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Spinal muscular atrophy: from animal model to clinical trial.
Funct Neurol. 2010 Apr-Jun;25(2):73-9.
Funct Neurol. 2010.
PMID: 20923604
Review.
Clinical Outcomes in Patients with Spinal Muscular Atrophy Type 1 Treated with Nusinersen.
de Holanda Mendonça R, Jorge Polido G, Ciro M, Jorge Fontoura Solla D, Conti Reed U, Zanoteli E.
de Holanda Mendonça R, et al. Among authors: conti reed u.
J Neuromuscul Dis. 2021;8(2):217-224. doi: 10.3233/JND-200533.
J Neuromuscul Dis. 2021.
PMID: 33459657
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A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms.
Sampedro Castañeda M, Zanoteli E, Scalco RS, Scaramuzzi V, Marques Caldas V, Conti Reed U, da Silva AMS, O'Callaghan B, Phadke R, Bugiardini E, Sud R, McCall S, Hanna MG, Poulsen H, Männikkö R, Matthews E.
Sampedro Castañeda M, et al. Among authors: conti reed u.
Brain. 2018 Dec 1;141(12):3308-3318. doi: 10.1093/brain/awy283.
Brain. 2018.
PMID: 30423015
Free PMC article.
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The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Rodríguez Cruz PM, Cossins J, Estephan EP, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Chow G, Carr A, Manzur A, Robb S, Munot P, Wei Liu W, Banka S, Fraser H, De Goede C, Zanoteli E, Conti Reed U, Sage A, Gratacos M, Macaya A, Dusl M, Senderek J, Töpf A, Hofer M, Knight R, Ramdas S, Jayawant S, Lochmüller H, Palace J, Beeson D.
Rodríguez Cruz PM, et al. Among authors: conti reed u.
Brain. 2019 Jun 1;142(6):1547-1560. doi: 10.1093/brain/awz107.
Brain. 2019.
PMID: 31081514
Free PMC article.
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