Jodi W. Chardon

Ottawa, ON, Canada

Last Updated: 09/26/2026

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Found 11 publications

Report on the 4th Ottawa International Conference on Neuromuscular Disease and Biology - September 5-7, 2017, Ottawa, Canada.

Report on the 4th Ottawa International Conference on Neuromuscular Disease and Biology - September 5-7, 2017, Ottawa, Canada.

Journal: Journal of neuromuscular diseases
Published: October 31, 2018

Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada.

Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada.

Journal: Journal of neuromuscular diseases
Published: November 18, 2016

Spinal Muscular Atrophy: More than a Disease of Motor Neurons?

Spinal Muscular Atrophy: More than a Disease of Motor Neurons?

Journal: Current molecular medicine
Published: July 12, 2016

Subcutaneous Immunoglobulin Therapy in the Chronic Management of Myasthenia Gravis: A Retrospective Cohort Study.

Subcutaneous Immunoglobulin Therapy in the Chronic Management of Myasthenia Gravis: A Retrospective Cohort Study.

Journal: PloS one
Published: March 09, 2016

Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.

Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.

Journal: American journal of medical genetics. Part A
Published: December 20, 2015

Autoimmune peripheral neuropathies.

Autoimmune peripheral neuropathies.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 23, 2015

Very late-onset Sandhoff disease presenting as Kennedy disease.

Very late-onset Sandhoff disease presenting as Kennedy disease.

Journal: Muscle & nerve
Published: December 15, 2014

LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tongues.

LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tongues.

Journal: Clinical genetics
Published: November 30, 2014

Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study.

Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study.

Journal: Clinical genetics
Published: April 23, 2014

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.

Journal: Orphanet journal of rare diseases
Published: July 04, 2012

Deletion of filamin A in two female patients with periventricular nodular heterotopia.

Deletion of filamin A in two female patients with periventricular nodular heterotopia.

Journal: American journal of medical genetics. Part A
Published: January 21, 2012
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Last Updated: 09/26/2026