432 results on '"Möslein, Gabriela"'
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2. Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes
3. Hereditäre Formen des Kolonkarzinoms und Präkanzerosen
4. Innovative Dynamik in der Erfassung und Behandlung erblicher Krebsprädisposition: Eine Synthese aus Genetik, Technologie, Interdisziplinarität, Patientenperspektive, KI-Potenzial und präventiver Medizin
5. Comparing continent ileostomy (CI) conversion to repair/redo IPAA: favorable outcomes
6. Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement
7. Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated 'Big Bang' pathway to CRC in three of the four Lynch syndromes
8. Delphi Initiative for Early-Onset Colorectal Cancer (DIRECt) International Management Guidelines
9. Hereditäre Formen des Kolonkarzinoms und Präkanzerosen
10. Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement
11. Salvage surgery for continent ileostomies (CI) after a first successful revision: more long-term blame on the reservoir than the nipple valve
12. The Different Immune Profiles of Normal Colonic Mucosa in Cancer-Free Lynch Syndrome Carriers and Lynch Syndrome Colorectal Cancer Patients
13. Hereditäre Aspekte des Kolonkarzinoms
14. Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision
15. Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes
16. Management of Hamartomatous Polyps
17. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
18. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
19. A narrative celebrating the recent contributions of women to colorectal surgery
20. Innovative dynamics in the detection and treatment of hereditary cancer predisposition
21. The Spigelman Staging System and the Risk of Duodenal and Papillary Cancer in Familial Adenomatous Polyposis. A Systematic Review and Meta-Analysis.
22. Kock-Pouch (kontinente Ileostomie)
23. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
24. Surgical Management of Hereditary Colorectal Cancer Syndromes
25. Comparing Continent Ileostomy (CI) Conversion to Repair/Redo IPAA: Favorable Outcomes
26. Management des Peutz-Jeghers-Syndroms
27. Female representation and position based on facts and members views in the European Society of Coloproctology (ESCP)
28. 28 Hereditäre kolorektale Karzinome
29. Colorectal Cancer Clinical Oncology
30. No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
31. Continent ileostomy and S‐pouch technique after ileal pouch−anal anastomosis failure: video correspondence of a case report and surgical details—a video vignette
32. Letter to the Editor-Recent advances in Lynch syndrome
33. Routine Virtual Ileostomy Following Restorative Proctocolectomy for Familial Adenomatous Polyposis
34. Supplementary Figure from Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up
35. Data from A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis
36. Data from Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up
37. Perspective on This Article from A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis
38. Supplementary Table 1 from Chromosomal Instability in MYH- and APC-Mutant Adenomatous Polyps
39. Impact of microsatellite status in early-onset colonic cancer
40. Correction to: Letter to the Editor—Recent advances in Lynch syndrome
41. Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
42. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
43. Chirurgische Prävention hereditärer gastrointestinaler Tumordispositionen: Syndromspezifische prophylaktische Indikationsstellung unter Berücksichtigung von Gen und Gender
44. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
45. Is HLA type a possible cancer risk modifier in Lynch syndrome?
46. FAP-Associated Desmoid Tumours
47. Colon Cancer
48. Chirurgische Aspekte zu Indikation und Technik bei Varianten der adenomatösen Polyposis
49. Surgical considerations in FAP-related pouch surgery: Could we do better?
50. Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients
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