Detalhe da pesquisa
1.
Coma in adult cerebral venous thrombosis: The BEAST study.
Eur J Neurol
; : e16311, 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38646961
2.
Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor.
Int J Mol Sci
; 24(18)2023 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37762470
3.
Genome-Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis.
Ann Neurol
; 90(5): 777-788, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459509
4.
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A.
Haemophilia
; 28(2): 270-277, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35182444
5.
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects.
Haematologica
; 104(10): 2084-2090, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30819905
6.
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.
Blood
; 127(23): 2924-33, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27060170
7.
Gene-Gene Interaction Between Factor-XI and ABO Genes in Cerebral Venous Thrombosis: The BEAST Study.
Neurology
; 102(11): e209445, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38759137
8.
Subjective Perception and Psychoacoustic Aspects of the Laryngectomee Voice: The Impact on Quality of Life.
J Pers Med
; 13(3)2023 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36983751
9.
Factor V Leiden but not the factor II 20210G>A mutation is a risk factor for premature coronary artery disease: a case-control study in Iran.
Res Pract Thromb Haemost
; 7(1): 100048, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36798900
10.
Age of onset of cerebral venous thrombosis: the BEAST study.
Eur Stroke J
; 8(1): 344-350, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37021156
11.
The role of serum free light chain as biomarker of Myasthenia Gravis.
Clin Chim Acta
; 528: 29-33, 2022 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35051425
12.
Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis.
PLoS One
; 16(10): e0258675, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662354
13.
Clinical Use of κ Free Light Chains Index as a Screening Test for Multiple Sclerosis.
Lab Med
; 51(4): 402-407, 2020 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31943078
14.
The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians.
J Clin Med
; 9(10)2020 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33096882
15.
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
Mol Immunol
; 45(13): 3536-44, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18586324
16.
Platelet to Lymphocyte Ratio and Neutrophil to Lymphocyte Ratio as Risk Factors for Venous Thrombosis.
Clin Appl Thromb Hemost
; 24(5): 808-814, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29088921
17.
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis.
Thromb Res
; 169: 76-81, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30029070
18.
Angioedema without urticaria: a large clinical survey.
CMAJ
; 175(9): 1065-70, 2006 Oct 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-17060655
19.
Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis.
PLoS One
; 11(3): e0151347, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26982741
20.
Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.
BMJ Open
; 6(11): e012351, 2016 11 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27881526