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Russell J M Lane

Showing results (1-10 of 5) with videos related to

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The Journal of Headache and Pain|April 10, 2013
Modified Valsalva test differentiates primary from secondary cough headacheRussell J M Lane, Paul T G Davies
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 9, 2008
A systematic review of antioxidant treatment for amyotrophic lateral sclerosis/motor neuron diseaseRichard W Orrell, Russell J M Lane, Mark Ross
Neuromuscular Disorders : NMD|August 30, 2011
Acetylcholine receptor antibodies in patients with genetic myopathies: clinical and biological significanceRussell J M Lane, Federico Roncaroli, Peter Charles, et al.
Primary Health Care Research & Development|June 1, 2018
The long and winding road: the journey taken by headache sufferers in search of helpPaul T G Davies, Russell J M Lane, Theresa Astbury, et al.
Neuromuscular Disorders : NMD|January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) geneHaiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
The Journal of Headache and Pain|April 10, 2013
Modified Valsalva test differentiates primary from secondary cough headacheRussell J M Lane, Paul T G Davies
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 9, 2008
A systematic review of antioxidant treatment for amyotrophic lateral sclerosis/motor neuron diseaseRichard W Orrell, Russell J M Lane, Mark Ross
Neuromuscular Disorders : NMD|August 30, 2011
Acetylcholine receptor antibodies in patients with genetic myopathies: clinical and biological significanceRussell J M Lane, Federico Roncaroli, Peter Charles, et al.
Primary Health Care Research & Development|June 1, 2018
The long and winding road: the journey taken by headache sufferers in search of helpPaul T G Davies, Russell J M Lane, Theresa Astbury, et al.
Neuromuscular Disorders : NMD|January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) geneHaiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Pageof 1