-
1
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder EH, Saunders AM, Strittmatter WJ, et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 1993;261:921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
-
2
-
-
0032739695
-
No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritance
-
Savioz A, Leuba G, Forsell C, et al. No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a swiss early-onset Alzheimer's disease family with a dominant mode of inheritance. Dement Geriatr Cogn Disord. 1999;10:431-436.
-
(1999)
Dement Geriatr Cogn Disord
, vol.10
, pp. 431-436
-
-
Savioz, A.1
Leuba, G.2
Forsell, C.3
-
3
-
-
0035860986
-
A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families
-
Athan ES, Williamson J, Ciappa A, et al. A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families. JAMA. 2001;286:2257-2263.
-
(2001)
JAMA
, vol.286
, pp. 2257-2263
-
-
Athan, E.S.1
Williamson, J.2
Ciappa, A.3
-
4
-
-
0028812820
-
Mutations of the presenilin I gene in families with early-onset Alzheimer's disease
-
Campion D, Flaman JM, Brice A, et al. Mutations of the presenilin I gene in families with early-onset Alzheimer's disease. Hum Mol Genet. 1995;4:2373-2377.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2373-2377
-
-
Campion, D.1
Flaman, J.M.2
Brice, A.3
-
5
-
-
0033358671
-
Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum
-
Campion D, Dumanchin C, Hannequin D, et al. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum. Am J Hum Genet. 1999;65:664-670.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 664-670
-
-
Campion, D.1
Dumanchin, C.2
Hannequin, D.3
-
6
-
-
0033909535
-
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes
-
Finckh U, Muller-Thomsen T, Mann U, et al. High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes. Am J Hum Genet. 2000;66:110-117.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 110-117
-
-
Finckh, U.1
Muller-Thomsen, T.2
Mann, U.3
-
7
-
-
0032544702
-
Familial Alzheimer's disease genes in Japanese
-
Kamimura K, Tanahashi H, Yamanaka H, Takahashi K, Asada T, Tabira T. Familial Alzheimer's disease genes in Japanese. J Neurol Sci. 1998;160:76-81.
-
(1998)
J Neurol Sci
, vol.160
, pp. 76-81
-
-
Kamimura, K.1
Tanahashi, H.2
Yamanaka, H.3
Takahashi, K.4
Asada, T.5
Tabira, T.6
-
8
-
-
6844255860
-
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease
-
Cruts M, van Duijn CM, Backhovens H, et al. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. Hum Mol Genet. 1998;7:43-51.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 43-51
-
-
Cruts, M.1
Van Duijn, C.M.2
Backhovens, H.3
-
9
-
-
28944440580
-
-
Antwerp, Belgium: Molecular Genetics Dept, Flanders Interuniversity Institute for Biotechnology, Born-Bunge Foundation, University of Antwerp
-
Cruts M. Alzheimer Disease Mutation Database. Antwerp, Belgium: Molecular Genetics Dept, Flanders Interuniversity Institute for Biotechnology, Born-Bunge Foundation, University of Antwerp; 2004.
-
(2004)
Alzheimer Disease Mutation Database
-
-
Cruts, M.1
-
10
-
-
0028883252
-
Molecular genetics of Alzheimer disease: Identification of genes and gene mutations
-
Van Broeckhoven CL. Molecular genetics of Alzheimer disease: identification of genes and gene mutations. Eur Neurol. 1995;35:8-19.
-
(1995)
Eur Neurol
, vol.35
, pp. 8-19
-
-
Van Broeckhoven, C.L.1
-
11
-
-
0037469171
-
Early onset familial Alzheimer's disease: Mutation frequency in 31 families
-
Janssen JC, Beck JA, Campbell TA, et al. Early onset familial Alzheimer's disease: mutation frequency in 31 families. Neurology. 2003;60:235-239.
-
(2003)
Neurology
, vol.60
, pp. 235-239
-
-
Janssen, J.C.1
Beck, J.A.2
Campbell, T.A.3
-
12
-
-
0033848935
-
Familial Alzheimer's disease: Site of mutation influences clinical phenotype
-
Lippa CF, Swearer JM, Kane KJ, et al. Familial Alzheimer's disease: site of mutation influences clinical phenotype. Ann Neurol. 2000;48:376-379.
-
(2000)
Ann Neurol
, vol.48
, pp. 376-379
-
-
Lippa, C.F.1
Swearer, J.M.2
Kane, K.J.3
-
13
-
-
0027426406
-
Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology
-
Mullan M, Houlden H, Crawford F, Kennedy A, Rogues P, Rossor M. Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology. Am J Med Genet. 1993;48:129-130.
-
(1993)
Am J Med Genet
, vol.48
, pp. 129-130
-
-
Mullan, M.1
Houlden, H.2
Crawford, F.3
Kennedy, A.4
Rogues, P.5
Rossor, M.6
-
14
-
-
0020040238
-
A new clinical scale for the staging of dementia
-
Hughes CP, Berg L, Danziger WL, Coben LA, Martin RL. A new clinical scale for the staging of dementia. Br J Psychiatry. 1982;140:566-572.
-
(1982)
Br J Psychiatry
, vol.140
, pp. 566-572
-
-
Hughes, C.P.1
Berg, L.2
Danziger, W.L.3
Coben, L.A.4
Martin, R.L.5
-
15
-
-
0027425211
-
The Clinical Dementia Rating (CDR): Current version and scoring rules
-
Morris JC. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology. 1993;43:2412-2414.
-
(1993)
Neurology
, vol.43
, pp. 2412-2414
-
-
Morris, J.C.1
-
16
-
-
0025863618
-
Neuropathological stageing of Alzheimer-related changes
-
Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol (Berl). 1991;824:239-259.
-
(1991)
Acta Neuropathol (Berl)
, vol.824
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
-
17
-
-
0006164301
-
Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop
-
McKeith IG, Galasko D, Kosaka K, et al. Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop. Neurology. 1996;47:1113-1124.
-
(1996)
Neurology
, vol.47
, pp. 1113-1124
-
-
McKeith, I.G.1
Galasko, D.2
Kosaka, K.3
-
19
-
-
84946642987
-
A standardized memory scale for clinical use
-
Wechsler D. A standardized memory scale for clinical use. J Psychol. 1945;19:87-95.
-
(1945)
J Psychol
, vol.19
, pp. 87-95
-
-
Wechsler, D.1
-
20
-
-
0033010135
-
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
-
Ezquerra M, Carnero C, Blesa R, Gelpi JL, Ballesta F, Oliva R. A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures. Neurology. 1999;52:566-570.
-
(1999)
Neurology
, vol.52
, pp. 566-570
-
-
Ezquerra, M.1
Carnero, C.2
Blesa, R.3
Gelpi, J.L.4
Ballesta, F.5
Oliva, R.6
-
21
-
-
0036845601
-
Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain
-
Lleo A, Blesa R, Queralt R, et al. Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain. Arch Neurol. 2002;59:1759-1763.
-
(2002)
Arch Neurol
, vol.59
, pp. 1759-1763
-
-
Lleo, A.1
Blesa, R.2
Queralt, R.3
-
22
-
-
7844246535
-
Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease
-
Taddei K, Kwok JB, Kril JJ, et al. Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease. Neuroreport. 1998;9:3335-3339.
-
(1998)
Neuroreport
, vol.9
, pp. 3335-3339
-
-
Taddei, K.1
Kwok, J.B.2
Kril, J.J.3
-
23
-
-
0035208657
-
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures
-
Takao M, Ghetti B, Murrell JR, et al. Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures. J Neuropathol Exp Neurol. 2001;60:1137-1152.
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 1137-1152
-
-
Takao, M.1
Ghetti, B.2
Murrell, J.R.3
-
24
-
-
0033762710
-
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations
-
Houlden H, Baker M, McGowan E, et al. Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. Ann Neurol. 2000;48:806-808.
-
(2000)
Ann Neurol
, vol.48
, pp. 806-808
-
-
Houlden, H.1
Baker, M.2
McGowan, E.3
-
25
-
-
6844240203
-
A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 28 years
-
Wisniewski T, Dowjat WK, Buxbaum JD, et al. A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 28 years. Neuroreport. 1998;9:217-221.
-
(1998)
Neuroreport
, vol.9
, pp. 217-221
-
-
Wisniewski, T.1
Dowjat, W.K.2
Buxbaum, J.D.3
-
26
-
-
0025959458
-
Early-onset Alzheimer's disease in 2 large Belgian families
-
Martin JJ, Gheuens J, Bruyland M, et al. Early-onset Alzheimer's disease in 2 large Belgian families. Neurology. 1991;41:62-68.
-
(1991)
Neurology
, vol.41
, pp. 62-68
-
-
Martin, J.J.1
Gheuens, J.2
Bruyland, M.3
-
27
-
-
0031820213
-
Presenilin 1 Met146Leu variant due to an A→T transversion in an early-onset familial Alzheimer's disease pedigree from Argentina
-
Morelli L, Prat MI, Levy E, Mangone CA, Castano EM. Presenilin 1 Met146Leu variant due to an A→T transversion in an early-onset familial Alzheimer's disease pedigree from Argentina. Clin Genet. 1998;53:469-473.
-
(1998)
Clin Genet
, vol.53
, pp. 469-473
-
-
Morelli, L.1
Prat, M.I.2
Levy, E.3
Mangone, C.A.4
Castano, E.M.5
-
28
-
-
0034041861
-
A novel presenilin 1 mutation (Leu166Arg) associated with early-onset Alzheimer disease
-
Ezquerra M, Carnero C, Blesa R, Oliva R. A novel presenilin 1 mutation (Leu166Arg) associated with early-onset Alzheimer disease. Arch Neurol. 2000;57:485-488.
-
(2000)
Arch Neurol
, vol.57
, pp. 485-488
-
-
Ezquerra, M.1
Carnero, C.2
Blesa, R.3
Oliva, R.4
-
29
-
-
0036063666
-
Very early-onset familial Alzheimer's disease: A novel presenilin 1 mutation
-
Goldman JS, Reed B, Gearhart R, Kramer JH, Miller BL. Very early-onset familial Alzheimer's disease: a novel presenilin 1 mutation. Int J Geriatr Psychiatry. 2002;17:649-651.
-
(2002)
Int J Geriatr Psychiatry
, vol.17
, pp. 649-651
-
-
Goldman, J.S.1
Reed, B.2
Gearhart, R.3
Kramer, J.H.4
Miller, B.L.5
-
30
-
-
0042385121
-
Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease
-
Miklossy J, Taddei K, Suva D, et al. Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease. Neurobiol Aging. 2003;24:655-662.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 655-662
-
-
Miklossy, J.1
Taddei, K.2
Suva, D.3
-
31
-
-
0035798271
-
A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies
-
Houlden H, Crook R, Dolan RJ, McLaughlin J, Revesz T, Hardy J. A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies. Neurosci Lett. 2001;313:93-95.
-
(2001)
Neurosci Lett
, vol.313
, pp. 93-95
-
-
Houlden, H.1
Crook, R.2
Dolan, R.J.3
McLaughlin, J.4
Revesz, T.5
Hardy, J.6
-
32
-
-
10144244629
-
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years
-
Campion D, Brice A, Dumanchin C, et al. A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years. Neuroreport. 1996;7:1582-1584.
-
(1996)
Neuroreport
, vol.7
, pp. 1582-1584
-
-
Campion, D.1
Brice, A.2
Dumanchin, C.3
-
33
-
-
8044251536
-
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients
-
Ikeda M, Sharma V, Sumi SM, et al. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. Ann Neurol. 1996;40:912-917.
-
(1996)
Ann Neurol
, vol.40
, pp. 912-917
-
-
Ikeda, M.1
Sharma, V.2
Sumi, S.M.3
-
34
-
-
0033776069
-
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease
-
Devi G, Fotiou A, Jyrinji D, et al. Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease. Arch Neurol. 2000;57:1454-1457.
-
(2000)
Arch Neurol
, vol.57
, pp. 1454-1457
-
-
Devi, G.1
Fotiou, A.2
Jyrinji, D.3
-
35
-
-
14844292710
-
A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease
-
Ishikawa A, Piao YS, Miyashita A, et al. A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease. Ann Neurol. 2005;57:429-434.
-
(2005)
Ann Neurol
, vol.57
, pp. 429-434
-
-
Ishikawa, A.1
Piao, Y.S.2
Miyashita, A.3
-
36
-
-
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
-
37
-
-
0028906390
-
Early onset Alzheimer's disease in a South American pedigree from Argentina
-
Mangone CA, Castano EM, Levy E, et al. Early onset Alzheimer's disease in a South American pedigree from Argentina. Acta Neurol Scand. 1995;91:6-13.
-
(1995)
Acta Neurol Scand
, vol.91
, pp. 6-13
-
-
Mangone, C.A.1
Castano, E.M.2
Levy, E.3
-
38
-
-
0034094214
-
Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene
-
Murrell JR, Hake AM, Quaid KA, Farlow MR, Ghetti B. Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene. Arch Neurol. 2000;57:885-887.
-
(2000)
Arch Neurol
, vol.57
, pp. 885-887
-
-
Murrell, J.R.1
Hake, A.M.2
Quaid, K.A.3
Farlow, M.R.4
Ghetti, B.5
-
39
-
-
0032611568
-
A Polish pedigree with Alzheimer's disease determined by a novel mutation in exon 12 of the presenilin 1 gene: Clinical and molecular characterization
-
Kowalska A, Forsell C, Florczak J, et al. A Polish pedigree with Alzheimer's disease determined by a novel mutation in exon 12 of the presenilin 1 gene: clinical and molecular characterization. Folia Neuropathol. 1999;37:57-61.
-
(1999)
Folia Neuropathol
, vol.37
, pp. 57-61
-
-
Kowalska, A.1
Forsell, C.2
Florczak, J.3
-
40
-
-
0007486598
-
A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimer's disease
-
Romero I, Jorgensen P, Bolwig G, et al. A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimer's disease. Neuroreport. 1999;10:2255-2260.
-
(1999)
Neuroreport
, vol.10
, pp. 2255-2260
-
-
Romero, I.1
Jorgensen, P.2
Bolwig, G.3
-
41
-
-
0032248908
-
Missense mutation in exon 11 (codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification
-
Besancon R, Lorenzi A, Cruts M, et al. Missense mutation in exon 11 (codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Hum Mutat. 1998;11:481.
-
(1998)
Hum Mutat
, vol.11
, pp. 481
-
-
Besancon, R.1
Lorenzi, A.2
Cruts, M.3
-
42
-
-
9344237637
-
Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease
-
Hutton M, Busfield F, Wragg M, et al. Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease. Neuroreport. 1996;7:801-805.
-
(1996)
Neuroreport
, vol.7
, pp. 801-805
-
-
Hutton, M.1
Busfield, F.2
Wragg, M.3
-
43
-
-
0034223610
-
A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease
-
Raux G, Gantier R, Martin C, et al. A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease. Hum Mutat. 2000;16:95.
-
(2000)
Hum Mutat
, vol.16
, pp. 95
-
-
Raux, G.1
Gantier, R.2
Martin, C.3
-
44
-
-
0037041304
-
Molecular evidence of presenilin 1 mutation in familial early onset dementia
-
Matsubara-Tsutsui M, Yasuda M, Yamagata H, et al. Molecular evidence of presenilin 1 mutation in familial early onset dementia. Am J Med Genet. 2002;114:292-298.
-
(2002)
Am J Med Genet
, vol.114
, pp. 292-298
-
-
Matsubara-Tsutsui, M.1
Yasuda, M.2
Yamagata, H.3
-
45
-
-
0344464874
-
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met233Leu)
-
Portet F, Dauvilliers Y, Campion D, et al. Very early onset AD with a de novo mutation in the presenilin 1 gene (Met233Leu). Neurology. 2003;61:1136-1137.
-
(2003)
Neurology
, vol.61
, pp. 1136-1137
-
-
Portet, F.1
Dauvilliers, Y.2
Campion, D.3
-
46
-
-
7744233995
-
A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis
-
Ataka S, Tomiyama T, Takuma H, et al. A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis. Arch Neurol. 2004;61:1773-1776.
-
(2004)
Arch Neurol
, vol.61
, pp. 1773-1776
-
-
Ataka, S.1
Tomiyama, T.2
Takuma, H.3
-
47
-
-
0034327364
-
Nonfibrillar diffuse amyloid deposition due to a γ42-secretase site mutation points to an essential role for N-truncated Aβ42 in Alzheimer's disease
-
Kumar-Singh S, De Jonghe C, Cruts M, et al. Nonfibrillar diffuse amyloid deposition due to a γ42-secretase site mutation points to an essential role for Ntruncated Aβ42 in Alzheimer's disease. Hum Mol Genet. 2000;9:2589-2598.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2589-2598
-
-
Kumar-Singh, S.1
De Jonghe, C.2
Cruts, M.3
-
49
-
-
19944428327
-
Pick bodies in a family with presenilin-1 Alzheimer's disease
-
Halliday GM, Song YJ, Lepar G, et al. Pick bodies in a family with presenilin-1 Alzheimer's disease. Ann Neurol. 2005;57:139-143.
-
(2005)
Ann Neurol
, vol.57
, pp. 139-143
-
-
Halliday, G.M.1
Song, Y.J.2
Lepar, G.3
-
50
-
-
0142125743
-
Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: A clinicopathological study of four autopsy cases
-
Yokota O, Terada S, Ishizu H, et al. Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: a clinicopathological study of four autopsy cases. Acta Neuropathol (Berl). 2003;106:348-356.
-
(2003)
Acta Neuropathol (Berl)
, vol.106
, pp. 348-356
-
-
Yokota, O.1
Terada, S.2
Ishizu, H.3
-
51
-
-
10544236903
-
Dementia with Lewy bodies: Reliability and validity of clinical and pathologic criteria
-
Mega MS, Masterman DL, Benson DF, et al. Dementia with Lewy bodies: reliability and validity of clinical and pathologic criteria. Neurology. 1996;47:1403-1409.
-
(1996)
Neurology
, vol.47
, pp. 1403-1409
-
-
Mega, M.S.1
Masterman, D.L.2
Benson, D.F.3
-
52
-
-
18344417178
-
Lewy bodies contain altered α-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes
-
Lippa CF, Fujiwara H, Mann DM, et al. Lewy bodies contain altered α-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes. Am J Pathol. 1998;153:1365-1370.
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(1998)
Am J Pathol
, vol.153
, pp. 1365-1370
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Lippa, C.F.1
Fujiwara, H.2
Mann, D.M.3
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