| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes
|
Khani, Marzieh
|
|
|
99 |
C |
p. 102.e1-102.e10
|
artikel
|
| 2 |
Contents
|
|
|
|
99 |
C |
p. OBC
|
artikel
|
| 3 |
Contents Continued
|
|
|
|
99 |
C |
p. 105
|
artikel
|
| 4 |
Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer’s disease
|
Hoogmartens, Julie
|
|
|
99 |
C |
p. 100.e17-100.e23
|
artikel
|
| 5 |
Disrupted ubiquitin proteasome system underlying tau accumulation in Alzheimer’s disease
|
Weng, Fang-lin
|
|
|
99 |
C |
p. 79-85
|
artikel
|
| 6 |
Dystrophic microglia are associated with neurodegenerative disease and not healthy aging in the human brain
|
Shahidehpour, Ryan K.
|
|
|
99 |
C |
p. 19-27
|
artikel
|
| 7 |
Editorial Advisory Board
|
|
|
|
99 |
C |
p. IFC
|
artikel
|
| 8 |
Effects and mechanisms of information saliency in enhancing value-based decision-making in younger and older adults
|
Chen, Hsiang-Yu
|
|
|
99 |
C |
p. 86-98
|
artikel
|
| 9 |
Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis
|
Ungaro, Carmine
|
|
|
99 |
C |
p. 99.e7-99.e14
|
artikel
|
| 10 |
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis
|
Teyssou, Elisa
|
|
|
99 |
C |
p. 102.e11-102.e20
|
artikel
|
| 11 |
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia
|
Rosas, Irene
|
|
|
99 |
C |
p. 99.e15-99.e22
|
artikel
|
| 12 |
Greater effect of polygenic risk score for Alzheimer's disease among younger cases who are apolipoprotein E-ε4 carriers
|
Fulton-Howard, Brian
|
|
|
99 |
C |
p. 101.e1-101.e9
|
artikel
|
| 13 |
Herpes simplex virus and Alzheimer's disease: a Mendelian randomization study
|
Kwok, Man Ki
|
|
|
99 |
C |
p. 101.e11-101.e13
|
artikel
|
| 14 |
Heterogenous deposition of β-amyloid in the brain of aged dogs
|
Mesquita, Laís L.R.
|
|
|
99 |
C |
p. 44-52
|
artikel
|
| 15 |
Impaired dopamine D3 and nicotinic acetylcholine receptor membrane localization in iPSCs-derived dopaminergic neurons from two Parkinson’s disease patients carrying the LRRK2 G2019S mutation
|
Bono, Federica
|
|
|
99 |
C |
p. 65-78
|
artikel
|
| 16 |
Longitudinal changes in network homogeneity in presymptomatic C9orf72 mutation carriers
|
Waugh, Rebecca E.
|
|
|
99 |
C |
p. 1-10
|
artikel
|
| 17 |
Mutation analysis of LRP10 in a large Chinese familial Parkinson disease cohort
|
Li, ChunYu
|
|
|
99 |
C |
p. 99.e1-99.e6
|
artikel
|
| 18 |
Negative screening for 12 rare LRRK2 pathogenic variants in a cohort of Nigerians with Parkinson's disease
|
Rizig, Mie
|
|
|
99 |
C |
p. 101.e15-101.e19
|
artikel
|
| 19 |
Reply: MELAS can be delineated from CADASIL by genotype and phenotype
|
Liao, Nai-Yi
|
|
|
99 |
C |
p. 104
|
artikel
|
| 20 |
The complement C7 variant rs3792646 is associated with amyotrophic lateral sclerosis in a Han Chinese population
|
He, Ji
|
|
|
99 |
C |
p. 103.e1-103.e7
|
artikel
|
| 21 |
The value of multimodal imaging with 123I-FP-CIT SPECT in differential diagnosis of dementia with Lewy bodies and Alzheimer's disease dementia
|
Miyagawa, Toji
|
|
|
99 |
C |
p. 11-18
|
artikel
|
| 22 |
Transfer learning for predicting conversion from mild cognitive impairment to dementia of Alzheimer's type based on a three-dimensional convolutional neural network
|
Bae, Jinhyeong
|
|
|
99 |
C |
p. 53-64
|
artikel
|
| 23 |
Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature
|
Swift, Imogen J.
|
|
|
99 |
C |
p. 100.e9-100.e15
|
artikel
|
| 24 |
Volumetric distribution of perivascular space in relation to mild cognitive impairment
|
Sepehrband, Farshid
|
|
|
99 |
C |
p. 28-43
|
artikel
|
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