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Tympanoplasty in a patient with hemophilia B
Auris Nasus Larynx, 1999We report the case of a 36-year-old hemophilia B who suffered from cholesteatoma and underwent tympanoplasty. Though the factor IX activity was less than 1% of normal before surgery, adequate replacement of factor IX led to the achievement of hemostasis during and after surgery.
Takashi Matsunaga +5 more
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Dental Extractions in Hemophilia A and B
JAMA: The Journal of the American Medical Association, 1971To the Editor.— In their article on the effective surgical treatment of patients with classic hemophilia and Christmas disease with human coagulation factor concentrates ( 214 : 1673,1970) Grant and Breckenridge also reported on uncomplicated dental extractions of deciduous and adult teeth in classic hemophilia and in Christmas disease with high ...
S. van Creveld, R. Buchner
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2009
Publisher Summary This chapter discusses the bleeding disorder known as hemophilia B. The disease results from a congenital deficiency or absence of Factor IX (FIX), leading to lifelong bleeding risk and it is X-linked recessive disorder and as such the majority of affected patients are male.
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Publisher Summary This chapter discusses the bleeding disorder known as hemophilia B. The disease results from a congenital deficiency or absence of Factor IX (FIX), leading to lifelong bleeding risk and it is X-linked recessive disorder and as such the majority of affected patients are male.
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Closing In on Treatment for Hemophilia B
New England Journal of Medicine, 2017Hemophilia is an X-linked recessive genetic bleeding disorder that occurs in two major forms. Approximately 80% of patients with hemophilia have mutations in the factor VIII clotting-factor gene (h...
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Hemophilia B Mutational Analysis
2003Since the cloning of the factor IX gene in 1982 (1), there have been several strategies employed for the identification of mutations in the mutationally heterogeneous hemophilia B population. Initially, such strategies inevitably employed Southern blotting to screen for gross deletions (2) or restriction site alterations (3), and cloning of the ...
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Molecular Analysis of Hemophilia B: »Greifswald Registry FIX Deficiency (Hemophilia B)«
2003Hemophilia B (HB) is due to multiple defects in the factor IX gene. More than 90% of mutants are single substitutions, small additions (
K. Wulff, F. H. Herrmann, W. Schröder
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Segregation analysis of hemophilia A and B.
American journal of human genetics, 1985We analyzed a sample of 1,485 families with hemophilia A and B and with unknown diagnosis. The frequency of sporadic cases was estimated to be .166 and .078 for the two types of hemophilia, respectively. The sex ratio of mutation rates did not differ significantly from unity. The average age of maternal grandfathers of probands at birth of mothers with
BARRAI, Italo Enrico +4 more
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Hemophilia B (Factor IX Deficiency).
Hematology/Oncology Clinics of North America, 2021R. Sidonio, L. Malec
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Hemophilia B Leyden and a Similar Variant of Hemophilia A
New England Journal of Medicine, 1982Inga Marie Nilsson, Rolf Ljung
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