-
1
-
-
0029914384
-
Dementia, and adult-onset unprovoked seizures
-
Hesdorffer DC, Hauser WA, Annegers JF, Kokmen E, Rocca WA. Dementia, and adult-onset unprovoked seizures. Neurology 1996; 46: 727-730
-
(1996)
Neurology
, vol.46
, pp. 727-730
-
-
Hesdorffer, D.C.1
Hauser, W.A.2
Annegers, J.F.3
Kokmen, E.4
Rocca, W.A.5
-
2
-
-
84875866043
-
Seizures in patients with Alzheimer's disease or vascular dementia: A population-based nested case-control analysis
-
Imfeld P, Bodmer M, Schuerch M, Jick SS, Meier CR. Seizures in patients with Alzheimer's disease or vascular dementia: a population-based nested case-control analysis. Epilepsia 2013; 54: 700-707
-
(2013)
Epilepsia
, vol.54
, pp. 700-707
-
-
Imfeld, P.1
Bodmer, M.2
Schuerch, M.3
Jick, S.S.4
Meier, C.R.5
-
4
-
-
0028139308
-
Seizures in Alzheimer's disease: Clinicopathologic study
-
Mendez MF, Catanzaro P, Doss RC, Arguello R, Frey WH. Seizures in Alzheimer's disease: clinicopathologic study. J Geriatr Psychiatry Neurol 1994; 7: 230-233
-
(1994)
J Geriatr Psychiatry Neurol
, vol.7
, pp. 230-233
-
-
Mendez, M.F.1
Catanzaro, P.2
Doss, R.C.3
Arguello, R.4
Frey, W.H.5
-
5
-
-
0024996068
-
Advanced Alzheimer's disease is a risk factor for lateonset seizures
-
Romanelli MF, Morris JC, Ashkin K, Coben LA. Advanced Alzheimer's disease is a risk factor for lateonset seizures. Arch Neurol 1990; 47: 847-850
-
(1990)
Arch Neurol
, vol.47
, pp. 847-850
-
-
Romanelli, M.F.1
Morris, J.C.2
Ashkin, K.3
Coben, L.A.4
-
6
-
-
68549089091
-
Seizures in Alzheimer disease: Who when, and how common?
-
Scarmeas N, Honig LS, Choi H, et al. Seizures in Alzheimer disease: who, when, and how common? Arch Neurol 2009; 66: 992-997
-
(2009)
Arch Neurol
, vol.66
, pp. 992-997
-
-
Scarmeas, N.1
Honig, L.S.2
Choi, H.3
-
7
-
-
84858610667
-
Incidence of new-onset seizures in mild to moderate Alzheimer disease
-
Irizarry MC, Jin S, He F, et al. Incidence of new-onset seizures in mild to moderate Alzheimer disease. Arch Neurol 2012; 69: 368-372
-
(2012)
Arch Neurol
, vol.69
, pp. 368-372
-
-
Irizarry, M.C.1
Jin, S.2
He, F.3
-
8
-
-
84862995971
-
The French series of autosomal dominant early onset Alzheimer's disease cases: Mutation spectrum, and cerebrospinal fluid biomarkers
-
Wallon D, Rousseau S, Rovelet-Lecrux A, et al. The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum, and cerebrospinal fluid biomarkers. J Alzheimers Dis 2012; 30: 847-856
-
(2012)
J Alzheimers Dis
, vol.30
, pp. 847-856
-
-
Wallon, D.1
Rousseau, S.2
Rovelet-Lecrux, A.3
-
9
-
-
84892733664
-
Presenilin-1 mutations in Alzheimer's disease: An update on genotype-phenotype relationships
-
Larner AJ. Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships. J Alzheimers Dis 2013; 37: 653-659
-
(2013)
J Alzheimers Dis
, vol.37
, pp. 653-659
-
-
Larner, A.J.1
-
10
-
-
84960211552
-
A systematic review of familial Alzheimer's disease: Differences in presentation of clinical features among three mutated genes, and potential ethnic differences
-
Shea YF, Chu LW, Chan AO, Ha J, Li Y, Song YQ. A systematic review of familial Alzheimer's disease: differences in presentation of clinical features among three mutated genes, and potential ethnic differences. J Formos Med Assoc 2016; 115: 67-75
-
(2016)
J Formos Med Assoc
, vol.115
, pp. 67-75
-
-
Shea, Y.F.1
Chu, L.W.2
Chan, A.O.3
Ha, J.4
Li, Y.5
Song, Y.Q.6
-
11
-
-
16344387731
-
Epileptic seizures, and epilepsy: Definitions proposed by the international league against epilepsy (ilae), and the international bureau for epilepsy (ibe
-
Fisher RS, van Emde Boas W, Blume W, et al. Epileptic seizures, and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE), and the International Bureau for Epilepsy (IBE). Epilepsia 2005; 46: 470-472
-
(2005)
Epilepsia
, vol.46
, pp. 470-472
-
-
Fisher, R.S.1
Van Emde Boas, W.2
Blume, W.3
-
12
-
-
77950857874
-
Revised terminology, and concepts for organization of seizures, and epilepsies: Report of the ilae commission on classification, and terminology 2005-2009
-
Berg AT, Berkovic SF, Brodie MJ, et al. Revised terminology, and concepts for organization of seizures, and epilepsies: report of the ILAE Commission on Classification, and Terminology, 2005-2009. Epilepsia 2010; 51: 676-685
-
(2010)
Epilepsia
, vol.51
, pp. 676-685
-
-
Berg, A.T.1
Berkovic, S.F.2
Brodie, M.J.3
-
13
-
-
0024317220
-
Commission on classification, and terminology of the international league against epilepsy
-
Proposal for revised classification of epilepsies, and epileptic syndromes
-
Proposal for revised classification of epilepsies, and epileptic syndromes. Commission on Classification, and Terminology of the International League Against Epilepsy. Epilepsia 1989; 30: 389-399
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
14
-
-
29444442794
-
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
-
Rovelet-Lecrux A, Hannequin D, Raux G, et al. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nat Genet 2006; 38: 24-26
-
(2006)
Nat Genet
, vol.38
, pp. 24-26
-
-
Rovelet-Lecrux, A.1
Hannequin, D.2
Raux, G.3
-
15
-
-
77950529014
-
Genetic screening of Alzheimer's disease genes in iberian, and african samples yields novel mutations in presenilins, and app
-
Guerreiro RJ, Baquero M, Blesa R, et al. Genetic screening of Alzheimer's disease genes in Iberian, and African samples yields novel mutations in presenilins, and APP. Neurobiol Aging 2010; 31: 725-731
-
(2010)
Neurobiol Aging
, vol.31
, pp. 725-731
-
-
Guerreiro, R.J.1
Baquero, M.2
Blesa, R.3
-
16
-
-
23244452355
-
Rate of progression differs in frontotemporal dementia, and Alzheimer disease
-
Rascovsky K, Salmon DP, Lipton AM, et al. Rate of progression differs in frontotemporal dementia, and Alzheimer disease. Neurology 2005; 65: 397-403
-
(2005)
Neurology
, vol.65
, pp. 397-403
-
-
Rascovsky, K.1
Salmon, D.P.2
Lipton, A.M.3
-
17
-
-
77951755286
-
Prevalence of superficial siderosis in patients with cerebral amyloid angiopathy
-
Linn J, Halpin A, Demaerel P, et al. Prevalence of superficial siderosis in patients with cerebral amyloid angiopathy. Neurology 2010; 74: 1346-1350
-
(2010)
Neurology
, vol.74
, pp. 1346-1350
-
-
Linn, J.1
Halpin, A.2
Demaerel, P.3
-
18
-
-
84858023462
-
Amyloid-b protein precursor gene expression in Alzheimer's disease, and other conditions
-
Pottier C, Wallon D, Lecrux AR, et al. Amyloid-b protein precursor gene expression in Alzheimer's disease, and other conditions. J Alzheimers Dis 2012; 28: 561-566
-
(2012)
J Alzheimers Dis
, vol.28
, pp. 561-566
-
-
Pottier, C.1
Wallon, D.2
Lecrux, A.R.3
-
19
-
-
33749066060
-
Phenotype associated with APP duplication in five families
-
Cabrejo L, Guyant-Maréchal L, Laquerrière A, et al. Phenotype associated with APP duplication in five families. Brain 2006; 129: 2966-2976
-
(2006)
Brain
, vol.129
, pp. 2966-2976
-
-
Cabrejo, L.1
Guyant-Maréchal, L.2
Laquerrière, A.3
-
20
-
-
63849331457
-
Intrafamilial diversity of phenotype associated with app duplication
-
Guyant-Marechal I, Berger E, Laquerriere A, et al. Intrafamilial diversity of phenotype associated with app duplication. Neurology 2008; 71: 1925-1926
-
(2008)
Neurology
, vol.71
, pp. 1925-1926
-
-
Guyant-Marechal, I.1
Berger, E.2
Laquerriere, A.3
-
21
-
-
84858129016
-
Down syndrome, and dementia: Seizures, and cognitive decline
-
Lott IT, Doran E, Nguyen VQ, Tournay A, Movsesyan N, Gillen DL. Down syndrome, and dementia: seizures, and cognitive decline. J Alzheimers Dis 2012; 29: 177-185
-
(2012)
J Alzheimers Dis
, vol.29
, pp. 177-185
-
-
Lott, I.T.1
Doran, E.2
Nguyen, V.Q.3
Tournay, A.4
Movsesyan, N.5
Gillen, D.L.6
-
22
-
-
0034975365
-
Amyloid angiopathy, and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease
-
Members of the Familial Alzheimer's Disease Pathology Study Group
-
Mann DM, Pickering-Brown SM, Takeuchi A, Iwatsubo T, Members of the Familial Alzheimer's Disease Pathology Study Group. Amyloid angiopathy, and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease. Am J Pathol 2001; 158: 2165-2175
-
(2001)
Am J Pathol
, vol.158
, pp. 2165-2175
-
-
Mann, D.M.1
Pickering-Brown, S.M.2
Takeuchi, A.3
Iwatsubo, T.4
-
23
-
-
84934441665
-
Quantifying biomarkers of cognitive dysfunction, and neuronal network hyperexcitability in mouse models of Alzheimer's disease: Depletion of calcium-dependent proteins, and inhibitory hippocampal remodeling
-
Palop JJ, Mucke L, Roberson ED. Quantifying biomarkers of cognitive dysfunction, and neuronal network hyperexcitability in mouse models of Alzheimer's disease: depletion of calcium-dependent proteins, and inhibitory hippocampal remodeling. Methods Mol Biol 2011; 670: 245-262
-
(2011)
Methods Mol Biol
, vol.670
, pp. 245-262
-
-
Palop, J.J.1
Mucke, L.2
Roberson, E.D.3
-
24
-
-
84896764452
-
Genetic suppression of transgenic APP rescues hypersynchronous network activity in a mouse model of Alzheimer's disease
-
Born HA, Kim JY, Savjani RR, et al. Genetic suppression of transgenic APP rescues hypersynchronous network activity in a mouse model of Alzheimer's disease. J Neurosci 2014; 34: 3826-3840
-
(2014)
J Neurosci
, vol.34
, pp. 3826-3840
-
-
Born, H.A.1
Kim, J.Y.2
Savjani, R.R.3
-
25
-
-
77954132249
-
Amyloid-beta-induced neuronal dysfunction in Alzheimer's disease: From synapses toward neural networks
-
Palop JJ, Mucke L. Amyloid-beta-induced neuronal dysfunction in Alzheimer's disease: from synapses toward neural networks. Nat Neurosci 2010; 13: 812-818
-
(2010)
Nat Neurosci
, vol.13
, pp. 812-818
-
-
Palop, J.J.1
Mucke, L.2
-
26
-
-
18044364799
-
Down syndrome Alzheimer's disease, and seizures
-
Menéndez M. Down syndrome, Alzheimer's disease, and seizures. Brain Dev 2005; 27: 246-252
-
(2005)
Brain Dev
, vol.27
, pp. 246-252
-
-
Menéndez, M.1
-
27
-
-
43849090365
-
Novel presenilin 1 variant (P117A) causing Alzheimer's disease in the fourth decade of life
-
Kauwe JS, Wang J, Chakraverty S, Goate AM, Henao-Martinez AF. Novel presenilin 1 variant (P117A) causing Alzheimer's disease in the fourth decade of life. Neurosci Lett 2008; 438: 257-259
-
(2008)
Neurosci Lett
, vol.438
, pp. 257-259
-
-
Kauwe, J.S.1
Wang, J.2
Chakraverty, S.3
Goate, A.M.4
Henao-Martinez, A.F.5
-
28
-
-
67149086705
-
Hereditary, and sporadic forms of Abetacerebrovascular amyloidosis, and relevant transgenic mouse models
-
Kumar-Singh S. Hereditary, and sporadic forms of Abetacerebrovascular amyloidosis, and relevant transgenic mouse models. Int J Mol Sci 2009; 10: 1872-1895
-
(2009)
Int J Mol Sci
, vol.10
, pp. 1872-1895
-
-
Kumar-Singh, S.1
-
29
-
-
47949125010
-
Mutational analysis in early-onset familial dementia in the Japanese population: The role of psen1, and mapt r406w mutations
-
Ikeuchi T, Kaneko H, Miyashita A, et al. Mutational analysis in early-onset familial dementia in the Japanese population: the role of PSEN1, and MAPT R406W mutations. Dement Geriatr Cogn Disord 2008; 26: 43-49
-
(2008)
Dement Geriatr Cogn Disord
, vol.26
, pp. 43-49
-
-
Ikeuchi, T.1
Kaneko, H.2
Miyashita, A.3
-
30
-
-
15244341378
-
Familial Alzheimer's disease presenilin 1 mutations cause alterations in the conformation of presenilin, and interactions with amyloid precursor protein
-
Berezovska O, Lleó A, Herl LD, et al. Familial Alzheimer's disease presenilin 1 mutations cause alterations in the conformation of presenilin, and interactions with amyloid precursor protein. J Neurosci 2005; 25: 3009-3017
-
(2005)
J Neurosci
, vol.25
, pp. 3009-3017
-
-
Berezovska, O.1
Lleó, A.2
Herl, L.D.3
-
31
-
-
67849085401
-
Genotype-phenotype relationships of presenilin-1 mutations in Alzheimer's disease: An update
-
Larner AJ, Doran M. Genotype-phenotype relationships of presenilin-1 mutations in Alzheimer's disease: an update. J Alzheimers Dis 2009; 17: 259-265
-
(2009)
J Alzheimers Dis
, vol.17
, pp. 259-265
-
-
Larner, A.J.1
Doran, M.2
-
32
-
-
79955625095
-
Presenilin-1 mutation Alzheimer's disease: A genetic epilepsy syndrome?
-
Larner AJ. Presenilin-1 mutation Alzheimer's disease: a genetic epilepsy syndrome? Epilepsy Behav 2011; 21: 20-22
-
(2011)
Epilepsy Behav
, vol.21
, pp. 20-22
-
-
Larner, A.J.1
-
33
-
-
77950815769
-
Alzheimer's disease phenotypes, and genotypes associated with mutations in presenilin 2
-
Jayadev S, Leverenz JB, Steinbart E, et al. Alzheimer's disease phenotypes, and genotypes associated with mutations in presenilin 2. Brain 2010; 133: 1143-1154
-
(2010)
Brain
, vol.133
, pp. 1143-1154
-
-
Jayadev, S.1
Leverenz, J.B.2
Steinbart, E.3
-
34
-
-
19944433121
-
An African American family with early-onset Alzheimer disease, and an APP (T714I) mutation
-
Edwards-Lee T, Ringman JM, Chung J, et al. An African American family with early-onset Alzheimer disease, and an APP (T714I) mutation. Neurology 2005; 64: 377-379
-
(2005)
Neurology
, vol.64
, pp. 377-379
-
-
Edwards-Lee, T.1
Ringman, J.M.2
Chung, J.3
-
35
-
-
84921292800
-
Seizures in Alzheimer's disease
-
Born HA. Seizures in Alzheimer's disease. Neuroscience 2015; 286: 251-263
-
(2015)
Neuroscience
, vol.286
, pp. 251-263
-
-
Born, H.A.1
-
36
-
-
84883759456
-
Seizures, and epileptiform activity in the early stages of Alzheimer disease
-
Vossel KA, Beagle AJ, Rabinovici GD, et al. Seizures, and epileptiform activity in the early stages of Alzheimer disease. JAMA Neurol 2013; 70: 1158-1166
-
(2013)
JAMA Neurol
, vol.70
, pp. 1158-1166
-
-
Vossel, K.A.1
Beagle, A.J.2
Rabinovici, G.D.3
-
37
-
-
20444390669
-
EEG in the diagnosis, classification, and management of patients with epilepsy
-
Smith SJ. EEG in the diagnosis, classification, and management of patients with epilepsy. J Neurol Neurosurg Psychiatry 2005; 76(suppl 2): 2-7
-
(2005)
J Neurol Neurosurg Psychiatry
, vol.76
, pp. 2-7
-
-
Smith, S.J.1
-
38
-
-
0036193906
-
Effects of psychotropic drugs on seizure threshold
-
Pisani F, Oteri G, Costa C, Di Raimondo G, Di Perri R. Effects of psychotropic drugs on seizure threshold. Drug Saf 2002; 25: 91-110
-
(2002)
Drug Saf
, vol.25
, pp. 91-110
-
-
Pisani, F.1
Oteri, G.2
Costa, C.3
Di Raimondo, G.4
Di Perri, R.5
-
39
-
-
84878794559
-
Developing an international network for Alzheimer research: The dominantly inherited Alzheimer network
-
Morris JC, Aisen PS, Bateman RJ, et al. Developing an international network for Alzheimer research: the Dominantly Inherited Alzheimer Network. Clin Investig 2012; 2: 975-984
-
(2012)
Clin Investig
, vol.2
, pp. 975-984
-
-
Morris, J.C.1
Aisen, P.S.2
Bateman, R.J.3
|