Chinnery, Patrick F., Crompton, Douglas E., Birchall, Daniel, Jackson, Margaret J., Coulthard, Alan, Lombès, Anne, ...
Neuroferritinopathy is a progressive potentially treatable adult-onset movement disorder caused by mutations in the ferritin light chain gene (FTL1). Features overlap with common extrapyramidal...
Chinnery, Patrick F., Crompton, Douglas E., Birchall, Daniel, Jackson, Margaret J., Coulthard, Alan, Lombès, Anne, ...
Neuroferritinopathy is a progressive potentially treatable adult-onset movement disorder caused by mutations in the ferritin light chain gene (FTL1). Features overlap with common extrapyramidal...
Preface – Special issue: Multiple system atrophy (2005)
Gilman, Sid, Quinn, Niall, Wenning, Gregor K., Colosimo, C.
Peer Reviewed
Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., ...
We have established that the frequency of LRRK2 mutations in a series of 118 cases of familial Parkinson's disease is 5.1%. In the largest family with autosomal dominant, late-onset Parkinson's...
Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., ...
We have established that the frequency of LRRK2 mutations in a series of 118 cases of familial Parkinson's disease is 5.1%. In the largest family with autosomal dominant, late-onset Parkinson's...
The syndrome of fixed dystonia: an evaluation of 103 patients (2004)
Schrag, Anette, Trimble, Michael, Quinn, Niall, Bhatia, Kailash
We describe the clinical features of 103 patients presenting with fixed dystonia and report the prospective assessment and investigation of 41 of them. Most patients were female (84%) and had a young...
The syndrome of fixed dystonia: an evaluation of 103 patients (2004)
Schrag, Anette, Trimble, Michael, Quinn, Niall, Bhatia, Kailash
We describe the clinical features of 103 patients presenting with fixed dystonia and report the prospective assessment and investigation of 41 of them. Most patients were female (84%) and had a young...
The syndrome of fixed dystonia: an evaluation of 103 patients (2004)
Schrag, Anette, Trimble, Michael, Quinn, Niall, Bhatia, Kailash
We describe the clinical features of 103 patients presenting with fixed dystonia and report the prospective assessment and investigation of 41 of them. Most patients were female (84%) and had a young...
Parkin disease: a phenotypic study of a large case series (2003)
Khan, Naheed L., Graham, Elizabeth, Critchley, Peter, Schrag, Anette E, Wood, Nicholas W., Lees, Andrew J., ...
Mutations in the parkin gene, PARK2, are a common cause of parkinsonism in familial as well as isolated cases with an age of onset
Parkin disease: a phenotypic study of a large case series (2003)
Khan, Naheed L., Graham, Elizabeth, Critchley, Peter, Schrag, Anette E, Wood, Nicholas W., Lees, Andrew J., ...
Mutations in the parkin gene, PARK2, are a common cause of parkinsonism in familial as well as isolated cases with an age of onset
Dyskinesias following neural transplantation in Parkinson's disease. (2002)
Hagell, Peter, Piccini, Paola, Björklund, Anders, Brundin, Patrik, Rehncrona, Stig, Widner, Håkan, ...
Severe dyskinesias during the 'off' phases (periods of increased Parkinson's disease (PD) disability) have been observed following intrastriatal transplantation of human embryonic mesencephalic...
Dyskinesias and motor fluctuations in Parkinson's disease: A community-based study (2000)
We investigated the prevalence of dyskinesias and motor fluctuations, and the factors determining their occurrence, in a community-based population of patients with Parkinson's disease. Among 124...
Consensus statement on the diagnosis of multiple system atrophy (1998)
Robertson, David, Schatz, Irwin, Oliver, Eugene, Fowler, Clare, Lantos, Peter, Klockgether, Thomas, ...
We report the results of a consensus conference on the diagnosis of multiple system atrophy (MSA). We describe the clinical features of the disease, which include four domains: autonomic...
Sawle, Guy V., Playford, E. Diane, Brooks, David J., Quinn, Niall, Frackowiak, Richard S. J.
Nine L-dopa naïve patients with clinically diagnosed parkinsonism were studied using positron emission tomography with 6-L-[18F]fluorodopa ([18F]dopa, a pre-synaptic tracer) and [11C]raclopride...