Jodi Warman Chardon profile picture

Contact Information

Jodi Warman Chardon, MD, MSc, FRCPC (Neurology)
613-798-5555 ext. 16221

Administrative Assistant
Amanda Paliotti
613-798-5555 ext. 16221


Selected Publications

McCurdy AR, Mielniczuk LM, Dennie C, Veinot JP, Warman Chardon J. Cardiac amyloidosis phenotype associated with a Glu89Lys transthyretin mutation. Canadian Journal of Cardiology . Forthcoming. 

Walker LA, Bourque P, Smith AM, Warman Chardon J. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) associated with progressive cognitive and behavioral deterioration. Neuropsychology. 2017 Mar;31(3):292-303. 
Bourque PR, Bourque G, Miller W, Woulfe J, Warman Chardon J. Combined isolated trigeminal and facial neuropathies from perineural invasion by squamous cell carcinoma: A case series and review of the literature. J Clin Neurosci. 2017 Jan;35:5-12. 

Yu YJ, Warman Chardon J, Bourque PR. Systematic analysis of clinical deficits in unilateral hypoglossal nerve palsy. Muscle Nerve. 2016 Dec;54(6):1055-1058.

Chrestian N, Dupré N, Gan-Or Z, Szuto A, Chen S, Venkitachalam A, Brisson JD, Warman-Chardon J, Ahmed S, Ashtiani S, MacDonald H, Mohsin N, Mourabit-Amari K, Provencher P, Boycott KM, Stavropoulos DJ, Dion PA, Ray PN, Suchowersky O, Rouleau GA, Yoon G. Clinical and genetic study of hereditary spastic paraplegia in Canada. Neurol Genet. 2016 Dec 5;3(1):e122.

Bourque PR, Warman Chardon J. A crucial first randomized controlled trial of thymectomy in non-thymomatous myasthenia gravis. J Thorac Dis. 2016 Oct;8(10):E1375-E1378. 
Kernohan KD, Cigana Schenkel L, Huang L, Smith A, Pare G, Ainsworth P; Care4Rare Canada Consortium., Boycott KM, Warman-Chardon J, Sadikovic B. Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. Clin Epigenetics. 2016 Sep 5;8:91. 

Nash LA, Burns JK, Chardon JW, Kothary R, Parks RJ. Spinal Muscular Atrophy: More than a Disease of Motor Neurons? Curr Mol Med. 2016;16(9):779-792. 

Chardon JW, Jasmin BJ, Kothary R, Parks RJ. Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada. J Neuromuscul Dis. 2016 Aug 30;3(3):431-442. 

Bourque PR, Pringle CE, Cameron W, Cowan J, Chardon JW. Subcutaneous Immunoglobulin Therapy in the Chronic Management of Myasthenia Gravis: A Retrospective Cohort Study. PLoS One. 2016 Aug 4;11(8):e0159993. 

Bourque PR, Nguyen TB, Zwicker J, Warman Chardon J. Marked enlargement of neck circumference from nerve hypertrophy in CIDP. Neurology. 2016 Jul 26;87(4):442. 

Armour CM, Smith A, Hartley T, Chardon JW, Sawyer S, Schwartzentruber J, Hennekam R, Majewski J, Bulman DE; FORGE Canada Consortium., Suri M, Boycott KM. Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events. Am J Med Genet A. 2016 Jul;170(7):1820-5. 

Lapalme-Remis S, Warman Chardon J, Bourque PR, Oboudiyat C. Diffuse leukoencephalopathy with spheroids presenting as primary progressive aphasia. Neurology. 2016 Apr 12;86(15):1464-5. 

Parker V, Warman Chardon J, Mills J, Goldsmith C, Bourque PR. Supramaximal Stimulus Intensity as a Diagnostic Tool in Chronic Demyelinating Neuropathy. Neurosci J. 2016;2016:6796270. 

Bourque PR, Shafi S, Jansen GH, McCurdy A, Warman Chardon J. Amyloid Neuropathy Following Domino Liver Transplantation: Response to Diflunisal. JAMA Neurol. 2016 Apr;73(4):477-8. 

Sawyer S, Hartley T, Dyment D, Beaulieu C, Schwartzentruber J, Smith A, Bedford M, Bernard G, Bernier F, Brais B, Bulman D, Warman Chardon J et al. (2015) Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care. Clin Genet. 2016 Mar;89(3):275-84

PubMed Listings

For more publications use this PubMed ID link.