Results 241 to 250 of about 118,583,499 (297)
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Pediatrics In Review, 2013
Hemophilia A (deficiency in factor [F] VIII) and hemophilia B (deficiency in FIX) are the most common serious congenital coagulation factor deficiencies. (Based on strong evidence) Hemophilia is a genetic disorder inherited in an Xlinked fashion. Both diseases cause similar bleeding diatheses, with the hallmark being hemarthroses.
Bree, Zimmerman, Leonard A, Valentino
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Hemophilia A (deficiency in factor [F] VIII) and hemophilia B (deficiency in FIX) are the most common serious congenital coagulation factor deficiencies. (Based on strong evidence) Hemophilia is a genetic disorder inherited in an Xlinked fashion. Both diseases cause similar bleeding diatheses, with the hallmark being hemarthroses.
Bree, Zimmerman, Leonard A, Valentino
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Journal of Small Animal Practice, 1967
Abstract— This study presents laboratory and clinical eveidence of canine hemophilia A in the Vizsla breed. The preparation and treatment with fresh frozen (‐197d̀C) normal canine plasma is reported.Résumé— Cette étude apporte le preuve par la clinique et les examens de laboratoire, de l'existence d'une hémophilic canine de type A dans la race Vizsla ...
R G, Buckner +3 more
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Abstract— This study presents laboratory and clinical eveidence of canine hemophilia A in the Vizsla breed. The preparation and treatment with fresh frozen (‐197d̀C) normal canine plasma is reported.Résumé— Cette étude apporte le preuve par la clinique et les examens de laboratoire, de l'existence d'une hémophilic canine de type A dans la race Vizsla ...
R G, Buckner +3 more
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Radiology, 1972
Knee arthrograms of 7 hemophilic children demonstrated the type and degree of joint changes. Synovial irregularity was infrequent and seemed unrelated to the degree of arthritis. Cartilaginous destruction did not always correlate with bone changes. Bone changes at some distance from the joints have long been recognized as the result of intraosseous ...
N R, Salerno, J F, Menges, P F, Borns
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Knee arthrograms of 7 hemophilic children demonstrated the type and degree of joint changes. Synovial irregularity was infrequent and seemed unrelated to the degree of arthritis. Cartilaginous destruction did not always correlate with bone changes. Bone changes at some distance from the joints have long been recognized as the result of intraosseous ...
N R, Salerno, J F, Menges, P F, Borns
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Current Opinion in Hematology, 1995
The treatment of hemophilia and conditions that frequently afflict hemophilic patients, such as arthropathy, HIV infection, and viral hepatitis, are discussed. Long-term prophylaxis with Factor VIII or IX is very successful at preventing disabling arthropathy.
S, Moll, G C, White
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The treatment of hemophilia and conditions that frequently afflict hemophilic patients, such as arthropathy, HIV infection, and viral hepatitis, are discussed. Long-term prophylaxis with Factor VIII or IX is very successful at preventing disabling arthropathy.
S, Moll, G C, White
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The American Journal of Medicine, 1965
Abstract A case of hemophilia (factor VIII deficiency) in a woman belonging to a large family of hemophilic subjects is presented. The clinical and laboratory findings in the proposita and in other carrier women and affected men in the kindred are discussed.
D Y, WHISSELL +4 more
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Abstract A case of hemophilia (factor VIII deficiency) in a woman belonging to a large family of hemophilic subjects is presented. The clinical and laboratory findings in the proposita and in other carrier women and affected men in the kindred are discussed.
D Y, WHISSELL +4 more
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Scientific American, 1965
O n April 7, 1853, Queen Victoria of England gave birth to the eighth of her nine childl'en. From the beginning the infant Leopold was sickly; his baptism was postponed for almost three months. It may be that the trauma of birth had resulted in hemor rhages. In any event it soon became evident that he had an unusual tendency to bleed even from trivial
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O n April 7, 1853, Queen Victoria of England gave birth to the eighth of her nine childl'en. From the beginning the infant Leopold was sickly; his baptism was postponed for almost three months. It may be that the trauma of birth had resulted in hemor rhages. In any event it soon became evident that he had an unusual tendency to bleed even from trivial
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The American Journal of Medicine, 1949
Abstract The history, clinical and laboratory findings are presented of a hemophilic boy who is one of presumably identical twins. His brother is entirely normal.
A J, QUICK, J P, CONWAY
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Abstract The history, clinical and laboratory findings are presented of a hemophilic boy who is one of presumably identical twins. His brother is entirely normal.
A J, QUICK, J P, CONWAY
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American Journal of Clinical Pathology, 1982
An acquired circulating inhibitor to Factor VIII:C was found in a 27-year-old postpartum woman who presented with ecchymoses and hematomas. Postpartum Factor VIII:C inhibitors can clinically manifest with signs and symptoms not unlike those in a classic hemophiliac.
B S, Shitamoto +2 more
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An acquired circulating inhibitor to Factor VIII:C was found in a 27-year-old postpartum woman who presented with ecchymoses and hematomas. Postpartum Factor VIII:C inhibitors can clinically manifest with signs and symptoms not unlike those in a classic hemophiliac.
B S, Shitamoto +2 more
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Thrombosis and Haemostasis, 1961
SummaryHemophilia A is reported in a Shetland sheepdog. The history, clotting defects and clinical course were similar to that seen in human hemophilia. As far as we know, no evidence of hemophilia has been reported in this breed. Bleeding episodes could be controlled by fresh frozen plasma given either intravenously or intraperitoneally.Due to the ...
H A, WURZEL, W C, LAWRENCE
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SummaryHemophilia A is reported in a Shetland sheepdog. The history, clotting defects and clinical course were similar to that seen in human hemophilia. As far as we know, no evidence of hemophilia has been reported in this breed. Bleeding episodes could be controlled by fresh frozen plasma given either intravenously or intraperitoneally.Due to the ...
H A, WURZEL, W C, LAWRENCE
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Seminars in Thrombosis and Hemostasis, 2012
Acquired hemophilia A is a rare, autoimmune disorder that is caused by autoantibodies that act as inhibitors to factor VIII. It is characterized by severe, unexpected bleeding that may be life-threatening. The incidence of acquired hemophilia A is ~ 0.2 to 1.48 cases per 1 million individuals per year.
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Acquired hemophilia A is a rare, autoimmune disorder that is caused by autoantibodies that act as inhibitors to factor VIII. It is characterized by severe, unexpected bleeding that may be life-threatening. The incidence of acquired hemophilia A is ~ 0.2 to 1.48 cases per 1 million individuals per year.
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