Muscle & Nerve: Vol 48, No 2

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Muscle & Nerve: Volume 48, Issue 2

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Table of Contents

Table of Contents

Between the Covers

Between the Covers August, 2013 Issue

Invited Review

Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations

Main Articles

Diagnostic value of high-resolution sonography in common fibular neuropathy at the fibular head

Isolated median neuropathy as the first symptom of leprosy

Origin of surface motor unit potentials in hypothenar motor unit number estimation

Far-field potentials in hypothenar motor unit number estimation

Symmetry of paraspinal muscle denervation in clinical lumbar spinal stenosis: Support for a hypothesis of posterior primary ramus stretching?

Experimental model of alcohol-related peripheral neuropathy

Electrophysiologic changes with incremental exercise in obstructive sleep apnea

Electrical muscle stimulation after immediate nerve repair reduces muscle atrophy without affecting reinnervation

Region-specific myoelectric manifestations of fatigue in human rectus femoris muscle

Spatial analysis of amyotrophic lateral sclerosis in Northern New England, USA, 1997–2009

H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patients

Guillain–Barré syndrome during childhood: Particular clinical and electrophysiological features

Cramps and small-fiber neuropathy

Selective stimulation of human tooth-pulp with a new stable method: Responses and validation

Differential Effects of a 5% lidocaine medicated patch in peripheral nerve injury

Diaphragm muscle atrophy in the mouse after long-term mechanical ventilation

Fast skeletal muscle troponin activator in the dy2J muscular dystrophy model

Sarcomere lengths in human extensor carpi radialis brevis measured by microendoscopy

Short Reports

Generating color-coded anatomic muscle maps for correlation of quantitative magnetic resonance imaging analysis with clinical examination in neuromuscular disorders

Spontaneous electromyographic activity of the tongue in amyotrophic lateral sclerosis

Motor unit loss and weakness in association with diabetic neuropathy in humans

Case of the Month

Lower motor neuron syndrome due to cauda equina hypertrophy with onion bulbs

Letter to the Editor

A patient with mutation in the SCN4A p.M1592v presenting with fixed weakness, rhabdomyolysis, and episodic worsening of weakness

Book Reviews

Electromyography and neuromuscular disorders: Clinical-electrophysiologic correlations, 3rd Edition edited by David C. Preston and Barbara E. Shapiro, 664 pp., Elsevier Saunders, 2012, $199

Atlas of Nerve Conduction Studies and Electromyography by A. Arturo Leis and Michael P. Schenk, 305 pp., New York, Oxford University Press, 2013

Erratum

Erratum to Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/myoshi myopathy necessitates mutational screen for diagnosis

This article corrects the following:

Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/myoshi myopathy necessitates mutational screen for diagnosis

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