nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
ACE variants and risk of intracerebral hemorrhage recurrence in amyloid angiopathy
|
Domingues-Montanari, Sophie |
|
2011 |
32 |
3 |
p. 551.e13-551.e22 5.509999994490001E24 p. |
artikel |
2 |
A de novo missense mutation of the FUS gene in a “true” sporadic ALS case
|
Chiò, Adriano |
|
2011 |
32 |
3 |
p. 553.e23-553.e26 5.52447E28 p. |
artikel |
3 |
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
|
Krüger, Rejko |
|
2011 |
32 |
3 |
p. 548.e9-548.e18 5.47999999452E20 p. |
artikel |
4 |
A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD)
|
Proitsi, P. |
|
2011 |
32 |
3 |
p. 434-442 9 p. |
artikel |
5 |
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease
|
Bekris, L.M. |
|
2011 |
32 |
3 |
p. 556.e13-556.e23 5.5599999994440004E25 p. |
artikel |
6 |
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis
|
Belzil, Véronique V. |
|
2011 |
32 |
3 |
p. 555.e13-555.e14 4.995E16 p. |
artikel |
7 |
A novel double mutation in FUS gene causing sporadic ALS
|
Robertson, J. |
|
2011 |
32 |
3 |
p. 553.e27-553.e30 5.5244700000000006E32 p. |
artikel |
8 |
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient
|
Corrado, Lucia |
|
2011 |
32 |
3 |
p. 552.e1-552.e6 5.51994481E8 p. |
artikel |
9 |
A novel presenilin 1 mutation, I202F occurring at a previously predicted pathogenic site causing autosomal dominant Alzheimer's disease
|
Church, Alistair |
|
2011 |
32 |
3 |
p. 556.e1-556.e2 50041 p. |
artikel |
10 |
Anti-inflammatory drugs reduce age-related decreases in brain volume in cognitively normal older adults
|
Walther, K. |
|
2011 |
32 |
3 |
p. 497-505 9 p. |
artikel |
11 |
APOE dependent-association of PPAR-γ genetic variants with Alzheimer's disease risk
|
Combarros, Onofre |
|
2011 |
32 |
3 |
p. 547.e1-547.e6 5.46994531E8 p. |
artikel |
12 |
Association of common KIBRA variants with episodic memory and AD risk
|
Burgess, Jeremy D. |
|
2011 |
32 |
3 |
p. 557.e1-557.e9 5.56999994431E11 p. |
artikel |
13 |
CALHM1 variant is not associated with Alzheimer's disease among Asians
|
Tan, E.K. |
|
2011 |
32 |
3 |
p. 546.e11-546.e12 4.91400000000001E14 p. |
artikel |
14 |
Contents
|
|
|
2011 |
32 |
3 |
p. 559-561 3 p. |
artikel |
15 |
Contents
|
|
|
2011 |
32 |
3 |
p. OBC- 1 p. |
artikel |
16 |
Cortical control of unilateral simple movement in healthy aging
|
Inuggi, Alberto |
|
2011 |
32 |
3 |
p. 524-538 15 p. |
artikel |
17 |
C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany
|
Drepper, Carsten |
|
2011 |
32 |
3 |
p. 548.e1-548.e4 5.474521E6 p. |
artikel |
18 |
Cyclophilin D deficiency improves mitochondrial function and learning/memory in aging Alzheimer disease mouse model
|
Du, Heng |
|
2011 |
32 |
3 |
p. 398-406 9 p. |
artikel |
19 |
Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy
|
Ezquerra, Mario |
|
2011 |
32 |
3 |
p. 547.e11-547.e16 5.4699453E18 p. |
artikel |
20 |
Editorial Advisory Board
|
|
|
2011 |
32 |
3 |
p. IFC- 1 p. |
artikel |
21 |
Emotional behavior in heterozygous rolling mouse Nagoya Cav2.1 channel mutant mice
|
Takahashi, Eiki |
|
2011 |
32 |
3 |
p. 486-496 11 p. |
artikel |
22 |
E-pub only of selected papers in Neurobiology of Aging
|
Coleman, Paul D. |
|
2011 |
32 |
3 |
p. 371- 1 p. |
artikel |
23 |
Exercise moderates age-related atrophy of the medial temporal lobe
|
Bugg, Julie M. |
|
2011 |
32 |
3 |
p. 506-514 9 p. |
artikel |
24 |
Five out of 16 plasma signaling proteins are enhanced in plasma of patients with mild cognitive impairment and Alzheimer's disease
|
Marksteiner, Josef |
|
2011 |
32 |
3 |
p. 539-540 2 p. |
artikel |
25 |
Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration
|
Borroni, Barbara |
|
2011 |
32 |
3 |
p. 555.e1-555.e8 5.5499994451E10 p. |
artikel |
26 |
FUS mutations in sporadic amyotrophic lateral sclerosis
|
Lai, Shiao-Lin |
|
2011 |
32 |
3 |
p. 550.e1-550.e4 5.494501E6 p. |
artikel |
27 |
FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS
|
Tsai, Ching-Paio |
|
2011 |
32 |
3 |
p. 553.e13-553.e21 5.5299999447E23 p. |
artikel |
28 |
Genetic variations in tau-tubulin kinase-1 are linked to Alzheimer's disease in a Spanish case-control cohort
|
Vázquez-Higuera, José Luis |
|
2011 |
32 |
3 |
p. 550.e5-550.e9 5.49945000001E11 p. |
artikel |
29 |
Genetic variations in the CLU and PICALM genes are associated with cognitive function in the oldest old
|
Mengel-From, Jonas |
|
2011 |
32 |
3 |
p. 554.e7-554.e11 5.5394460000001E13 p. |
artikel |
30 |
Glutamate transporter variants reduce glutamate uptake in Alzheimer's disease
|
Scott, Heather A. |
|
2011 |
32 |
3 |
p. 553.e1-553.e11 5.5299999994471E13 p. |
artikel |
31 |
GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort
|
Kalinderi, Kallirhoe |
|
2011 |
32 |
3 |
p. 546.e1-546.e5 5.4594541E7 p. |
artikel |
32 |
IGF-I gene variability is associated with an increased risk for AD
|
Vargas, Teo |
|
2011 |
32 |
3 |
p. 556.e3-556.e11 5.5599999444001E13 p. |
artikel |
33 |
Impaired neurogenesis, neuronal loss, and brain functional deficits in the APPxPS1-Ki mouse model of Alzheimer's disease
|
Faure, A. |
|
2011 |
32 |
3 |
p. 407-418 12 p. |
artikel |
34 |
Lack of association of PON polymorphisms with sporadic ALS in an Italian population
|
Ricci, Claudia |
|
2011 |
32 |
3 |
p. 552.e7-552.e13 5.519994480000001E15 p. |
artikel |
35 |
Lack of evidence to support the association of polymorphisms within the alpha- and beta-secretase genes (ADAM10/BACE1) with Alzheimer's disease
|
Laws, S.M. |
|
2011 |
32 |
3 |
p. 541-543 3 p. |
artikel |
36 |
Mechanisms of AD neurodegeneration may be independent of Aβ and its derivatives
|
Robakis, Nikolaos K. |
|
2011 |
32 |
3 |
p. 372-379 8 p. |
artikel |
37 |
Memory activation in healthy nonagenarians
|
Beeri, Michal Schnaider |
|
2011 |
32 |
3 |
p. 515-523 9 p. |
artikel |
38 |
Microglia activation mediates fibrillar amyloid-β toxicity in the aged primate cortex
|
Leung, Elaine |
|
2011 |
32 |
3 |
p. 387-397 11 p. |
artikel |
39 |
Midlife homocysteine and late-life dementia in women. A prospective population study
|
Zylberstein, Dimitri E. |
|
2011 |
32 |
3 |
p. 380-386 7 p. |
artikel |
40 |
Mutational analysis of parkin and PINK1 in multiple system atrophy
|
Brooks, Janet A. |
|
2011 |
32 |
3 |
p. 548.e5-548.e7 5.425200001E9 p. |
artikel |
41 |
Neuron–glia interactions underlie ALS-like axonal cytoskeletal pathology
|
King, A.E. |
|
2011 |
32 |
3 |
p. 459-469 11 p. |
artikel |
42 |
Neurotrophic signaling molecules associated with cholinergic damage in young and aged rats: Environmental enrichment as potential therapeutic agent
|
Paban, Véronique |
|
2011 |
32 |
3 |
p. 470-485 16 p. |
artikel |
43 |
NEW evidences for fractalkine/CX3CL1 involved in substantia nigral microglial activation and behavioral changes in a rat model of Parkinson's disease
|
Shan, Sun |
|
2011 |
32 |
3 |
p. 443-458 16 p. |
artikel |
44 |
No association between high temperature requirement 1 (HTRA1) gene polymorphisms and Alzheimer's disease
|
Turunen, Mari |
|
2011 |
32 |
3 |
p. 547.e7-547.e9 5.41530000001E11 p. |
artikel |
45 |
No association of psychosis in Alzheimer disease with neurodegenerative pathway genes
|
DeMichele-Sweet, Mary Ann A. |
|
2011 |
32 |
3 |
p. 555.e9-555.e11 5.4945000000001E13 p. |
artikel |
46 |
No association of Tachykinin receptor 2 (TACR2) polymorphisms with Alzheimer's disease
|
Friedrich, P. |
|
2011 |
32 |
3 |
p. 544-545 2 p. |
artikel |
47 |
No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort
|
Fernández-Santiago, Rubén |
|
2011 |
32 |
3 |
p. 551.e1-551.e4 5.504491E6 p. |
artikel |
48 |
NOS3 gene rs1799983 polymorphism and incident dementia in elderly stroke survivors
|
Morris, Christopher M. |
|
2011 |
32 |
3 |
p. 554.e1-554.e6 5.53994461E8 p. |
artikel |
49 |
Role of BDNF val66met polymorphism on the association between physical activity and incident dementia
|
Kim, Jae-Min |
|
2011 |
32 |
3 |
p. 551.e5-551.e12 5.50999944900001E14 p. |
artikel |
50 |
Screening of OPTN in French familial amyotrophic lateral sclerosis
|
Millecamps, Stéphanie |
|
2011 |
32 |
3 |
p. 557.e11-557.e13 5.514300000000001E15 p. |
artikel |
51 |
Tau inclusions in retinal ganglion cells of human P301S tau transgenic mice: Effects on axonal viability
|
Gasparini, Laura |
|
2011 |
32 |
3 |
p. 419-433 15 p. |
artikel |
52 |
Tenomodulin variants, APOE and Alzheimer's disease in a Finnish case–control cohort
|
Tolppanen, Anna-Maija |
|
2011 |
32 |
3 |
p. 546.e7-546.e9 5.40540000001E11 p. |
artikel |
53 |
Variation in the CBP gene involved in epigenetic control associates with cognitive function
|
Trompet, Stella |
|
2011 |
32 |
3 |
p. 549.e1-549.e8 5.4899994511E10 p. |
artikel |