The clinical and neurophysiological findings in a patient with a typical st
iff-man syndrome and their three-year evolution are described. The patient
had high titers of anti-glutamic acid decarboxylase antibodies in both seru
m and cerebrospinal fluid. Magnetic resonance imaging (MRI) of brain and sp
inal cord was normal. Transcranial magnetic stimulation (TMS) revealed a di
stinctive motor evoked potential (MEP) pattern in proximal lower limb muscl
es consisting of markedly increased MEP amplitudes and MEP/M ratios, reduce
d excitability thresholds, and absent silent period. However, MEP latencies
, central and peripheral conduction times and amplitudes obtained by magnet
ic spinal root stimulation were normal. Treatment with benzodiazepine and b
aclofen normalized both the clinical picture and the MEP values. TMS may be
useful both as a diagnostic tool and to monitor the response to drug treat
ment.