Neuropathology underlying clinical variability in patients with synucleinopathies
Abnormal aggregates of the synaptic protein, α-synuclein, are the dominant pathology in
syndromes known as the synucleinopathies. The cellular aggregation of the protein occurs in …
syndromes known as the synucleinopathies. The cellular aggregation of the protein occurs in …
Research in motion: the enigma of Parkinson's disease pathology spread
P Brundin, JY Li, JL Holton, O Lindvall… - Nature Reviews …, 2008 - nature.com
Neuropathological changes in Parkinson's disease progress slowly and spread according to
a characteristic pattern. Recent papers have shed light on this progression of pathology by …
a characteristic pattern. Recent papers have shed light on this progression of pathology by …
The neuropathology, pathophysiology and genetics of multiple system atrophy
… Professor Revesz and Dr Holton are supported by the Alzheimer's Research UK, the
Progressive Supranuclear Palsy (Europe) Association and Brain Net Europe. Professor Lees and …
Progressive Supranuclear Palsy (Europe) Association and Brain Net Europe. Professor Lees and …
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
JY Li, E Englund, JL Holton, D Soulet, P Hagell… - Nature medicine, 2008 - nature.com
Two subjects with Parkinson's disease who had long-term survival of transplanted fetal
mesencephalic dopaminergic neurons (11–16 years) developed α-synuclein–positive Lewy …
mesencephalic dopaminergic neurons (11–16 years) developed α-synuclein–positive Lewy …
A common LRRK2 mutation in idiopathic Parkinson's disease
…, V Bonifati, NP Quinn, J Lynch, DG Healy, JL Holton… - The Lancet, 2005 - thelancet.com
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have been shown to cause
autosomal dominant Parkinson's disease. Few mutations in this gene have been identified. We …
autosomal dominant Parkinson's disease. Few mutations in this gene have been identified. We …
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
The clinical diagnosis of progressive supranuclear palsy (PSP) relies on the identification of
characteristic signs and symptoms. A proportion of pathologically diagnosed cases do not …
characteristic signs and symptoms. A proportion of pathologically diagnosed cases do not …
Lewy-and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?
The relative importance of Lewy- and Alzheimer-type pathologies to dementia in Parkinson's
disease remains unclear. We have examined the combined associations of α-synuclein, tau …
disease remains unclear. We have examined the combined associations of α-synuclein, tau …
A clinico-pathological study of subtypes in Parkinson's disease
M Selikhova, DR Williams, PA Kempster, JL Holton… - Brain, 2009 - academic.oup.com
We have carried out a systematic review of the case files of 242 donors with pathologically
verified Parkinson's disease at the Queen Square Brain Bank for Neurological Disorders in an …
verified Parkinson's disease at the Queen Square Brain Bank for Neurological Disorders in an …
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations
…, L Kilford, DG Healy, NW Wood, AJ Lees, JL Holton… - Brain, 2004 - academic.oup.com
Multiple system atrophy (MSA) has varying clinical (MSA-P versus MSA-C) and pathological
[striatonigral degeneration (SND) versus olivopontocerebellar atrophy (OPCA)] phenotypes. …
[striatonigral degeneration (SND) versus olivopontocerebellar atrophy (OPCA)] phenotypes. …
[HTML][HTML] α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
We report a British family with young-onset Parkinson’s disease (PD) and a G51D SNCA
mutation that segregates with the disease. Family history was consistent with autosomal …
mutation that segregates with the disease. Family history was consistent with autosomal …