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151. Epidemiologic study on survival of chronic myeloid leukemia and Ph+ acute lymphoblastic leukemia patients with BCR-ABL T315I mutation

152. TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs)

153. Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis

159. Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

160. The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

161. Transcriptomic and genomic heterogeneity in blastic plasmacytoid dendritic cell neoplasms: from ontogeny to oncogenesis.

164. Chromothripsis and Genomic Complexity As Pejorative Prognostic Markers in Pediatric and Adult T-ALL

165. Somatic Mutations and DNA Hypermethylation at Enhancers and Promoters Identify Distinct Subtypes within Lower-Risk Myelodysplastic Syndromes

166. Involvement of the JAK-STAT Pathway in the Molecular Landscape of Fusion-Free Myeloid Neoplasms with Eosinophilia

167. Venetoclax in Combination with Intermediate Doses of Cytarabine in Consolidation Phase for Acute Myeloid Leukemia Patients in First Complete Remission; Results of the Part 1 of the Phase 1/2 Multicentric Covenidac Study

169. Current Results of Intensive Therapy in Younger Adults with Acute Myeloid Leukemia (AML): The Large Randomized French Backbone Intergroup (BIG)-1 Study on Behalf of the Filo, ALFA, and SFGM-TC Study Groups

173. Imatinib plus peginterferon alfa-2a in chronic myeloid leukemia

174. MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome

176. Fractionated gemtuzumab ozogamicin and standard dose cytarabine produced prolonged second remissions in patients over the age of 55 years with acute myeloid leukemia in late first relapse

177. Prognostic impact of RUNX1mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group

178. Genetic identification of patients with AML older than 60 years achieving long-term survival with intensive chemotherapy

179. Optical genome mapping, a promising alternative to gold standard cytogenetic approaches in a series of acute lymphoblastic leukemias

180. Characterisation of Asp669Tyr Piezo1 cation channel activity in red blood cells: an unexpected phenotype

181. The Impact of DNMT3A Status on NPM1 MRD Predictive Value and Survival in Elderly AML Patients Treated Intensively

183. Hereditary Predisposition to Acute Myeloid Leukemia in Older Adults

185. Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia

186. Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia

187. Biomarkers of Gemtuzumab Ozogamicin Response for Acute Myeloid Leukemia Treatment

188. Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients

191. Prognostic significance of concurrent gene mutations in intensively treated patients with IDH-mutated AML, an ALFA study

192. Minimal residual disease monitoring in acute myeloid leukemia with non-A/B/D-NPM1 mutations by digital polymerase chain reaction: feasibility and clinical use

193. The Folate Cycle Enzyme MTHFR Is a Critical Regulator of Cell Response to MYC-Targeting Therapies

194. Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia

195. Outcome of older patients with acute myeloid leukemia in first relapse

197. Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia

198. Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2and DDX41

200. Impact of DNMT3a Status on Post Induction NPM1 MRD Predictive Value on Survival in Elderly AML Patients Treated Intensively

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