157 results on '"Brozou, Triantafyllia"'
Search Results
2. ATM germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignancies
Catalog
Books, media, physical & digital resources
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
5. Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia
6. Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency
7. Patterns and temporal trends in the incidence of childhood and adolescence cancer in Cyprus 1998–2017: A population-based study from the Cyprus Paediatric Oncology Registry
8. Alpha/beta values in pediatric medulloblastoma: implications for tailored approaches in radiation oncology.
9. Second-look surgery after pediatric brain tumor resection – Single center analysis of morbidity and volumetric efficacy
10. Increasing incidence and survival of paediatric and adolescent thyroid cancer in Cyprus 1998–2017: A population-based study from the Cyprus Pediatric Oncology Registry
11. Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer
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
15. Pediatric thyroid cancer in Cyprus 1998-2017, incidence, trends, survival: A population-based study from the Cyprus Pediatric Oncology Registry
16. Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants
17. Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes
18. Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients
19. Family-based germline sequencing in children with cancer
20. Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6
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.
23. Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations
24. Genetic predisposition in children with cancer – affected families' acceptance of Trio-WES
25. Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome
26. Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies
27. Reply to: Comments on “The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients”
28. The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients
29. Handlungsempfehlung nach der AWMF-Leitlinie „Leitsymptome und Diagnostik der ZNS-Tumoren im Kindes- und Jugendalter“
30. The Role of Adult Cancer Predisposition Genes in Hematological Malignancies of Childhood
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
35. Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents
36. The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients.
37. Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents.
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
39. Die Rolle von genetischer Prädisposition bei Krebserkrankungen im Kindesalter
40. Recurrent Germline Variant in the Cohesin Complex Gene RAD21 Predisposes Children to Lymphoblastic Leukemia and Lymphoma
41. Novel Germline POT1 Variant Predisposes to Childhood Acute Myeloid Leukemia
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
44. High-Hyperdiploid Acute Lymphoblastic Leukemia in Children with LZTR1 Germline Variants
45. ATM Germline Pathogenic Variants Affect Treatment Outcomes in Children with Acute Lymphoblastic Leukemia/Lymphoma and Ataxia Telangiectasia
46. Correction to: Genetic predisposition in children with cancer – affected families' acceptance of Trio-WES
47. QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum
48. Germline Mutations in children with malignancies
49. Family Trio-Based Whole Genome Optical Mapping Identifies Candidate Structural Variations Predisposing Children to Acute Lymphoblastic Leukemia
50. QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum.
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.