Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology-Reference-Cited by-同舟云学术

Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology

Published:2024-03-26 Issue:5 Volume:204 Page:1714-1731
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Platton Sean¹^ORCID,Baker Peter²^ORCID,Bowyer Annette³^ORCID,Keenan Catriona⁴^ORCID,Lawrence Caroline⁵^ORCID,Lester Will⁶^ORCID,Riddell Anne⁷^ORCID,Sutherland Megan⁸^ORCID

Affiliation:

1. Royal London Hospital Haemophilia Centre London UK

2. Oxford Haemophilia and Thrombosis Centre Nuffield Orthopaedic Hospital Oxford UK

3. Department of Coagulation Royal Hallamshire Hospital Sheffield UK

4. Department of Haematology & the National Coagulation Centre St. James's Hospital Dublin Ireland

5. Department of Haematology Glasgow Royal Infirmary Glasgow UK

6. Haemophilia Unit University Hospitals Birmingham UK

7. Katharine Dormandy Haemophilia Centre Royal Free Hospital London UK

8. North West Genomic Laboratory Hub Manchester University NHS Foundation Trust Manchester UK

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.19385

Reference151 articles.

1. The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology

2. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

3. Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)

4. (ACGS) A.f.C.G.S.ACGS best practice guidelines for variant classification in rare disease[Internet]. ACGS;2020. [cited 2023 Aug 1]. Available from:https://www.acgs.uk.com/quality/best‐practice‐guidelines/

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