Results 201 to 210 of about 45,170 (249)
Citation clarification regarding feline eltrombopag in the "ACVIM consensus statement on the treatment of immune thrombocytopenia in dogs and cats". [PDF]
J Vet Intern MedKim J, Kwak D.
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Die ITP ist eine erworbene Thrombozytopenie, verursacht durch eine Autoimmunreaktion gegen Thrombozyten und Megakaryozyten. Unterschieden wird eine primäre Form, bei der keine auslösende Ursache erkennbar ist, von sekundären Formen, ausgelöst z. B. durch
Meyer, Oliver +16 more
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Idiopathic thrombocytopenic purpura (ITP): Is there a genetic predisposition?
Pediatric Blood and Cancer, 2006 Idiopathic thrombocytopenic purpura (ITP) is a diagnosis of exclusion. It is unknown, whether familial ITP exists. Familial cases would make a genetic susceptibility for ITP possible.
Thomas 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
Sherwood Hachtman, Dima Sinapova
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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
Sherwood Hachtman, Dima Sinapova
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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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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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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
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STIMULATED MEGAKARYOCYTES ARE FOUND IN CHILDHOOD ITP BUT NOT IN ADULT ITP
Thrombosis and Haemostasis, 1987ITP is thought to be caused primarily by peripheral platelet destruction, but recent work has suggested that platelet production may also be impaired. Although the clinical course in children usually differs from that in adults, no distinctions have been established with regard to marrow characteristics.
R F Levine, P K Shoff
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Hematology, 2006
Abstract Immune (or idiopathic) thrombocytopenic purpura (ITP) is commonly encountered by the practicing hematologist. Clinical management decisions have traditionally been guided by individual training and past experience. Input from the literature has been more from observational reports of case series than from scientific results of ...
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Abstract Immune (or idiopathic) thrombocytopenic purpura (ITP) is commonly encountered by the practicing hematologist. Clinical management decisions have traditionally been guided by individual training and past experience. Input from the literature has been more from observational reports of case series than from scientific results of ...
openaire +2 more sources