Alberto Aleman

Alberto-Aleman-web

Working Group Member

Neurologist, The Ottawa Hospital


NMD4C Involvement: Pillar 2: Clinical Research, Pillar 3: Clinical Practice Research

Email Alberto

Biography

Dr. Aleman 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. Aleman completed a neuromuscular fellowship at The Hospital for Sick Children and is currently a neurologist at The Ottawa Hospital. Within the NMD4C, Dr. Aleman is a member of the Curriculum Development working group.


Recent Publications

Bastianelli, C, Araujo, M, Cataldi, L, Aleman, A, Olleta, C, Pineda, M et al.. Scientific societies in health education and promotion in the school setting. Arch Argent Pediatr. 2025. e202410603 PMID:40526472

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. 22143602251336076 PMID:40356341

Liu, M, Chambers, A, Chambers, B, Aleman, A, Stift, M, Mamonova, K et al.. SNP-RFLP Markers for the Study of Arabidopsis lyrata. Ecol Evol. 2025.15 (4)e71056 PMID:40270795

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

Aleman, A, Arteaga, MC, Gasca-Pineda, J, Bello-Bedoy, R. Divergent lineages in a young species: The case of datilillo (Yucca valida), a broadly distributed plant from the Baja California Peninsula. Am J Bot. 2024.111 (9)e16385 PMID:39113241

Baranello, G, Neurodevelopment in SMA Working Group. The emerging spectrum of neurodevelopmental comorbidities in early-onset Spinal Muscular Atrophy. Eur J Paediatr Neurol. 2024.48 67-68 PMID:38043384

Sondheimer, N, Aleman, A, Cameron, J, Gonorazky, H, Sabha, N, Oliveira, P et al.. Biallelic pathogenic variants in the mitochondrial form of phosphoenolpyruvate carboxykinase cause peripheral neuropathy. HGG Adv. 2023.4 (2)100182 PMID:36845668

See more on PubMed