164 results on '"Guerrini-Rousseau, Léa"'
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2. Specific brain MRI features of constitutional mismatch repair deficiency syndrome in children with high-grade gliomas
3. Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients
4. Report of the sixth meeting of the European Consortium ‘Care for CMMRD’ (C4CMMRD), Paris, France, November 16th 2022
5. Imaging features to distinguish posterior fossa ependymoma subgroups
6. Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.
7. Pediatric high-grade glioma MYCN is frequently associated with Li-Fraumeni syndrome
8. The role of cancer predisposition syndrome in children and adolescents with very rare tumours
9. Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency
10. Li–Fraumeni‐associated osteosarcomas: The French experience.
11. Comprehensive analysis of constitutional mismatch repair deficiency‐associated non‐Hodgkin lymphomas in a global cohort.
12. Biallelic Germline BRCA1 Frameshift Mutations Associated with Isolated Diminished Ovarian Reserve.
13. Postzygotic mosaicism of SMARCB1 variants in patients with rhabdoid tumors: A not-so-rare condition exposing to successive tumors.
14. Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Paris, France, November 16th 2022.
15. Medulloblastomas with ELP1 pathogenic variants: a weakly penetrant syndrome with a restricted spectrum in a limited age window
16. Long-Term Weight Gain in Children with Craniopharyngioma
17. Immunohistochemistry as a tool to identify ELP1-associated medulloblastoma
18. Medulloblastomas with ELP1 pathogenic variants: A weakly penetrant syndrome with a restricted spectrum in a limited age window
19. Family history of cancer and the risk of childhood brain tumors : a pooled analysis of the ESCALE and ESTELLE studies (SFCE)
20. Traitement des douleurs de mucite : actualités et perspectives
21. Les auteurs
22. Family history of cancer and the risk of childhood brain tumors: a pooled analysis of the ESCALE and ESTELLE studies (SFCE)
23. Parental smoking, maternal alcohol, coffee and tea consumption and the risk of childhood brain tumours : the ESTELLE and ESCALE studies (SFCE, France)
24. Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiency
25. Imaging features to distinguish posterior fossa ependymoma subgroups
26. Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiency.
27. ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management
28. Chapitre 20. Les tumeurs cérébrales chez l’enfant
29. Assessment of Puberty and Hypothalamic–Pituitary–Gonadal Axis Function After Childhood Brain Tumor Treatment
30. GH and Childhood-onset Craniopharyngioma: When to Initiate GH Replacement Therapy?
31. Maternal residential pesticide use during pregnancy and risk of malignant childhood brain tumors: A pooled analysis of the ESCALE and ESTELLE studies (SFCE)
32. GH and Childhood-onset Craniopharyngioma: When to Initiate GH Replacement Therapy?
33. Cancer risk and tumour spectrum in 172 patients with a germlineSUFUpathogenic variation: a collaborative study of the SIOPE Host Genome Working Group
34. MEDB-84. The French experience of ELP1-related medulloblastomas
35. High Prevalence of Early Endocrine Disorders After Childhood Brain Tumors in a Large Cohort
36. EPCO-03. GLIOMA ONCOGENESIS IN THE CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY (CMMRD) SYNDROME
37. Pediatric brain tumors as a developmental disease
38. Additional file 16 of Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions
39. Additional file 8 of Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions
40. Additional file 7 of Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions
41. Additional file 6 of Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions
42. Additional file 5 of Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions
43. A novel case of cribriform neuroepithelial tumor: A potential diagnostic pitfall in the ventricular system
44. Clinical and molecular analysis of smoothened inhibitors in Sonic Hedgehog medulloblastoma
45. Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5
46. Prognostic Clinical and Biologic Features for Overall Survival after Relapse in Childhood Medulloblastoma
47. MBCL-02. ROLE OF PREOPERATIVE CHEMOTHERAPY IN METASTATIC MEDULLOBLASTOMA: A COMPARATIVE STUDY IN 92 CHILDREN
48. RARE-21. CANCER SPECTRUM IN GERMLINE SUFU MUTATION CARRIERS: A COLLABORATIVE PROJECT OF THE SIOPE HOST GENOME WORKING GROUP
49. Role of neoadjuvant chemotherapy in metastatic medulloblastoma: a comparative study in 92 children
50. Constitutional mismatch repair deficiency-associated brain tumors: Report from the European C4CMMRD consortium
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