| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of A673T variant in APP gene indicates an alternative protective mechanism contributing to longevity in Chinese individuals
|
Liu, Yao-Wen
|
|
|
35 |
4 |
p. 935.e11-935.e12
|
artikel
|
| 2 |
Aging is associated with changes in the neural circuits underlying empathy
|
Chen, Yao-Chu
|
|
|
35 |
4 |
p. 827-836
|
artikel
|
| 3 |
Apolipoprotein E genotype influences spatial distribution of cerebral microbleeds
|
Loehrer, Elizabeth
|
|
|
35 |
4 |
p. 899-905
|
artikel
|
| 4 |
A role for the neurexin–neuroligin complex in Alzheimer's disease
|
Sindi, Ikhlas A.
|
|
|
35 |
4 |
p. 746-756
|
artikel
|
| 5 |
Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies
|
Liu, Guiyou
|
|
|
35 |
4 |
p. 786-792
|
artikel
|
| 6 |
Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease
|
Li, Yuanzhe
|
|
|
35 |
4 |
p. 935.e3-935.e8
|
artikel
|
| 7 |
Contents
|
|
|
|
35 |
4 |
p. OBC
|
artikel
|
| 8 |
Contents continued
|
|
|
|
35 |
4 |
p. 938-939
|
artikel
|
| 9 |
Copper pathology in vulnerable brain regions in Parkinson's disease
|
Davies, Katherine M.
|
|
|
35 |
4 |
p. 858-866
|
artikel
|
| 10 |
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
|
Ticozzi, Nicola
|
|
|
35 |
4 |
p. 936.e13-936.e17
|
artikel
|
| 11 |
Corticosteroid treatment of Alzheimer's disease: is S100A9/Mrp14 a key target?
|
Kametani, Fuyuki
|
|
|
35 |
4 |
p. e11-e12
|
artikel
|
| 12 |
Disentangling the effects of age and APOE on neuropathology and late life cognitive decline
|
Yu, Lei
|
|
|
35 |
4 |
p. 819-826
|
artikel
|
| 13 |
DNAJ mutations are rare in Chinese Parkinson's disease patients and controls
|
Foo, Jia Nee
|
|
|
35 |
4 |
p. 935.e1-935.e2
|
artikel
|
| 14 |
Editorial Advisory Board
|
|
|
|
35 |
4 |
p. IFC
|
artikel
|
| 15 |
Epigenetically regulated microRNAs in Alzheimer's disease
|
Van den Hove, Daniel L.
|
|
|
35 |
4 |
p. 731-745
|
artikel
|
| 16 |
Evaluating noncoding nucleotide repeat expansions in amyotrophic lateral sclerosis
|
Figley, Matthew D.
|
|
|
35 |
4 |
p. 936.e1-936.e4
|
artikel
|
| 17 |
Evaluation of late-onset Alzheimer disease genetic susceptibility risks in a Canadian population
|
Omoumi, Ardeshir
|
|
|
35 |
4 |
p. 936.e5-936.e12
|
artikel
|
| 18 |
Functional connectivity and graph theory in preclinical Alzheimer's disease
|
Brier, Matthew R.
|
|
|
35 |
4 |
p. 757-768
|
artikel
|
| 19 |
Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation
|
Crespo, Ângela C.
|
|
|
35 |
4 |
p. 777-785
|
artikel
|
| 20 |
Genetic variation in PICALM and Alzheimer's disease risk in Han Chinese
|
Jiang, Teng
|
|
|
35 |
4 |
p. 934.e1-934.e3
|
artikel
|
| 21 |
Heritability of brain volumes in older adults: the Older Australian Twins Study
|
Batouli, Seyed Amir Hossein
|
|
|
35 |
4 |
p. 937.e5-937.e18
|
artikel
|
| 22 |
Heterozygous TREM2 mutations in frontotemporal dementia
|
Borroni, Barbara
|
|
|
35 |
4 |
p. 934.e7-934.e10
|
artikel
|
| 23 |
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
|
Le Ber, Isabelle
|
|
|
35 |
4 |
p. 934.e5-934.e6
|
artikel
|
| 24 |
Human superoxide dismutase 1 overexpression in motor neurons of Caenorhabditis elegans causes axon guidance defect and neurodegeneration
|
Li, Jia
|
|
|
35 |
4 |
p. 837-846
|
artikel
|
| 25 |
Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China
|
Jiao, Bin
|
|
|
35 |
4 |
p. 936.e19-936.e22
|
artikel
|
| 26 |
Increased pro–nerve growth factor and decreased brain-derived neurotrophic factor in non–Alzheimer's disease tauopathies
|
Belrose, Jillian C.
|
|
|
35 |
4 |
p. 926-933
|
artikel
|
| 27 |
Management of the aging risk factor for Parkinson's disease
|
Phillipson, Oliver T.
|
|
|
35 |
4 |
p. 847-857
|
artikel
|
| 28 |
Markers of cholesterol transport are associated with amyloid deposition in the brain
|
Hughes, Timothy M.
|
|
|
35 |
4 |
p. 802-807
|
artikel
|
| 29 |
Neuroprotective effects of the amylin analogue pramlintide on Alzheimer's disease pathogenesis and cognition
|
Adler, Brittany L.
|
|
|
35 |
4 |
p. 793-801
|
artikel
|
| 30 |
Operationalizing hippocampal volume as an enrichment biomarker for amnestic mild cognitive impairment trials: effect of algorithm, test-retest variability, and cut point on trial cost, duration, and sample size
|
Yu, Peng
|
|
|
35 |
4 |
p. 808-818
|
artikel
|
| 31 |
Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
|
Turner, Bradley J.
|
|
|
35 |
4 |
p. 906-915
|
artikel
|
| 32 |
Pathogenic effects of amyotrophic lateral sclerosis-linked mutation in D-amino acid oxidase are mediated by D-serine
|
Paul, Praveen
|
|
|
35 |
4 |
p. 876-885
|
artikel
|
| 33 |
PGRN haploinsufficiency increased Wnt5a signaling in peripheral cells from frontotemporal lobar degeneration-progranulin mutation carriers
|
Alquézar, Carolina
|
|
|
35 |
4 |
p. 886-898
|
artikel
|
| 34 |
Positron emission tomography imaging of 5-hydroxytryptamine1B receptors in Parkinson's disease
|
Varrone, Andrea
|
|
|
35 |
4 |
p. 867-875
|
artikel
|
| 35 |
Regional white matter hyperintensities: aging, Alzheimer's disease risk, and cognitive function
|
Birdsill, Alex C.
|
|
|
35 |
4 |
p. 769-776
|
artikel
|
| 36 |
Resting state functional connectivity alterations in primary lateral sclerosis
|
Agosta, Federica
|
|
|
35 |
4 |
p. 916-925
|
artikel
|
| 37 |
SLC1A2 rs3794087 does not associate with essential tremor
|
Ross, Jay P.
|
|
|
35 |
4 |
p. 935.e9-935.e10
|
artikel
|
| 38 |
Tissue transglutaminase in Alzheimer's disease – facts and fiction: a reply to “Tissue transglutaminase is a biochemical marker for Alzheimer's disease”
|
Wolf, Johannes
|
|
|
35 |
4 |
p. e5-e9
|
artikel
|
| 39 |
Tissue transglutaminase is a biochemical marker for Alzheimer's disease
|
Wilhelmus, Micha M.M.
|
|
|
35 |
4 |
p. e3-e4
|
artikel
|
| 40 |
Triggering receptor expressed on myeloid cells 2 variant is rare in late-onset Alzheimer's disease in Han Chinese individuals
|
Yu, Jin-Tai
|
|
|
35 |
4 |
p. 937.e1-937.e3
|
artikel
|
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