Risk of perinatal intracranial hemorrhage and role of prenatal genetic testing in individuals with type 3 von Willebrand disease-Reference-Cited by-同舟云学术

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Risk of perinatal intracranial hemorrhage and role of prenatal genetic testing in individuals with type 3 von Willebrand disease

Published:2020-10 Issue:10 Volume:18 Page:2779-2780
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Warad Deepti¹²^ORCID,Ismail Maryama³,Rusk Dawn²,Rodriguez Vilmarie²,Pruthi Rajiv K.¹⁴^ORCID

Affiliation:

1. Special Coagulation Laboratory Division of Hematopathology Mayo Clinic Rochester MinnesotaUSA

2. Division of Pediatric Hematology Oncology Mayo Clinic Rochester MinnesotaUSA

3. Mayo Medical School Mayo Clinic Rochester MinnesotaUSA

4. Division of Hematology Mayo Clinic Rochester MinnesotaUSA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.15000

Reference6 articles.

1. Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study;Tosetto A;J Thromb Haemost,2020

2. Management of Inheritedvon Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients

3. Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease

4. Diagnosis of Inherited von Willebrand Disease: A Clinical Perspective

5. http://www.vwf.group.shef.ac.uk/vwd.html

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