Diagnosis and management of Becker muscular dystrophy: the French guidelines.
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J Neurol. 2023 Oct;270(10):4763-4781. doi: 10.1007/s00415-023-11837-5. Epub 2023 Jul 9.
An update on Becker muscular dystrophy.
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Curr Opin Neurol. 2023 Oct 1;36(5):450-454. doi: 10.1097/WCO.0000000000001191. Epub 2023 Aug 21.
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy.
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J Med Genet. 2007 Jun;44(6):368-72. doi: 10.1136/jmg.2006.047464. Epub 2007 Jan 26.
A Review of Muscular Dystrophies.
Hoang T, Dowdy RAE.
Anesth Prog. 2024 May 3;71(1):44-52. doi: 10.2344/673191.
Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.
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Muscle Nerve. 2006 Aug;34(2):135-44. doi: 10.1002/mus.20586.
Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy.
Duan D.
Mol Ther. 2018 Oct 3;26(10):2337-2356. doi: 10.1016/j.ymthe.2018.07.011. Epub 2018 Jul 17.
The importance of genetic diagnosis for Duchenne muscular dystrophy.
Aartsma-Rus A, Ginjaar IB, Bushby K.
J Med Genet. 2016 Mar;53(3):145-51. doi: 10.1136/jmedgenet-2015-103387. Epub 2016 Jan 11.
Dystrophin-Deficient Cardiomyopathy.
Kamdar F, Garry DJ.
J Am Coll Cardiol. 2016 May 31;67(21):2533-46. doi: 10.1016/j.jacc.2016.02.081.
Duchenne and Becker muscular dystrophy: Cellular mechanisms, image analysis, and computational models: A review.
Escobar-Huertas JF, Vaca-González JJ, Guevara JM, Ramirez-Martinez AM, Trabelsi O, Garzón-Alvarado DA.
Cytoskeleton (Hoboken). 2024 Jun-Jul;81(6-7):269-286. doi: 10.1002/cm.21826. Epub 2024 Jan 15.
Becker muscular dystrophy: case report, review of the literature, and analysis of differentially expressed hub genes.
Li M, Han Y, Wang S, Yu Y, Liu M, Xia Y, Weng Z, Zhou L, He X, Wang J, He Z, Yu L, Zha Y.
Neurol Sci. 2022 Jan;43(1):243-253. doi: 10.1007/s10072-021-05499-2. Epub 2021 Nov 3.
