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You searched for: Author/Creator Tarnopolsky, Mark

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1. A novel multisystem disease associated with recessive mutations in the tyrosyl‐tRNA synthetase (YARS) gene. Issue 1 (15th September 2016)

2. A phase 3 randomized study evaluating sialic acid extended-release for GNE myopathy. (30th April 2019)

4. Altered PLP1 splicing causes hypomyelination of early myelinating structures. Issue 6 (1st May 2015)

5. Anti–Valosin‐Containing Protein (VCP/p97) Autoantibodies in Inclusion Body Myositis and Other Inflammatory Myopathies. Issue 1 (14th November 2022)

6. BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes. Issue 1 (December 2018)

7. Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Issue 3 (29th November 2022)

8. Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Issue 8 (29th September 2020)

9. Clinical features related to statin‐associated muscle symptoms. Issue 5 (11th January 2019)

10. Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project. Issue 3 (16th March 2017)