Alberto Aleman
Neurologist
Email AlbertoDr. Alemán graduated from medical school at University of Buenos Aires. He completed his residency in adult neurology and he was chief of residents at the Hospital Privado de Comunidad; and afterward he became a permanent Staff in the Insituto Médico de Alta Complejidad in Argentina.
Dr. Alemán completed a neuromuscular fellowship at The Hospital for Sick Children and is currently a neurologist at The Ottawa Hospital.
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Recent publications
Machado, J, Zwicker, J, Bourque, PR, Lochmüller, H, Warman-Chardon, J, Aleman, A et al.. Cramps as the initial presentation of CANVAS/RFC1-related disorder. J Neuromuscul Dis. 2026. 22143602261485644 PMID:42758088
Mah, JK, Gonorazky, HD, Nigro, E, Lochmüller, H, Alemán, A, Yaworski, A et al.. Vamorolone Safety, Pharmacokinetics, and Exploratory Efficacy in Duchenne Muscular Dystrophy: A Phase II, Nonrandomized, Multiple-Dose Study in 2-<4-Year-Old Boys. Neurology. 2026.106 (11)e218066 PMID:42139656
Lochmüller, H, Gonorazky, H, Nigro, E, Mah, JK, Alemán, A, Yaworski, A et al.. Results of a phase II open-label, multiple-dose study of vamorolone (VBP15-006) in 7- to < 18-year-old boys with duchenne muscular dystrophy. J Neurol. 2026.273 (3) PMID:41774261
Alawneh, I, Alemán, A, Nigro, E, Bouchard, M, Gonorazky, HD. Pediatric Cohort of Charcot-Marie-Tooth Disease: Clinical Features and Genetic Distribution. Neurol Genet. 2026.12 (1)e200339 PMID:41450731
O'Connell, C, Rodrigue, X, Hodgkinson, V, Henley, K, Slayter, J, Aleman, A et al.. Thinking outside the box: A re-evaluation of Canadian recommended outcome measures in adult spinal muscular atrophy - report of a national consensus workshop. J Neuromuscul Dis. 2025.12 (5)699-710 PMID:40356341
Estévez-Arias, B, Matalonga, L, Yubero, D, Polavarapu, K, Codina, A, Ortez, C et al.. Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases. Eur J Hum Genet. 2024. PMID:39658675
Kraft, F, Rodriguez-Aliaga, P, Yuan, W, Franken, L, Zajt, K, Hasan, D et al.. Brain malformations and seizures by impaired chaperonin function of TRiC. Science. 2024.386 (6721)516-525 PMID:39480921
Landfeldt, E, Alemán, A, Abner, S, Zhang, R, Werner, C, Tomazos, I et al.. Predictors of cardiac disease in duchenne muscular dystrophy: a systematic review and evidence grading. Orphanet J Rare Dis. 2024.19 (1)359 PMID:39342355
Estévez-Arias, B, Matalonga, L, Yubero, D, Polavarapu, K, Codina, A, Ortez, C et al.. Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases. Eur J Hum Genet. 2025.33 (2)239-247 PMID:39333429
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