Clinical development of novel therapies for Duchenne muscular dystrophy—Current and future
Author:
Affiliation:
1. Department of Molecular Therapy National Institute of Neuroscience, National Center of Neurology and Psychiatry Tokyo Japan
Funder
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ncn3.12691
Reference43 articles.
1. Indicators for ventilator use in Duchenne muscular dystrophy
2. A longitudinal cause-of-death analysis of patients with Duchenne muscular dystrophy
3. Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan
4. Clinical and genetic characterization of manifesting carriers of DMD mutations
5. Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular Dystrophy
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1. AMONDYS 45 (Casimersen), a Novel Antisense Phosphorodiamidate Morpholino Oligomer: Clinical Considerations for Treatment in Duchenne Muscular Dystrophy;Cureus;2023-12-28
2. Establishment of a Triple Quadrupole HPLC-MS Quantitation Method for Dystrophin Protein in Mouse and Human Skeletal Muscle;International Journal of Molecular Sciences;2023-12-25
3. Cardiac therapies for Duchenne muscular dystrophy;Therapeutic Advances in Neurological Disorders;2023-01
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