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2. ATM germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignancies

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3. Integrative multi-omics reveals two biologically distinct groups of pilocytic astrocytoma

4. A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children

6. Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency

8. Alpha/beta values in pediatric medulloblastoma: implications for tailored approaches in radiation oncology.

12. Flash survey on severe acute respiratory syndrome coronavirus-2 infections in paediatric patients on anticancer treatment

13. Supratentorial ependymoma in childhood: more than just RELA or YAP

14. ATMgerm line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignancies

16. Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants

18. Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients

21. Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia

22. Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients.

26. Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies

31. Deciphering the Somatic and Germline Structural Variation Landscape in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia By Whole Genome Optical Mapping

32. Clinical criteria for genetic testing in pediatric oncology show a low specificity and miss every 4thchild carrying a cancer predisposition

33. Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma

34. Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma

36. The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients.

38. Multimodal Treatment of Nasopharyngeal Carcinoma in Children, Adolescents and Young Adults-Extended Follow-Up of the NPC-2003-GPOH Study Cohort and Patients of the Interim Cohort

40. Recurrent Germline Variant in the Cohesin Complex Gene RAD21 Predisposes Children to Lymphoblastic Leukemia and Lymphoma

42. Germline POT1 Deregulation Can Predispose to Myeloid Malignancies in Childhood

43. Paediatric Cancer Predisposition Documentation Tool – Standardized Reporting Form for Children and Adolescents With Suspected Cancer Predisposition Syndrome

45. ATM Germline Pathogenic Variants Affect Treatment Outcomes in Children with Acute Lymphoblastic Leukemia/Lymphoma and Ataxia Telangiectasia

47. QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum

50. QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum.