Cam-Tu Émilie Nguyen

Cam-Tu-3x2

Working Group Member

Pediatric Neurologist, CHU Sainte-Justine, Université de Montréal

Medical Director of the Neuromuscular clinic, Marie Enfant Rehabilitation Centre of CHU Sainte-Justine | Neuromuscular and EMG fellowship director at CHU Sainte-Justine


NMD4C Working Group(s): Early-Career Working Group

Email Cam-Tu Émilie

Biography

Dr. Cam-Tu Émilie Nguyen is a pediatric neurologist specialized in neuromuscular disorders and neuromuscular and EMG fellowship director at CHU Sainte-Justine in Montreal. Dr. Nguyen is also the medical director of the Neuromuscular clinic at Marie Enfant Rehabilitation Centre of CHU Sainte-Justine. Dr. Nguyen completed a fellowship in EMG and neuromuscular disorders at McGill University, the London Health Sciences Centre under Dr. Craig Campbell’s supervision, and The Hospital for Sick Children (SickKids).

Dr. Nguyen received an EMG Diploma from the Canadian Society of Clinical Neurophysiologists (CSCN), and was the recipient of the CSCN Fellowship in Neuromuscular Medicine & Electromyography in 2015.She is an early-career member of the NMD4C, and sits on the early-career working group.

Watch Dr. Nguyen’s feature in Radio-Canada Découvert’s ‘Thérapie à 2,8 millions $’ on the topic of Zolgensma and Spinal muscular atrophy in Quebec. This recording is available in French.


Recent Publications

Yazdani, PA, St-Jean, ML, Matovic, S, Spahr, A, Tran, LT, Boucher, RM et al.. The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study. J Child Neurol. 2023. 8830738231176672 PMID:37225698

Allen, NM, O'Rahelly, M, Eymard, B, Chouchane, M, Hahn, A, Kearns, G et al.. The emerging spectrum of foetal acetylcholine receptor antibody-associated disorders (FARAD). Brain. 2023. PMID:37186601

Derksen, A, Shih, HY, Forget, D, Darbelli, L, Tran, LT, Poitras, C et al.. Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease. HGG Adv. 2021.2 (3)100034 PMID:35047835

Amir Yazdani, P, St-Jean, ML, Matovic, S, Spahr, A, Tran, LT, Boucher, RM et al.. Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic. J Child Neurol. 2022.37 (4)237-245 PMID:34986037

Prasad, M, Glueck, M, Ceballos-Saenz, D, Zapata-Aldana, E, Johnson, N, Campbell, C et al.. A Phenotypic Description of Congenital Myotonic Dystrophy using PhenoStacks. J Neuromuscul Dis. 2019.6 (3)341-347 PMID:31227653

Feichtinger, RG, Mucha, BE, Hengel, H, Orfi, Z, Makowski, C, Dort, J et al.. Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy. Genet Med. 2019.21 (11)2521-2531 PMID:31092906

Remtulla, S, Emilie Nguyen, CT, Prasad, C, Campbell, C. Twinkle-Associated Mitochondrial DNA Depletion. Pediatr Neurol. 2019.90 61-65 PMID:30391088

Mercuri, E, Darras, BT, Chiriboga, CA, Day, JW, Campbell, C, Connolly, AM et al.. Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy. N Engl J Med. 2018.378 (7)625-635 PMID:29443664

Nguyen, CE, Campbell, C. Myotonic dystrophy type 1. CMAJ. 2016.188 (14)1033 PMID:27270116

Ciarallo, A, Nguyen, CT, Stein, L. Interventional radiology: from idea to device to patient. Mcgill J Med. 2007.10 (2)144-8 PMID:18523536

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