Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ann T. Harrington"'
Autor:
Alison M Barnard, Rebecca J Willcocks, Erika L Finanger, Michael J Daniels, William T Triplett, William D Rooney, Donovan J Lott, Sean C Forbes, Dah-Jyuu Wang, Claudia R Senesac, Ann T Harrington, Richard S Finkel, Barry S Russman, Barry J Byrne, Gihan I Tennekoon, Glenn A Walter, H Lee Sweeney, Krista Vandenborne
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0194283 (2018)
OBJECTIVE:To provide evidence for quantitative magnetic resonance (qMR) biomarkers in Duchenne muscular dystrophy by investigating the relationship between qMR measures of lower extremity muscle pathology and functional endpoints in a large ambulator
Externí odkaz:
https://doaj.org/article/e8dfd05ea09445269c042c5cef248456
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
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 ((
Autor:
Kavya S. Nair, Donovan J. Lott, Sean C. Forbes, Alison M. Barnard, Rebecca J. Willcocks, Claudia R. Senesac, Michael J. Daniels, Ann T. Harrington, Gihan I. Tennekoon, Kirsten Zilke, Erika L. Finanger, Richard S. Finkel, William D. Rooney, Glenn A. Walter, Krista Vandenborne
Publikováno v:
J Neuromuscul Dis
Background: Muscles of boys with Duchenne muscular dystrophy (DMD) are progressively replaced by fatty fibrous tissues, and weakness leads to loss of ambulation (LoA). Step activity (SA) monitoring is a quantitative measure of real-world ambulatory f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23bf53acba5f02477e41717786060e87
https://europepmc.org/articles/PMC9257666/
https://europepmc.org/articles/PMC9257666/
Autor:
Rebecca J. Willcocks, Alison M. Barnard, Ryan J. Wortman, Claudia R. Senesac, Donovan J. Lott, Ann T. Harrington, Kirsten L. Zilke, Sean C. Forbes, William D. Rooney, Dah-Jyuu Wang, Erika L. Finanger, Gihan I. Tennekoon, Michael J. Daniels, William T. Triplett, Glenn A. Walter, Krista Vandenborne
Publikováno v:
J Neuromuscul Dis
Background: Joint contractures are common in boys and men with Duchenne muscular dystrophy (DMD), and management of contractures is an important part of care. The optimal methods to prevent and treat contractures are controversial, and the natural hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6e8403247af5ae280303c8b5186f09
https://europepmc.org/articles/PMC9257436/
https://europepmc.org/articles/PMC9257436/
Autor:
Amy Waldman, Tracy Kornafel, Geraldine Liu, Ann T. Harrington, Laura Adang, Samuel R. Pierce, Amanda K. Jan, Adeline Vanderver, Elizabeth Ballance, Francesco Gavazzi, Scott A. Lorch, Allan M. Glanzman, Sara B. DeMauro, Justine Shults
Publikováno v:
Pediatr Neurol
Background Leukodystrophies are a rare class of disorders characterized by severe neuromotor disability. There is a strong need for research regarding the functional status of people with leukodystrophy which is limited by the need for in-person asse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc15934b5f2fdea939d8cd9af53dd41c
https://europepmc.org/articles/PMC8629609/
https://europepmc.org/articles/PMC8629609/
Autor:
Rebecca J. Willcocks, G. Tennekoon, Sean C. Forbes, Krista Vandenborne, Harneet Arora, H. Lee Sweeney, Dah Jyuu Wang, Ann T. Harrington, Alison M. Barnard, Erika Finanger, Glenn A. Walter, Michael J. Daniels, Saptarshi Chakraborty, William D. Rooney, Claudia R. Senesac, William T. Triplett, Donovan J. Lott
Publikováno v:
Neurology
ObjectiveTo investigate the potential of lower extremity magnetic resonance (MR) biomarkers to serve as endpoints in clinical trials of therapeutics for Duchenne muscular dystrophy (DMD) by characterizing the longitudinal progression of MR biomarkers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::659cb500027f7455a0603f37b0d0b54e
https://europepmc.org/articles/PMC7238941/
https://europepmc.org/articles/PMC7238941/
Autor:
Barry J. Byrne, William T. Triplett, Ann T. Harrington, Glenn A. Walter, Krista Vandenborne, Claudia R. Senesac, Rebecca J. Willcocks, Michael J. Daniels, Harneet Arora, Gihan Tennekoon, Barry S. Russman, H. Lee Sweeney, Dandan Xu, Richard S. Finkel, Donovan J. Lott, Kirsten L. Zilke, Erika Finanger
Publikováno v:
Muscle & Nerve. 58:631-638
Introduction Tests of ambulatory function are common clinical trial endpoints in Duchenne muscular dystrophy (DMD). Using these tests, the ImagingDMD study has generated a large data set that can describe the contemporary natural history of DMD in 5-
Autor:
Thomas A. Miller, Robin S Schlosser, Nicholas Dagincourt, Teresa Barnard, Victoria L. Pemberton, Ann T. Harrington, Linda M. Lambert, Janine Wood, Felicia L Trachtenberg, Kaitlyn Daniels, Shelley Andreas
Publikováno v:
Cardiology in the Young. 27:1361-1368
ObjectiveThe aim of this study was to evaluate the safety and feasibility of a passive range of motion exercise programme for infants with CHD.Study designThis non-randomised pilot study enrolled 20 neonates following Stage I palliation for single-ve
Autor:
Rebecca J. Willcocks, Claudia R. Senesac, Richard S. Finkel, William D. Rooney, Glenn A. Walter, Erika Finanger, Michael J. Daniels, William T. Triplett, Barry J. Byrne, Gihan Tennekoon, Sean C. Forbes, Krista Vandenborne, H. Lee Sweeney, Donovan J. Lott, Ann T. Harrington, Dah Jyuu Wang, Barry S. Russman
Publikováno v:
Annals of Neurology. 79:535-547
Objective The aim of this study was to describe Duchenne muscular dystrophy (DMD) disease progression in the lower extremity muscles over 12 months using quantitative magnetic resonance (MR) biomarkers, collected across three sites in a large cohort.