Suchergebnisse - "Rey, Gaëlle"

PubPharm (10)

1

Allogeneic hematopoietic stem cell transplantation for adults with therapy-related acute myeloid leukaemia : a retrospective multicentre study on behalf of the SFGM-TC

enthalten in: Bone marrow transplantation | 2023

von Rey, G. | Daguenet, E. | Bonjean, P. | +27

2

Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Therapy-Related Acute Myeloid Leukemia: a Retrospective Multicentre Study on behalf of the SFGM-TC

enthalten in: ResearchSquare.com | 2023

von Tavernier, E. | Rey, G. | Daguenet, E. | +27

3

Late relapse after hematopoietic stem cell transplantation for acute leukemia : a retrospective study by SFGM-TC

enthalten in: Transplantation and cellular therapy | 2023

von Kaphan, E. | Bettega, F. | Forcade, E. | +38

4

New drug approval : Asciminib for the treatment of adult patients with Ph+ CML previously treated with two or more tyrosine kinase inhibitors

enthalten in: Bulletin du cancer | 2023

von Rey, G. | Rousselot, P.

5

Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing : A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants

enthalten in: Molecular diagnosis & therapy | 2022

von Janin, A. | Perouse de Montclos, T. | Nguyen, K. | +12

6

Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants

enthalten in: Molecular diagnosis & therapy | 2022

von Janin, A. | Perouse de Montclos, T. | Nguyen, K. | +12

7

Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants

enthalten in: Molecular diagnosis & therapy | 2022

von Janin, A. | Perouse de Montclos, T. | Nguyen, K. | +12

8

Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants

enthalten in: Molecular diagnosis & therapy | 2022

von Janin, A. | Perouse de Montclos, T. | Nguyen, K. | +12

9

A novel synonymous variant in exon 1 of GNAS gene results in a cryptic splice site and causes pseudohypoparathyroidism type 1A and pseudo-pseudohypoparathyroidism in a French family

enthalten in: Bone reports | 2021

von Apetrei, A. | Molin, A. | Gruchy, N. | +6

10

Bee Cluster 3D: A system to monitor the temperature in a hive over time

enthalten in: arXiv.org | 2021

von Besson, O. | Mugnier, H. | Neveux, A. | +2

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