نتایج جستجو برای: hemophilia b

تعداد نتایج: 904114  

Journal: :Molecular therapy. Methods & clinical development 2016
Allison M Lytle Harrison C Brown Na Yoon Paik Kristopher A Knight J Fraser Wright H Trent Spencer Christopher B Doering

Immune responses to coagulation factors VIII (FVIII) and IX (FIX) represent primary obstacles to hemophilia treatment. Previously, we showed that hematopoietic stem cell (HSC) retroviral gene therapy induces immune nonresponsiveness to FVIII in both naive and preimmunized murine hemophilia A settings. Liver-directed adeno-associated viral (AAV)-FIX vector gene transfer achieved similar results ...

Journal: :The Journal of Thoracic and Cardiovascular Surgery 1975

Journal: :Journal of Veterinary Medical Science 2006

Journal: :Blood 1979
S H Goodnight C W Britell K D Wuepper B Osterud

A persistent low-titer factor IX Inhibitor was discovered in a patIent with severe hemophllia B. The Inhibitor was very likely an immunoglobulin, since it was present in serum, was not dialyzable, retained its potency after heating to 56#{176}C, and was bound by staphylococcal protein A (SPA). When the hemophilia B patient with the inhibItor was given therapeutic infusions of factor Ix concentr...

2017
Davod Javanmard Masood Ziaee Hadi Ghaffari Mohammad Hasan Namaei Ahmad Tavakoli Hamidreza Mollaei Mohsen Moghoofei Helya Sadat Mortazavi Seyed Hamidreza Monavari

Background Human parvovirus B19 (B19V) is one of the smallest DNA viruses and shows great resistance to most disinfectants. Therefore, it is one of the common contaminant pathogens present in blood and plasma products. Parvovirus 4 (PARV4) is a newly identified parvovirus, which is also prevalent in parenteral transmission. In this study, we aimed to evaluate the prevalence of B19V and PARV4 DN...

2015
Hee Young Ju Hye Lim Jang Young Shil Park

BACKGROUND Inhibitory antibodies to factor VIII (FVIII) or IX (FIX) are important issues when managing patients with hemophilia A or B. Advances in bypassing agents such as recombinant activated FVII (rFVIIa) and activated prothrombin complex concentrates (APCC) have enabled the aggressive management of hemophilia with inhibitors during emergency or elective surgery. This study provides an upda...

Journal: :The Journal of clinical investigation 2009
Betsy T Kren Gretchen M Unger Lucas Sjeklocha Alycia A Trossen Vicci Korman Brenda M Diethelm-Okita Mark T Reding Clifford J Steer

Liver sinusoidal endothelial cells are a major endogenous source of Factor VIII (FVIII), lack of which causes the human congenital bleeding disorder hemophilia A. Despite extensive efforts, gene therapy using viral vectors has shown little success in clinical hemophilia trials. Here we achieved cell type-specific gene targeting using hyaluronan- and asialoorosomucoid-coated nanocapsules, genera...

Journal: :P & T : a peer-reviewed journal for formulary management 2013
Walter Alexander

We review key sessions on Hodgkin's lymphoma, diffuse large B-cell lymphoma, thromboembolism, hemophilia, sickle cell disease, and chronic lymphocytic leukemia.

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