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1.

Screening for von Willebrand disease does not impact posttonsillectomy bleeding in a low-risk population.

Digiandomenico, Stefanie; Conley, Stephen F; Johnson, Victoria P; Christopherson, Pamela A; Haberichter, Sandra L; Zhang, Jian; Simpson, Pippa; Abshire, Thomas C; Montgomery, Robert R; Flood, Veronica H.

Pediatr Blood Cancer ; 68(12): e29371, 2021 12.

Artículo en Inglés | MEDLINE | ID: mdl-34606172

2.

The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease.

Flood, Veronica H; Garcia, Jessica; Haberichter, Sandra L.

Curr Opin Hematol ; 26(5): 331-335, 2019 09.

Artículo en Inglés | MEDLINE | ID: mdl-31261173

3.

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.

Flood, Veronica H; Christopherson, Pamela A; Gill, Joan Cox; Friedman, Kenneth D; Haberichter, Sandra L; Bellissimo, Daniel B; Udani, Rupa A; Dasgupta, Mahua; Hoffmann, Raymond G; Ragni, Margaret V; Shapiro, Amy D; Lusher, Jeanne M; Lentz, Steven R; Abshire, Thomas C; Leissinger, Cindy; Hoots, W Keith; Manco-Johnson, Marilyn J; Gruppo, Ralph A; Boggio, Lisa N; Montgomery, Kate T; Goodeve, Anne C; James, Paula D; Lillicrap, David; Peake, Ian R; Montgomery, Robert R.

Blood ; 127(20): 2481-8, 2016 05 19.

Artículo en Inglés | MEDLINE | ID: mdl-26862110

4.

von Willebrand factor propeptide: biology and clinical utility.

Haberichter, Sandra L.

Blood ; 126(15): 1753-61, 2015 Oct 08.

Artículo en Inglés | MEDLINE | ID: mdl-26215113

5.

VWF propeptide in defining VWD subtypes.

Haberichter, Sandra L.

Blood ; 125(19): 2882-3, 2015 May 07.

Artículo en Inglés | MEDLINE | ID: mdl-25953977

6.

Crucial role for the VWF A1 domain in binding to type IV collagen.

Flood, Veronica H; Schlauderaff, Abraham C; Haberichter, Sandra L; Slobodianuk, Tricia L; Jacobi, Paula M; Bellissimo, Daniel B; Christopherson, Pamela A; Friedman, Kenneth D; Gill, Joan Cox; Hoffmann, Raymond G; Montgomery, Robert R.

Blood ; 125(14): 2297-304, 2015 Apr 02.

Artículo en Inglés | MEDLINE | ID: mdl-25662333

7.

Allosteric activation of ADAMTS13 by von Willebrand factor.

Muia, Joshua; Zhu, Jian; Gupta, Garima; Haberichter, Sandra L; Friedman, Kenneth D; Feys, Hendrik B; Deforche, Louis; Vanhoorelbeke, Karen; Westfield, Lisa A; Roth, Robyn; Tolia, Niraj Harish; Heuser, John E; Sadler, J Evan.

Proc Natl Acad Sci U S A ; 111(52): 18584-9, 2014 Dec 30.

Artículo en Inglés | MEDLINE | ID: mdl-25512528

8.

G protein-dependent basal and evoked endothelial cell vWF secretion.

Rusu, Luiza; Andreeva, Alexandra; Visintine, David J; Kim, Kyungho; Vogel, Stephen M; Stojanovic-Terpo, Aleksandra; Chernaya, Olga; Liu, Guoquan; Bakhshi, Farnaz R; Haberichter, Sandra L; Iwanari, Hiroko; Kusano-Arai, Osamu; Suzuki, Nobuchika; Hamakubo, Takao; Kozasa, Tohru; Cho, Jaehyung; Du, Xiaoping; Minshall, Richard D.

Blood ; 123(3): 442-50, 2014 Jan 16.

Artículo en Inglés | MEDLINE | ID: mdl-24081657

9.

No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation.

Flood, Veronica H; Friedman, Kenneth D; Gill, Joan Cox; Haberichter, Sandra L; Christopherson, Pamela A; Branchford, Brian R; Hoffmann, Raymond G; Abshire, Thomas C; Dunn, Amy L; Di Paola, Jorge A; Hoots, W Keith; Brown, Deborah L; Leissinger, Cindy; Lusher, Jeanne M; Ragni, Margaret V; Shapiro, Amy D; Montgomery, Robert R.

Blood ; 121(18): 3742-4, 2013 May 02.

Artículo en Inglés | MEDLINE | ID: mdl-23520336

10.

The B subunits of Shiga-like toxins induce regulated VWF secretion in a phospholipase D1-dependent manner.

Huang, Jing; Haberichter, Sandra L; Sadler, J Evan.

Blood ; 120(5): 1143-9, 2012 Aug 02.

Artículo en Inglés | MEDLINE | ID: mdl-22718838

11.

Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storage.

Jacobi, Paula M; Gill, Joan Cox; Flood, Veronica H; Jakab, David A; Friedman, Kenneth D; Haberichter, Sandra L.

Blood ; 119(19): 4543-53, 2012 May 10.

Artículo en Inglés | MEDLINE | ID: mdl-22431572

12.

VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

Bellissimo, Daniel B; Christopherson, Pamela A; Flood, Veronica H; Gill, Joan Cox; Friedman, Kenneth D; Haberichter, Sandra L; Shapiro, Amy D; Abshire, Thomas C; Leissinger, Cindy; Hoots, W Keith; Lusher, Jeanne M; Ragni, Margaret V; Montgomery, Robert R.

Blood ; 119(9): 2135-40, 2012 Mar 01.

Artículo en Inglés | MEDLINE | ID: mdl-22197721

13.

The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change.

Christopherson, Pamela A; Tijet, Nathalie; Haberichter, Sandra L; Flood, Veronica H; Ross, Justyne; Notley, Colleen; Rawley, Orla; Montgomery, Robert R; James, Paula D; Lillicrap, David.

J Thromb Haemost ; 22(3): 666-675, 2024 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-38040335

14.

Distinguishing ASH Clinical Practice Guidelines from Other Forms of ASH Clinical Advice.

Cuker, Adam; Kunkle, Robert; Bercovitz, Rachel Sara; Byrne, Michael T; Djulbegovic, Benjamin; Haberichter, Sandra L; Holter-Chakrabarty, Jennifer; Lottenberg, Richard; Pai, Menaka; Rezende, Suely Meireles; Seftel, Matthew D; Silverstein, Roy L; Terrell, Deirdra R; Cheung, Matthew C.

Blood Adv ; 2024 Apr 09.

Artículo en Inglés | MEDLINE | ID: mdl-38593461

15.

Collagen binding provides a sensitive screen for variant von Willebrand disease.

Flood, Veronica H; Gill, Joan Cox; Friedman, Kenneth D; Christopherson, Pamela A; Jacobi, Paula M; Hoffmann, Raymond G; Montgomery, Robert R; Haberichter, Sandra L.

Clin Chem ; 59(4): 684-91, 2013 Apr.

Artículo en Inglés | 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.

Flood, Veronica H; Gill, Joan Cox; Morateck, Patricia A; Christopherson, Pamela A; Friedman, Kenneth D; Haberichter, Sandra L; Hoffmann, Raymond G; Montgomery, Robert R.

Blood ; 117(6): e67-74, 2011 Feb 10.

Artículo en Inglés | MEDLINE | ID: mdl-21148813

17.

Enhanced VWF clearance in low VWF pathogenesis: limitations of the VWFpp/VWF:Ag ratio and clinical significance.

Doherty, Dearbhla; Byrne, Mary; Nolan, Margaret; O'Sullivan, Jamie M; Ryan, Kevin; O'Connell, Niamh M; Haberichter, Sandra L; Christopherson, Pamela A; Di Paola, Jorge; James, Paula D; O'Donnell, James S.

Blood Adv ; 7(3): 302-308, 2023 02 14.

Artículo en Inglés | 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.

Sadler, Brooke; Christopherson, Pamela A; Perry, Crystal L; Bellissimo, Daniel B; Haberichter, Sandra L; Haller, Gabe; Antunes, Lilian; Flood, Veronica H; Di Paola, Jorge; Montgomery, Robert R.

Res Pract Thromb Haemost ; 7(7): 102232, 2023 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-38077814

19.

The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.

Haberichter, Sandra L; Budde, Ulrich; Obser, Tobias; Schneppenheim, Sonja; Wermes, Cornelia; Schneppenheim, Reinhard.

Blood ; 115(22): 4580-7, 2010 Jun 03.

Artículo en Inglés | MEDLINE | ID: mdl-20335223

20.

Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor.

Flood, Veronica H; Gill, Joan Cox; Morateck, Patricia A; Christopherson, Pamela A; Friedman, Kenneth D; Haberichter, Sandra L; Branchford, Brian R; Hoffmann, Raymond G; Abshire, Thomas C; Di Paola, Jorge A; Hoots, W Keith; Leissinger, Cindy; Lusher, Jeanne M; Ragni, Margaret V; Shapiro, Amy D; Montgomery, Robert R.

Blood ; 116(2): 280-6, 2010 Jul 15.

Artículo en Inglés | MEDLINE | ID: mdl-20231421

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