Results 161 to 170 of about 1,080,266 (216)

Drug-free remission of immune thrombocytopenic purpura following resection of perihilar cholangiocarcinoma: a case report. [PDF]

J Surg Case Rep
Sakuma M, Takahashi D, Kamei K, Takayama Y, Takahashi T, Aoyama H, Hosoi T, Maeda A.   +7 more
europepmc   +1 more source

Emperipolesis in immune thrombocytopenic purpura

Indian Journal of Pathology and Microbiology, 2009
Aslan Deniz
doaj  

Correction to: Double-territory STEMI with cardiogenic shock in immune thrombocytopenic purpura with severe thrombocytopenia-a case report. [PDF]

Eur Heart J Case Rep
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
  +7 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
  +5 more sources

Immune thrombocytopenic purpura

The Indian Journal of Pediatrics, 2008
Immune thrombocytopenic purpura (ITP) is the commonest cause of sudden onset thrombocytopenia in a healthy child. The condition is frequently preceded by a viral infection. The hematological parameters are essentially normal except a low platelet count. Bone marrow examination is not routinely indicated except in specific situations.
V, Gupta, V, Tilak, B D, Bhatia
openaire   +2 more sources

The geoepidemiology of immune thrombocytopenic purpura

Autoimmunity Reviews, 2010
First described in 1735 (Watson-Williams et al., 1958), immune-mediated platelet destruction is a phenomenon of protean associations that has historically varied in its definition. Recently, consensus guidelines were proposed for a standardized system of nomenclature that preserves the acronym "ITP" but encompasses a number of causes of immune-mediated
Sean, Deane, Suzanne S, Teuber, M Eric, Gershwin   +2 more
openaire   +2 more sources

Immune thrombocytopenic purpura in adults

Current Opinion in Hematology, 2007
A review of recent studies was conducted to determine if guidelines promulgated by the American Society of Hematology and the British Committee for Standards in Haematology need to be updated as these were based mainly on expert opinion rather than outcomes derived from clinical trials.Recent studies suggest that most patients with immune ...
Bertrand, Godeau, Drew, Provan, James, Bussel   +2 more
openaire   +2 more sources