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1. Treatment of tailgut cysts by extended distal rectal segmental resection with rectoanal anastomosis

2. Prevalence of Lynch syndrome in unselected patients with endometrial or ovarian cancer

3. An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis

4. Is there still a place for adrenal venous sampling in the diagnostic localization of pheochromocytoma?

5. S3-Leitlinie 'Magenkarzinom'

6. Mutational status ofKITandPDGFRAand expression of PDGFRA are not associated with prognosis after curative resection of primary gastrointestinal stromal tumors (GISTs)

7. Erbliche Tumoren im Gastrointestinaltrakt

8. N-Acetyltransferase (NAT) 2 acetylator status and age of tumour onset in patients with sporadic and familial, microsatellite stable (MSS) colorectal cancer

9. Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients

10. Resektionsausmaß und Therapiekonzept bei hereditärem, nicht Polyposis-assoziiertem kolorektalem Karzinom (HNPCC) – Indexpatient: chirurgische Strategie

11. Perspektiven der Molekular-/Gendiagnostik in der Gastroenterologie am Beispiel des vererbbaren kolorektalen Karzinoms

12. Loss of MSH3 Protein Expression Is Frequent in MLH1-Deficient Colorectal Cancer and Is Associated with Disease Progression

13. Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability

14. Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome

15. Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers

16. Chirurgische Konzepte und Strategien bei Kolonadenomen und Polyposissyndromen

17. Band 18, Heft 2, Juni 2002

18. Involvement ofhMSH6in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation

19. Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two families

20. Band 24, Supplement 5, September 2001

21. Hereditäre kolorektale Karzinome – Überlegung zu präventiven chirurgischen Maßnahmen

22. Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

23. Präventive Chirurgie des vererbten colorectalen Carcinoms als Folge molekularer Diagnostik

24. Molekularbiologie in der Viszeralchirurgie – prädiktive Diagnostik hereditärer Tumoren

25. Epithelioid hemangiosarcoma of the rectum

26. Colorectal liver metastases: an update on palliative treatment options

27. Mutational status of KIT and PDGFRA and expression of PDGFRA are not associated with prognosis after curative resection of primary gastrointestinal stromal tumors (GISTs)

28. PDGFRA-overexpression is associated with a favourable prognosis after resection of primary gastrointestinal stromal tumors — an analysis of mutation and expression status of KIT and PDGFR-alpha in 109 resected patients

29. Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations

31. Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation

32. Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer

33. Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations

34. Können die molekulargenetischen Kenntnisse aus dem Studium des erblichen Karzinoms auf das sporadische kolorektale Karzinom übertragen werden? / Is Molecular Genetic Knowledge of Hereditary Colorectal Carcinomas Transferable to Sporadic Carcinomas?

35. An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer

36. ERBB2 gene as a potential therapeutic target in small bowel adenocarcinoma

37. Techniken und Strategien zur Identifizierung von Mutationen, die zum Hereditary Nonpolyposis Colorectal Cancer Syndrome (HNPCC Syndrom) prädisponieren

38. Ten novelMSH2andMLH1germline mutations in families with HNPCC

39. Identification of six novelMSH2andMLH1germline mutations in HNPCC

40. Near-complete association between microsatellite instability and abnormal immunostaining of the mismatch repair proteins hMSH2, hMSH6, hMLH1 and hPMS2 and involvement of hMSH6 in sporadic and hereditary colorectal cancers

41. Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer

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