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1. The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients

7. Genetic counselling legislation and practice in cancer in EU Member States

9. Results of a 1-year quality-improvement process to reduce door-to-needle time in acute ischemic stroke with MRI screening

14. Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome.

15. High yield of surveillance in patients diagnosed with constitutional mismatch repair deficiency

19. Seroprevalencia de Toxoplasma gondiien Gallus domesticus en La Habana, Cuba

22. The multinational second Diabetes, Attitudes, Wishes and Needs study: results of the French survey

23. The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients

27. Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

29. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

35. Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort

38. Grounding Language to Autonomously-Acquired Skills via Goal Generation

40. Recommendations to improve identification of hereditary and familial colorectal cancer in Europe

41. Peutz-Jeghers syndrome: a systematic review and recommendations for management

43. Development of a Tool to Measure the Clinical Response to Biologic Therapy in Uncontrolled Severe Asthma: The FEV1, Exacerbations, Oral Corticosteroids, Symptoms Score

44. GENOTYPE-PHENOTYPE ASSOCIATIONS PROVIDE A RATIONAL TO IDENTIFY POTENTIALLY ACTIONABLE VUS

46. Guidelines for the clinical management of familial adenomatous polyposis (FAP)

47. Language-Conditioned Goal Generation: a New Approach to Language Grounding for RL

48. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

49. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

50. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.

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