Results 201 to 210 of about 153,671 (233)
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British Journal of Haematology, 2011
SummaryA clinical syndrome of bleeding and purpura consistent with a diagnosis of immune thrombocytopenia (ITP) was described by Werlhof long before platelets were identified as the cellular component of blood playing an essential role in primary haemostasis.
Roberto, Stasi, Adrian C, Newland
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SummaryA clinical syndrome of bleeding and purpura consistent with a diagnosis of immune thrombocytopenia (ITP) was described by Werlhof long before platelets were identified as the cellular component of blood playing an essential role in primary haemostasis.
Roberto, Stasi, Adrian C, Newland
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Blut, 1989
Chronic ITP is a syndrome of destructive thrombocytopenia due in most cases to antiplatelet autoantibodies. In the present studies we have studied 74 patients with chronic ITP using a new immunobead assay. Of these, 59 (79.7%) had demonstrable platelet-associated autoantibodies: 48 against platelet glycoprotein IIb/IIIa and 11 against glycoprotein Ib ...
P, Tani, P, Berchtold, R, McMillan
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Chronic ITP is a syndrome of destructive thrombocytopenia due in most cases to antiplatelet autoantibodies. In the present studies we have studied 74 patients with chronic ITP using a new immunobead assay. Of these, 59 (79.7%) had demonstrable platelet-associated autoantibodies: 48 against platelet glycoprotein IIb/IIIa and 11 against glycoprotein Ib ...
P, Tani, P, Berchtold, R, McMillan
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An update on pediatric ITP: differentiating primary ITP, IPD, and PID
Blood, 2022AbstractImmune thrombocytopenia (ITP) is the most common acquired thrombocytopenia in children and is caused by immune-mediated decreased platelet production and increased platelet destruction. In the absence of a diagnostic test, ITP must be differentiated from other thrombocytopenic disorders, including inherited platelet disorders.
Rachael F. Grace, Michele P. Lambert
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Immune Thrombocytopenic Purpura ITP
Vox Sanguinis, 1998AbstractImmune thrombocytopenic purpura ITP is characterized by early platelet destruction due to an unbalanced immune response. In acute ITP, a transient increase of HLA‐DR molecules has been detected while in individuals with chronic ITP, in addition, increased serum concentrations of IL‐2 and other cytokines reflecting in vivo T‐cell activation have
P, Imbach, T, Kühne
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The Journal of Symbolic Logic, 2019
Abstract $ISP$ cannot hold at the first or second successor of a singular strong limit of countable cofinality; on the other hand, we force a failure of “strong ${\rm{SCH}}$ ” across a cardinal where $ITP$ holds.
Hachtman, Sherwood, Sinapova, Dima
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Abstract $ISP$ cannot hold at the first or second successor of a singular strong limit of countable cofinality; on the other hand, we force a failure of “strong ${\rm{SCH}}$ ” across a cardinal where $ITP$ holds.
Hachtman, Sherwood, Sinapova, Dima
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Blood, 2013
![Figure][1] A 23-year-old primigravida woman presented with recurrent mucocutaneous bleeding since the age of 7 years. She was diagnosed with acute immune-mediated thrombocytopenia (ITP), and splenectomy was performed in 2006 after failure to respond to steroid therapy.
Bushra, Moiz, Anila, Rashid
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![Figure][1] A 23-year-old primigravida woman presented with recurrent mucocutaneous bleeding since the age of 7 years. She was diagnosed with acute immune-mediated thrombocytopenia (ITP), and splenectomy was performed in 2006 after failure to respond to steroid therapy.
Bushra, Moiz, Anila, Rashid
openaire +2 more sources