Detalhe da pesquisa
1.
Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding.
Platelets
; 30(1): 56-65, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30520671
2.
Antiplatelet drugs block platelet activation by VITT patient serum.
Blood
; 138(25): 2733-2740, 2021 12 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34375398
3.
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay.
Blood
; 123(8): e11-22, 2014 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24408324
4.
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects.
Haematologica
; 101(10): 1170-1179, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27479822
5.
Mutation in GNE is associated with severe congenital thrombocytopenia.
Blood
; 132(17): 1855-1858, 2018 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29941673
6.
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects.
Blood
; 122(25): 4090-3, 2013 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24100448
7.
High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders.
Haematologica
; 105(3): e124-e128, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31221775
8.
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?
Br J Haematol
; 165(2): 193-203, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24479992
9.
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel.
Blood
; 120(25): 5041-9, 2012 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-23002116
10.
Comprehensive functional characterization of a novel ANO6 variant in a new patient with Scott syndrome.
J Thromb Haemost
; 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38492852
11.
Health-related quality of life following valoctocogene roxaparvovec gene therapy for severe hemophilia A in the phase 3 trial GENEr8-1.
J Thromb Haemost
; 21(12): 3450-3462, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37678546
12.
Analysis of preplatelets and their barbell platelet derivatives by imaging flow cytometry.
Blood Adv
; 6(9): 2932-2946, 2022 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35042240
13.
Anti-platelet factor 4 immunoglobulin G levels in vaccine-induced immune thrombocytopenia and thrombosis: Persistent positivity through 7 months.
Res Pract Thromb Haemost
; 6(3): e12707, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35515079
14.
ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?St. Anne's College, Oxford, 6-9th September 2016.
Platelets
; 27(8): 719-721, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27841701
15.
Management of surgery, menorrhagia and child-birth for patients with unclassified bleeding disorders: a systematic review of cohort studies.
Blood Coagul Fibrinolysis
; 32(6): 366-372, 2021 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33973892
16.
A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia.
Res Pract Thromb Haemost
; 2(4): 640-652, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30349881
17.
Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome and evaluation of dosing regimens.
Blood Adv
; 1(15): 1159-1166, 2017 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29296757
18.
Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.
Thromb Haemost
; 113(4): 826-37, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25567036
19.
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.
J Clin Invest
; 125(9): 3600-5, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26280575
20.
Kikuchi-Fujimoto disease: a rare but important differential diagnosis for lymphadenopathy.
BMJ Case Rep
; 20142014 Sep 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25199195