Literature DB >> 28476066

Angiodysplasia in von Willebrand Disease: Understanding the Clinical and Basic Science.

Soundarya Selvam1, Paula James1,2.   

Abstract

Severe and intractable gastrointestinal bleeding caused by angiodysplasia is a debilitating problem for up to 20% of patients with von Willebrand disease (VWD). Currently, the lack of an optimal treatment for this recurrent problem presents an ongoing challenge for many physicians in their management of affected patients. Over the past few years, studies have pointed to a regulatory role for the hemostatic protein, von Willebrand factor (VWF), in angiogenesis, providing a novel target for the modulation of vessel development. This article will review the clinical implications and molecular pathology of angiodysplasia in VWD. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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Year:  2017        PMID: 28476066      PMCID: PMC5949878          DOI: 10.1055/s-0037-1599145

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  100 in total

1.  Increased expression of angiogenic factors in human colonic angiodysplasia.

Authors:  F Junquera; E Saperas; I de Torres; M T Vidal; J R Malagelada
Journal:  Am J Gastroenterol       Date:  1999-04       Impact factor: 10.864

Review 2.  New model of tumor angiogenesis: dynamic balance between vessel regression and growth mediated by angiopoietins and VEGF.

Authors:  J Holash; S J Wiegand; G D Yancopoulos
Journal:  Oncogene       Date:  1999-09-20       Impact factor: 9.867

3.  Acquired von Willebrand syndrome: data from an international registry.

Authors:  A B Federici; J H Rand; P Bucciarelli; U Budde; P J van Genderen; H Mohri; D Meyer; F Rodeghiero; J E Sadler
Journal:  Thromb Haemost       Date:  2000-08       Impact factor: 5.249

Review 4.  Heyde syndrome: a common diagnosis in older patients with severe aortic stenosis.

Authors:  M W Massyn; S A Khan
Journal:  Age Ageing       Date:  2009-03-10       Impact factor: 10.668

5.  Acquired von Willebrand syndrome in aortic stenosis.

Authors:  André Vincentelli; Sophie Susen; Thierry Le Tourneau; Isabelle Six; Olivier Fabre; Francis Juthier; Anne Bauters; Christophe Decoene; Jenny Goudemand; Alain Prat; Brigitte Jude
Journal:  N Engl J Med       Date:  2003-07-24       Impact factor: 91.245

Review 6.  von Willebrand factor assembly and secretion.

Authors:  J E Sadler
Journal:  J Thromb Haemost       Date:  2009-07       Impact factor: 5.824

Review 7.  Biochemistry and genetics of von Willebrand factor.

Authors:  J E Sadler
Journal:  Annu Rev Biochem       Date:  1998       Impact factor: 23.643

8.  Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor.

Authors:  Grégoire Michaux; Lindsay J Hewlett; Sarah L Messenger; Anne C Goodeve; Ian R Peake; Martina E Daly; Daniel F Cutler
Journal:  Blood       Date:  2003-06-05       Impact factor: 22.113

9.  Acquired von Willebrand's syndrome due to an inhibitor of IgG specific for von Willebrand's factor in polycythemia rubra vera.

Authors:  H Mohri; T Ohkubo
Journal:  Acta Haematol       Date:  1987       Impact factor: 2.195

10.  Immunolocalization of von Willebrand protein in Weibel-Palade bodies of human endothelial cells.

Authors:  D D Wagner; J B Olmsted; V J Marder
Journal:  J Cell Biol       Date:  1982-10       Impact factor: 10.539

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  4 in total

1.  Significant gynecological bleeding in women with low von Willebrand factor levels.

Authors:  Michelle Lavin; Sonia Aguila; Niall Dalton; Margaret Nolan; Mary Byrne; Kevin Ryan; Barry White; Niamh M O'Connell; Jamie M O'Sullivan; Jorge Di Paola; Paula D James; James S O'Donnell
Journal:  Blood Adv       Date:  2018-07-24

2.  Characterization of a Porcine Model for Von Willebrand Disease Type 1 and 3 Regarding Expression of Angiogenic Mediators in the Nonpregnant Female Reproductive Tract.

Authors:  Hanna Allerkamp; Stefanie Lehner; Mahnaz Ekhlasi-Hundrieser; Carsten Detering; Christiane Pfarrer; Mario von Depka Prondzinski
Journal:  Comp Med       Date:  2019-09-16       Impact factor: 0.982

3.  Variability of von Willebrand factor-related parameters in endothelial colony forming cells.

Authors:  Annika de Jong; Ester Weijers; Richard Dirven; Suzan de Boer; Jasmin Streur; Jeroen Eikenboom
Journal:  J Thromb Haemost       Date:  2019-07-22       Impact factor: 5.824

4.  Ex vivo Improvement of a von Willebrand Disease Type 2A Phenotype Using an Allele-Specific Small-Interfering RNA.

Authors:  Annika de Jong; Richard J Dirven; Johan Boender; Ferdows Atiq; Seyed Yahya Anvar; Frank W G Leebeek; Bart J M van Vlijmen; Jeroen Eikenboom
Journal:  Thromb Haemost       Date:  2020-08-15       Impact factor: 5.249

  4 in total

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