Results 221 to 230 of about 61,273 (263)

Association of Cognitive Impairment with Reduced Health-Related Quality of Life and Depression Among Survivors of Thrombotic Thrombocytopenic Purpura. [PDF]

Hematol Rep
Selvakumar S, Yu J, Meade J, Chaturvedi S.   +3 more
europepmc   +1 more source

Prevalence and characteristics of acute ischemic stroke and intracranial hemorrhage in patients with immune thrombocytopenic purpura and immune thrombotic thrombocytopenic purpura: a systematic review and meta-analysis. [PDF]

Neurol Res Pract
Ahmad SA, Liu O, Feng A, Kalra A, Dev A, Spann M, Gusdon AM, Chaturvedi S, Cho SM.   +8 more
europepmc   +1 more source

Acquired thrombotic thrombocytopenic purpura of unidentified pathophysiology in patients with severe disease: completing the landscape of thrombotic thrombocytopenic purpura. [PDF]

Haematologica
Joly BS, Leclercq M, Benhamou Y, Veyradier A, Coppo P.   +4 more
europepmc   +1 more source

Recurrent Idiopathic Thrombocytopenic Purpura Associated With Splenosis: A Case Report. [PDF]

Cureus
Mejia JL, Mejia Sierra L.
europepmc   +1 more source

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THROMBOHEMOLYTIC THROMBOCYTOPENIC PURPURA

Archives of Internal Medicine, 1954
THE DISEASE thrombotic thrombocytopenic purpura refers to a condition characterized by an unusual triad: hemolytic anemia, thrombocytopenic purpura, and multiple hyaline thrombi throughout the small vessels of the body. The occurrence of thrombi in cranial blood vessels gives rise to the characteristic cerebral symptoms.
E, ADELSON, E J, HEITZMAN, J F, FENNESSEY   +2 more
openaire   +2 more sources

Immune Thrombocytopenic Purpura

Hematology/Oncology Clinics of North America, 2007
Immune thrombocytopenic purpura (ITP) is an autoantibody-mediated thrombocytopenic disorder in which accelerated destruction of platelets occurs; platelet production may also be impaired by these antibodies. ITP is characterized by mucocutaneous bleeding. Rarely, more severe hemorrhages, such as intracranial hemorrhage, may occur. Traditional therapies,
Bethan, Psaila, James B, Bussel
openaire   +2 more sources

Immune Thrombocytopenic Purpura

New England Journal of Medicine, 2002
Immune thrombocytopenic purpura, which may lead to bleeding, is typically caused by antibodies directed against the platelet glycoprotein IIb/IIIa complex. Since the management of the disorder is different for children and adults, the authors of this up-to-date review provide separate sections on the two age groups.
Douglas B, Cines, Victor S, Blanchette
openaire   +4 more sources