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Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America.
Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
This report presents the work of the Task Force and proposes classification systems and definitions of response to therapy designed to achieve more uniformity in recording and reporting clinical trials and outcomes research.
Guillain-Barré syndrome and variants.
Chronic inflammatory demyelinating polyradiculoneuropathy. Clinical characteristics, course, and recommendations for diagnostic criteria.
- R. Barohn, J. Kissel, J. R. Warmolts, J. Mendell
- Medicine, PsychologyArchives of neurology
- 1 August 1989
It is suggested that chronic inflammatory demyelinating polyradiculoneuropathy may be more heterogeneous than previously emphasized and proposed diagnostic criteria that allow for the heterogeneity but at the same time provide for a more consistent approach to better establish the natural history of this condition.
Distal acquired demyelinating symmetric neuropathy
Distinguishing acquired demyelinating neuropathies by phenotype can often predict the presence of IgM kappa M-proteins, anti-MAG antibodies, and responses to immunomodulating therapy.
Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis.
An innate immune response characterized by plasmacytoid dendritic cell infiltration and interferon-alpha/beta inducible gene and protein expression may be an important part of the pathogenesis of dermatomyositis, as it appears to be in systemic lupus erythematosus.
Muscle Pain: Understanding its Nature, Diagnosis, and Treatment
- R. Barohn
- 1 February 2002
Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial