39 results on '"Brozou, Triantafyllia"'
Search Results
2. Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants
3. Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients
4. Integrative multi-omics reveals two biologically distinct groups of pilocytic astrocytoma
5. Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia
6. A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children
7. Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia
8. Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency
9. Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies
10. Reply to: Comments on “The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients”
11. The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients
12. The Role of Adult Cancer Predisposition Genes in Hematological Malignancies of Childhood
13. Deciphering the Somatic and Germline Structural Variation Landscape in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia By Whole Genome Optical Mapping
14. Clinical criteria for genetic testing in pediatric oncology show a low specificity and miss every 4thchild carrying a cancer predisposition
15. 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
16. Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma
17. Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents
18. 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
19. Die Rolle von genetischer Prädisposition bei Krebserkrankungen im Kindesalter
20. Second-look surgery after pediatric brain tumor resection – Single center analysis of morbidity and volumetric efficacy
21. Recurrent Germline Variant in the Cohesin Complex Gene RAD21 Predisposes Children to Lymphoblastic Leukemia and Lymphoma
22. Novel Germline POT1 Variant Predisposes to Childhood Acute Myeloid Leukemia
23. Germline POT1 Deregulation Can Predispose to Myeloid Malignancies in Childhood
24. Increasing incidence and survival of paediatric and adolescent thyroid cancer in Cyprus 1998–2017: A population-based study from the Cyprus Pediatric Oncology Registry
25. Paediatric Cancer Predisposition Documentation Tool – Standardized Reporting Form for Children and Adolescents With Suspected Cancer Predisposition Syndrome
26. Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer
27. Supratentorial ependymoma in childhood: more than just RELA or YAP
28. QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum
29. Flash survey on severe acute respiratory syndrome coronavirus-2 infections in paediatric patients on anticancer treatment
30. Family Trio-Based Whole Genome Optical Mapping Identifies Candidate Structural Variations Predisposing Children to Acute Lymphoblastic Leukemia
31. Handlungsempfehlung nach der AWMF-Leitlinie „Leitsymptome und Diagnostik der ZNS-Tumoren im Kindes- und Jugendalter“
32. Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes
33. Family-based germline sequencing in children with cancer
34. Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6
35. Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations
36. Correction to: Genetic predisposition in children with cancer – affected families' acceptance of Trio-WES
37. Genetic predisposition in children with cancer – affected families' acceptance of Trio-WES
38. Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome
39. Postoperative spinal infection mimicking systemic vasculitis with titanium-spinal implants
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