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351 results on '"Fenneteau, Odile"'

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1. Plasmodium ovale spp dhfr mutations associated with reduced susceptibility to pyrimethamine in sub-Saharan Africa: a retrospective genetic epidemiology and functional study

2. Childhood Langerhans cell histiocytosis hematological involvement: severity associated with BRAFV600E loads

4. Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia

5. Plasmodium ovale spp dhfr mutations associated with reduced susceptibility to pyrimethamine in sub-Saharan Africa: a retrospective genetic epidemiology and functional study

8. Genome-edited, donor-derived allogeneic anti-CD19 chimeric antigen receptor T cells in paediatric and adult B-cell acute lymphoblastic leukaemia: results of two phase 1 studies

10. Despite mutation acquisition in hematopoietic stem cells, JMML-propagating cells are not always restricted to this compartment

11. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome

12. Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome

16. CD36 cell surface expression as a surrogate marker to identify ABL/JAK-class kinase fusions in pediatric BCP-ALL

17. Relevance of Howell‐Jolly body counts for measuring spleen function in sickle cell disease

19. The Morphologic Spectrum of Myelokathexis in WHIM Syndrome and Germline CXCR4 Variants: New Insights into Cellular Changes in the Bone Marrow and Peripheral Blood

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

24. GATA-1 Defects in Diamond-Blackfan Anemia : Phenotypic Characterization Points to a Specific Subset of Disease

25. Perls' Stain Guidelines from the French-Speaking Cellular Hematology Group (GFHC).

26. GATA-1 Defects in Diamond–Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

33. Two Distinct Fetal-Type Signatures Caracterise Juvenile Myelomonocytic Leukemia

36. Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity

38. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

39. Juvenile myelomonocytic leukaemia and Noonan syndrome

40. Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis

42. Leukaemic transformation in a 10‐year‐old girl with SRP54 congenital neutropenia.

43. Platelet Morphology Analysis

44. Case Report: Targeting 2 Antigens as a Promising Strategy in Mixed Phenotype Acute Leukemia: Combination of Blinatumomab With Gemtuzumab Ozogamicin in an Infant With a KMT2A-Rearranged Leukemia

49. JMML Fetal Identity Results Either from Retention of a Physiologic Signature or Aberrant Activation of Master Oncofetal Regulators

50. How Many Patients Have Congenital Neutropenia? a Population-Based Estimation from the Nationwide French Severe Chronic Neutropenia Registry

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