Suchergebnisse - "Favier, Remi"

PubPharm (148)

41

Eltrombopag to Treat Thrombocytopenia During Last Month of Pregnancy in a Woman With MYH9-Related Disease : A Case Report

enthalten in: A&A practice | 2018

von Favier, R. | De Carne, C. | Elefant, E. | +3

42

Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

enthalten in: Circulation | 2017

von Hadinnapola, C. | Bleda, M. | Haimel, M. | +141

CommentIn: Circulation. 2017 Nov 21;136(21):2034-2036. - PMID 29158214

43

ACTN1-related Macrothrombocytopenia : A Novel Entity in the Progressing Field of Pediatric Thrombocytopenia

enthalten in: Journal of pediatric hematology/oncology | 2017

von Boutroux, H. | David, B. | Guéguen, P. | +4

44

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

enthalten in: Haematologica | 2017

von Orsini, S. | Noris, P. | Bury, L. | +34

45

Acquired TET2 mutation in one patient with familial platelet disorder with predisposition to AML led to the development of pre-leukaemic clone resulting in T2-ALL and AML-M0

enthalten in: Journal of cellular and molecular medicine | 2017

von Manchev, V. | Bouzid, H. | Antony-Debré, I. | +13

46

Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors

enthalten in: Haematologica | 2017

von Poggi, M. | Canault, M. | Favier, M. | +24

47

Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

enthalten in: American journal of human genetics | 2017

von Arno, G. | Carss, K. | Hull, S. | +114

48

Identification of MPL R102P Mutation in Hereditary Thrombocytosis

enthalten in: Frontiers in endocrinology | 2017

von Bellanné-Chantelot, C. | Mosca, M. | Marty, C. | +3

49

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

enthalten in: American journal of human genetics | 2017

von Carss, K. | Arno, G. | Erwood, M. | +135

50

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

enthalten in: American journal of human genetics | 2017

von Carss, K. | Arno, G. | Erwood, M. | +98