Ahmad M, ElRasoul A, Sedayou R, Tamboosi M, Mahroos H, Alrashed S
J Int Med Res. 2024; 52(12):3000605241305252.
PMID: 39719075
PMC: 11683810.
DOI: 10.1177/03000605241305252.
Birnkrant D, Black J, Sheehan D, Baker H, DiBartolo M, Katz S
Paediatr Drugs. 2024; 27(2):143-159.
PMID: 39707120
PMC: 11829838.
DOI: 10.1007/s40272-024-00673-3.
Spagnoli C, Adorisio R, Bello L, DAmico A, DAngelo M, Pane M
Acta Myol. 2024; 43(3):102-107.
PMID: 39468966
PMC: 11537712.
DOI: 10.36185/2532-1900-447.
Pijeira Perez Y, Hughes D
Pharmacoeconomics. 2024; 42(12):1373-1394.
PMID: 39249730
PMC: 11564307.
DOI: 10.1007/s40273-024-01418-3.
Hwu W
J Biomed Sci. 2024; 31(1):79.
PMID: 39138523
PMC: 11321167.
DOI: 10.1186/s12929-024-01070-1.
Promising therapeutic approaches of utrophin replacing dystrophin in the treatment of Duchenne muscular dystrophy.
Wu R, Song Y, Wu S, Chen Y
Fundam Res. 2024; 2(6):885-893.
PMID: 38933385
PMC: 11197810.
DOI: 10.1016/j.fmre.2022.07.004.
Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis.
Landfeldt E, Aleman A, Abner S, Zhang R, Werner C, Tomazos I
J Neuromuscul Dis. 2024; 11(3):579-612.
PMID: 38669554
PMC: 11091649.
DOI: 10.3233/JND-230220.
The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy.
Swiderski K, Chan A, Herold M, Kueh A, Chung J, Hardee J
Dis Model Mech. 2024; 17(4).
PMID: 38602028
PMC: 11095634.
DOI: 10.1242/dmm.050502.
The complex landscape of DMD mutations: moving towards personalized medicine.
Gatto F, Benemei S, Piluso G, Bello L
Front Genet. 2024; 15:1360224.
PMID: 38596212
PMC: 11002111.
DOI: 10.3389/fgene.2024.1360224.
Treatment with ataluren in four symptomatic Duchenne carriers. A pilot study.
Dori A, Scutifero M, Passamano L, Zoppi D, Ruggiero L, Trabacca A
Acta Myol. 2024; 43(1):8-15.
PMID: 38586166
PMC: 10997039.
DOI: 10.36185/2532-1900-398.
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience.
Spagnoli C, Adorisio R, Bello L, DAmico A, DAngelo M, Pane M
Acta Myol. 2024; 42(4):118-122.
PMID: 38406379
PMC: 10883323.
DOI: 10.36185/2532-1900-396.
The role of ataluren in the treatment of ambulatory and non-ambulatory children with nonsense mutation duchenne muscular dystrophy - a consensus derived using a modified Delphi methodology in Eastern Europe, Greece, Israel and Sweden.
Golli T, Jurikova L, Sejersen T, Dixon C
BMC Neurol. 2024; 24(1):73.
PMID: 38383326
PMC: 10880248.
DOI: 10.1186/s12883-024-03570-x.
AMONDYS 45 (Casimersen), a Novel Antisense Phosphorodiamidate Morpholino Oligomer: Clinical Considerations for Treatment in Duchenne Muscular Dystrophy.
Vasterling M, Maitski R, Davis B, Barnes J, Kelkar R, Klapper R
Cureus. 2024; 15(12):e51237.
PMID: 38283433
PMC: 10821770.
DOI: 10.7759/cureus.51237.
Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.
Li S, Li J, Shi W, Nie Z, Zhang S, Ma F
Biomolecules. 2023; 13(6).
PMID: 37371567
PMC: 10296333.
DOI: 10.3390/biom13060988.
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study.
Brogna C, Pane M, Coratti G, DAmico A, Pegoraro E, Bello L
Children (Basel). 2023; 10(4).
PMID: 37189996
PMC: 10136754.
DOI: 10.3390/children10040746.
Safety and effectiveness of ataluren in patients with nonsense mutation DMD in the STRIDE Registry compared with the CINRG Duchenne Natural History Study (2015-2022): 2022 interim analysis.
Mercuri E, Osorio A, Muntoni F, Buccella F, Desguerre I, Kirschner J
J Neurol. 2023; 270(8):3896-3913.
PMID: 37115359
PMC: 10141820.
DOI: 10.1007/s00415-023-11687-1.
Recent Trends in Antisense Therapies for Duchenne Muscular Dystrophy.
Wilton-Clark H, Yokota T
Pharmaceutics. 2023; 15(3).
PMID: 36986639
PMC: 10054484.
DOI: 10.3390/pharmaceutics15030778.
Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy.
Araujo A, Morales Saute J, Fortes C, Franca Jr M, Pereira J, Albuquerque M
Arq Neuropsiquiatr. 2023; 81(1):81-94.
PMID: 36918011
PMC: 10014210.
DOI: 10.1055/s-0043-1761466.
Natural History and Real-World Data in Rare Diseases: Applications, Limitations, and Future Perspectives.
Liu J, Barrett J, Leonardi E, Lee L, Roychoudhury S, Chen Y
J Clin Pharmacol. 2022; 62 Suppl 2:S38-S55.
PMID: 36461748
PMC: 10107901.
DOI: 10.1002/jcph.2134.
PTC124 Rescues Nonsense Mutation of Two Tumor Suppressor Genes and to Repress HNSCC Cell Proliferation.
Wu M, Lu R, Yu S, Tsai Y, Lin Y, Bai Z
Biomedicines. 2022; 10(11).
PMID: 36428516
PMC: 9687978.
DOI: 10.3390/biomedicines10112948.