Incidence of adult primary immune thrombocytopenia in England—An update

Author:

Doobaree Indraraj Umesh1ORCID,Conway Katherine2ORCID,Miah Haroon3ORCID,Miah Atiqa4ORCID,Makris Michael5ORCID,Hill Quentin6ORCID,Cooper Nicola7,Bradbury Charlotte8ORCID,Newland Adrian3ORCID,Provan Drew3ORCID,McDonald Vickie4,

Affiliation:

1. Certara EVA London UK

2. West Sussex University Hospital Worthing West Sussex UK

3. Department of Immunobiology, Blizard Institute Queen Mary University of London London UK

4. Department of Clinical Haematology Royal London Hospital, Barts Health Trust London UK

5. University of Sheffield Sheffield UK

6. Leeds Teaching Hospitals Leeds UK

7. Department of Immunology and Inflammation Imperial College London London UK

8. Faculty of Health Sciences University of Bristol Bristol UK

Funder

GlaxoSmithKline

Novartis

Publisher

Wiley

Subject

Hematology,General Medicine

Reference38 articles.

1. The ITP syndrome: pathogenic and clinical diversity

2. Cellular immune dysfunction in immune thrombocytopenia (ITP)

3. Treatment, platelet count pattern and comorbidities among primary immune thrombocytopenia (ITP) patients seen in routine clinical practice: data from the United Kingdom immune thrombocytopenia (UK ITP) registry;Doobaree U;Blood,2017

4. Incidence and 10-Year Survival of Intracerebral Hemorrhage in a Population-Based Registry

5. Bleeding in primary immune thrombocytopenia: who are most at risk?;Doobaree U;Haematologica,2017

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