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24. Surgical correction of a ventricular septal defect in a child with spinal muscular atrophy type 2 treated with nusinersen sodium: a case report. Biçer M; Kozan Ş; Öztürk F; Akçay AA J Cardiothorac Surg; 2023 Feb; 18(1):68. PubMed ID: 36759863 [TBL] [Abstract][Full Text] [Related]
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26. Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family. Shaw PJ; Ince PG; Goodship J; Burn J; Slade J; Bates D; Medwin DG Neurology; 1992 Aug; 42(8):1477-80. PubMed ID: 1641139 [TBL] [Abstract][Full Text] [Related]
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32. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy. Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481 [TBL] [Abstract][Full Text] [Related]
33. A new form of infantile spinal muscular atrophy. García-Alix A; Rodriguez JI; Quero J J Med Genet; 1992 Mar; 29(3):215. PubMed ID: 1552561 [No Abstract] [Full Text] [Related]
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35. Childhood progressive spinal muscular atrophy with facioscapulo-humeral predominance, sensory and autonomic involvement and optic atrophy. Schmitt HP; Härle M; Koelfen W; Nissen KH Brain Dev; 1994; 16(5):386-92. PubMed ID: 7892958 [TBL] [Abstract][Full Text] [Related]
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