Objectives: The authors report the results of detailed investigations into the motor function of a patient who, after a heavy drinking binge and subsequent unconsciousness, respiratory acidosis, and initial recovery, developed parkinsonism characterised by hypophonic speech and palilalia, ''fast micrographia'', impaired postural reflexes, and brady/akinesia in proximal (but not distal) alternating upper limb movements. Methods: In addition to brain magnetic resonance imaging (MRI), different aspects of motor function were investigated using reaction time (RT) tasks, pegboard and finger tapping tasks, flex and squeeze tasks, movement related cortical potentials (MRCPs), and contingent negative variation (CNV). Cognitive function was also assessed. The results were compared to those previously reported in patients with Parkinson's disease (PD). Results: Brain MRI showed isolated and bilateral globus pallidus (GP) lesions covering mainly the external parts (GPe). These lesions were most probably secondary to respiratory acidosis, as other investigations failed to reveal an alternative cause. The results of the RT tasks showed that the patient had difficulties in preparing and maintaining preparation for a forthcoming movement. MRCP and CNV studies were in line with this, as the early component of the MRCP and CNV were absent prior to movement. The patient's performance on pegboard and finger tapping, and flex and squeeze tasks was normal when performed with one hand, but clearly deteriorated when using both hands simultaneously or sequentially. Conclusions: In general, the present results were similar to those reported previously in patients with PD. This provides further indirect evidence that the output of globus pallidus is of major importance in abnormal motor function in PD. The possible similarities of the functional status of GP in PD and our case are discussed.T here is considerable interest in the pathophysiology of motor dysfunction in different basal ganglia diseases, especially in idiopathic Parkinson's disease. Preparation and execution of voluntary movements assessed using different reaction time paradigms, 1-3 or through recording of movement related cortical potentials (MRCP) [4][5][6] have been extensively studied in PD. The overall conclusion is that the preparation, initiation, and the execution of voluntary movements are slow or abnormal in patients compared with healthy control subjects.7 It is also known that bradykinesia in PD becomes more prominent by repetitive, simultaneous, or sequential movements.7 Despite these interesting results, it has been very difficult to examine the role of individual nuclei in the pathophysiology of motor dysfunction in PD, as the underlying alterations in different pathways and nuclei are complex in this disease. 8 9 Although the gross morphology of the globus pallidus (GP) is normal, 10 it is widely accepted that the abnormal functional output of GP is one of the major contributors to motor dysfunction in PD.8 9 The renaissance in the surgical treatment of PD ...