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Showing results (191-200 of 345) with videos related to

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Journal of Clinical Neuromuscular Disease|August 28, 2012
Facial onset sensorimotor neuronopathy syndrome: a case seriesDobrin Dobrev, Richard J Barohn, Neil E Anderson, et al.
Neurology|July 13, 2000
Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of AmericaA Jaretzki, R J Barohn, R M Ernstoff, et al.
Journal of Visualized Experiments : Jove|February 25, 2020
Use of Capillary Electrophoresis Immunoassay to Search for Potential Biomarkers of Amyotrophic Lateral Sclerosis in Human PlateletsJessica M Sage, LaSharice Hall, April McVey, et al.
Physical Therapy|July 16, 2016
Activity for Diabetic Polyneuropathy (ADAPT): Study Design and Protocol for a 2-Site Randomized Controlled TrialPatricia M Kluding, J Robinson Singleton, Mamatha Pasnoor, et al.
Muscle & Nerve|September 25, 2003
Late-onset distal muscular dystrophy affecting the posterior calvesJonathan S Katz, Thomas A Rando, Richard J Barohn, et al.
Neurology|February 28, 2002
Axonal multifocal motor neuropathy without conduction block or other features of demyelinationJ S Katz, R J Barohn, S Kojan, et al.
Neurology|November 9, 2005
Bilateral isolated phrenic neuropathy causing painless bilateral diaphragmatic paralysisP T Lin, P-B Andersson, B J Distad, et al.
Muscle & Nerve|December 17, 2011
Consensus treatment recommendations for late-onset Pompe diseaseEdward J Cupler, Kenneth I Berger, Robert T Leshner, et al.
Annals of Neurology|October 1, 1996
Inclusion body myositis: clinical and pathological boundariesA A Amato, G S Gronseth, C E Jackson, et al.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Pageof 35

Showing results (191-200 of 345) with videos related to

Sort By:
Pageof 35
Journal of Clinical Neuromuscular Disease|August 28, 2012
Facial onset sensorimotor neuronopathy syndrome: a case seriesDobrin Dobrev, Richard J Barohn, Neil E Anderson, et al.
Neurology|July 13, 2000
Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of AmericaA Jaretzki, R J Barohn, R M Ernstoff, et al.
Journal of Visualized Experiments : Jove|February 25, 2020
Use of Capillary Electrophoresis Immunoassay to Search for Potential Biomarkers of Amyotrophic Lateral Sclerosis in Human PlateletsJessica M Sage, LaSharice Hall, April McVey, et al.
Physical Therapy|July 16, 2016
Activity for Diabetic Polyneuropathy (ADAPT): Study Design and Protocol for a 2-Site Randomized Controlled TrialPatricia M Kluding, J Robinson Singleton, Mamatha Pasnoor, et al.
Muscle & Nerve|September 25, 2003
Late-onset distal muscular dystrophy affecting the posterior calvesJonathan S Katz, Thomas A Rando, Richard J Barohn, et al.
Neurology|February 28, 2002
Axonal multifocal motor neuropathy without conduction block or other features of demyelinationJ S Katz, R J Barohn, S Kojan, et al.
Neurology|November 9, 2005
Bilateral isolated phrenic neuropathy causing painless bilateral diaphragmatic paralysisP T Lin, P-B Andersson, B J Distad, et al.
Muscle & Nerve|December 17, 2011
Consensus treatment recommendations for late-onset Pompe diseaseEdward J Cupler, Kenneth I Berger, Robert T Leshner, et al.
Annals of Neurology|October 1, 1996
Inclusion body myositis: clinical and pathological boundariesA A Amato, G S Gronseth, C E Jackson, et al.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Pageof 35