Recent Publications

Ederer, IA, Spennato, S, Nguyen, CT, Wehle, A, Wachtel, C, Kiehlmann, M et al.. A Single-Center 10-Year Experience of 180 Transmasculine Patients Undergoing Gender-Affirming Mastectomy While Continuing Masculinizing Hormone Replacement Therapy. Aesthetic Plast Surg. 2022. PMID:36510021

Bich, TA, Vuong, NL, Cam Tu, NCHTN, Truong, TM, Trung, LV. Long-Term Survival of Patients After Total Pharyngolaryngoesophagectomy With Gastric Pull-Up Reconstruction for Hypopharyngeal or Laryngeal Cancer Invading Cervical Esophagus. Ann Otol Rhinol Laryngol. 2022. 34894221098802 PMID:35656819

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

Finkel, RS, McDonald, CM, Lee Sweeney, H, Finanger, E, Neil Knierbein, E, Wagner, KR et al.. A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial. J Neuromuscul Dis. 2021.8 (5)769-784 PMID:34120912

Hodgkinson, VL, Oskoui, M, Lounsberry, J, M'Dahoma, S, Butler, E, Campbell, C et al.. A National Spinal Muscular Atrophy Registry for Real-World Evidence. Can J Neurol Sci. 2020.47 (6)810-815 PMID:32493524

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

Lopes, F, Miguet, M, Mucha, BE, Gauthier, J, Saillour, V, Nguyen, CÉ et al.. MYOD1 involvement in myopathy. Eur J Neurol. 2018.25 (12)e123-e124 PMID:30403323

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

Zapata-Aldana, E, Kim, DD, Remtulla, S, Prasad, C, Nguyen, CT, Campbell, C et al.. Further delineation of TBCK - Infantile hypotonia with psychomotor retardation and characteristic facies type 3. Eur J Med Genet. 2019.62 (4)273-277 PMID:30103036

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

Amburgey, K, Tsuchiya, E, de Chastonay, S, Glueck, M, Alverez, R, Nguyen, CT et al.. A natural history study of X-linked myotubular myopathy. Neurology. 2017.89 (13)1355-1364 PMID:28842446

Prasad, M, Hicks, R, MacKay, M, Nguyen, CT, Campbell, C. Developmental Milestones and Quality of Life Assessment in a Congenital Myotonic Dystrophy Cohort. J Neuromuscul Dis. 2016.3 (3)405-412 PMID:27854230

El-Aloul, B, Altamirano-Diaz, L, Zapata-Aldana, E, Rodrigues, R, Malvankar-Mehta, MS, Nguyen, CT et al.. Pharmacological therapy for the prevention and management of cardiomyopathy in Duchenne muscular dystrophy: A systematic review. Neuromuscul Disord. 2017.27 (1)4-14 PMID:27815032

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

Nguyen, CT, Faingold, R. Cavernous sinus thrombosis secondary to sinusitis: a rare and life-threatening complication. Pediatr Radiol. 2009.39 (6)633 PMID:19172257