Results 181 to 190 of about 43,474 (218)

Assessing treatment response in thrombotic thrombocytopenic purpura: Beyond the platelet count. [PDF]

Hematol Transfus Cell Ther
Martins de Oliveira Filho C, Bode-Sojobi I, Lam BD, Conrad S, Berry J, Carney BJ.   +5 more
europepmc   +1 more source

Overcoming Cytomegalovirus Induced Immune Thrombocytopenia in Immunocompetent Adults - A Case of Antiviral Therapy Efficacy. [PDF]

Am J Case Rep
Baddam S, Thiriveedi M, Patel S.
europepmc   +1 more source

Effectiveness and Safety of Respiratory Syncytial Virus Vaccine for US Adults Aged 60 Years or Older.

JAMA Netw Open
Fry SE, Terebuh P, Kaelber DC, Xu R, Davis PB.   +4 more
europepmc   +1 more source

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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   +5 more sources

Thrombotic Thrombocytopenic Purpura [PDF]

Thrombosis and Haemostasis, 1995
Recent studies indicate that CRTTP patients have excessive shear stress-induced platelet aggregation that is associated with the presence of ULvWF multimers in their plasma and increased vWF-binding to their platelets by flow cytometry. In these CRTTP patients, relapses, excessive shear-aggregation and the presence in their plasma of ULvWF forms are ...
openaire   +3 more sources

Congenital thrombocytopenic purpura

The Journal of Pediatrics, 1947
Summary Congenital thrombocytopenic purpura has occurred as a familial condition in three successive children of a mother previously splenectomized for thrombocytopenic purpura. In each of these children there has been a gradual spontaneous recovery to a normal blood picture during the first 2 months of life, and following recovery there has been no ...
Benjamin Berman, Janet Talmadge
openaire   +3 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,
James B. Bussel, Bethan Psaila
openaire   +3 more sources

Idiopathic Thrombocytopenic Purpura

Postgraduate Medicine, 1962
The acute form of ITP may be drug-induced or may follow infection or exposure to chemicals. The chronic form represents a self-perpetuating immunologic (auto-immune) disorder, at times associated with chronic lymphatic leukemia and other disorders. In some cases, it may be a prodrome of systemic lupus, to which it seems to be closely related.
openaire   +4 more sources

Idiopathic thrombocytopenic purpura [PDF]

The American Journal of Medicine, 1983
Idiopathic thrombocytopenic purpura occurs at all ages, in acute and chronic forms. Children mainly have the acute form, which usually follows a recent viral illness, occurs equally in both sexes, and generally resolves within six months. Chronic idiopathic thrombocytopenic purpura occurs more often in adults, often has an insidious onset, and shows a ...
Abdus Saleem, Terry R. Burns
openaire   +2 more sources