Research Output per year
Research Output per year
Personal profile
Research interests
neuromuscular disorders, muscular dystrophy, hereditary disease, peripheral neuropathy, amyotrophic lateral sclerosis
Areas of Clinical Interest
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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Dive into the research topics where Richard Sommerville is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Research Output
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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
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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
9 Scopus citations -
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 1 2017, (Accepted/In press) In : Trends in Cardiovascular Medicine.Research output: Contribution to journal › Article
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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
11 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
223 Scopus citations