| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aging reduces the sensitivity to the reinforcing efficacy of morphine
|
Bongiovanni, Angela R.
|
|
|
97 |
C |
p. 28-32
|
artikel
|
| 2 |
Alterations of GABA B receptors in the APP/PS1 mouse model of Alzheimer's disease
|
Salazar, Arnold M.
|
|
|
97 |
C |
p. 129-143
|
artikel
|
| 3 |
Alzheimer amyloid-β- peptide disrupts membrane localization of glucose transporter 1 in astrocytes: implications for glucose levels in brain and blood
|
Hendrix, Rachel D.
|
|
|
97 |
C |
p. 73-88
|
artikel
|
| 4 |
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
|
Brown, Emmeline E.
|
|
|
97 |
C |
p. 148.e17-148.e24
|
artikel
|
| 5 |
Aquaporin-4 polymorphisms predict amyloid burden and clinical outcome in the Alzheimer's disease spectrum
|
Chandra, Avinash
|
|
|
97 |
C |
p. 1-9
|
artikel
|
| 6 |
Association between telomere length and Parkinson's disease: a Mendelian randomization study
|
Chen, Ruoqing
|
|
|
97 |
C |
p. 144.e9-144.e11
|
artikel
|
| 7 |
Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases
|
Bartoletti-Stella, Anna
|
|
|
97 |
C |
p. 145.e7-145.e15
|
artikel
|
| 8 |
Cognitive and neuroimaging profiles of older adults with dual decline in memory and gait speed
|
Tian, Qu
|
|
|
97 |
C |
p. 49-55
|
artikel
|
| 9 |
Contents
|
|
|
|
97 |
C |
p. OBC
|
artikel
|
| 10 |
Contents Continued
|
|
|
|
97 |
C |
p. 150-151
|
artikel
|
| 11 |
Editorial Advisory Board
|
|
|
|
97 |
C |
p. IFC
|
artikel
|
| 12 |
Extrastriatal SPECT-DAT uptake correlates with clinical and biological features of de novo Parkinson's disease
|
Sampedro, Frederic
|
|
|
97 |
C |
p. 120-128
|
artikel
|
| 13 |
Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China
|
Yang, Lu
|
|
|
97 |
C |
p. 149.e1-149.e8
|
artikel
|
| 14 |
Genes containing hexanucleotide repeats resembling C9ORF72 and expressed in the central nervous system are frequent in the human genome
|
Vourc’h, Patrick
|
|
|
97 |
C |
p. 148.e1-148.e7
|
artikel
|
| 15 |
Genetic and functional analysis of KIF5A variants in Japanese patients with sporadic amyotrophic lateral sclerosis
|
Nakamura, Ryoichi
|
|
|
97 |
C |
p. 147.e11-147.e17
|
artikel
|
| 16 |
Increased isoform-specific phosphodiesterase 4D expression is associated with pathology and cognitive impairment in Alzheimer’s disease
|
Paes, Dean
|
|
|
97 |
C |
p. 56-64
|
artikel
|
| 17 |
Longitudinal trajectories of hippocampal volume in middle to older age community dwelling individuals
|
Fraser, Mark A.
|
|
|
97 |
C |
p. 97-105
|
artikel
|
| 18 |
Mendelian randomization integrating GWAS and mQTL data identified novel pleiotropic DNA methylation loci for neuropathology of Alzheimer’s disease
|
Liu, Di
|
|
|
97 |
C |
p. 18-27
|
artikel
|
| 19 |
Mesial temporal tau is related to worse cognitive performance and greater neocortical tau load in amyloid-β–negative cognitively normal individuals
|
Groot, Colin
|
|
|
97 |
C |
p. 41-48
|
artikel
|
| 20 |
Metabolic syndrome and its components in relation to in vivo brain amyloid and neurodegeneration in late middle age
|
Palta, Priya
|
|
|
97 |
C |
p. 89-96
|
artikel
|
| 21 |
Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype
|
Liao, Nai-Yi
|
|
|
97 |
C |
p. 145.e5-145.e6
|
artikel
|
| 22 |
Neural correlates of post-retrieval monitoring in older adults are preserved under divided attention, but are decoupled from memory performance
|
Horne, Erin D.
|
|
|
97 |
C |
p. 106-119
|
artikel
|
| 23 |
Neuronal densities and vascular pathology in the hippocampal formation in CADASIL
|
Yamamoto, Yumi
|
|
|
97 |
C |
p. 33-40
|
artikel
|
| 24 |
Neuronal insulin signaling and brain structure in nondemented older adults: the Atherosclerosis Risk in Communities Study
|
Walker, Keenan A.
|
|
|
97 |
C |
p. 65-72
|
artikel
|
| 25 |
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
|
Koçoğlu, Cemile
|
|
|
97 |
C |
p. 145.e1-145.e4
|
artikel
|
| 26 |
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophy
|
Xu, Keqin
|
|
|
97 |
C |
p. 144.e5-144.e7
|
artikel
|
| 27 |
PLA2G6 variants associated with the number of affected alleles in Parkinson’s disease in Japan
|
Daida, Kensuke
|
|
|
97 |
C |
p. 147.e1-147.e9
|
artikel
|
| 28 |
Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China
|
Ni, Jie
|
|
|
97 |
C |
p. 145.e17-145.e22
|
artikel
|
| 29 |
TBK1 variants in Chinese patients with amyotrophic lateral sclerosis
|
Liu, Xiaolu
|
|
|
97 |
C |
p. 149.e9-149.e15
|
artikel
|
| 30 |
The age-dependent associations of white matter hyperintensities and neurofilament light in early- and late-stage Alzheimer's disease
|
Walsh, Phoebe
|
|
|
97 |
C |
p. 10-17
|
artikel
|
| 31 |
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1
|
Hayashida, Arisa
|
|
|
97 |
C |
p. 146.e1-146.e13
|
artikel
|
| 32 |
The role of RHOT1 and RHOT2 genetic variation on Parkinson disease risk and onset
|
Periñán, María Teresa
|
|
|
97 |
C |
p. 144.e1-144.e3
|
artikel
|
| 33 |
Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients
|
Mol, Merel O.
|
|
|
97 |
C |
p. 148.e9-148.e16
|
artikel
|
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