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1992 | 1 |
2014 | 1 |
2023 | 1 |
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Page 1
Electrophysiological Characterization of a MYH7 Variant with Tremor Phenotype.
Mov Disord Clin Pract. 2023 Mar 14;10(4):646-651. doi: 10.1002/mdc3.13664. eCollection 2023 Apr.
Mov Disord Clin Pract. 2023.
PMID: 37070061
Free PMC article.
Ataluren treatment of patients with nonsense mutation dystrophinopathy.
Bushby K, Finkel R, Wong B, Barohn R, Campbell C, Comi GP, Connolly AM, Day JW, Flanigan KM, Goemans N, Jones KJ, Mercuri E, Quinlivan R, Renfroe JB, Russman B, Ryan MM, Tulinius M, Voit T, Moore SA, Lee Sweeney H, Abresch RT, Coleman KL, Eagle M, Florence J, Gappmaier E, Glanzman AM, Henricson E, Barth J, Elfring GL, Reha A, Spiegel RJ, O'donnell MW, Peltz SW, Mcdonald CM; PTC124-GD-007-DMD STUDY GROUP.
Bushby K, et al.
Muscle Nerve. 2014 Oct;50(4):477-87. doi: 10.1002/mus.24332.
Muscle Nerve. 2014.
PMID: 25042182
Free PMC article.
Clinical Trial.
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Spinal muscular atrophy: new thoughts on the pathogenesis and classification schema.
Russman BS, Iannacone ST, Buncher CR, Samaha FJ, White M, Perkins B, Zimmerman L, Smith C, Burhans K, Barker L.
Russman BS, et al. Among authors: iannacone st.
J Child Neurol. 1992 Oct;7(4):347-53. doi: 10.1177/088307389200700403.
J Child Neurol. 1992.
PMID: 1469240
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