Zobrazeno 1 - 10
of 129
pro vyhledávání: '"McVie-Wylie A"'
Autor:
Sanford L. Boye, Catherine O’Riordan, James Morris, Michael Lukason, David Compton, Rena Baek, Dana M. Elmore, James.J. Peterson, Diego Fajardo, K. Tyler McCullough, Abraham Scaria, Alison McVie-Wylie, Shannon E. Boye
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 28, Iss , Pp 129-145 (2023)
Mutations in GUCY2D are associated with severe early-onset retinal dystrophy, Leber congenital amaurosis type 1 (LCA1), a leading cause of blindness in children. Despite a high degree of visual disturbance stemming from photoreceptor dysfunction, pat
Externí odkaz:
https://doaj.org/article/a3ce88c96c0141e087c17132b69d17e5
Autor:
Boye, Sanford L., O’Riordan, Catherine, Morris, James, Lukason, Michael, Compton, David, Baek, Rena, Elmore, Dana M., Peterson, James.J., Fajardo, Diego, McCullough, K. Tyler, Scaria, Abraham, McVie-Wylie, Alison, Boye, Shannon E.
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 9 March 2023 28:129-145
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1999 Aug 01. 96(16), 8861-8866.
Externí odkaz:
https://www.jstor.org/stable/48239
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 8, Iss C, Pp 48-50 (2016)
Correlations between angiotensin-converting enzyme (ACE) genotype (I/I, I/D, D/D), disease severity at baseline and response to enzyme replacement therapy (ERT) were assessed in the Pompe disease Late-Onset Treatment Study (LOTS). No correlations wer
Externí odkaz:
https://doaj.org/article/23ef5675789a48d4a06699465a80b3cc
Autor:
Nelson, Carol A., Hunter, R. Bridge, Quigley, Lindsay A., Girgenrath, Stefan, Weber, William D., McCullough, Jennifer A., Dinardo, Carol J., Keefe, Kelly A., Ceci, Lorena, Clayton, Nicholas P., McVie-Wylie, Alison, Cheng, Seng H., Leonard, John P., Wentworth, Bruce M.
Publikováno v:
In The American Journal of Pathology 2011 178(6):2611-2621
Autor:
R. Bradley Troxler, Marta Sabbadini, Neerja Gupta, David Kronn, Ankit K. Desai, Katalin Scherer, Susan M. Richards, Alison McVie-Wylie, Priya S. Kishnani, Reeval Segel, Langston Sherry, Alexandra Joseph, Pranoot Tanpaiboon, William B. Rizzo, Crystal Sung, Seymour Packman, Sheela Nampoothiri, Zoheb B. Kazi, Omar A. Abdul-Rahman, Annette Feigenbaum, Dmitriy Niyazov
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Purpose: To investigate immune tolerance induction with transient low-dose methotrexate (TLD-MTX) initiated with recombinant human acid α-glucosidase (rhGAA), in treatment-naïve cross-reactive immunologic material (CRIM)-positive infantile-onset Po
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Autor:
Ashe, K., Taylor, K.M., Chu, Q., Meyers, E., Ellis, A., Jingozyan, V., Klinger, K., Finn, P.F., Cooper, C.G.F., Chuang, W., Marshall, J., McVie-Wylie, A.J., McPherson, J.M., Mattaliano, R.J., Cheng, S.H., Scheule, R.K., Moreland, R.J.
Publikováno v:
In Clinical Therapeutics 2011 33(6) Supplement:S31-S31
Autor:
D'Angona, Alida, LaCasse, Emily, Finn, Patrick, Phillips, Lucy, Ziegler, Robin, Matthews, Doug, Andrews, Laura, McVie-Wylie, Alison
Publikováno v:
In Clinical Therapeutics 2011 33(6) Supplement:S32-S32
Autor:
Palermo, A., Palmer, R., So, K., Zhang, M., Richards, B., Shah, S., Finn, P., Oba-Shinjo, S., Pescatori, M., Marie, S., McVie-Wylie, A., Mattaliano, R., Pomponio, R., Madden, S., Klinger, K.
Publikováno v:
In Clinical Therapeutics 2011 33(6) Supplement:S25-S25