|
1
|
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
|
PLoS Pathog
|
2007
|
1.97
|
|
2
|
Progressive supranuclear palsy and Parkinson's disease in a family with a new mutation in the tau gene.
|
Ann Neurol
|
2004
|
1.51
|
|
3
|
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features.
|
Acta Neuropathol
|
2010
|
1.16
|
|
4
|
A new function of microtubule-associated protein tau: involvement in chromosome stability.
|
Cell Cycle
|
2008
|
0.98
|
|
5
|
Specific recognition of biologically active amyloid-β oligomers by a new surface plasmon resonance-based immunoassay and an in vivo assay in Caenorhabditis elegans.
|
J Biol Chem
|
2012
|
0.97
|
|
6
|
A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype.
|
J Alzheimers Dis
|
2009
|
0.96
|
|
7
|
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.
|
Brain Pathol
|
2012
|
0.90
|
|
8
|
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38.
|
Acta Neuropathol
|
2012
|
0.86
|
|
9
|
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
|
Arch Neurol
|
2010
|
0.85
|
|
10
|
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration.
|
Neurol Sci
|
2011
|
0.84
|
|
11
|
Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patients.
|
Mov Disord
|
2010
|
0.83
|
|
12
|
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.
|
J Neuropathol Exp Neurol
|
2005
|
0.81
|
|
13
|
Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.
|
Neurol Sci
|
2009
|
0.80
|
|
14
|
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
|
Brain Pathol
|
2013
|
0.79
|
|
15
|
Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family.
|
Neurol Sci
|
2008
|
0.77
|
|
16
|
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients.
|
J Neuropathol Exp Neurol
|
2002
|
0.77
|
|
17
|
Familial frontotemporal dementia associated with the novel MAPT mutation T427M.
|
J Neurol
|
2005
|
0.77
|
|
18
|
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
|
BMJ Case Rep
|
2009
|
0.75
|
|
19
|
Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.
|
Neurology
|
2004
|
0.75
|
|
20
|
Synchronization of cortisol circadian rhythm by the pineal hormone melatonin in untreatable metastatic solid tumor patients and its possible prognostic significance on tumor progression.
|
In Vivo
|
2010
|
0.75
|
|
21
|
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.
|
J Neurol Sci
|
2010
|
0.75
|