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                             45 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia Ferrari, Raffaele
2015
36 10 p. 2904.e13-2904.e26
2.9039999999997098E29 p.
artikel
2 Altered age-related changes in bioenergetic properties and mitochondrial morphology in fibroblasts from sporadic amyotrophic lateral sclerosis patients Allen, Scott P.
2015
36 10 p. 2893-2903
11 p.
artikel
3 Association of plasma β-amyloid with MRI markers of structural brain aging the 3-City Dijon study Kaffashian, Sara
2015
36 10 p. 2663-2670
8 p.
artikel
4 A switch in the mode of the sodium/calcium exchanger underlies an age-related increase in the slow afterhyperpolarization Scutt, Greg
2015
36 10 p. 2838-2849
12 p.
artikel
5 ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry Borghero, Giuseppe
2015
36 10 p. 2906.e1-2906.e5
2.90570941E8 p.
artikel
6 Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome Schupf, Nicole
2015
36 10 p. 2907.e1-2907.e10
2.9069999970931E13 p.
artikel
7 Cell adhesion molecule pathway genes are regulated by cis-regulatory SNPs and show significantly altered expression in Alzheimer's disease brains Bao, Xinjie
2015
36 10 p. 2904.e1-2904.e7
2.9039970961E10 p.
artikel
8 Cerebral amyloid angiopathy and its co-occurrence with Alzheimer's disease and other cerebrovascular neuropathologic changes Brenowitz, Willa D.
2015
36 10 p. 2702-2708
7 p.
artikel
9 Contents 2015
36 10 p. OBC-
1 p.
artikel
10 Contents continued 2015
36 10 p. 2910-2911
2 p.
artikel
11 C9ORF72 hexanucleotide repeat expansion in ALS patients from the Central European Russia population Abramycheva, Natalya Y.
2015
36 10 p. 2908.e5-2908.e9
2.907709200001E12 p.
artikel
12 Decreased theta power at encoding and cognitive mapping deficits in elderly individuals during a spatial memory task Lithfous, Ségolène
2015
36 10 p. 2821-2829
9 p.
artikel
13 Disruption of cholinergic neurotransmission exacerbates Aβ-related cognitive impairment in preclinical Alzheimer's disease Lim, Yen Ying
2015
36 10 p. 2709-2715
7 p.
artikel
14 Editorial Advisory Board 2015
36 10 p. IFC-
1 p.
artikel
15 Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease Yuan, Lamei
2015
36 10 p. 2907.e11-2907.e12
2.616300000000001E15 p.
artikel
16 Heritability of telomere length in a study of long-lived families Honig, Lawrence S.
2015
36 10 p. 2785-2790
6 p.
artikel
17 Herpes simplex virus type 2 infection induces AD-like neurodegeneration markers in human neuroblastoma cells Kristen, Henrike
2015
36 10 p. 2737-2747
11 p.
artikel
18 HFE p.H63D polymorphism does not influence ALS phenotype and survival Chiò, Adriano
2015
36 10 p. 2906.e7-2906.e11
2.90570940000001E14 p.
artikel
19 Identification of PSEN2 mutation p.N141I in Argentine pedigrees with early-onset familial Alzheimer's disease Muchnik, Carolina
2015
36 10 p. 2674-2677.e1
24097 p.
artikel
20 Increased levels of plasma amyloid-beta are related to cortical thinning and cognitive decline in cognitively normal elderly subjects Llado-Saz, Sandra
2015
36 10 p. 2791-2797
7 p.
artikel
21 Inherited mtDNA variations are not strong risk factors in human prion disease Hudson, Gavin
2015
36 10 p. 2908.e1-2908.e3
2.878921E6 p.
artikel
22 Inhibition of aberrant complement activation by a dimer of acetylsalicylic acid Lee, Moonhee
2015
36 10 p. 2748-2756
9 p.
artikel
23 Inhibition of JAK2 attenuates the increase in inflammatory markers in microglia from APP/PS1 mice Jones, Raasay S.
2015
36 10 p. 2716-2724
9 p.
artikel
24 Inhibition of Tnf-α R1 signaling can rescue functional cortical plasticity impaired in early post-stroke period Liguz-Lecznar, Monika
2015
36 10 p. 2877-2884
8 p.
artikel
25 Loss of functional connectivity is greater outside the default mode network in nonfamilial early-onset Alzheimer's disease variants Lehmann, Manja
2015
36 10 p. 2678-2686
9 p.
artikel
26 LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population Li, Kai
2015
36 10 p. 2908.e11-2908.e15
2.9077092E18 p.
artikel
27 Mitochondrial decline precedes phenotype development in the complement factor H mouse model of retinal degeneration but can be corrected by near infrared light Calaza, Karin C.
2015
36 10 p. 2869-2876
8 p.
artikel
28 Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population Chen, Kai-Hsiang
2015
36 10 p. 2905.e7-2905.e8
2.61450000001E11 p.
artikel
29 Mutation analysis of C9orf72 in patients with corticobasal syndrome Anor, Cassandra J.
2015
36 10 p. 2905.e1-2905.e5
2.90470951E8 p.
artikel
30 Neurofilament light gene deletion exacerbates amyloid, dystrophic neurite, and synaptic pathology in the APP/PS1 transgenic model of Alzheimer's disease Fernandez-Martos, Carmen M.
2015
36 10 p. 2757-2767
11 p.
artikel
31 Neuropathologic correlates of regional brain volumes in a community cohort of older adults Kotrotsou, Aikaterini
2015
36 10 p. 2798-2805
8 p.
artikel
32 Nonlinear cerebral atrophy patterns across the Alzheimer's disease continuum: impact of APOE4 genotype Gispert, J.D.
2015
36 10 p. 2687-2701
15 p.
artikel
33 Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease Achouri-Rassas, Afef
2015
36 10 p. 2904.e9-2904.e11
2.87496000000001E14 p.
artikel
34 PCC characteristics at rest in 10-year memory decliners Bernard, Charlotte
2015
36 10 p. 2812-2820
9 p.
artikel
35 Plasma amyloid β—quo vadis? Zetterberg, Henrik
2015
36 10 p. 2671-2673
3 p.
artikel
36 Progressive age-related changes in sleep and EEG profiles in the PLB1Triple mouse model of Alzheimer’s disease Jyoti, Amar
2015
36 10 p. 2768-2784
17 p.
artikel
37 RNF8 deficiency results in neurodegeneration in mice Ouyang, Siwei
2015
36 10 p. 2850-2860
11 p.
artikel
38 Role of brain infarcts in behavioral variant frontotemporal dementia Torralva, Teresa
2015
36 10 p. 2861-2868
8 p.
artikel
39 The amyloid precursor protein (APP) intracellular domain regulates translation of p44, a short isoform of p53, through an IRES-dependent mechanism Li, Mi
2015
36 10 p. 2725-2736
12 p.
artikel
40 The APP A673T frequency differs between Nordic countries Mengel-From, Jonas
2015
36 10 p. 2909.e1-2909.e4
2.9060911E7 p.
artikel
41 The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients Wong, Chun Hao
2015
36 10 p. 2908.e17-2908.e18
2.6172E21 p.
artikel
42 Therapeutic potentials of human adipose-derived stem cells on the mouse model of Parkinson's disease Choi, Hee Soon
2015
36 10 p. 2885-2892
8 p.
artikel
43 The relation of structural integrity and task-related functional connectivity in the aging brain Burianová, Hana
2015
36 10 p. 2830-2837
8 p.
artikel
44 Total MRI load of cerebral small vessel disease and cognitive ability in older people Staals, Julie
2015
36 10 p. 2806-2811
6 p.
artikel
45 Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts Simón-Sánchez, Javier
2015
36 10 p. 2907.e13-2907.e17
2.9067093E20 p.
artikel
                             45 gevonden resultaten
 
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