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137 results on '"Brouzes, Chantal"'

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1. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

2. Immunopathologie de l’intestin grêle

4. Comprehensive genetic profiling reveals frequent alterations of driver genes on the X chromosome in extranodal NK/T-cell lymphoma

5. KIR3DL2 contributes to the typing of acute adult T-cell leukemia and is a potential therapeutic target

6. Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial

7. Optical genome mapping refines cytogenetic diagnostics, prognostic stratification and provides new molecular insights in adult MDS/AML patients

8. Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia

9. Bone Marrow

10. A novel pediatric polycystic lung disease caused by CCR2 deficiency

11. P1166: BRIGATINIB IN PATIENTS WITH ALK-POSITIVE ANAPLASTIC LARGE CELL LYMPHOMA WHO HAVE FAILED BRENTUXIMAB VEDOTIN

12. Bone Marrow

13. X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

14. Frequent Alterations of Driver Genes in Chromosome X and Their Clinical Relevance in Extranodal NK/T-Cell Lymphoma

15. Perls’ Stain Guidelines from the French-Speaking Cellular Hematology Group (GFHC)

16. The Eatl-001 Trial: Results of a Phase 2 Study of Brentuximab Vedotin and CHP Followed By Consolidation with High-Dose Therapy - Autologous Stem-Cell Transplantation (HDT-ASCT) in the Frontline Treatment of Patients with Enteropathy-Associated T-Cell Lymphoma

17. Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia

18. Peripheral blood 8 colour flow cytometry monitoring of hairy cell leukaemia allows detection of high-risk patients

21. Occurrence of myelodysplastic syndrome in 2 patients with reticular dysgenesis

22. Standardization of Flow Cytometric Immunophenotyping for Hematological Malignancies: The FranceFlow Group Experience

23. GDF15 and Erythroferrone Mark Erythropoietic Response to ACE-011 (Sotatercept) in Thalassemia

25. Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study

26. Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study

28. Type I interferon-mediated autoinflammation due to DNase II deficiency

29. The First Two Years of Life in Sickle Cell Anemia Infants: Results of a Comprehensive Longitudinal Study

32. Midostaurin in Advanced Systemic Mastocytosis

33. A French National Survey on Clotting Disorders in Mastocytosis

35. Adult T-Cell Leukemia/Lymphoma in a Caucasian Patient After Sexual Transmission of Human T-Cell Lymphotropic Virus Type 1

36. BRAFV600E Mutation in a Histiocytic Sarcoma Arising From Hairy Cell Leukemia

37. Treatment of Advanced Systemic Mastocytosis with PKC412: The French Compassionate Use Programme Experience and Historical Comparison

38. Peripheral blood 8 colour flow cytometry monitoring of hairy cell leukaemia allows detection of high‐risk patients

42. Methodological aspects of minimal residual disease assessment by flow cytometry in acute lymphoblastic leukemia: A french multicenter study.

44. Deciphering leukemic B-cell chronic lymphoproliferative disorders

46. KIR3DL2 contributes to the typing of acute-type adult T-cell leukemia and is a potential therapeutic target.

47. Treatment of Advanced Systemic Mastocytosis with PKC412: The French Compassionate Use Programme Experience and Historical Comparison

48. Type I interferon-mediated autoinflammation due to DNase II deficiency

49. Hepatosplenic T-cell lymphoma displays an original oyster-shell cytological pattern and a genomic profile distinct from that of γδ T-cell large granular lymphocytic leukemia.

50. [Anemia in adult and child].

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