Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Megan, Iammarino"'
Autor:
Yiwen Dong, Megan Iammarino, Jingxiao Liu, Jesse Codling, Jonathon Fagert, Mostafa Mirshekari, Linda Lowes, Pei Zhang, Hae Young Noh
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Muscular dystrophies (MD) are a group of genetic neuromuscular disorders that cause progressive weakness and loss of muscles over time, influencing 1 in 3500–5000 children worldwide. New and exciting treatment options have led to a critica
Externí odkaz:
https://doaj.org/article/630fe936f3d44c4dbc89bdcf34a70cf4
Autor:
Kevin A. Strauss, Vincent J. Carson, Emilienne Bolettieri, Mariah Everett, Ashton Bollinger, Lauren E. Bowser, Keturah Beiler, Millie Young, Simon Edvardson, Nitay Fraenkel, Adele D'Amico, Enrico Bertini, Lokesh Lingappa, Devyani Chowdhury, Linda P. Lowes, Megan Iammarino, Lindsay N. Alfano, Karlla W. Brigatti
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 11, Pp 1972-1984 (2023)
ABSTRACT Objective We created WiTNNess as a hybrid prospective/cross‐sectional observational study to simulate a clinical trial for infantile‐onset TNNT1 myopathy. Our aims were to identify populations for future trial enrollment, rehearse outcom
Externí odkaz:
https://doaj.org/article/aed2e23aa754450b8426dda69cb75b30
Autor:
Kevin M. Flanigan, Tatyana A. Vetter, Tabatha R. Simmons, Megan Iammarino, Emma C. Frair, Federica Rinaldi, Louis G. Chicoine, Johan Harris, John P. Cheatham, Sharon L. Cheatham, Brian Boe, Megan A. Waldrop, Deborah A. Zygmunt, Davin Packer, Paul T. Martin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 27, Iss , Pp 47-60 (2022)
In a phase 1/2, open-label dose escalation trial, we delivered rAAVrh74.MCK.GALGT2 (also B4GALNT2) bilaterally to the legs of two boys with Duchenne muscular dystrophy using intravascular limb infusion. Subject 1 (age 8.9 years at dosing) received 2.
Externí odkaz:
https://doaj.org/article/5d4cb4d3fc0f4849bd3ccf973f1e61e1
Autor:
Erin O’Rourke, Jerry R. Mendell, Zarife Sahenk, Kelly J. Lehman, Linda P. Lowes, Natalie F. Reash, Megan Iammarino, Lindsay Alfano, Sarah Lewis, Kathleen Church, Richard Shell, Rachael A. Potter, Danielle Griffin, Mark J. Hogan, Shufang Wang, Stefanie Mason, Eddie Darton, Louise Rodino-Klapac
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100342- (2023)
Externí odkaz:
https://doaj.org/article/fb9e1b284811470595a4cfbc12d4ff7e
Autor:
Marielle G. Contesse, Linda P. Lowes, Michelle K. White, Laura Dalle Pazze, Christine McSherry, Lindsay N. Alfano, Megan Iammarino, Natalie Reash, Kelly Bonarrigo, Michael Kiefer, Katie Laubscher, Melissa McIntyre, Shelley Mockler, Leslie Nelson, Leslie Vogel, Mindy G. Leffler
Publikováno v:
PLoS ONE, Vol 17, Iss 4 (2022)
Background Patients with Duchenne muscular dystrophy (DMD) adopt compensatory movement patterns as muscles weaken. The Duchenne Video Assessment (DVA) measures patient ease of movement through identification of compensatory movement patterns. The DVA
Externí odkaz:
https://doaj.org/article/44aeb7ead2724744905f9707b48739a3
Autor:
Jerry Mendell, Perry Shieh, Zarife Sahenk, Kelly Lehman, Linda Lowes, Natalie Reash, Megan Iammarino, Lindsay Alfano, Brenna Sabo, Jeremy Woods, Christy Skura, Howard Mao, Loretta Staudt, Rachael Potter, Danielle Griffin, Sarah Lewis, Shufang Wang, Tejdip Singh, Louise Rodino-Klapac
Publikováno v:
Thursday, April 27.
Autor:
Jerry Mendell, Zarife Sahenk, Kelly Lehman, Linda Lowes, Natalie Reash, Megan Iammarino, Lindsay Alfano, Sarah Lewis, Kathleen Church, Richard Shell, Rachael Potter, Danielle Griffin, Mark Hogan, Shufang Wang, Stefanie Mason, Eddie Darton, Louise Rodino-Klapac
Publikováno v:
Sunday, April 23.
Autor:
Marielle G. Contesse, Linda P. Lowes, Michelle K. White, Laura Dalle Pazze, Christine McSherry, Lindsay N. Alfano, Megan Iammarino, Natalie Reash, Kelly Bonarrigo, Michael Kiefer, Katie Laubscher, Melissa McIntyre, Shelley Mockler, Leslie Nelson, Leslie Vogel, Mindy G. Leffler
Publikováno v:
PloS one. 17(4)
BackgroundPatients with Duchenne muscular dystrophy (DMD) adopt compensatory movement patterns as muscles weaken. The Duchenne Video Assessment (DVA) measures patient ease of movement through identification of compensatory movement patterns. The DVA
Autor:
Kevin M, Flanigan, Tatyana A, Vetter, Tabatha R, Simmons, Megan, Iammarino, Emma C, Frair, Federica, Rinaldi, Louis G, Chicoine, Johan, Harris, John P, Cheatham, Sharon L, Cheatham, Brian, Boe, Megan A, Waldrop, Deborah A, Zygmunt, Davin, Packer, Paul T, Martin
Publikováno v:
Molecular therapy. Methodsclinical development. 27
In a phase 1/2, open-label dose escalation trial, we delivered rAAVrh74.MCK.
Autor:
HAE YOUNG NOH, Pei Zhang, Megan Iammarino, Linda Lowes, Mostafa Mirshekari, Jonathon Fagert, Jingxiao Liu, Joanna Jiaqi Zou, Yiwen Dong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::158b050c64c8614976e52532c385c30a
https://doi.org/10.26226/morressier.612f6737bc981037241008a7
https://doi.org/10.26226/morressier.612f6737bc981037241008a7