Results 241 to 250 of about 2,583,576 (275)
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JAMA: The Journal of the American Medical Association, 1983
Reproduction rates in 294 men with severe hemophilia, 327 of their mothers, and 215 of their sisters were compared with Vital Statistics data for the general US population matched for exact age, calendar year between 1940 and 1977, and, for women, parity.
Robert B. Francis, Carol K. Kasper
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Reproduction rates in 294 men with severe hemophilia, 327 of their mothers, and 215 of their sisters were compared with Vital Statistics data for the general US population matched for exact age, calendar year between 1940 and 1977, and, for women, parity.
Robert B. Francis, Carol K. Kasper
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Pseudotumor of hemophilia in the mandible of a patient with hemophilia A
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2012Hemophilic pseudotumor is a rare lesion that is essentially a progressive, slowly expanding, encapsulated hematoma. It is estimated to affect 1% to 2% of severe hemophiliacs. The majority of hemophilic pseudotumors occur within soft tissues (intramuscular) and long bones of adult males. Fewer than 20 cases have been reported in the maxillofacial region.
Roger R. Throndson+3 more
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2013
Recent advances in the management of patients with hemophilia have led to significantly improved outcomes. Transmission of infectious diseases through blood product administration and severe arthropathies from recurrent joint bleeds are now rare.
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Recent advances in the management of patients with hemophilia have led to significantly improved outcomes. Transmission of infectious diseases through blood product administration and severe arthropathies from recurrent joint bleeds are now rare.
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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.
Gilbert C. White, Stephan Moll
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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.
Gilbert C. White, Stephan Moll
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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. M. Bird+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. M. Bird+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 ...
Job F. Menges+2 more
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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 ...
Job F. Menges+2 more
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Seminars in Arthritis and Rheumatism, 1972
Abstract The severe and progressive permanent crippling defects that develop in the child with severe hemophilia are no longer inevitable. Although the prophylactic administration of deficient factor on a daily basis by intravenous injection to the young child suffering from hemophilia is economically and logistically prohibitive in most instances ...
Corning Benton+2 more
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Abstract The severe and progressive permanent crippling defects that develop in the child with severe hemophilia are no longer inevitable. Although the prophylactic administration of deficient factor on a daily basis by intravenous injection to the young child suffering from hemophilia is economically and logistically prohibitive in most instances ...
Corning Benton+2 more
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Pediatrics, 1986
To the Editor.— I enjoyed reading the paper by Aronis et al,1 and would like to bring to your attention that we have also recently observed leukemia in two patients with hemophilia A and B, 10 and 1½ years of age, respectively.2 Because commercial factor VIII and IX were not used and only blood, fresh frozen plasma, and plasma were given
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To the Editor.— I enjoyed reading the paper by Aronis et al,1 and would like to bring to your attention that we have also recently observed leukemia in two patients with hemophilia A and B, 10 and 1½ years of age, respectively.2 Because commercial factor VIII and IX were not used and only blood, fresh frozen plasma, and plasma were given
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Journal of Pediatric Surgery, 1968
Abstract The second successfully resected intussusception in a hemophiliac is reported. The mainstay of the antihemophilic therapy was cryoprecipitated globulin, an easily prepared blood fraction containing the antihemophilic globulin from 500 ml. of blood in a volume of 30 ml.
Kenneth E. Miller, David L. Collins
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Abstract The second successfully resected intussusception in a hemophiliac is reported. The mainstay of the antihemophilic therapy was cryoprecipitated globulin, an easily prepared blood fraction containing the antihemophilic globulin from 500 ml. of blood in a volume of 30 ml.
Kenneth E. Miller, David L. Collins
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