Muscle & Nerve: Vol 23, No 2

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Muscle & Nerve: Volume 23, Issue 2

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Editorial

The challenge of CMTX and connexin 32 mutations

Prognosis of neuropathy with monoclonal gammopathy

Invited Review

The surgical treatment of spasticity

Main Articles

Long-term clinical and neurophysiological follow-up of patients with peripheral, neuropathy associated with benign monoclonal gammopathy†

Muscle phosphorus magnetic resonance spectroscopy oxidative indices correlate with physical activity

Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease

Tolerability of recombinant-methionyl human neurotrophin-3 (r-metHuNT3) in healthy subjects

Statistical motor unit number estimation: Reproducibility and sources of error in patients with amyotrophic lateral sclerosis

Abnormal movements in complex regional pain syndrome: Assessment of their nature

Impact of plasma exchange on indices of demyelination in chronic inflammatory demyelinating polyradiculoneuropathy

Usefulness of hand rehabilitation after carpal tunnel surgery

Macro-EMG and muscle biopsy of paretic foot dorsiflexors in Charcot–Marie–Tooth disease

Malignant hyperthermia: Fatigue characteristics of skeletal muscle

Relation between maximum discharge rates on electromyography and motor unit number estimates

HGF is an autocrine growth factor for skeletal muscle satellite cells in vitro

Thalamic potentials evoked by motor point stimulation

Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease)

Quantitative analysis of reflex inhibition in single motor units in human masseter muscle: Effects of stimulus intensity

Short Reports

Isolated superior oblique palsies with electrophysiologically documented brainstem lesions

Brachial plexopathy in diabetic ketoacidosis

Focal myopathy induced by chronic heroin injection is reversible

Stability of N20 onset or peak latency in median somatosensory evoked potentials

Cases of the Month

Chronic demyelinating hypertrophic brachial plexus neuropathy

Rhabdomyolysis as the presenting manifestation of calciphylaxis

Letters to the Editor

ALS and myasthenia: An unusual association in a patient treated with riluzole

Clinical improvement following interferon-α alone as an initial treatment in CIDP

Muscle fiber conduction velocity in arg1239his mutation in hypokalemic periodic paralysis

Book Review

Book review

Regular Features

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Long-term clinical and neurophysiological follow-up of patients with peripheral, neuropathy associated with benign monoclonal gammopathy ^†