980 results on '"DONADIEU, Jean"'
Search Results
2. The ouroboros of autoimmunity
3. Indeterminate DC histiocytosis is distinct from LCH and often associated with other hematopoietic neoplasms
4. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
5. A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome
6. Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop
7. OCT2 expression in histiocytoses
8. Childhood Langerhans cell histiocytosis hematological involvement: severity associated with BRAFV600E loads
9. Lineage switching of the cellular distribution of BRAFV600E in multisystem Langerhans cell histiocytosis
10. Eye movement abnormalities in neurodegenerative langerhans cell histiocytosis
11. Stem Cell Transplantation in Patients Affected by Shwachman-Diamond Syndrome: Expert Consensus and Recommendations From the EBMT Severe Aplastic Anaemia Working Party
12. Langerhans cell histiocytosis and associated malignancies: A retrospective analysis of 270 patients
13. Heterozygous variants of CLPB are a cause of severe congenital neutropenia
14. ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition
15. Establishment of MOS-SF36 percentile ranks in the general youth French population
16. Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect
17. Juvenile Xanthogranuloma of the Head and Neck: Imaging Findings in 11 Cases
18. Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell Histiocytosis
19. Histiocytosis
20. CXCR4 signaling controls dendritic cell location and activation at steady state and in inflammation
21. High frequency of clonal hematopoiesis in Erdheim-Chester disease
22. Infectious and digestive complications in glycogen storage disease type Ib: Study of a French cohort
23. Lung Involvement in Destombes-Rosai-Dorfman Disease: Clinical and Radiological Features and Response to the MEK Inhibitor Cobimetinib
24. CXCR4 Antagonist in HPV5-Associated Perianal Squamous-Cell Carcinoma
25. CXCR4 WHIM syndrome is a cancer predisposition condition for virus‐induced malignancies
26. Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for the Treatment of Participants With WHIM Syndrome: Investigational Assessment of Lymphocyte Subpopulations in Peripheral Blood
27. Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance
28. Somatic genetic rescue of a germline ribosome assembly defect
29. Management of Gorham Stout disease with skull-base defects: Case series of six children and literature review
30. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
31. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
32. Childhood pulmonary Langerhans cell histiocytosis: a comprehensive clinical-histopathological and BRAFV600E mutation study from the French national cohort
33. Atteintes ostéoarticulaires au cours des histiocytoses
34. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
35. 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
36. Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome
37. Temporomandibular joint anomalies in pediatric craniofacial Gorham-Stout disease
38. Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease
39. Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia
40. 7 Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for Treatment of Patients With WHIM Syndrome: Preliminary Results From Ongoing Open-Label Extension Period of Continuous Mavorixafor Treatment
41. Lung transplantation as a rescue option in childhood critical pulmonary Langerhans cell histiocytosis
42. Comment on “Subcutaneous administration of cytarabine for pediatric patients with Langerhans cell histiocytosis decreases burden of patient travel and infusion center utilization”
43. P1058: CHILDHOOD-ONSET ERDHEIM-CHESTER DISEASE IN THE MOLECULAR ERA: CLINICAL PHENOTYPE AND LONG-TERM OUTCOME OF 21 PATIENTS
44. How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome
45. Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies
46. Histiocytoses: emerging neoplasia behind inflammation
47. Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study
48. Central nervous system involvement in Erdheim-Chester disease: An observational cohort study
49. Neurohistiocytose langerhansienne
50. Histiocytose langerhansienne de l’enfant
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.