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1. Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWP

2. Indeterminate DC histiocytosis is distinct from LCH and often associated with other hematopoietic neoplasms

3. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition

4. A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome

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

6. Lineage switching of the cellular distribution of BRAFV600E in multisystem Langerhans cell histiocytosis

9. ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

11. Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect

13. High frequency of clonal hematopoiesis in Erdheim-Chester disease

15. Somatic genetic rescue of a germline ribosome assembly defect

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

17. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition

18. Validation of Liquid Chromatography Coupled with Tandem Mass Spectrometry for the Determination of 12 Tyrosine Kinase Inhibitors (TKIs) and Their Application to Therapeutic Drug Monitoring in Adult and Pediatric Populations

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

21. P1058: CHILDHOOD-ONSET ERDHEIM-CHESTER DISEASE IN THE MOLECULAR ERA: CLINICAL PHENOTYPE AND LONG-TERM OUTCOME OF 21 PATIENTS

23. Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study

24. Childhood-onset Erdheim-Chester Disease in the molecular era: clinical phenotype and long-term outcome of 21 patients

25. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages

27. Validation of Liquid Chromatography Coupled with Tandem Mass Spectrometry for the Determination of 12 Tyrosine Kinase Inhibitors (TKIs) and Their Application to Therapeutic Drug Monitoring in Adult and Pediatric Populations.

28. Somatic genetic alterations predict hematological progression in GATA2 deficiency

29. Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation

30. Severe chronic primary neutropenia in adults: report on a series of 108 patients

32. Molecular and clinicopathologic characterization of pediatric histiocytoses

36. Oral SGLT2 Inhibitors in Glycogen Storage Disease Type Ib and G6PC3-Deficiency. Preliminary Results from an Off-Label Study of 21 Patients

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

38. Association of both Langerhans cell histiocytosis and Erdheim-Chester disease linked to the BRAFV600E mutation

39. Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis

43. Lineage-switching of the cellular distribution of BRAFV600E in multisystem Langerhans cell histiocytosis

46. High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia

47. Molecular and clinicopathologic characterization of pediatric histiocytoses.

48. ALK-positive histiocytosis:a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

49. ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

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