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European Journal of Neurology|November 29, 2013
Low dose bromocriptine-induced pleural effusion and pleuropulmonary fibrosisE R Brunt, M J Boeree
Brain : a Journal of Neurology|October 1, 1990
Familial paroxysmal kinesigenic ataxia and continuous myokymiaE R Brunt, T W van Weerden
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1995
Unique myoclonic pattern in corticobasal degenerationE R Brunt, T W van Weerden, J Pruim, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 17, 2002
A six-month multicentre, double-blind, bromocriptine-controlled study of the safety and efficacy of ropinirole in the treatment of patients with Parkinson's disease not optimally controlled by L-dopaE R Brunt, D J Brooks, A D Korczyn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 1998
Ropinirole versus bromocriptine in the treatment of early Parkinson's disease: a 6-month interim report of a 3-year study. 053 Study GroupA D Korczyn, D J Brooks, E R Brunt, et al.
Neurology|August 3, 1999
A 3-year randomized trial of ropinirole and bromocriptine in early Parkinson's disease. The 053 Study GroupA D Korczyn, E R Brunt, J P Larsen, et al.
Brain : a Journal of Neurology|August 17, 2002
Spinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleusU Rüb, R A I de Vos, C Schultz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 1998
Ropinirole in the treatment of early Parkinson's disease: a 6-month interim report of a 5-year levodopa-controlled study. 056 Study GroupO Rascol, D J Brooks, E R Brunt, et al.
The European Journal of Neuroscience|August 24, 2010
Levels of DNAJB family members (HSP40) correlate with disease onset in patients with spinocerebellar ataxia type 3M P Zijlstra, M A Rujano, M A Van Waarde, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
The human premotor oculomotor brainstem system - can it help to understand oculomotor symptoms in Huntington's disease?U Rüb, H Heinsen, E R Brunt, et al.
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