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. 2016 Nov 22;14(1):78–90. doi: 10.1007/s13311-016-0492-9

Table 1.

Peripheral axonal excitability findings in neuromuscular disorders

Disease Excitability findings References
Strength-duration time constant Recovery cycle Threshold electrotonus and I/V relationship
Motor neuron disease Prolonged Increased superexcitability Increased TEd and TEh [68, 58, 61, 76]
Kennedy’s disease Prolonged Minor changes Increased hyperpolarizing I/V slope; increased TEd [116]
Multifocal motor neuropathy No change Decreased RRP; increased superexcitability Increased TEd and TEh; decreased resting I/V slope [14, 139, 140]
Chronic inflammatory demyelinating polyneuropathy Reduced Variability with disease stage—decreased recovery cycle parameters or no changes Variability with disease stage—increased TEd and TEh or no changes [140, 142, 144, 145]
Spinal muscular atrophy Prolonged in severe disease Increased subexcitability in severe disease Increased TEd and TEh; decreased resting I/V slope in severe disease [12, 61]
Acquired neuromyotonia No change Increased subexcitability or no change No change [15, 135]
Benign cramp fasciculation syndrome No change No change No changes in conventional measures; decreased TEh at −70 and −100% [136, 137]

I/V = current threshold relationship; TEh = threshold electrotonus (hyperpolarizing direction); TEd = threshold electrotonus (depolarizing direction); RRP = relative refractory period