Results 161 to 170 of about 3,107 (209)
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Glanzmann's thrombasthenia revisited
The Journal of Emergency Medicine, 1996Glanzmann's thrombasthenia is a rare thrombocytopathy that has been associated with fatal bleeding. This disorder is characterized by a defect in platelet aggregation. Platelet counts, morphologies, prothrombin times, and activated partial thromboplastin times are normal, however, the bleeding time is markedly prolonged.
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Glanzmann’s Thrombasthenia: Identification of 19 New Mutations in 30 Patients
Maurizio Margaglione +2 more
exaly +1 more source
[Life threatening menorrhagia in thrombasthenia. (Glanzmann-Naegeli) thrombasthenia].
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1992Glanzmann's Thrombasthenia is a rare inherited disorder of platelet aggregation with normal platelet count and humoral coagulation. It is caused by the deficiency or functional disorder of platelet membrane glycoproteins IIb und IIIa. This complex is considered to be a receptor for fibrinogen.
K, Schnell +5 more
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Glanzmann's thrombasthenia and puerperium
International Journal of Gynecology & Obstetrics, 1997E, Capuzzo, F, Polatti, C, Zara
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FAMILIAL GLANZMANN’S THROMBASTHENIA
Mayo Clinic Proceedings, 1964L L, FRIEDMAN +4 more
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