Zobrazeno 1 - 10
of 37
pro vyhledávání: '"John F. Brandsema"'
Autor:
Rebecca J. Willcocks, Alison M. Barnard, Michael J. Daniels, Sean C. Forbes, William T. Triplett, John F. Brandsema, Erika L. Finanger, William D. Rooney, Sarah Kim, Dah‐Jyuu Wang, Donovan J. Lott, Claudia R. Senesac, Glenn A. Walter, H. Lee Sweeney, Krista Vandenborne
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 1, Pp 67-78 (2024)
Abstract Objective Magnetic resonance (MR) measures of muscle quality are highly sensitive to disease progression and predictive of meaningful functional milestones in Duchenne muscular dystrophy (DMD). This investigation aimed to establish the repro
Externí odkaz:
https://doaj.org/article/4a848dd8b4bb4a98b68cbbe201dd5627
Autor:
Erika J. Mejia, Kimberly Y. Lin, Oluwatimilehin Okunowo, Katherine A. Iacobellis, Susan E. Matesanz, John F. Brandsema, Carol A. Wittlieb‐Weber, Hannah Katcoff, Heather Griffis, Jonathan B. Edelson
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 8 (2022)
Background Duchenne and Becker muscular dystrophy are progressive disorders associated with cardiac mortality. Guidelines recommend routine surveillance; we assess cardiac resource use and identify gaps in care delivery. Methods and Results Male pati
Externí odkaz:
https://doaj.org/article/104c62123f5d4c9a9700c826e2679049
Autor:
Francesco Muntoni, Michela Guglieri, Jean K. Mah, Kathryn R. Wagner, John F. Brandsema, Russell J. Butterfield, Craig M. McDonald, Anna G. Mayhew, Jeffrey P. Palmer, Shannon Marraffino, Lawrence Charnas, Eugenio Mercuri
Publikováno v:
PLoS ONE, Vol 17, Iss 8 (2022)
Introduction The North Star Ambulatory Assessment (NSAA) tool is a key instrument for measuring clinical outcomes in patients with Duchenne muscular dystrophy (DMD). To gain a better understanding of the longitudinal utility of the NSAA, we evaluated
Externí odkaz:
https://doaj.org/article/fde97ba947ad4ba8aef682b8dd0767d2
Autor:
Anne M. Connolly, Craig M. Zaidman, John F. Brandsema, Han C. Phan, Cuixia Tian, Xueping Zhang, Jack Li, Mark D. Eisner, Ewa Carrier
Publikováno v:
Journal of Neuromuscular Diseases. :1-15
BACKGROUND: Duchenne muscular dystrophy (DMD) is a neuromuscular disease stemming from dystrophin gene mutations. Lack of dystrophin leads to progressive muscle damage and replacement of muscle with fibrotic and adipose tissue. Pamrevlumab (FG-3019),
Autor:
Richard S. Finkel, Basil T. Darras, Jerry R. Mendell, John W. Day, Nancy L. Kuntz, Anne M. Connolly, Craig M. Zaidman, Thomas O. Crawford, Russell J. Butterfield, Perry B. Shieh, Gihan Tennekoon, John F. Brandsema, Susan T. Iannaccone, John Shoffner, Sarah Kavanagh, Thomas A. Macek, Sitra Tauscher-Wisniewski
Publikováno v:
Journal of Neuromuscular Diseases. 10:389-404
Background: Spinal muscular atrophy (SMA) is a neuromuscular disorder arising from biallelic non-functional survival motor neuron 1 (SMN1) genes with variable copies of partially functional SMN2 gene. Intrathecal onasemnogene abeparvovec administrati
Autor:
John F. Brandsema, Matthew Ginsberg, Hideki Hoshino, Masakazu Mimaki, Satoru Nagata, Vamshi Rao, Katherine Ruzhansky, Niraja Suresh, Emmanuelle Tiongson, Hideo Yamanouchi, Glen Frick, Eden Hicks, Serena Liao, James Howard
Publikováno v:
Sunday, April 23.
Autor:
Nancy Kuntz, Julie Parsons, John F. Brandsema, Crystal Proud, Richard Finkel, Kathryn Swoboda, Ricardo Masson, Yingying Liu, Corinne Makepeace, Angela Paradis, Zdenek Berger, Kathleen Somera-Molina
Publikováno v:
Tuesday, April 25.
Autor:
Sarah P. Sherlock, Jeffrey Palmer, Kathryn R. Wagner, Hoda Z. Abdel-Hamid, Enrico Bertini, Cuixia Tian, Jean K. Mah, Anna Kostera-Pruszczyk, Francesco Muntoni, Michela Guglieri, John F. Brandsema, Eugenio Mercuri, Russell J. Butterfield, Craig M. McDonald, Lawrence Charnas, Shannon Marraffino
Publikováno v:
Journal of Neurology. 269:4421-4435
Duchenne muscular dystrophy (DMD) is a progressive, neuromuscular disorder caused by mutations in the DMD gene that results in a lack of functional dystrophin protein. Herein, we report the use of quantitative magnetic resonance imaging (MRI) measure
Autor:
John F. Brandsema, Susan E. Matesanz
Publikováno v:
Pulmonary Assessment and Management of Patients with Pediatric Neuromuscular Disease ISBN: 9780323957472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d65d8b784200c5ed5730c850be889f6
https://doi.org/10.1016/b978-0-323-95747-2.00011-2
https://doi.org/10.1016/b978-0-323-95747-2.00011-2
Autor:
Jason Ackrivo, Reshma Amin, Heather Boas, John F. Brandsema, Pi Chun Cheng, Jonathan Finder, Robert J. Graham, Neepa Gurbani, Sherri Lynne Katz, Oren Kupfer, Jia Liu, Susan E. Matesanz, Oscar Henry Mayer, Kristen Miller, John E. Pascoe, Gregory Redding, Hemant Sawnani, Richard Shell, Jenny Yue Shi, Aaron St-Laurent, Michael A. Storey, Danna Tauber, Federica Trucco, Katharine Tsukahara, David Zielinski
Publikováno v:
Pulmonary Assessment and Management of Patients with Pediatric Neuromuscular Disease ISBN: 9780323957472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::543e5a52d53fdc95fb9498d150650e7e
https://doi.org/10.1016/b978-0-323-95747-2.09992-4
https://doi.org/10.1016/b978-0-323-95747-2.09992-4