Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Dah-Jyuu Wang"'
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:
Andrew J. Degnan, Victor M. Ho-Fung, Rebecca C. Ahrens-Nicklas, Christian A. Barrera, Suraj D. Serai, Dah-Jyuu Wang, Can Ficicioglu
Publikováno v:
Insights into Imaging, Vol 10, Iss 1, Pp 1-19 (2019)
Abstract Gaucher disease is an inherited metabolic disorder resulting in deficiency of lysosomal enzyme β-glucocerebrosidase causing the accumulation of abnormal macrophages (“Gaucher cells”) within multiple organs, most conspicuously affecting
Externí odkaz:
https://doaj.org/article/0f344bca3c1d4b459ab938f4eb4842c5
Autor:
Jeremy S. Francis, PhD, Ireneusz Wojtas, PhD, Vladimir Markov, MD, Steven J. Gray, PhD, Thomas J. McCown, PhD, R. Jude Samulski, PhD, Larissa T. Bilaniuk, MD, Dah-Jyuu Wang, PhD, Darryl C. De Vivo, MD, Christopher G. Janson, MD, Paola Leone, PhD
Publikováno v:
Neurobiology of Disease, Vol 96, Iss , Pp 323-334 (2016)
Breakdown of neuro-glial N-acetyl-aspartate (NAA) metabolism results in the failure of developmental myelination, manifest in the congenital pediatric leukodystrophy Canavan disease caused by mutations to the sole NAA catabolizing enzyme aspartoacyla
Externí odkaz:
https://doaj.org/article/36bbbc38714a4910a6a154ba0ec668da
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
Publikováno v:
Journal of Central Nervous System Disease, Vol 2013, Iss 5, Pp 25-30 (2013)
Externí odkaz:
https://doaj.org/article/c76ca43179e2438fb41c87ceb1b50db9
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
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/
Publikováno v:
Journal of Central Nervous System Disease, Vol 2012, Iss 4, Pp 73-79 (2012)
Externí odkaz:
https://doaj.org/article/c9c20509b03548c8af659012913daa4c
Autor:
Suraj D. Serai, Can Ficicioglu, Rebecca C. Ahrens-Nicklas, Andrew J. Degnan, Dah Jyuu Wang, Victor Ho-Fung, Christian A. Barrera
Publikováno v:
Insights into Imaging, Vol 10, Iss 1, Pp 1-19 (2019)
Insights into Imaging
Insights into Imaging
Gaucher disease is an inherited metabolic disorder resulting in deficiency of lysosomal enzyme β-glucocerebrosidase causing the accumulation of abnormal macrophages (“Gaucher cells”) within multiple organs, most conspicuously affecting the liver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68445e5d681be2c4fe1f8e7e9cce482d
http://link.springer.com/article/10.1186/s13244-019-0743-5
http://link.springer.com/article/10.1186/s13244-019-0743-5