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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 2 |
2019 | 2 |
2020 | 2 |
2021 | 1 |
2023 | 1 |
2024 | 0 |
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6 results
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Page 1
Posterior Spinal Fusion Surgery for Neuromuscular Disease Patients with Severe Scoliosis Whose Cobb Angle Was over 100 Degrees.
Medicina (Kaunas). 2023 Jun 5;59(6):1090. doi: 10.3390/medicina59061090.
Medicina (Kaunas). 2023.
PMID: 37374294
Free PMC article.
Limitations of posterior spinal fusion to L5 for flaccid neuromuscular scoliosis focusing on pelvic obliquity.
Saito W, Inoue G, Shirasawa E, Imura T, Nakazawa T, Miyagi M, Kawakubo A, Uchida K, Kotani T, Akazawa T, Takaso M.
Saito W, et al.
Spine Deform. 2021 Mar;9(2):559-565. doi: 10.1007/s43390-020-00214-1. Epub 2020 Oct 2.
Spine Deform. 2021.
PMID: 33006744
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Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy.
Okubo M, Noguchi S, Hayashi S, Nakamura H, Komaki H, Matsuo M, Nishino I.
Okubo M, et al.
Hum Genet. 2020 Feb;139(2):247-255. doi: 10.1007/s00439-019-02107-4. Epub 2020 Jan 9.
Hum Genet. 2020.
PMID: 31919629
Free PMC article.
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COX6A2 variants cause a muscle-specific cytochrome c oxidase deficiency.
Inoue M, Uchino S, Iida A, Noguchi S, Hayashi S, Takahashi T, Fujii K, Komaki H, Takeshita E, Nonaka I, Okada Y, Yoshizawa T, Van Lommel L, Schuit F, Goto YI, Mimaki M, Nishino I.
Inoue M, et al.
Ann Neurol. 2019 Aug;86(2):193-202. doi: 10.1002/ana.25517. Epub 2019 Jul 2.
Ann Neurol. 2019.
PMID: 31155743
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Emery-Dreifuss muscular dystrophy-related myopathy with TMEM43 mutations.
Mukai T, Mori-Yoshimura M, Nishikawa A, Hokkoku K, Sonoo M, Nishino I, Takahashi Y.
Mukai T, et al.
Muscle Nerve. 2019 Feb;59(2):E5-E7. doi: 10.1002/mus.26355. Epub 2018 Nov 13.
Muscle Nerve. 2019.
PMID: 30311943
No abstract available.
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Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis.
Shimizu-Motohashi Y, Murakami T, Kimura E, Komaki H, Watanabe N.
Shimizu-Motohashi Y, et al.
Orphanet J Rare Dis. 2018 Jun 15;13(1):93. doi: 10.1186/s13023-018-0834-2.
Orphanet J Rare Dis. 2018.
PMID: 29907124
Free PMC article.
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