Results 291 to 300 of about 283,642 (353)
Mevalonic acid exerts procoagulant effect by potentiating factor Xa. [PDF]
Niu L +12 more
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Venous Thromboembolism in Inherited Platelet Disorders: A Clinical Challenge. [PDF]
Paciullo F +4 more
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Immune Thrombocytopenia and Type 1 von Willebrand Disease in a Patient With a Femoral Fracture: A Case Report. [PDF]
Ferreira A, Roberto A.
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The correlation of lupus anticoagulant and anticardiolipin antibodies with hematological parameters and clinical findings in sickle cell disease at steady state phase. [PDF]
Almorish MA +11 more
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The Enumeration of the Blood-Platelets in Mental Disorders
On looking through the literature relating to the blood-picture in various types of mental disorders, one finds that most workers have confined themselves to the red and white cells only. Relatively little attention has been given to the study of the third element of the blood, namely, the blood-platelet.
D. K. Bruce
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Familial Bleeding Disorder with a Moderate Thrombocytopenia and Giant Blood Platelets
Among 10 siblings in an otherwise healthy family two sisters had experienced serious bleeding tendency from early childhood. They were moderately thrombocytopenic, their primary bleeding time was prolonged, and splenectomy had been performed in both without effect. One of them, now aged 66, was admitted because of recurrent episodes of life‐threatening
S A, Evensen +3 more
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Studies on human blood platelets in affective disorder
Psychopharmacology, 1979Platelets were examined to enable a simultaneous investigation to be made of indolylamine and electrolyte metabolism in affective disorder. No significant differences were detected in either platelet membrane ATPase or adenyl cyclase specific activity in any of the groups of patients studied, when compared with appropriate controls.
M, Scott, H W, Reading, J B, Loudon
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[Blood platelet changes in myeloproliferative disorders].
Minerva medica, 1988Morphofunctional alterations to the platelets in myeloproliferative disorders (MPD), conditions featuring clonal rearrangement of the haemopoietic stem-cell, were examined. These platelet anomalies including morphological alterations, acquired storage pool disease, membrane alterations, altered arachidonic acid metabolism and structural alterations to ...
G, D'Angelo, D, Calvano, C, Giardini
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