Suchergebnisse - "Bury, Loredana"

PubPharm (66)

1

Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework

enthalten in: Journal of thrombosis and haemostasis : JTH | 2024

von Ross, J. | Mohan, S. | Zhang, J. | +20

2

Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool - LABoratory tests substudy) : communication from the Platelet Physiology ISTH-SSC

enthalten in: Research and practice in thrombosis and haemostasis | 2024

von Gresele, P. | Falcinelli, E. | Bury, L. | +14

3

Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders : Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617

enthalten in: Journal of thrombosis and haemostasis : JTH | 2023

von Megy, K. | Downes, K. | Morel-Kopp, M. | +13

ErratumFor: J Thromb Haemost. 2021 Oct;19(10):2612-2617. - PMID 34355501

4

Usefulness of global tests of primary hemostasis in the initial screening of mild/moderate bleeding disorders for orienting towards von Willebrand disease or inherited platelet functions disorders

enthalten in: Thrombosis research | 2023

von Baccolo, A. | Falcinelli, E. | Mezzasoma, A. | +4

5

Platelet dysfunction in platelet-type von Willebrand disease due to the constitutive triggering of the Lyn-PECAM1 inhibitory pathway

enthalten in: Haematologica | 2022

von Bury, L. | Falcinelli, E. | Mezzasoma, A. | +3

6

Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation

enthalten in: Haematologica | 2022

von Purgatorio, G. | Piselli, E. | Guglielmini, G. | +8

7

A p.Arg127Gln variant in GPIbα LRR5 allosterically enhances affinity for VWF : a novel form of platelet-type VWD

enthalten in: Blood advances | 2022

von Bury, L. | Falcinelli, E. | Kuchi Bhotla, H. | +6

8

F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes

enthalten in: Journal of thrombosis and haemostasis : JTH | 2022

von Branchini, A. | Morfini, M. | Lunghi, B. | +26

9

F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes

enthalten in: Journal of Thrombosis and Haemostasis | 2022

von Branchini, A. | Morfini, M. | Lunghi, B. | +12

10

Expanding the genetic spectrum of TUBB1-related thrombocytopenia

enthalten in: Blood advances | 2021

von Palma-Barqueros, V. | Bury, L. | Kunishima, S. | +17

ErratumIn: Blood Adv. 2023 Mar 28;7(6):877. - PMID 36920438

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