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Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
Preclinical and clinical gene therapy for haemophiliaM K L Chuah, D Collen, T VandendriesscheJournal of Thrombosis and Haemostasis : JTH|July 23, 2003
Gene therapy for the hemophiliasT VandenDriessche, D Collen, M K L ChuahBulletin Et Memoires De L'Academie Royale De Medecine De Belgique|April 15, 2008
Gene therapy for haemophilia "A" and "B": efficacy, safety and immune consequencesM K L Chuah, T VandendriesscheHaemophilia : the Official Journal of the World Federation of Hemophilia|February 1, 2003
Bone marrow mesenchymal cells for haemophilia A gene therapy using retroviral vectors with modified long-terminal repeatsA Van Damme, M K L Chuah, F Dell'accio, et al.The Journal of Gene Medicine|March 28, 2001
Gene therapy for hemophiliaM K Chuah, D Collen, T VandenDriesscheCurrent Gene Therapy|July 12, 2002
Viral vector-mediated gene therapy for hemophiliaT VandenDriessche, D Collen, M K ChuahHuman Gene Therapy|March 21, 1998
Bone marrow stromal cells as targets for gene therapy of hemophilia AM K Chuah, H Brems, V Vanslembrouck, et al.Journal of Thrombosis and Haemostasis : JTH|September 28, 2006
Efficacy and safety of adeno-associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapyT Vandendriessche, L Thorrez, A Acosta-Sanchez, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1999
Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient miceT VandenDriessche, V Vanslembrouck, I Goovaerts, et al.Human Gene Therapy|April 11, 2000
Long-term persistence of human bone marrow stromal cells transduced with factor VIII-retroviral vectors and transient production of therapeutic levels of human factor VIII in nonmyeloablated immunodeficient miceM K Chuah, A Van Damme, H Zwinnen, et al.Pageof 58