Research output per year
Research output per year
Personal profile
Research interests
neuromuscular disorders, muscular dystrophy, hereditary disease, peripheral neuropathy, amyotrophic lateral sclerosis
Clinical interests
Immune and inflammatory diseases of muscle and nerve, polymyositis, Charcot-Marie-Tooth diseases, motor neuron diseases, spinomuscular atrophy, muscular dystrophy, mitochondrial disorders, metabolic myopathy, myelopathy, ataxia, neurological paraneoplastic syndromes, fatigue, myalgias
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Comments on Letter to the Editor entitled: “Role of electrophysiological evaluation for the best device choice to prevent sudden cardiac death in patients with Myotonic Dystrophy Type1 and Emery Dreifuss Muscular Dystrophy”
Sommerville, R. B., Vincenti, M. G., Winborn, K., Casey, A., Stitziel, N. O., Connolly, A. M. & Mann, D. L., Jan 2021, In: Trends in Cardiovascular Medicine. 31, 1, p. e3Research output: Contribution to journal › Letter › peer-review
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Rapid Recovery with Plasma Exchange in Acute Motor Axonal Neuropathy with Reversible Conduction Failure
Burford, M., Chou, C. A., Sommerville, R. B. & Bucelli, R. C., Sep 1 2019, In: Journal of clinical neuromuscular disease. 21, 1, p. 35-41 7 p.Research output: Contribution to journal › Review article › peer-review
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CANOMAD and other chronic ataxic neuropathies with disialosyl antibodies (CANDA)
Garcia-Santibanez, R., Zaidman, C. M., Sommerville, R. B., Lopate, G., Weihl, C. C., Pestronk, A. & Bucelli, R. C., Jun 1 2018, In: Journal of Neurology. 265, 6, p. 1402-1409 8 p.Research output: Contribution to journal › Article › peer-review
26 Scopus citations -
Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders
Sommerville, R. B., Vincenti, M. G., Winborn, K., Casey, A., Stitziel, N. O., Connolly, A. M. & Mann, D. L., Jan 1 2017, In: Trends in Cardiovascular Medicine. 27, 1, p. 51-58 8 p.Research output: Contribution to journal › Review article › peer-review
17 Scopus citations -
Ataluren treatment of patients with nonsense mutation dystrophinopathy
FOR THE PTC124-GD-007-DMD STUDY GROUP, Oct 1 2014, In: Muscle and Nerve. 50, 4, p. 477-487 11 p.Research output: Contribution to journal › Article › peer-review
Open Access293 Scopus citations