Detalhe da pesquisa
1.
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome.
Blood
; 136(17): 1956-1967, 2020 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32693407
2.
Platelet dysfunction in platelet-type von Willebrand disease due to the constitutive triggering of the Lyn-PECAM1 inhibitory pathway.
Haematologica
; 107(7): 1643-1654, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34407603
3.
Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation.
Haematologica
; 107(5): 1072-1085, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233447
4.
Association of Neutrophil Activation, More Than Platelet Activation, With Thrombotic Complications in Coronavirus Disease 2019.
J Infect Dis
; 223(6): 933-944, 2021 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33280009
5.
Long-term treatment with thalidomide for severe recurrent hemorrhage from intestinal angiodysplasia in Glanzmann Thrombasthenia.
Platelets
; 32(2): 288-291, 2021 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32200672
6.
Search for SARS-CoV-2 RNA in platelets from COVID-19 patients.
Platelets
; 32(2): 284-287, 2021 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33349108
7.
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.
Hum Mutat
; 41(1): 277-290, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31562665
8.
Prochemerin cleavage by factor XIa links coagulation and inflammation.
Blood
; 131(3): 353-364, 2018 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29158361
9.
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study.
Haematologica
; 105(7): 1948-1956, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31558677
10.
A novel mechanism regulating human platelet activation by MMP-2-mediated PAR1 biased signaling.
Blood
; 129(7): 883-895, 2017 02 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28034890
11.
Mechanisms of thrombocytopenia in platelet-type von Willebrand disease.
Haematologica
; 104(7): 1473-1481, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30655369
12.
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Blood
; 127(23): 2791-803, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27084890
13.
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.
Haematologica
; 102(7): 1192-1203, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385783
14.
Inherited Platelet Function Disorders: Algorithms for Phenotypic and Genetic Investigation.
Semin Thromb Hemost
; 42(3): 292-305, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26962877
15.
Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia.
Haematologica
; 101(1): 46-56, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26452979
16.
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders.
Br J Haematol
; 170(4): 559-63, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25899604
17.
Of mice and men: genes relevant to thrombosis and bleeding.
Blood
; 132(24): 2532-2534, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30545893
18.
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.
Haematologica
; 99(8): 1387-94, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24763399
19.
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.
Res Pract Thromb Haemost
; 8(1): 102305, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38292347
20.
Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework.
J Thromb Haemost
; 22(3): 645-665, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38016518