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Thrombasthenia
Known as:
glanzmann's disease
, PLATELET GLYCOPROTEIN IIb-IIIa DEFICIENCY
, Glanzmann's thrombasthenia
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A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and…
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National Institutes of Health
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Related topics
Related topics
21 relations
Autosomal recessive inheritance
Bernard-Soulier Syndrome
Epistaxis
Gastrointestinal Hemorrhage
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Broader (1)
Blood Platelet Disorders
Narrower (3)
Glanzmann Thrombasthenia, Autosomal Dominant
Glanzmann Thrombasthenia, Type A
Schlegelberger Grote syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2005
Highly Cited
2005
Critical Role of β3 Integrin in Experimental Postmenopausal Osteoporosis
Haibo Zhao
,
H. Kitaura
,
M. Sands
,
F. Ross
,
S. Teitelbaum
,
D. Novack
2005
Corpus ID: 904228
We show that mice lacking β3 integrin are protected from OVX‐induced bone loss. Using a lentiviral‐based strategy to express β3…
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Highly Cited
2004
Highly Cited
2004
Release of soluble CD40 ligand after platelet activation: studies on the solubilization phase.
K. Otterdal
,
T. Pedersen
,
N. Solum
Thrombosis Research
2004
Corpus ID: 10520747
Highly Cited
2003
Highly Cited
2003
Increased local procoagulant action: a mechanism contributing to the favorable hemostatic effect of recombinant FVIIa in PLT disorders
A. Galán
,
R. Tonda
,
M. Pino
,
J. Reverter
,
A. Ordinas
,
G. Escolar
Transfusion
2003
Corpus ID: 22220427
BACKGROUND: Recombinant FVIIa (rFVIIa) has been shown to improve hemostasis in patients with thrombocytopenia and to prevent or…
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Highly Cited
1991
Highly Cited
1991
Involvement of platelet glycoprotein IIb-IIIa (alpha IIb-beta 3 integrin) in thrombin-induced synthesis of phosphatidylinositol 3',4'-bisphosphate.
C. Sultan
,
M. Plantavid
,
+6 authors
H. Chap
Journal of Biological Chemistry
1991
Corpus ID: 22500477
Highly Cited
1986
Highly Cited
1986
Acquired thrombasthenia due to GPIIb/IIIa-specific platelet autoantibodies.
H. Niessner
,
K. Clemetson
,
S. Panzer
,
C. Mueller-Eckhardt
,
S. Santoso
,
P. Bettelheim
Blood
1986
Corpus ID: 7886393
An otherwise healthy woman developed a hemorrhagic diathesis with fluctuating clinical symptoms and laboratory findings, but…
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Highly Cited
1983
Highly Cited
1983
Characteristics of platelet aggregation induced by the monoclonal antibody ALB6 (acute lymphoblastic leukemia antigen p 24)
C. Boucheix
,
C. Soria
,
+5 authors
C. Rosenfeld
FEBS Letters
1983
Corpus ID: 28401216
Highly Cited
1980
Highly Cited
1980
Binding of radioiodinated human von Willebrand factor to Bernard-Soulier, thrombasthenic and von Willebrand's disease platelets.
J. Moake
,
J. Olson
,
J. H. Troll
,
S. Tang
,
T. Funicella
,
D. Peterson
Thrombosis Research
1980
Corpus ID: 41890372
Highly Cited
1977
Highly Cited
1977
Thromboxane Synthesis and the Platelet Release Reaction in Bernard‐Soulier Syndrome, Thrombasthenia Glanzmann and Hermansky‐Pudlak Syndrome
C. Malmsten
,
H. Kindahl
,
B. Samuelsson
,
S. Levy‐toledano
,
G. Tobelem
,
J. Caen
British Journal of Haematology
1977
Corpus ID: 39420217
Thromboxane (TX) synthesis was investigated in some characterized platelet disorders and correlated with release of ADP or [14C…
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Highly Cited
1974
Highly Cited
1974
Factor-VIII-related antigen in platelets.
M. Howard
,
D. Montgomery
,
R. Hardisty
Thrombosis Research
1974
Corpus ID: 8427680
Highly Cited
1972
Highly Cited
1972
PLASMA PROTEIN REQUIREMENTS FOR HUMAN PLATELET AGGREGATION
N. Bang
,
R. O. Heidenreich
,
C. W. Trygstad
Annals of the New York Academy of Sciences
1972
Corpus ID: 39161568
1. Three cationic proteins–fibrinogen, Hageman factor, and gamma globulin‐are all capable of restoring aggregation capability of…
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