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A Founder FACTOR VIII Mutation, Valine 2016 to Alanine, in a Population with extraordinarily High Prevalence of Mild Hemophilia A
Manual sobre Hemofilias
Safety and Efficacy Studies of AAV-MEDIATED, LIVER-DIRECTED Gene Transfer for Hemophilia B
Analysis of FACTOR VIII Inhibitors Using V gene Phage Display
Complete and sustained Phenotypic Correction Hemophilia B Mice After Hepatic Gene Tranfer of a High-expressing Human FACTOR IX Plasmid
Dose Resonse of rhFVIIa Concentrate on Homostasis in Uremic Blood
Pre-clinica Efficacy and Safety Studies of a Gutlees Adenovirus Vector (MAXADFVIII) for Tretment of Hemophilia A
A Site Between Residues 50 and 67 on GPIIIa is Recognized by Antibodies (Abs) from three Patients with Quinine-induced Thrombocytopenia
Hemophilia: treatment options in the twenty-first century
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