Electromyography (EMG) is the most common procedure for screening pati
ents with myopathies and remains the most important technique for asse
ssing the course of the disease over time. Fibrillation potentials, po
sitive sharp waves, myotonic or complex repetitive discharges, as well
as polyphasic potentials are non specific and can occur in both myopa
thic and neurogenic lesions. The most sensitive and specific parameter
for myopathy in conventional EMG is the decreased duration of motor u
nit potentials (MUP), but this can also be seen in disorders of the te
rminal motor fibers or the neuromuscular junction. More advanced techn
iques such as single fiber EMG, macro EMG, scanning EMG and turns/ampl
itude analysis have opened additional possibilities for analysis of th
e motor unit and the interference pattern, by which both the sensitivi
ty to early changes and specificity for myopathic alterations is incre
ased. The importance of combining different techniques to improve diag
nostic yield and specificity is stressed.