Results 11 to 20 of about 50 (50)
Hereditary disorders of blood coagulation factors amongst Jews! [PDF]
Journal of Clinical Research and Reports, 2020 This is picked up on routine bloods such as partial thromboplastin times. The prothrombin time is usually normal. There is no excess bleeding after trauma. They may however still bleed excessively after surgery. In terms of treatment or therapy the factor XI level must be kept at greater than 30 % with fresh frozen plasma 5-20 ml./kg./ day.
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Blood Coagulation Studies of Various Hematological Disorders
Japanese Journal of Medicine, 1963 We have carried out blood coagulation studies of various hematological disorders encountered routinely, in which hemorrhagic diathesis is the cardinal symptom and also it has important influence upon the prognosis of the diseases. Those which we studied are mainly acute leukemia, idiopathic thrombocytopenic purpura (ITP) and aplastic anemia, and ...
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Gerinnungsstörungen in graviditate [PDF]
Gynecologic and Obstetric Investigation, 1968 H Graeff, W Kuhn
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Physiology and Disorders of Blood Coagulation
International Journal of Clinical Practice, 1954 openaire +2 more sources
Human Blood Coagulation and its Disorders [PDF]
Journal of Clinical Pathology, 1958 openaire +2 more sources
HUMAN BLOOD COAGULATION AND ITS DISORDERS [PDF]
Journal of Clinical Pathology, 1963 openaire +2 more sources
Blood coagulation studies of various hematological disorders.
Nagoya journal of medical science, 1966 openaire +3 more sources
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Blood Coagulation and Hemophilioid Disorders
Postgraduate Medicine, 1968Hereditary bleeder states and syndromes of diffuse intravascular clotting are considered from the standpoint of laboratory diagnosis and the physiologic principles on which management is based. Availability of antihemophilic factor concentrates has revolutionized treatment of hemophilia A.
H R Roberts, K M Brinkhous
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HEMORRHAGIC THROMBOCYTHEMIA [PDF]
A.M.A. Archives of Internal Medicine, 1956 AS WOULD BE anticipated, disorders with moderately increased blood platelet levels are often characterized by thrombotic complications. Paradoxically, massive increases in the platelet count are more frequently associated with a hemorrhagic disorder.1Thus, such diseases as polycythemia vera, chronic granulocytic leukemia, and essential thrombocythemia ...
Samuel Melamed +2 more
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INTRACRANIAL HAEMORRHAGE IN DISORDERS OF BLOOD COAGULATION
Australian and New Zealand Journal of Surgery, 1960Summary The chief disorders of blood coagulation are discussed as predisposing or complicating factors in intracranial haemorrhage. Six cases of intracranial haemorrhage associated with various coagulation defects (haemophilia, hypoprothrombinaemia, and platelet deficiencies) are presented. Their management is discussed.
Donald Simpson, H. N. Robson
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