Detalhe da pesquisa
1.
Glanzmann Thrombasthenia 10 Years Later: Progress Made and Future Directions.
Semin Thromb Hemost
; 2024 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38499192
2.
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.
Haematologica
; 108(3): 772-784, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35638551
3.
Platelet glycoprotein VI promotes metastasis through interaction with cancer cell-derived galectin-3.
Blood
; 135(14): 1146-1160, 2020 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32040544
4.
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy.
Haematologica
; 106(2): 337-350, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33147934
5.
A mutation of the human EPHB2 gene leads to a major platelet functional defect.
Blood
; 132(19): 2067-2077, 2018 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30213874
6.
Inherited thrombocytopenias: history, advances and perspectives.
Haematologica
; 105(8): 2004-2019, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32527953
7.
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.
Blood
; 127(23): 2903-14, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26912466
8.
The GPIIb-IIIa defect of platelets in Glanzmann thrombasthenia.
Haematologica
; 108(4): 937-938, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37002607
9.
Personal reflections on the early contributions of Gus Born to platelet research.
Platelets
; : 1-5, 2018 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30183446
10.
Marked bleeding diathesis in patients with platelet dysfunction due to a novel mutation in RASGRP2, encoding CalDAG-GEFI (p.Gly305Asp).
Platelets
; 29(1): 84-86, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28726538
11.
Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors.
Haematologica
; 102(2): 282-294, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27663637
12.
Linkage disequilibrium amongst ITGA2B and ITGB3 gene variants in patients with Glanzmann thrombasthenia confirms that most disease-causing mutations are recent.
Br J Haematol
; 175(4): 686-695, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27469266
13.
Should any genetic defect affecting α-granules in platelets be classified as gray platelet syndrome?
Am J Hematol
; 91(7): 714-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26971401
14.
Expanding the Mutation Spectrum Affecting αIIbß3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort.
Hum Mutat
; 36(5): 548-61, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25728920
15.
Procoagulant platelets form an α-granule protein-covered "cap" on their surface that promotes their attachment to aggregates.
J Biol Chem
; 288(41): 29621-32, 2013 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23995838
16.
Congenital platelet disorders and understanding of platelet function.
Br J Haematol
; 165(2): 165-78, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24286193
17.
Platelet membrane glycoproteins: a historical review.
Semin Thromb Hemost
; 40(5): 577-84, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24967889
18.
Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?
Haematologica
; 104(6): 1103-1105, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152089
19.
Glanzmann thrombasthenia: state of the art and future directions.
Semin Thromb Hemost
; 39(6): 642-55, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23929305
20.
Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models.
Blood
; 118(23): 5996-6005, 2011 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21917754