Detalhe da pesquisa
1.
Screening for von Willebrand disease does not impact posttonsillectomy bleeding in a low-risk population.
Pediatr Blood Cancer
; 68(12): e29371, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34606172
2.
The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease.
Curr Opin Hematol
; 26(5): 331-335, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31261173
3.
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.
Blood
; 127(20): 2481-8, 2016 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-26862110
4.
von Willebrand factor propeptide: biology and clinical utility.
Blood
; 126(15): 1753-61, 2015 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26215113
5.
VWF propeptide in defining VWD subtypes.
Blood
; 125(19): 2882-3, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25953977
6.
Crucial role for the VWF A1 domain in binding to type IV collagen.
Blood
; 125(14): 2297-304, 2015 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25662333
7.
Allosteric activation of ADAMTS13 by von Willebrand factor.
Proc Natl Acad Sci U S A
; 111(52): 18584-9, 2014 Dec 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25512528
8.
G protein-dependent basal and evoked endothelial cell vWF secretion.
Blood
; 123(3): 442-50, 2014 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24081657
9.
No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation.
Blood
; 121(18): 3742-4, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23520336
10.
The B subunits of Shiga-like toxins induce regulated VWF secretion in a phospholipase D1-dependent manner.
Blood
; 120(5): 1143-9, 2012 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718838
11.
Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storage.
Blood
; 119(19): 4543-53, 2012 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22431572
12.
VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.
Blood
; 119(9): 2135-40, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22197721
13.
The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change.
J Thromb Haemost
; 22(3): 666-675, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38040335
14.
Distinguishing ASH Clinical Practice Guidelines from Other Forms of ASH Clinical Advice.
Blood Adv
; 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38593461
15.
Collagen binding provides a sensitive screen for variant von Willebrand disease.
Clin Chem
; 59(4): 684-91, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23340442
16.
Gain-of-function GPIb ELISA assay for VWF activity in the Zimmerman Program for the Molecular and Clinical Biology of VWD.
Blood
; 117(6): e67-74, 2011 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21148813
17.
Enhanced VWF clearance in low VWF pathogenesis: limitations of the VWFpp/VWF:Ag ratio and clinical significance.
Blood Adv
; 7(3): 302-308, 2023 02 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35523118
18.
Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type.
Res Pract Thromb Haemost
; 7(7): 102232, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-38077814
19.
The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.
Blood
; 115(22): 4580-7, 2010 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-20335223
20.
Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor.
Blood
; 116(2): 280-6, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20231421