Detalhe da pesquisa
1.
Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene.
Neuropathol Appl Neurobiol
; 41(5): 601-12, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25185840
2.
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
Nat Genet
; 38(5): 515-7, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16604074
3.
The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons.
J Neurosci
; 33(26): 10790-801, 2013 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-23804100
4.
Microangiopathy in the cerebellum of patients with mitochondrial DNA disease.
Brain
; 135(Pt 6): 1736-50, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22577219
5.
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.
Brain
; 135(Pt 1): 62-71, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22189570
6.
Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death.
Acta Neuropathol
; 122(1): 75-86, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21541762
7.
Pathological correlates of frontotemporal lobar degeneration in the elderly.
Acta Neuropathol
; 121(3): 365-71, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20978901
8.
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
Acta Neuropathol
; 122(1): 99-110, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21424531
9.
Dementia with Lewy bodies: a comparison of clinical diagnosis, FP-CIT single photon emission computed tomography imaging and autopsy.
J Neurol Neurosurg Psychiatry
; 78(11): 1176-81, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17353255
10.
A harmonized classification system for FTLD-TDP pathology.
Acta Neuropathol
; 122(1): 111-3, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21644037
11.
Clinicians' ability to diagnose dementia with Lewy bodies is not affected by ß-amyloid load.
Neurology
; 84(5): 496-9, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25552579
12.
Neuropathological substrates of psychiatric symptoms in prospectively studied patients with autopsy-confirmed dementia with lewy bodies.
Am J Psychiatry
; 161(5): 843-9, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15121649
13.
Muscarinic receptors in basal ganglia in dementia with Lewy bodies, Parkinson's disease and Alzheimer's disease.
J Chem Neuroanat
; 25(3): 161-73, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12706204
14.
Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.
Neurosci Lett
; 341(3): 177-80, 2003 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-12697277
15.
Nicotinic acetylcholine receptor immunohistochemistry in Alzheimer's disease and dementia with Lewy bodies: differential neuronal and astroglial pathology.
J Neurol Sci
; 225(1-2): 39-49, 2004 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15465084
16.
Anti-GQ1b ganglioside positive Miller Fisher syndrome - evidence of paranodal pathology on nerve biopsy.
J Neuromuscul Dis
; 1(2): 191-195, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-27858774
17.
Frontotemporal dementia and its subtypes: a genome-wide association study.
Lancet Neurol
; 13(7): 686-99, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24943344
18.
Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study.
J Neuropathol Exp Neurol
; 72(2): 164-75, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23334599
19.
Synaptic proteins and choline acetyltransferase loss in visual cortex in dementia with Lewy bodies.
J Neuropathol Exp Neurol
; 72(1): 53-60, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23242284
20.
Mitochondrial DNA deletions cause the biochemical defect observed in Alzheimer's disease.
Neurobiol Aging
; 33(9): 2210-4, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21925769