Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Donovan J. Lott"'
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:
Abhinandan Batra, Alison M. Barnard, Donovan J. Lott, Rebecca J. Willcocks, Sean C. Forbes, Saptarshi Chakraborty, Michael J. Daniels, Jannik Arbogast, William Triplett, Erik K. Henricson, Jonathan G. Dayan, Carsten Schmalfuss, Lee Sweeney, Barry J. Byrne, Craig M. McDonald, Krista Vandenborne, Glenn A. Walter
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background The lack of dystrophin in cardiomyocytes in Duchenne muscular dystrophy (DMD) is associated with progressive decline in cardiac function eventually leading to death by 20–40 years of age. The aim of this prospective study was to
Externí odkaz:
https://doaj.org/article/4f3246949aea4b8fb84745347438167c
Autor:
Charles A Thornton, Richard Thomas Moxley, Katy Eichinger, Chad Heatwole, Laurence Mignon, W David Arnold, Tetsuo Ashizawa, John W Day, Gersham Dent, Matthew K Tanner, Tina Duong, Ericka P Greene, Laura Herbelin, Nicholas E Johnson, Wendy King, John T Kissel, Doris G Leung, Donovan J Lott, Daniel A Norris, Evan M Pucillo, Wendy Schell, Jeffrey M Statland, Nikia Stinson, Sub H Subramony, Shuting Xia, Kathie M Bishop, C Frank Bennett
Publikováno v:
The Lancet Neurology. 22:218-228
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06edbb966b88ee3a85a273542b721585
https://doi.org/10.1016/s1474-4422(23)00001-7
https://doi.org/10.1016/s1474-4422(23)00001-7
Autor:
Julien, Louis, Sam, Bennett, Daniel J, Owens, Eve, Tiollier, Franck, Brocherie, Marcelo A. S., Carneiro, Paulo Ricardo P., Nunes, Bruna, Costa, Pâmela, Castro-e-Souza, Luís A., Lima, Felipe, Lisboa, Gersiel, Oliveira-Júnior, Witalo, Kassiano, Edilson S., Cyrino, Fábio L., Orsatti, Arthur Henrique, Bossi, Guilherme, Matta, Géssyca, Tolomeu de Oliveira, Ferreira, Renato Melo, Everton, Rocha Soares, Bruno, Ocelli Ungheri, Matheus, Daros Pinto, James L., Nuzzo, Christopher, Latella, Daniel, van den Hoek, Alistair, Mallard, Jemima, Spathis, Justin A., DeBlauw, Stephen J., Ives, Nicholas, Ravanelli, Benjamin J., Narang, Tadej, Debevec, Liliana C., Baptista, Ana Isabel, Padrão, José, Oliveira, Jorge, Mota, Rodrigo, Zacca, Pantelis T., Nikolaidis, Donovan J., Lott, Sean C., Forbes, Korey, Cooke, Tanja, Taivassalo, Steven J., Elmer, John J., Durocher, Ricardo J., Fernandes, Gonçalo, Silva, Mário J., Costa
Publikováno v:
Journal of applied physiology (Bethesda, Md. : 1985). 133(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081640de8ae2cb5e74ec169077b998e3
https://pubmed.ncbi.nlm.nih.gov/36074923
https://pubmed.ncbi.nlm.nih.gov/36074923
Autor:
Alison M Barnard, David W Hammers, William T Triplett, Sarah Kim, Sean C Forbes, Rebecca J Willcocks, Michael J Daniels, Claudia R Senesac, Donovan J Lott, Ishu Arpan, William D Rooney, Richard T Wang, Stanley F Nelson, H Lee Sweeney, Krista Vandenborne, Glenn A Walter
Publikováno v:
Neurology
Background and Objectives:Duchenne muscular dystrophy (DMD) is a progressive muscle degenerative disorder with a well-characterized disease phenotype but considerable interindividual heterogeneity that is not well understood. The aim of the study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69bd59c400a798777962bdaf85f08030
https://doi.org/10.1212/wnl.0000000000201163
https://doi.org/10.1212/wnl.0000000000201163
Autor:
Emily J. Griffis, Waniiku A. Makumi, Hannah M. Sweatland, Kimberly J. Stubbs, Tanja Taivassalo, Donovan J. Lott, Warren E. Dixon
Publikováno v:
2022 IEEE Conference on Control Technology and Applications (CCTA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f94a1d770f7560f372d001ffa89e3f95
https://doi.org/10.1109/ccta49430.2022.9966066
https://doi.org/10.1109/ccta49430.2022.9966066
Autor:
Barry J. Byrne, Hyunjun Park, Glenn A. Walter, Donovan J. Lott, Tanja Taivassalo, Zahra Moslemi, Krista Vandenborne, Abhinandan Batra, Korey D. Cooke, Sean C. Forbes
Publikováno v:
Muscle Nerve
INTRODUCTION: This two-part study explored the safety, feasibility, and efficacy of a mild-moderate resistance isometric leg exercise program in ambulatory boys with Duchenne Muscular Dystrophy (DMD). METHODS: First, we used a dose escalation paradig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15660fb52c883285d2c9d366525ef43b
https://doi.org/10.1002/mus.27137
https://doi.org/10.1002/mus.27137
Autor:
Glenn A. Walter, Alison M. Barnard, Kirsten L. Zilke, Rebecca J. Willcocks, Kavya S Nair, Claudia R. Senesac, William D. Rooney, Krista Vandenborne, Ann T. Harrington, Donovan J. Lott
Publikováno v:
Phys Ther
Duchenne muscular dystrophy (DMD) is a muscle degenerative disorder that manifests in early childhood and results in progressive muscle weakness. Physical therapists have long been an important component of the multidisciplinary team caring for peopl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98727169da0f2689e49acdc7a6e66e8c
https://doi.org/10.1093/ptj/pzaa140
https://doi.org/10.1093/ptj/pzaa140
Autor:
Ann T. Harrington, John F. Brandsema, Glenn A. Walter, Rebecca J. Willcocks, Harneet Arora, Michael J. Daniels, William T. Triplett, Gihan Tennekoon, Krista Vandenborne, Claudia R. Senesac, Erika Finanger, H. Lee Sweeney, Alison M. Barnard, Donovan J. Lott, William D. Rooney, Sean C. Forbes, Dah Jyuu Wang, Umar Alabasi
Publikováno v:
Radiology
BACKGROUND: Upper extremity MRI and proton MR spectroscopy are increasingly considered to be outcome measures in Duchenne muscular dystrophy (DMD) clinical trials. PURPOSE: To demonstrate the feasibility of acquiring upper extremity MRI and proton ((
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f308dc946b30fa57f404285eb7254d08
https://doi.org/10.1148/radiol.2020192210
https://doi.org/10.1148/radiol.2020192210
Autor:
William T. Triplett, Sean C. Forbes, Barry S. Russman, Claudia R. Senesac, G. Tennekoon, Harneet Arora, Rebecca J. Willcocks, Erika Finanger, Michael J. Daniels, Dah Jyuu Wang, Richard S. Finkel, William D. Rooney, Yosef A. Berlow, Elliott O'Brien, Donovan J. Lott, Saptarshi Chakraborty, Brendan Moloney, Alison M. Barnard, Krista Vandenborne, H. Lee Sweeney, Ishu Arpan, Glenn A. Walter
Publikováno v:
Neurology
ObjectiveTo quantify disease progression in individuals with Duchenne muscular dystrophy (DMD) using magnetic resonance biomarkers of leg muscles.MethodsMRI and magnetic resonance spectroscopy (MRS) biomarkers were acquired from 104 participants with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3801c2c1126305e4799fbcff5f53a6ac
https://doi.org/10.1212/wnl.0000000000009244
https://doi.org/10.1212/wnl.0000000000009244