Suchergebnisse - "Raffoux, Emmanuel"

PubPharm (276)

1

Germline CHEK2 mutations in patients with myeloid neoplasms

enthalten in: Leukemia | 2024

von Freiman, L. | Larcher, L. | Tueur, G. | +10

2

Blinatumomab Consolidation for Adult B-Cell Acute Lymphoblastic Leukemia in First and Second Complete Remission

enthalten in: Blood advances | 2024

von Urbino, I. | Lengliné, E. | Rabian, F. | +13

3

Comparative clinical and molecular landscape of primary and secondary myelofibrosis : Superior performance of MIPSS70+ v2.0 over MYSEC-PM

enthalten in: American journal of hematology | 2024

von Guerra, M. | Pasquer, H. | Daltro de Oliveira, R. | +14

4

Nilotinib with or without cytarabine for Philadelphia positive acute lymphoblastic leukemia

enthalten in: Blood | 2024

von Chalandon, Y. | Rousselot, P. | Chevret, S. | +27

5

Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification

enthalten in: Leukemia | 2024

von Pasquer, H. | Daltro de Oliveira, R. | Vasseur, L. | +20

6

Hypomethylating agent monotherapy in core binding factor acute myeloid leukemia : a French multicentric retrospective study

enthalten in: Annals of hematology | 2024

von Gabellier, L. | Peterlin, P. | Thepot, S. | +16

7

Tyrosine Kinase Inhibitor Discontinuation in Chronic Myeloid Leukemia : Strategies to Optimize Success and New Directions

enthalten in: Current hematologic malignancy reports | 2024

von Rea, D. | Fodil, S. | Lengline, E. | +2

8

Life-threatening complications and intensive care unit management in patients treated with blinatumomab for B-cell acute lymphoblastic leukemia

enthalten in: Critical care (London, England) | 2024

von Urbino, I. | Lengliné, E. | Valade, S. | +6

9

Genetic alterations and MRD refine risk assessment for KMT2A-rearranged B-cell precursor ALL in adults : a GRAALL study

enthalten in: Blood | 2023

von Kim, R. | Bergugnat, H. | Pastoret, C. | +29

CommentIn: Blood. 2023 Nov 23;142(21):1764-1766. - PMID 37995105

10

Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis

enthalten in: Haematologica | 2023

von Delamare, M. | Le Roy, A. | Pacault, M. | +63

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[28]