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2. Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency

3. NASPGHAN Annual Meeting Abstracts

4. Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance

6. Management of Familial Adenomatous Polyposis in Children and Adolescents: Position Paper From the ESPGHAN Polyposis Working Group

7. NASPGHAN Annual Meeting Abstracts

10. GE-09 * COMBINED HEREDITARY AND SOMATIC MUTATIONS OF REPLICATION ERROR REPAIR GENES RESULT IN RAPID ONSET OF ULTRA-HYPERMUTATED MALIGNANT BRAIN TUMORS IN CHILDREN

11. RADIOLOGY

12. HIGH GRADE GLIOMAS AND DIPG

13. EPIDEMIOLOGY

19. Epstein-Barr virus infection in transplant recipients: Summary of a workshop on surveillance, prevention and treatment

22. Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control study.

23. Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group.

24. Clinical Updates and Surveillance Recommendations for DNA Replication Repair Deficiency Syndromes in Children and Young Adults.

25. Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study.

26. Polyps and Polyposis Syndromes in Children: Novel Endoscopic Considerations.

27. Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset.

28. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.

29. Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency.

30. Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance.

31. Mutations in the RAS/MAPK Pathway Drive Replication Repair-Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition.

32. DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells.

33. ACG Clinical Report and Recommendations on Transition of Care in Children and Adolescents With Hereditary Polyposis Syndromes.

34. Cancers from Novel Pole -Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade.

35. Position paper: Challenges and specific strategies for constitutional mismatch repair deficiency syndrome in low-resource settings.

36. Ongoing issues with the management of children with Constitutional Mismatch Repair Deficiency syndrome.

37. Management of Peutz-Jeghers Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group.

38. Management of Juvenile Polyposis Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group.

39. Functional Repair Assay for the Diagnosis of Constitutional Mismatch Repair Deficiency From Non-Neoplastic Tissue.

40. Role of video capsule endoscopy in patients with constitutional mismatch repair deficiency (CMMRD) syndrome: report from the International CMMRD Consortium.

41. A Toddler With Treatment-Resistant Iron Deficiency Anemia.

42. Comprehensive Analysis of Hypermutation in Human Cancer.

43. Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.

44. Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency.

45. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium.

46. High frequency of mismatch repair deficiency among pediatric high grade gliomas in Jordan.

47. Management of Acute Myeloblastic Leukemia in a Child With Biallelic Mismatch Repair Deficiency.

48. Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.

49. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.

50. Unifying diagnosis for adenomatous polyps, café-au-lait macules, and a brain mass?

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