PMID: 25477341

2

Serum tests for diagnosis and follow-up of hepatocellular carcinoma after treatment.

Trojan J, Raedle J, Zeuzem S. Trojan J, et al. Digestion. 1998 Jul;59 Suppl 2:72-4. doi: 10.1159/000051429. Digestion. 1998. PMID: 9718428 Review. No abstract available.

3

[Mutated serine-threonine kinase gene (STK11) is the cause of Peutz-Jeghers syndrome].

Trojan J, Raedle J, Zeuzem S. Trojan J, et al. Z Gastroenterol. 1998 Sep;36(9):871-3. Z Gastroenterol. 1998. PMID: 9795419 German. No abstract available.

4

Rapid microsatellite analysis of paraffin embedded tumour specimens from patients with hereditary non-polyposis colorectal cancer.

Raedle J, Brieger A, Trojan J, Herrmann G, Zeuzem S. Raedle J, et al. Among authors: trojan j. J Clin Pathol. 1998 Aug;51(8):621-2. doi: 10.1136/jcp.51.8.621. J Clin Pathol. 1998. PMID: 9828824 Free PMC article.

5

Limited value of fluorine-18-fluorodeoxyglucose PET for the differential diagnosis of focal liver lesions in patients with chronic hepatitis C virus infection.

Schröder O, Trojan J, Zeuzem S, Baum RP. Schröder O, et al. Among authors: trojan j. Nuklearmedizin. 1998;37(8):279-85. Nuklearmedizin. 1998. PMID: 9868710

6

Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.

Trojan J, Brieger A, Raedle J, Roth WK, Zeuzem S. Trojan J, et al. Am J Gastroenterol. 1999 Jan;94(1):257-61. doi: 10.1111/j.1572-0241.1999.00810.x. Am J Gastroenterol. 1999. PMID: 9934767

7

Evaluation of rapid microsatellite analysis of paraffin-embedded specimens in screening for hereditary nonpolyposis colorectal cancer.

Raedle J, Brieger A, Trojan J, Hardt T, Herrmann G, Zeuzem S. Raedle J, et al. Among authors: trojan j. Mod Pathol. 1999 May;12(5):485-91. Mod Pathol. 1999. PMID: 10349986

8

[Pathogenetic germ-line mutation in patients with hereditary nonpolyposis colorectal carcinoma (HNPCC)].

Trojan J, Raedle J, Zeuzem S. Trojan J, et al. Z Gastroenterol. 1999 Apr;37(4):321-4. Z Gastroenterol. 1999. PMID: 10378370 German. No abstract available.

9

Identification of germline mutations in hereditary nonpolyposis colorectal cancer using base excision sequence scanning analysis.

Brieger A, Trojan J, Raedle J, Roth WK, Zeuzem S. Brieger A, et al. Among authors: trojan j. Clin Chem. 1999 Sep;45(9):1564-7. Clin Chem. 1999. PMID: 10471663 No abstract available.

10

Cystic adrenal lymphangioma: incidental diagnosis on abdominal sonography.

Trojan J, Schwarz W, Zeuzem S, Dietrich CF. Trojan J, et al. AJR Am J Roentgenol. 2000 Apr;174(4):1164-5. doi: 10.2214/ajr.174.4.1741164. AJR Am J Roentgenol. 2000. PMID: 10749271 No abstract available.

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