Results 271 to 280 of about 82,032 (316)
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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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Pediatric Hemophilia: A Review
Seminars in Thrombosis and Hemostasis, 2011The hemophilias are the most common X-linked inherited bleeding disorders, which if not properly managed can lead to chronic disease and lifelong disabilities. The challenges and issues in newborns are different from that in older children and adults.
Roshni, Kulkarni, J Michael, Soucie
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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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Archives of Pediatrics & Adolescent Medicine, 1957
It is now possible to distinguish several disorders of blood coagulation within the condition previously designated as hemophilia, and to identify each as being characterized by defective production of thromboplastin. Whether the latter results from a quantitative deficiency in one of several substances or from the presence of an inhibitor of that ...
M C, HARMON, A, ZIPURSKY, M E, LAHEY
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It is now possible to distinguish several disorders of blood coagulation within the condition previously designated as hemophilia, and to identify each as being characterized by defective production of thromboplastin. Whether the latter results from a quantitative deficiency in one of several substances or from the presence of an inhibitor of that ...
M C, HARMON, A, ZIPURSKY, M E, LAHEY
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Aesthetic Plastic Surgery, 2007
Major surgical procedures can be performed safely for hemophiliacs provided the clotting factors are adequate. However, rhinoplasty, an elective facial procedure, has not yet been evaluated in this group of patients. The authors present a hemophilia A patient who underwent rhinoplasty for cosmetic reasons.
Zafer, Ozsoy +4 more
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Major surgical procedures can be performed safely for hemophiliacs provided the clotting factors are adequate. However, rhinoplasty, an elective facial procedure, has not yet been evaluated in this group of patients. The authors present a hemophilia A patient who underwent rhinoplasty for cosmetic reasons.
Zafer, Ozsoy +4 more
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Hemophilia and cancer: A new challenge for hemophilia centers
Cancer Treatment Reviews, 2009The improved life expectancy of hemophilia patients due to the advances in hemophilia care and factor replacement therapy has permitted to hemophiliacs to reach an older age. As a consequence, age-related diseases, such as cardiovascular disorders and cancer, have been increasingly recognized in such patients. In particular, the management of cancer in
Massimo, Franchini +8 more
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Hemophilia A and Hemophilia B: Different Types of Diseases?
Seminars in Thrombosis and Hemostasis, 2013Hemophilia A and B are traditionally considered clinically indistinguishable; however, differences in bleeding frequency, clinical scores, use of prophylaxis, and need for orthopedic surgery have been reported, suggesting that the bleeding tendency associated with factor IX deficiency may be less severe with consequent better outcomes in the long term ...
Elena, Santagostino +1 more
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Oral Surgery, Oral Medicine, Oral Pathology, 1969
B M, Lyons, B J, Blankenship, R A, Stout
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B M, Lyons, B J, Blankenship, R A, Stout
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Annals of Hematology
Hemophilia A (HA) is an X-chromosome-linked recessive genetic disorder. Female carriers may have bleeding symptoms, but rarely have moderate or severe disease. We identified a female patient with moderate HA by pedigree tracking and genetic testing in a HA family involving consanguineous marriage.
Jie Wang +11 more
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Hemophilia A (HA) is an X-chromosome-linked recessive genetic disorder. Female carriers may have bleeding symptoms, but rarely have moderate or severe disease. We identified a female patient with moderate HA by pedigree tracking and genetic testing in a HA family involving consanguineous marriage.
Jie Wang +11 more
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