566 results on '"Morreau, H."'
Search Results
2. A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
3. The BMP pathway either enhances or inhibits the Wnt pathway depending on the SMAD4 and p53 status in CRC.
4. Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients.
5. Scoring the tumor-stroma ratio in colon cancer: procedure and recommendations
6. Molecular alterations associated with liver metastases development in colorectal cancer patients
7. COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer
8. Practical guidance for mismatch repair-deficiency testing in endometrial cancer
9. Surveillance for pancreatic cancer in high-risk individuals leads to improved outcomes: a propensity score-matched analysis
10. Cost-effectiveness of pancreas surveillance
11. Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis
12. Safety and efficacy of the addition of simvastatin to cetuximab in previously treated KRAS mutant metastatic colorectal cancer patients
13. Mismatch repair deficiency and MUTYH variants in small intestine-neuroendocrine tumors
14. APCmosaicism, not always isolated: two first-degree relatives with apparently distinctAPCmosaicism
15. 1750P Molecular genotyping in refractory thyroid cancers: Results of a European survey
16. Dual role of LOH at MMR loci in hereditary non-polyposis colorectal cancer?
17. Mosaic APC mutations in patients with mild polyposis phenotypes
18. Expression and genomic profiling of colorectal cancer
19. Duodenal carcinoma in MUTYH-associated polyposis
20. Dendritic cells in colorectal cancer correlate with other tumor-infiltrating immune cells
21. Mutational Analyses of EGFR and Downstream Pathways in Adrenocortical Carcinoma: Correlation with Mitotane Response and Survival
22. The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) – Results of an international collaborative study
23. Prognostic relevance of occult tumour cells in lymph nodes in colorectal cancer
24. ESMO-ESP - Molecular diagnostics for personalized cancer treatment
25. PTEN in colorectal cancer: a report on two Cowden syndrome patients
26. Increased frequency of 20q gain and copy-neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas
27. New treatment modalities in advanced thyroid cancer
28. High detection rate of adenomas in familial colorectal cancer
29. 594P The Drug Rediscovery Protocol (DRUP): Results of the first 500 treated patients
30. A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
31. The feasibility and reliability of sentinel node mapping in colorectal cancer
32. High frequency of copy-neutral LOH in MUTYH-associated polyposis carcinomas#
33. Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas
34. Single nucleotide polymorphism array analysis of chromosomal instability patterns discriminates rectal adenomas from carcinomas
35. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis
36. Clinical aspects of SDHA-related pheochromocytoma and paraganglioma; a nationwide study
37. Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
38. Extending the p16-Leiden tumour spectrum by respiratory tract tumours
39. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
40. Surveillance for Familial Pancreatic Cancer
41. Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree
42. Somatic mutation profiles in primary colorectal cancers and matching ovarian metastases: Identification of driver and passenger mutations
43. Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study (vol 103, pg 438, 2018)
44. Dilemmas for the pathologist in the oncologic assessment of pancreatoduodenectomy specimens
45. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (vol 117, pg 1215, 2017)
46. Targetable gene fusions identified in radioactive iodine refractory advanced thyroid carcinoma
47. Diagnostic value of ultra-deep targeted next-generation sequencing in patients with suspect pancreatic and periampullary lesions
48. Immunophenotypes in young-onset colorectal cancer
49. Predictive Biomarkers for Short-Term Survival After Curative Intent Pancreatic Cancer Surgery: Identifying the Biologically Ill-Fated
50. Tumor biology and surgical aspects of R1 resection in pancreatic cancer surgery
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