Results 211 to 220 of about 95,790 (243)
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Lipoprotein disorder in brain infarction and hemorrhage

International Journal of Clinical & Laboratory Research, 1998
The cholesterol, triglyceride, and apolipoprotein B content of very low-, intermediate-, low-, and high-density lipoprotein fractions (separated by ultracentrifugation) and plasma were measured in healthy controls and patients with atherothrombotic infarction (26), lacunar infarction (26), and brain hemorrhage (14). In both atherothrombotic and lacunar
M. Kobayashi   +9 more
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THE TREATMENT OF HEMORRHAGIC DISORDERS

JAMA: The Journal of the American Medical Association, 1913
Within the past few years, chiefly because of better knowledge of the physiology of the blood, much new light has been thrown on a group of diseases which have always aroused great interest, but whose pathology has been obscure, and whose treatment has been exceedingly unsatisfactory.
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Congenital Hemorrhagic Disorders in Jordan

Thrombosis and Haemostasis, 1984
SummaryThe results of a three year prospective study of inherited bleeding syndromes in Jordan is presented. There were 112 patients from 64 families. Of these there were 42 patients with hemophilia A, 23 with Glanzmann’s thrombasthenia, 22 with von Willebrand’s disease, 11 with Christmas disease, 6 with hypofibrinogenemia, 3 with afibrinogenemia, 2 ...
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Treatment of Hemorrhagic Disorders

JAMA: The Journal of the American Medical Association, 1969
Since there have been at least ten other books on bleeding and coagulation disorders published in the 60's, one might well ask, "Why another?" Several answers are forthcoming: (1) Some facets of specific therapy, such as the use of cryoprecipitated antihemophilic factor in classic hemophilia, the use of heparin in defibrination syndromes, and the use ...
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Maternal Coagulation Disorders and Postpartum Hemorrhage

Clinical Obstetrics & Gynecology, 2010
Disorders of coagulation are relatively uncommon as a sole cause of postpartum hemorrhage. Coagulation disturbances should be suspected in patients with a family history of such abnormalities and patients with a history of menorrhagia. Clinical circumstances may also suggest coagulation defect as a cause of postpartum hemorrhage.
Robert M. Silver, Heather Major
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Hemorrhagic Disorders Associated with Thrombolytic Therapy

Critical Care Nursing Clinics of North America, 2000
Thrombolytic treatment for AMI, acute ischemic stroke, and massive pulmonary embolism has shown significant benefit. Along with the potential increase in perfusion and decrease in cell death, however, comes potential complications. Bleeding is the most common complication associated with thrombolytic therapy regardless of the particular agent and can ...
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Laboratory Diagnosis of Hemorrhagic and Thrombotic Disorders

Hematology/Oncology Clinics of North America, 1994
The study of hemostasis is a rapidly expanding field. Not only are new disorders being elucidated almost monthly, but also new proteins and interrelationships between known proteins are being reported continuously. These factors make the study of hemostatic disorders at once both exhilarating and challenging.
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Thalamic hemorrhage with neglect and memory disorder

Journal of the Neurological Sciences, 1986
A patient with right thalamic hemorrhage developed left-sided hemi-inattention, indifference, motor neglect, and hypokinesia. He also developed a severe memory deficit at the time of hemorrhage. Observations in this patient suggest that, in addition to a syndrome of neglect and hypokinesia, an amnesic syndrome can arise from unilateral lesions ...
Scott B. Tucker   +2 more
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Clinical Approach to the Patient With a Hemorrhagic Disorder

Postgraduate Medicine, 1960
Diagnosis of hemorrhagic disorders depends heavily on results of laboratory examinations; however, a sound and thorough clinical approach is also important. The proper clinical approach should first reveal whether or not an abnormality in hemostasis exists.
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Some complications of the therapy of hemorrhagic disorders

Disease-a-Month, 1993
The principal mode for treating disorders of hemostasis is correction of the patient's functional defect by transfusions of appropriate fractions of normal plasma or transfusions of platelets. Two major complications of such therapy are the transmission of infectious diseases, particularly hepatitis and the acquired immune deficiency syndrome (AIDS ...
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