OSLER'S DISEASE WITH IMPAIRED ADHESION AND AGGREGATION OF PLATELETS
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0954-6820.1974.tb00982.x/fullpdf
Reference24 articles.
1. On the pathogenesis of hepatic changes in teleangiectasia hereditaria haemorrhagica (Morbus Osler-Rendu-Weber);Angervall;Acta path. microbiol. scand.,1954
2. Arteriovenous pulmonary aneurysms in Osier's disease (Telangiectasia hereditaria haemorrhagica);Bergqvist;Acta med. scand.,1962
3. A new method for enumeration of platelets;Björkman;Acta haemat. (Basel),1959
4. Aggregation of blood platelets by adenosine diphosphate and its reversal;Born;Nature (Lond.),1962
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1. The bleeding diathesis in patients with hereditary haemorrhagic telangiectasia is not due to impaired platelet function;Orphanet Journal of Rare Diseases;2023-11-14
2. CONJUNCTIVAL BLEEDING IN OSLER'S DISEASE WITH ASSOCIATED PLATELET DYSFUNCTION: A Case Report;Acta Ophthalmologica;2009-05-27
3. Hereditary hemorrhagic telangiectasis treated by the harmonic scalpel;Head & Neck;2003-03-20
4. Splenomegaly and chronic disseminated intravascular coagulation in Osler-Weber-Rendu disease: A case report;American Journal of Hematology;2000
5. Hereditary Hemorrhagic Telangiectasia Response to Aminocaproic Acid Treatment;Thrombosis Research;1999-10
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