Zobrazeno 1 - 10
of 19
pro vyhledávání: '"M. J. Manco-Johnson"'
Choosing outcome assessment tools in haemophilia care and research : A multidisciplinary perspective
Autor:
K, Fischer, P, Poonnoose, A L, Dunn, P, Babyn, M J, Manco-Johnson, J A, David, J, van der Net, B, Feldman, K, Berger, M, Carcao, P, de Kleijn, M, Silva, P, Hilliard, A, Doria, A, Srivastava, V, Blanchette, Runhui, Wu
Publikováno v:
Haemophilia, 23(1), 11–24. Wiley-Blackwell
Introduction The implementation of early long-term, regular clotting factor concentrate (CFC) replacement therapy (‘prophylaxis’) has made it possible to offer boys with haemophilia a near normal life. Many different regimens have reported favour
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c9690f6dbb0e69760e5b3fb9d04752
https://dspace.library.uu.nl/handle/1874/353328
https://dspace.library.uu.nl/handle/1874/353328
Autor:
B, Lundin, M L, Manco-Johnson, D M, Ignas, R, Moineddin, V S, Blanchette, A L, Dunn, S V, Gibikote, S N, Keshava, R, Ljung, M J, Manco-Johnson, S F, Miller, G E, Rivard, A S, Doria, Marijke, van den Berg
Publikováno v:
Haemophilia. 18:962-970
Evaluation of prophylactic treatment of haemophilia requires sensitive methods. To design and test a new magnetic resonance imaging (MRI) scale for haemophilic arthropathy, two scales of a combined MRI scoring scheme were merged into a single scale w
Autor:
M L Manco-Johnson, Leonard A. Valentino, Desiree Medeiros, Prasad Mathew, Amy D. Shapiro, Nattee Narkbunnam, J. Michael Soucie, Brenda Riske, Harlan Austin, Gregory Thomas, Ray F. Kilcoyne, Linda J. Jacobson, Genlin Hu, W. Keith Hoots, L. J. Jacobson, Paul E. Monahan, Michael Recht, Sharon Funk, Donna DiMichele, J. David Ingram, Diane J. Nugent, Richard Jude Samulski, Bruce L. Evatt, Thomas C. Abshire, Deborah L Brown, Shirley Bleak, Alan R. Cohen, Aravind Asokan, Alexis A. Thompson, Michele R. Hacker, Marilyn J. Manco-Johnson, Alison Matsunaga, George R. Buchanan, Cindy A. Leissinger, M. J. Manco-Johnson, Chengwen Li, Kevin McRedmond
Publikováno v:
Gene therapy. 19(3)
Recombinant adeno-associated virus (rAAV) is a promising gene delivery vector and has recently been used in patients with hemophilia. One limitation of AAV application is that most humans have experienced wild-type AAV serotype 2 exposure, which freq
Autor:
V S, Blanchette, M J, Manco-Johnson
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16
For patients with haemophilia, the development of inhibitors complicates treatment, and inhibitor patients may thus have a range of unmet needs. Although successful inhibitor eradication will render patients responsive to factor replacement therapy,
Autor:
N A, Goldenberg, M J, Manco-Johnson
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 14(6)
Severe protein C deficiency (i.e. protein C activity1 IU dL(-1)) is a rare autosomal recessive disorder that usually presents in the neonatal period with purpura fulminans (PF) and severe disseminated intravascular coagulation (DIC), often with conco
Autor:
M J, Manco-Johnson, V S, Blanchette
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9
Arthropathy is associated with the greatest cost and morbidity to persons with haemophilia. Clinical protocols have been developed empirically to prevent or retard the development of joint disease using routine infusions of replacement factor concent
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9
A survey was conducted in 2002 to determine the pattern of factor prophylaxis use in boysor=18 years of age with haemophilia followed in North American treatment centres. Responses were obtained from 4553 cases (74% haemophilia A, 26% haemophilia B).
Autor:
M J, Manco-Johnson, R, Nuss
Publikováno v:
Advances in pediatrics. 48
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 6(6)
With the heightened interest in protocols to prevent or treat complications of haemophilia related to recurrent haemarthroses, there is a need for sensitive joint-evaluation tools. The World Federation of Haemophilia (WFH) Physical Joint Examination
Autor:
M J, Manco-Johnson
Publikováno v:
Thrombosis and haemostasis. 78(1)
In both children and neonates with venous thrombosis, one or more predisposing risk factors can generally be identified. Underlying prothrombotic medical conditions are common in these patients. In addition, a "trigger factor" such as a catheter, sur