Modeling disease trajectory in Duchenne muscular dystrophy

scientific article published on 17 March 2020

Modeling disease trajectory in Duchenne muscular dystrophy is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1212/WNL.0000000000009244
P932PMC publication ID7251517
P698PubMed publication ID32184340

P50authorYosef A BerlowQ90407710
Saptarshi ChakrabortyQ90407714
P2093author name stringH Lee Sweeney
Dah-Jyuu Wang
Michael J Daniels
William D Rooney
Claudia Senesac
Glenn A Walter
Krista Vandenborne
Sean C Forbes
Donovan J Lott
Richard Finkel
Rebecca J Willcocks
Barry S Russman
Gihan Tennekoon
Elliott O'Brien
Erika L Finanger
Ishu Arpan
William T Triplett
Harneet Arora
Brendan Moloney
Alison Barnard
P2860cites workDystrophin: the protein product of the Duchenne muscular dystrophy locusQ29618077
Skeletal muscles of ambulant children with Duchenne muscular dystrophy: validation of multicenter study of evaluation with MR imaging and MR spectroscopyQ30546319
Chemical shift-based MRI to measure fat fractions in dystrophic skeletal muscleQ30665063
Quantitative Skeletal Muscle MRI: Part 2, MR Spectroscopy and T2 Relaxation Time Mapping-Comparison Between Boys With Duchenne Muscular Dystrophy and Healthy BoysQ30982305
Magnetic resonance imaging of skeletal muscle diseaseQ31115497
Notch signaling deficiency underlies age-dependent depletion of satellite cells in muscular dystrophy.Q33935640
Examination of effects of corticosteroids on skeletal muscles of boys with DMD using MRI and MRS.Q34171004
Human soleus muscle: a comparison of fiber composition and enzyme activities with other leg musclesQ34205271
A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophyQ34417832
Muscular dystrophies and the dystrophin-glycoprotein complexQ34425741
Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle BiopsiesQ34518069
The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophyQ36842039
Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large duchenne muscular dystrophy cohort.Q37114363
MRI quantifies neuromuscular disease progressionQ37123866
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophyQ37633713
Use of skeletal muscle MRI in diagnosis and monitoring disease progression in Duchenne muscular dystrophyQ37975308
Stakeholder cooperation to overcome challenges in orphan medicine development: the example of Duchenne muscular dystrophy.Q38865431
Pharmacological advances for treatment in Duchenne muscular dystrophyQ39293658
Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophyQ42368601
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function MeasureQ43454569
High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy.Q44239685
Cerebral metabolism in man after acute stroke: new observations using localized proton NMR spectroscopyQ45410633
Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study.Q45935564
Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.Q45966003
Deflazacort use in Duchenne muscular dystrophy: an 8-year follow-upQ46750138
Regional metabolite concentrations in human brain as determined by quantitative localized proton MRS.Q48560409
A short protocol for muscle MRI in children with muscular dystrophies.Q53667939
Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy.Q55282480
Necroptosis mediates myofibre death in dystrophin-deficient miceQ58759838
Report on the workshop: Meaningful outcome measures for Duchenne muscular dystrophy, London, UK, 30–31 January 2017Q59876191
Long-term benefit from prednisone therapy in Duchenne muscular dystrophyQ67767537
The muscular dystrophiesQ77731754
Quantitative MRI and loss of free ambulation in Duchenne muscular dystrophyQ85398934
P921main subjectDuchenne muscular dystrophyQ1648484
P577publication date2020-03-17
P1433published inNeurologyQ1161692
P1476titleModeling disease trajectory in Duchenne muscular dystrophy

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