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Thrombocytopenia 10
- ... of thrombocytopenia. The estimated incidence of X-linked thrombocytopenia is between 1 and 10 per million males worldwide; this condition is rarer ... families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Pathology. ... 10.1080/00313020410001692521. Citation on PubMed Imai K, Morio ...
- ... D, Newland AC. Current Management of Primary Immune Thrombocytopenia. Adv Ther. 2015 Oct;32(10):875-87. doi: 10.1007/s12325-015-0251- ... on the investigation and management of primary immune thrombocytopenia. Blood. 2010 Jan 14;115(2):168-86. doi: 10.1182/blood-2009-06-225565. Epub 2009 Oct ...
- ... Cleveland Clinic [Internet]. Cleveland (OH): Cleveland Clinic; c2024. Thrombocytopenia: Overview; [cited 2024 Apr 09]; [about 10 screens]. Available from: https://my.clevelandclinic.org/health/diseases/14430-thrombocytopenia Gernsheimer T, James AH, Stasi R. How I ...
- ... No abstract available. Citation on PubMed Toriello HV. Thrombocytopenia-absent radius syndrome. Semin Thromb Hemost. 2011 Sep;37(6):707-12. doi: 10.1055/s-0031-1291381. Epub 2011 Nov 18. ...
- ... Mutation in GNE is associated with severe congenital thrombocytopenia. Blood. 2018 Oct 25;132(17):1855-1858. doi: 10.1182/blood-2018-04-847798. Epub 2018 Jun ...
- ... PD, Balamohan SM, Raskind WH, Kacena MA. Inherited thrombocytopenia due to GATA-1 mutations. Semin Thromb Hemost. 2011 Sep;37(6):682-9. doi: 10.1055/s-0031-1291378. Epub 2011 Nov 18. ...
- Coronavirus Disease 2019 (COVID-19) Vaccine Safety (Centers for Disease Control and Prevention)COVID-19 Vaccines/Related Issues ... COVID-19 Vaccines ... Centers for Disease Control and Prevention ... Learn safety information about the COVID-19 vaccine
- ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98(6):868-74. doi: 10.3324/haematol.2012.075861. Epub 2012 Oct 25. ...
- ... phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and alpha-granule deficiency. Haematologica. 2013 Jun;98(6):868-74. doi: 10.3324/haematol.2012.075861. Epub 2012 Oct 25. ...
- ... L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis. Br J Haematol. 2013 Feb;160(4):521-9. doi: 10.1111/bjh.12160. Epub 2012 Dec 17. Citation ...