Combined effects of two mutations in von Willebrand disease 2M phenotype-Reference-Cited by-同舟云学术

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Combined effects of two mutations in von Willebrand disease 2M phenotype

Published:2017-12-20 Issue:1 Volume:2 Page:162-167
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Res Pract Thromb Haemost

Author:

Woods Adriana I.¹,Paiva Juvenal²,Kempfer Ana C.¹,Primrose Debora M.³,Blanco Alicia N.²,Sanchez-Luceros Analía¹²,Lazzari María A.¹

Affiliation:

1. Laboratorio de Hemostasia y Trombosis; IMEX-CONICET-Academia Nacional de Medicina; Buenos Aires Argentina

2. Departamento de Hemostasia y Trombosis; Instituto de Investigaciones Hematológicas; Academia Nacional de Medicina; Buenos Aires Argentina

3. Facultad de Agronomía y Ciencias Agroalimentarias; Universidad de Morón; Buenos Aires Argentina

Funder

Consejo Nacional de Investigaciones Científicas y Técnicas

Fundación René Barón

Academia Nacional de Medicina

Publisher

Wiley

Subject

Hematology

Reference25 articles.

1. VWF collagen (types III and VI)-binding defects in a cohort of type 2M VWD patients - a strategy for improvement of a challenging diagnosis;Fidalgo;Haemophilia,2017

2. Clinical and laboratory phenotype variability in type 2M von Willebrand disease;Doruelo;J Thromb Haemost,2017

3. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders;Rodeghiero;J Thromb Haemost,2010

4. A simple visual assessment technique to discriminate between menorrhagia and normal menstrual blood loss;Janssen;Obstet Gynecol,1995

5. The partial thromboplastin time with kaolin. A simple screening test for first stage plasma clotting factor deficiencies;Proctor;Am J Clin Pathol,1961

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Type 2A and 2M von Willebrand Disease: Differences in Phenotypic Parameters According to the Affected Domain by Disease-Causing Variants and Assessment of Pathophysiological Mechanisms;Seminars in Thrombosis and Hemostasis;2021-06-15

2. Genetic variants of VWF gene in type 2 von Willebrand disease;Haemophilia;2019-02-28

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