Zhao Y, Wang Y, Tulehalede A, Meng Z, Xu L, Bai H
Int J Mol Sci. 2025; 26(4).
PMID: 40003927
PMC: 11854990.
DOI: 10.3390/ijms26041459.
da Silva J, Nogueira M, da Silva Y, Nogueira F, Canedo N, Carneiro K
Sci Rep. 2025; 15(1):3293.
PMID: 39865125
PMC: 11770181.
DOI: 10.1038/s41598-025-87995-5.
Barak S, Ackerman Laufer S, Gudinsky Elyashiv M, Rubinstein-Shatz S, Davidson R, Kaplan T
PLoS One. 2025; 20(1):e0317006.
PMID: 39808623
PMC: 11731756.
DOI: 10.1371/journal.pone.0317006.
Luglio A, Maggi E, Riviello F, Conforti A, Sorrentino U, Zuccarello D
Genes (Basel). 2024; 15(11).
PMID: 39596609
PMC: 11593801.
DOI: 10.3390/genes15111409.
Ge L, Yang Y, Yang Y, Chen Y, Tao N, Zhang L
Open Med (Wars). 2024; 19(1):20240916.
PMID: 39588385
PMC: 11587917.
DOI: 10.1515/med-2024-0916.
A Review of Muscular Dystrophies.
Hoang T, Dowdy R
Anesth Prog. 2024; 71(1):44-52.
PMID: 39503119
PMC: 11101287.
DOI: 10.2344/673191.
Comprehensive quantitative magnetic resonance imaging assessment of skeletal muscle pathophysiology in golden retriever muscular dystrophy: Insights from multicomponent water T2 and extracellular volume fraction.
Caldas de Almeida Araujo E, Barthelemy I, Fromes Y, Baudin P, Blot S, Reyngoudt H
NMR Biomed. 2024; 38(1):e5278.
PMID: 39434514
PMC: 11602680.
DOI: 10.1002/nbm.5278.
Antisense oligonucleotides and their applications in rare neurological diseases.
McDowall S, Aung-Htut M, Wilton S, Li D
Front Neurosci. 2024; 18:1414658.
PMID: 39376536
PMC: 11456401.
DOI: 10.3389/fnins.2024.1414658.
Muscular dystrophy patients show low exercise-induced blood flow in muscles with normal strength.
Gera O, Shavit-Stein E, Amichai T, Chapman J, Chorin O, Greenbaum L
Ann Clin Transl Neurol. 2024; 11(11):2866-2876.
PMID: 39250335
PMC: 11572729.
DOI: 10.1002/acn3.52194.
A Systematic Review on the Application of Virtual Reality for Muscular Dystrophy Rehabilitation: Motor Learning Benefits.
Kiper P, Federico S, Szczepanska-Gieracha J, Szary P, Wrzeciono A, Mazurek J
Life (Basel). 2024; 14(7).
PMID: 39063545
PMC: 11278510.
DOI: 10.3390/life14070790.
Cardiomyopathy in Duchenne Muscular Dystrophy and the Potential for Mitochondrial Therapeutics to Improve Treatment Response.
Gandhi S, Sweeney H, Hart C, Han R, Perry C
Cells. 2024; 13(14.
PMID: 39056750
PMC: 11274633.
DOI: 10.3390/cells13141168.
Comprehensive review of adverse reactions and toxicology in ASO-based therapies for Duchenne Muscular Dystrophy: From FDA-approved drugs to peptide-conjugated ASO.
Haque U, Kohut M, Yokota T
Curr Res Toxicol. 2024; 7:100182.
PMID: 38983605
PMC: 11231654.
DOI: 10.1016/j.crtox.2024.100182.
CISD3/MiNT is required for complex I function, mitochondrial integrity, and skeletal muscle maintenance.
Nechushtai R, Rowland L, Karmi O, Marjault H, Nguyen T, Mittal S
Proc Natl Acad Sci U S A. 2024; 121(22):e2405123121.
PMID: 38781208
PMC: 11145280.
DOI: 10.1073/pnas.2405123121.
Identification of novel variations in three cases with rare inherited neuromuscular disorder.
Chen W, Yuan Y, Hu K, Sun D, Wang S, He Q
Exp Ther Med. 2024; 27(6):270.
PMID: 38756899
PMC: 11097291.
DOI: 10.3892/etm.2024.12558.
Clinical Scoring Tool for Diagnosis of Dystrophinopathies: Can the Tool Finish the Job?.
Hiew F
Ann Indian Acad Neurol. 2024; 27(2):118-119.
PMID: 38751931
PMC: 11093167.
DOI: 10.4103/aian.aian_682_23.
Cross-species modeling of muscular dystrophy in Caenorhabditis elegans using patient-derived extracellular vesicles.
Shalash R, Levi-Ferber M, Cohen C, Dori A, Brodie C, Henis-Korenblit S
Dis Model Mech. 2024; 17(3).
PMID: 38501170
PMC: 11007864.
DOI: 10.1242/dmm.050412.
Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of Disease.
McDonald C, Camino E, Escandon R, Finkel R, Fischer R, Flanigan K
J Neuromuscul Dis. 2024; 11(2):499-523.
PMID: 38363616
PMC: 10977441.
DOI: 10.3233/JND-230219.
Use of plasmapheresis to lower anti-AAV antibodies in nonhuman primates with pre-existing immunity to AAVrh74.
Potter R, Peterson E, Griffin D, Cooper Olson G, Lewis S, Cochran K
Mol Ther Methods Clin Dev. 2024; 32(1):101195.
PMID: 38327805
PMC: 10847772.
DOI: 10.1016/j.omtm.2024.101195.
deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis.
Fortunato F, Tonelli L, Farne M, Selvatici R, Ferlini A
Front Neurol. 2024; 14:1288721.
PMID: 38288333
PMC: 10823016.
DOI: 10.3389/fneur.2023.1288721.
Regulation of Satellite Cells Functions during Skeletal Muscle Regeneration: A Critical Step in Physiological and Pathological Conditions.
Careccia G, Mangiavini L, Cirillo F
Int J Mol Sci. 2024; 25(1).
PMID: 38203683
PMC: 10778731.
DOI: 10.3390/ijms25010512.