Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Trusha T. Patel"'
Autor:
Baodong Sun, Suhrad G. Banugaria, Sean N. Prater, Trusha T. Patel, Keri Fredrickson, Douglas J. Ringler, Antonin de Fougerolles, Amy S. Rosenberg, Herman Waldmann, Priya S. Kishnani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 446-450 (2014)
Approximately 35–40% of patients with classic infantile Pompe disease treated with enzyme replacement therapy (ERT) develop high, sustained antibody titers against the therapeutic enzyme alglucosidase alfa, which abrogates the treatment efficacy. I
Externí odkaz:
https://doaj.org/article/e2218e4187334a8baee1035af47e2f37
Autor:
Suhrad G Banugaria, Sean N Prater, Trusha T Patel, Stephanie M Dearmey, Christie Milleson, Kathryn B Sheets, Deeksha S Bali, Catherine W Rehder, Julian A J Raiman, Raymond A Wang, Francois Labarthe, Joel Charrow, Paul Harmatz, Pranesh Chakraborty, Amy S Rosenberg, Priya S Kishnani
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67052 (2013)
Although enzyme replacement therapy (ERT) is a highly effective therapy, CRIM-negative (CN) infantile Pompe disease (IPD) patients typically mount a strong immune response which abrogates the efficacy of ERT, resulting in clinical decline and death.
Externí odkaz:
https://doaj.org/article/18fa0e438966415a88a3734dd619fdd0
Publikováno v:
Molecular Genetics and Metabolism. 107:244
Autor:
Patel, Trusha T., Banugaria, Suhrad G., Frush, Donald P., Enterline, David S., Tanpaiboon, Pranoot, Kishnani, Priya S.
Publikováno v:
Muscle & Nerve; Apr2013, Vol. 47 Issue 4, p613-615, 2p
Publikováno v:
JAMA Pediatrics; Aug2018, Vol. 172 Issue 8, p721-722, 2p