Research Topics
Species | T FoltynieSummaryAffiliation: University of Cambridge Country: UK Publications
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Detail Information
Publications
Vascular parkinsonism: a review of the precision and frequency of the diagnosisThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, Cambridge, UK
Neuroepidemiology 21:1-7. 2002....
Cognitive deficits and psychosis in Parkinson's disease: a review of pathophysiology and therapeutic optionsCaroline H Williams-Gray
Cambridge Centre for Brain Repair, University of Cambridge, Cambridge, UK
CNS Drugs 20:477-505. 2006..Modafinil improves alertness in Parkinson's disease and warrants further investigation to establish its effects on cognitive performance...
The frequency and validity of self-reported diagnosis of Parkinson's Disease in the UK elderly: MRC CFAS cohortThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, Forvie Site, Robinson Way, Cambridge, CB2 2PY, UK
BMC Neurol 6:29. 2006..Estimates of the incidence and prevalence of chronic diseases can be made using established cohort studies but these estimates may have lower reliability if based purely on self-reported diagnosis...
The BDNF Val66Met polymorphism has a gender specific influence on planning ability in Parkinson's diseaseThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, Forvie Site, Robinson Way, Cambridge CB2 2PY, UK
J Neurol 252:833-8. 2005..We speculate that BDNF may interact with dopaminergic transmission and dopamine receptor stimulation in the frontostriatal circuitry, with subsequent consequences on cognition in Parkinson's disease...
A genome wide linkage disequilibrium screen in Parkinson's diseaseThomas Foltynie
Dept of Neurology, University of Cambridge, Cambridge, CB2 2PY, UK
J Neurol 252:597-602. 2005..Subgroup analysis of the most promising marker shows some evidence that microsatellite marker D1S2886 is associated with familial forms of the disease...
Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphismThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, United Kingdom
Mov Disord 19:885-91. 2004..We suggest that polymorphisms of common genes, which regulate central nervous system dopaminergic transmission, can influence some of the phenotypic manifestations of PD...
The cognitive ability of an incident cohort of Parkinson's patients in the UK. The CamPaIGN studyThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, Forvie Site, Robinson Way, Cambridge CB2 2PY, UK
Brain 127:550-60. 2004....
The genetic basis of Parkinson's diseaseT Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, Cambridge, UK
J Neurol Neurosurg Psychiatry 73:363-70. 2002..The identification of such susceptibility genes will eventually enable us to more accurately classify this complex disease...
Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohortC H Williams-Gray
Cambridge Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Forvie Site, Robinson Way, Cambridge CB2 2PY, UK
J Neurol Neurosurg Psychiatry 77:665-7. 2006..The true prevalence of the mutation in idiopathic disease, its penetrance, and the phenotypic heterogeneity of associated cases have important implications for genetic screening in the clinical field...
BDNF val66met influences time to onset of levodopa induced dyskinesia in Parkinson's diseaseT Foltynie
Cambridge Centre for Brain Repair, Cambridge, UK
J Neurol Neurosurg Psychiatry 80:141-4. 2009..There is accumulating evidence that LID develop due to abnormal synaptic plasticity, which is in turn influenced by the release of brain derived neurotrophic factor (BDNF)...
Evolution of cognitive dysfunction in an incident Parkinson's disease cohortC H Williams-Gray
Cambridge Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Forvie Site, Robinson Way, Cambridge, CB2 2PY, UK
Brain 130:1787-98. 2007..Furthermore, given that these predictors of dementia are readily measurable within just a few minutes in a clinical setting, our work may ultimately have practical implications in terms of guiding prognosis in individual patients...
Saccadic latency distributions in Parkinson's disease and the effects of L-dopaA W Michell
Cambridge Centre for Brain Repair, Forvie Site, Robinson Way, CB2 2PY, Cambridge, UK
Exp Brain Res 174:7-18. 2006....
Heterogeneity of Parkinson's disease in the early clinical stages using a data driven approachS J G Lewis
Cambridge Centre for Brain Repair, Forvie Site, Addenbrooke s Hospital, Cambridge, CB2 2PY, UK
J Neurol Neurosurg Psychiatry 76:343-8. 2005..To investigate the heterogeneity of idiopathic Parkinson's disease (PD) in a data driven manner among a cohort of patients in the early clinical stages of the disease meeting established diagnostic criteria...
Biomarkers and Parkinson's diseaseA W Michell
Cambridge Centre for Brain Repair, Forvie Site, Robinson Way, CB2 2PY, UK
Brain 127:1693-705. 2004..In this review we discuss the current potential biomarkers for Parkinson's disease, highlight the problems with their use, and conclude with a discussion of future alternatives...
A genome-wide screen for association in Hungarian multiple sclerosisCecilia Rajda
Department of Neurology, University of Szeged, Semmelweis u. 6, H-6725 Szeged, Hungary
J Neuroimmunol 143:84-7. 2003..These markers were typed in DNA pools that consisted of 88 MS patients (cases), and 128 unrelated controls. Based on a stringent selection criterion, we obtained 33 markers suggesting association with the disease...
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris
Department of Clinical Neurosciences Neurology Unit, University of Cambridge, Cambridge, United Kingdom
Ann Neurol 62:145-53. 2007..We investigated the genetic basis of susceptibility to and cognitive heterogeneity of this disease...
The heterogeneity of idiopathic Parkinson's diseaseThomas Foltynie
Cambridge Centre for Brain Repair, University of Cambridge, UK
J Neurol 249:138-45. 2002....
A whole genome association study in multiple sclerosis patients from north PortugalBerta Martins Silva
Pathology and Molecular Immunology Department, Instituto Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal
J Neuroimmunol 143:116-9. 2003..When compared to a physical map three regions were found with two of these markers less than 1.5 Mb apart: chromosomes 6p21.3 (the MHC region), 6q14.1 and 7q34...
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy
Department of Molecular Neuroscience, Institute of Neurology, University College London, London, United Kingdom
Ann Neurol 59:627-33. 2006..The strongest evidence comes from a meta-analysis of small studies that reported the S18Y polymorphism as protective against PD, after pooling studies of white and Asian subjects. Here, we present data that challenge this association...
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PDAngela Pyle
Mitochondrial Research Group, The University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom
Ann Neurol 57:564-7. 2005....
The future challenges in Parkinson's diseaseRoger A Barker
Cambridge Centre for Brain Repair and Department of Neurology, Forvie Site, Robinson Way, Cambridge, CB2 2PY, UK
J Neurol 251:361-5. 2004
No alterations in alpha-synuclein gene dosage observed in sporadic Parkinson's diseaseCaroline H Williams-Gray
Mov Disord 21:731-2. 2006
