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Hemophilia A

Known as: Classic Hemophilia, Hemophilia As, Haemophilia 
An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited… Expand
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Hemophilia is a rare disorder that is complex to diagnose and to manage. These evidence-based guidelines offer practical… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Hemophilia B, an X-linked disorder, is ideally suited for gene therapy. We investigated the use of a new gene therapy… Expand
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Highly Cited
2009
Highly Cited
2009
One of the conclusions of the subcommittee meeting on Lupus Anticoagulant/Phospholipid dependent antibodies, held in Geneva on… Expand
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Review
2004
Review
2004
From Kleinman Biomedical Research, Victoria, British Columbia, Canada; the University of British Columbia, Vancouver, British… Expand
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Highly Cited
2003
Highly Cited
2003
Hemophilia B is an X-linked coagulopathy caused by absence of functional coagulation factor IX (F.IX). Previously, we established… Expand
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Review
2001
Review
2001
Of the various types of hemophilia, the most common of these lifelong bleeding disorders are due to an inherited deficiency of… Expand
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Highly Cited
2000
Highly Cited
2000
Pre-clinical studies in mice and haemophilic dogs have shown that introduction of an adeno-associated viral (AAV) vector encoding… Expand
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Highly Cited
1997
Highly Cited
1997
The critical role of chemokine receptors (CCR5 and CXCR4) in human immunodeficiency virus-type 1 (HIV-1) infection and… Expand
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Highly Cited
1996
Highly Cited
1996
The chemokine receptor 5 (CKR5) protein serves as a secondary receptor on CD4+ T lymphocytes for certain strains of human… Expand
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Highly Cited
1992
Highly Cited
1992
In Sweden, prophylactic treatment of boys with severe haemophilia has been practised since 1958 in an attempt to convert the… Expand
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