-
1
-
-
0034828250
-
Familial cerebral amyloid angiopathy related to stroke and dementia
-
Frangione B, Revesz T, Vidal R, et al. Familial cerebral amyloid angiopathy related to stroke and dementia. Amyloid 2001;8Suppl 1:36-42
-
(2001)
Amyloid
, vol.8
, Issue.SUPPL. 1
, pp. 36-42
-
-
Frangione, B.1
Revesz, T.2
Vidal, R.3
-
2
-
-
0037038813
-
Amyloidosis and Alzheimer's disease
-
Ghiso J, Frangione B. Amyloidosis and Alzheimer's disease. Adv Drug Deliv Rev 2002;54:1539-51
-
(2002)
Adv Drug Deliv Rev
, vol.54
, pp. 1539-1551
-
-
Ghiso, J.1
Frangione, B.2
-
3
-
-
0023254674
-
Cerebral amyloid angiopathy. A critical review
-
Vinters HV. Cerebral amyloid angiopathy. A critical review. Stroke 1987;18:311-24
-
(1987)
Stroke
, vol.18
, pp. 311-324
-
-
Vinters, H.V.1
-
4
-
-
84889148670
-
Familial and sporadic cerebral amyloid angiopathies associated with dementia and the BRI dementias
-
Esiri MM, Lee V-MY, Trojanowski JQ, eds. Cambridge: Cambridge University Press, in press
-
Plant GT, Ghiso J, Holton JL, Frangione B, Revesz T. Familial and sporadic cerebral amyloid angiopathies associated with dementia and the BRI dementias. In: Esiri MM, Lee V-MY, Trojanowski JQ, eds. The neuropathology of dementia. Cambridge: Cambridge University Press, in press
-
The Neuropathology of Dementia
-
-
Plant, G.T.1
Ghiso, J.2
Holton, J.L.3
Frangione, B.4
Revesz, T.5
-
5
-
-
0036019162
-
Sporadic and familial cerebral amyloid angiopathies
-
Revesz T, Holton JL, Lashley T, et al. Sporadic and familial cerebral amyloid angiopathies. Brain Pathol 2002;12:343-57
-
(2002)
Brain Pathol
, vol.12
, pp. 343-357
-
-
Revesz, T.1
Holton, J.L.2
Lashley, T.3
-
6
-
-
0001458616
-
Neuropathologic features and grading of Alzheimer-related and sporadic CAA
-
Verbeek MM, de Waal RMW, Vinters HV, eds. Dordrecht: Kluwer Academic Publishers
-
Vinters HV, Vonsattel JP. Neuropathologic features and grading of Alzheimer-related and sporadic CAA. In: Verbeek MM, de Waal RMW, Vinters HV, eds. Cerebral amyloid angiopathy in Alzheimer's disease and related disorders. Dordrecht: Kluwer Academic Publishers, 2000;137-55
-
(2000)
Cerebral Amyloid Angiopathy in Alzheimer's Disease and Related Disorders
, pp. 137-155
-
-
Vinters, H.V.1
Vonsattel, J.P.2
-
7
-
-
0026004781
-
Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study
-
Vonsattel JP, Myers RH, Hedley-Whyte ET, Ropper AH, Bird ED, Richardson EP Jr. Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study. Ann Neurol 1991;30:637-49
-
(1991)
Ann Neurol
, vol.30
, pp. 637-649
-
-
Vonsattel, J.P.1
Myers, R.H.2
Hedley-Whyte, E.T.3
Ropper, A.H.4
Bird, E.D.5
Richardson E.P., Jr.6
-
8
-
-
0035137042
-
Regional distribution of amyloid-BRI deposition and its association with neurofibrillary degeneration in familial British dementia
-
Holton JL, Ghiso J, Lashley T, et al. Regional distribution of amyloid-BRI deposition and its association with neurofibrillary degeneration in familial British dementia. Am J Pathol 2001;158:515-26
-
(2001)
Am J Pathol
, vol.158
, pp. 515-526
-
-
Holton, J.L.1
Ghiso, J.2
Lashley, T.3
-
9
-
-
0036194067
-
Familial Danish dementia: A novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta
-
Holton JL, Lashley T, Ghiso J, et al. Familial Danish dementia: A novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta. J Neuropathol Exp Neurol 2002;61:254-67
-
(2002)
J Neuropathol Exp Neurol
, vol.61
, pp. 254-267
-
-
Holton, J.L.1
Lashley, T.2
Ghiso, J.3
-
10
-
-
0036096013
-
Genetic and environmental risk factors for intracerebral hemorrhage: Preliminary results of a population-based study
-
Woo D, Sauerbeck LR, Kissela BM, et al. Genetic and environmental risk factors for intracerebral hemorrhage: Preliminary results of a population-based study. Stroke 2002;33:1190-95
-
(2002)
Stroke
, vol.33
, pp. 1190-1195
-
-
Woo, D.1
Sauerbeck, L.R.2
Kissela, B.M.3
-
11
-
-
0009735077
-
Clinical aspects and diagnostic criteria of sporadic CAA-related hemorrhage
-
Verbeek MM, de Waal RMW, Vinters HV, eds. Dordrecht: Kluwer Academic Publishers
-
Greenberg, SM. Clinical aspects and diagnostic criteria of sporadic CAA-related hemorrhage. In: Verbeek MM, de Waal RMW, Vinters HV, eds. Cerebral amyloid angiopathy in Alzheimer's disease and related disorders. Dordrecht: Kluwer Academic Publishers, 2000;3-19
-
(2000)
Cerebral Amyloid Angiopathy in Alzheimer's Disease and Related Disorders
, pp. 3-19
-
-
Greenberg, S.M.1
-
12
-
-
0037062566
-
Cerebral amyloid angiopathy and cognitive function: The HAAS autopsy study
-
Pfeifer LA, White LR, Ross GW, Petrovitch H, Launer LJ. Cerebral amyloid angiopathy and cognitive function: The HAAS autopsy study. Neurology 2002;58:1629-34
-
(2002)
Neurology
, vol.58
, pp. 1629-1634
-
-
Pfeifer, L.A.1
White, L.R.2
Ross, G.W.3
Petrovitch, H.4
Launer, L.J.5
-
13
-
-
0035282982
-
Spontaneous hemorrhagic stroke in a mouse model of cerebral amyloid angiopathy
-
Winkler DT, Bondolfi L, Herzig MC, et al. Spontaneous hemorrhagic stroke in a mouse model of cerebral amyloid angiopathy. J Neurosci 2001;21:1619-27
-
(2001)
J Neurosci
, vol.21
, pp. 1619-1627
-
-
Winkler, D.T.1
Bondolfi, L.2
Herzig, M.C.3
-
14
-
-
0033804862
-
Cerebral beta amyloid angiopathy is a risk factor for cerebral ischemic infarction. A case control study in human brain biopsies
-
Cadavid D, Mena H, Koeller K, Frommelt RA. Cerebral beta amyloid angiopathy is a risk factor for cerebral ischemic infarction. A case control study in human brain biopsies. J Neuropathol Exp Neurol 2000;59:768-73
-
(2000)
J Neuropathol Exp Neurol
, vol.59
, pp. 768-773
-
-
Cadavid, D.1
Mena, H.2
Koeller, K.3
Frommelt, R.A.4
-
15
-
-
0035203856
-
Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles
-
Natte R, Maat-Schieman ML, Haan J, Bornebroek M, Roos RA, van Duinen SG. Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles. Ann Neurol 2001;50:765-72
-
(2001)
Ann Neurol
, vol.50
, pp. 765-772
-
-
Natte, R.1
Maat-Schieman, M.L.2
Haan, J.3
Bornebroek, M.4
Roos, R.A.5
Van Duinen, S.G.6
-
16
-
-
0034982951
-
Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy
-
Grabowski TJ, Cho HS, Vonsattel JP, Rebeck GW, Greenberg SM. Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy. Ann Neurol 2001;49:697-705
-
(2001)
Ann Neurol
, vol.49
, pp. 697-705
-
-
Grabowski, T.J.1
Cho, H.S.2
Vonsattel, J.P.3
Rebeck, G.W.4
Greenberg, S.M.5
-
17
-
-
0035090079
-
Analysis of cerebral amyloid angiopathy in a transgenic mouse model of Alzheimer disease using in vivo multiphoton microscopy
-
Kimchi EY, Kajdasz S, Bacskai BJ, Hyman BT. Analysis of cerebral amyloid angiopathy in a transgenic mouse model of Alzheimer disease using in vivo multiphoton microscopy. J Neuropathol Exp Neurol 2001;60:274-79
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 274-279
-
-
Kimchi, E.Y.1
Kajdasz, S.2
Bacskai, B.J.3
Hyman, B.T.4
-
18
-
-
0036447712
-
Proinflammatory and vasoactive effects of Abeta in the cerebrovasculature
-
Townsend KP, Obregon D, Quadros A, et al. Proinflammatory and vasoactive effects of Abeta in the cerebrovasculature. Ann N Y Acad Sci 2002;977:65-76
-
(2002)
Ann N Y Acad Sci
, vol.977
, pp. 65-76
-
-
Townsend, K.P.1
Obregon, D.2
Quadros, A.3
-
19
-
-
0036451721
-
Risk factors for cerebral amyloid angiopathy in the elderly
-
Yamada M. Risk factors for cerebral amyloid angiopathy in the elderly. Ann N Y Acad Sci 2002;977:37-44
-
(2002)
Ann N Y Acad Sci
, vol.977
, pp. 37-44
-
-
Yamada, M.1
-
20
-
-
0029973286
-
Cerebral amyloid angiopathy in the brains of patients with Alzheimer's disease: The CERAD experience, Part XV
-
Ellis RJ, Olichney JM, Thal LJ, et al. Cerebral amyloid angiopathy in the brains of patients with Alzheimer's disease: The CERAD experience, Part XV. Neurology 1996;46:1592-96
-
(1996)
Neurology
, vol.46
, pp. 1592-1596
-
-
Ellis, R.J.1
Olichney, J.M.2
Thal, L.J.3
-
21
-
-
0028991404
-
Apolipoprotein E epsilon 4 and cerebral hemorrhage associated with amyloid angiopathy
-
Greenberg SM, Rebeck GW, Vonsattel JP, Gomez-Isla T, Hyman BT. Apolipoprotein E epsilon 4 and cerebral hemorrhage associated with amyloid angiopathy. Ann Neurol 1995;38:254-59
-
(1995)
Ann Neurol
, vol.38
, pp. 254-259
-
-
Greenberg, S.M.1
Rebeck, G.W.2
Vonsattel, J.P.3
Gomez-Isla, T.4
Hyman, B.T.5
-
22
-
-
0029665096
-
Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer's disease
-
Premkumar DR, Cohen DL, Hedera P, Friedland RP, Kalaria RN. Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer's disease. Am J Pathol 1996;148:2083-95
-
(1996)
Am J Pathol
, vol.148
, pp. 2083-2095
-
-
Premkumar, D.R.1
Cohen, D.L.2
Hedera, P.3
Friedland, R.P.4
Kalaria, R.N.5
-
23
-
-
0031942889
-
Progression of cerebral amyloid angiopathy: Accumulation of amyloid-beta40 in affected vessels
-
Alonzo NC, Hyman BT, Rebeck GW, Greenberg SM. Progression of cerebral amyloid angiopathy: Accumulation of amyloid-beta40 in affected vessels. J Neuropathol Exp Neurol 1998;57:353-59
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 353-359
-
-
Alonzo, N.C.1
Hyman, B.T.2
Rebeck, G.W.3
Greenberg, S.M.4
-
24
-
-
0030610591
-
High frequency of apolipoprotein E epsilon 2 allele in hemorrhage due to cerebral amyloid angiopathy
-
Nicoll JA, Burnett C, Love S, et al. High frequency of apolipoprotein E epsilon 2 allele in hemorrhage due to cerebral amyloid angiopathy. Ann Neurol 1997;41:716-21
-
(1997)
Ann Neurol
, vol.41
, pp. 716-721
-
-
Nicoll, J.A.1
Burnett, C.2
Love, S.3
-
25
-
-
0035066332
-
Alzheimer's disease: Genes, proteins, and therapy
-
Selkoe DJ. Alzheimer's disease: Genes, proteins, and therapy. Physiol Rev 2001;81:741-66
-
(2001)
Physiol Rev
, vol.81
, pp. 741-766
-
-
Selkoe, D.J.1
-
26
-
-
0036545673
-
APOE polymorphism and clinical duration determine regional neuropathology in Swedish APP(670, 671) mutation carriers: Implications for late-onset Alzheimer's disease
-
Bogdanovic N, Corder E, Lannfelt L, Winblad B. APOE polymorphism and clinical duration determine regional neuropathology in Swedish APP(670, 671) mutation carriers: Implications for late-onset Alzheimer's disease. J Cell Mol Med 2002;6:199-214
-
(2002)
J Cell Mol Med
, vol.6
, pp. 199-214
-
-
Bogdanovic, N.1
Corder, E.2
Lannfelt, L.3
Winblad, B.4
-
27
-
-
0029869667
-
Predominant deposition of amyloid-beta(42(43)) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene
-
Mann DMA, Iwatsubo T, IHARA Y, et al. Predominant deposition of amyloid-beta(42(43)) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene. Am J Pathol 1996;148:1257-66
-
(1996)
Am J Pathol
, vol.148
, pp. 1257-1266
-
-
Mann, D.M.A.1
Iwatsubo, T.2
Ihara, Y.3
-
28
-
-
0025296269
-
Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type
-
Levy E, Carman MD, Fernandez-Madrid IJ, et al. Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. Science 1990;248:1124-26
-
(1990)
Science
, vol.248
, pp. 1124-1126
-
-
Levy, E.1
Carman, M.D.2
Fernandez-Madrid, I.J.3
-
29
-
-
0029927290
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II - A review of histopathological aspects
-
Maat-Schieman ML, van Duinen SG, Bornebroek M, Haan J, Roos RA. Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II - A review of histopathological aspects. Brain Pathol 1996;6:115-20
-
(1996)
Brain Pathol
, vol.6
, pp. 115-120
-
-
Maat-Schieman, M.L.1
Van Duinen, S.G.2
Bornebroek, M.3
Haan, J.4
Roos, R.A.5
-
30
-
-
0036968368
-
Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric
-
Kumar-Singh S, Cras P, Wang R, et al. Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric. Am J Pathol 2002;161:507-20
-
(2002)
Am J Pathol
, vol.161
, pp. 507-520
-
-
Kumar-Singh, S.1
Cras, P.2
Wang, R.3
-
31
-
-
0034662929
-
BACE2, a beta-secretase homolog, cleaves at the beta site and within the amyloid-beta region of the amyloid-beta precursor protein
-
Farzan M, Schnitzler CE, Vasilieva N, Leung D, Choe H. BACE2, a beta-secretase homolog, cleaves at the beta site and within the amyloid-beta region of the amyloid-beta precursor protein. Proc Natl Acad Sci U S A 2000;97:9712-17
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 9712-9717
-
-
Farzan, M.1
Schnitzler, C.E.2
Vasilieva, N.3
Leung, D.4
Choe, H.5
-
32
-
-
0034975365
-
Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease
-
Mann DM, Pickering-Brown SM, Takeuchi A, Iwatsubo T. Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease. Am J Pathol 2001;158:2165-75
-
(2001)
Am J Pathol
, vol.158
, pp. 2165-2175
-
-
Mann, D.M.1
Pickering-Brown, S.M.2
Takeuchi, A.3
Iwatsubo, T.4
-
33
-
-
0035831499
-
A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques
-
Steiner H, Revesz T, Neumann M, et al. A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques. J Biol Chem 2001;276:7233-39
-
(2001)
J Biol Chem
, vol.276
, pp. 7233-7239
-
-
Steiner, H.1
Revesz, T.2
Neumann, M.3
-
34
-
-
0036938641
-
A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: Presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum
-
Takao M, Ghetti B, Hayakawa I. et al. A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: Presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum. Acta Neuropathol (Berl) 2002;104:155-70
-
(2002)
Acta Neuropathol (Berl)
, vol.104
, pp. 155-170
-
-
Takao, M.1
Ghetti, B.2
Hayakawa, I.3
-
35
-
-
0031941389
-
Amyloid angiopathy in a Volga German family with Alzheimer's disease and a presenilin-2 mutation (N141I)
-
Nochlin D, Bird TD, Nemens EJ, Ball MJ, Sumi SM. Amyloid angiopathy in a Volga German family with Alzheimer's disease and a presenilin-2 mutation (N141I). Ann Neurol 1998;43:131-35
-
(1998)
Ann Neurol
, vol.43
, pp. 131-135
-
-
Nochlin, D.1
Bird, T.D.2
Nemens, E.J.3
Ball, M.J.4
Sumi, S.M.5
-
36
-
-
0030330082
-
Apolipoprotein E. amyloidogenesis
-
Frangione B, Castano EM, Wisniewski T, Ghiso J, Prelli F, Vidal R. Apolipoprotein E and amyloidogenesis. Ciba Found Symp 1996;199:132-41
-
(1996)
Ciba Found Symp
, vol.199
, pp. 132-141
-
-
Frangione, B.1
Castano, E.M.2
Wisniewski, T.3
Ghiso, J.4
Prelli, F.5
Vidal, R.6
-
37
-
-
0029774196
-
The length of amyloid-beta in hereditary cerebral hemorrhage with amyloidosis, Dutch type. Implications for the role of amyloid-beta 1-42 in Alzheimer's disease
-
Castano EM, Prelli F, Soto C, et al. The length of amyloid-beta in hereditary cerebral hemorrhage with amyloidosis, Dutch type. Implications for the role of amyloid-beta 1-42 in Alzheimer's disease. J Biol Chem 1996;271:32185-91
-
(1996)
J Biol Chem
, vol.271
, pp. 32185-32191
-
-
Castano, E.M.1
Prelli, F.2
Soto, C.3
-
38
-
-
0033809909
-
Prominent cerebral amyloid angiopathy in transgenic mice overexpressing the London mutant of human APP in neurons
-
Van Dorpe J, Smeijers L, Dewachter I, et al. Prominent cerebral amyloid angiopathy in transgenic mice overexpressing the London mutant of human APP in neurons. Am J Pathol 2000;157:1283-98
-
(2000)
Am J Pathol
, vol.157
, pp. 1283-1298
-
-
Van Dorpe, J.1
Smeijers, L.2
Dewachter, I.3
-
39
-
-
0344431341
-
Structural neurology: Are seeds at the root of neuronal degeneration?
-
Lansbury PT. Structural neurology: Are seeds at the root of neuronal degeneration? Neuron 1997;19:1151-54
-
(1997)
Neuron
, vol.19
, pp. 1151-1154
-
-
Lansbury, P.T.1
-
40
-
-
0031985080
-
N-terminal heterogeneity of parenchymal and cerebrovascular Abeta deposits
-
Tekirian TL, Saido TC, Markesbery WR, et al. N-terminal heterogeneity of parenchymal and cerebrovascular Abeta deposits. J Neuropathol Exp Neurol 1998;57:76-94
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 76-94
-
-
Tekirian, T.L.1
Saido, T.C.2
Markesbery, W.R.3
-
41
-
-
0025075723
-
Expression of a normal and variant Alzheimer's beta-protein gene in amyloid of hereditary cerebral hemorrhage, Dutch type: DNA and protein diagnostic assays
-
Prelli F, Levy E, van Duinen SG, Bots GT, Luyendijk W, Frangione B. Expression of a normal and variant Alzheimer's beta-protein gene in amyloid of hereditary cerebral hemorrhage, Dutch type: DNA and protein diagnostic assays. Biochem Biophys Res Commun 1990;170:301-7
-
(1990)
Biochem Biophys Res Commun
, vol.170
, pp. 301-307
-
-
Prelli, F.1
Levy, E.2
Van Duinen, S.G.3
Bots, G.T.4
Luyendijk, W.5
Frangione, B.6
-
42
-
-
0035980088
-
Pathogenic effects of D23N Iowa mutant amyloid beta-protein
-
Van Nostrand WE, Melchor JP, Cho HS, Greenberg SM, Rebeck GW. Pathogenic effects of D23N Iowa mutant amyloid beta-protein. J Biol Chem 2001;276:32860-66
-
(2001)
J Biol Chem
, vol.276
, pp. 32860-32866
-
-
Van Nostrand, W.E.1
Melchor, J.P.2
Cho, H.S.3
Greenberg, S.M.4
Rebeck, G.W.5
-
43
-
-
0034282630
-
Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells
-
Miravalle L, Tokuda T, Chiarle R, et al. Substitutions at codon 22 of Alzheimer's abeta peptide induce diverse conformational changes and apoptotic effects in human cerebral endothelial cells. J Biol Chem 2000;275:27110-16
-
(2000)
J Biol Chem
, vol.275
, pp. 27110-27116
-
-
Miravalle, L.1
Tokuda, T.2
Chiarle, R.3
-
44
-
-
0031791971
-
Distribution of A beta-associated proteins in cerebrovascular amyloid of Alzheimer's disease
-
Verbeek MM, Otte-Holler I, Veerhuis R, Ruiter DJ, de Waal RM. Distribution of A beta-associated proteins in cerebrovascular amyloid of Alzheimer's disease. Acta Neuropathol (Berl) 1998;96:628-36
-
(1998)
Acta Neuropathol (Berl)
, vol.96
, pp. 628-636
-
-
Verbeek, M.M.1
Otte-Holler, I.2
Veerhuis, R.3
Ruiter, D.J.4
De Waal, R.M.5
-
45
-
-
0011766298
-
Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)
-
Ghiso J, Jensson O, Frangione B. Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C). Proc Natl Acad Sci U S A 1986;83:2974-78
-
(1986)
Proc Natl Acad Sci U S A
, vol.83
, pp. 2974-2978
-
-
Ghiso, J.1
Jensson, O.2
Frangione, B.3
-
46
-
-
0024504095
-
Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases
-
Levy E, Lopez-Otin C, Ghiso J, Geltner D, Frangione B. Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases. J Exp Med 1989;169:1771-78
-
(1989)
J Exp Med
, vol.169
, pp. 1771-1778
-
-
Levy, E.1
Lopez-Otin, C.2
Ghiso, J.3
Geltner, D.4
Frangione, B.5
-
47
-
-
0035093468
-
The cerebral hemorrhage-producing cystatin C variant (L68Q) in extracellular fluids
-
Bjarnadottir M, Nilsson C, Lindstrom V, et al. The cerebral hemorrhage-producing cystatin C variant (L68Q) in extracellular fluids. Amyloid 2001;8:1-10
-
(2001)
Amyloid
, vol.8
, pp. 1-10
-
-
Bjarnadottir, M.1
Nilsson, C.2
Lindstrom, V.3
-
48
-
-
0035047801
-
Distinct properties of wild-type and the amyloidogenic human cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type
-
Calero M, Pawlik M, Soto C, et al. Distinct properties of wild-type and the amyloidogenic human cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type. J Neurochem 2001;77:628-37
-
(2001)
J Neurochem
, vol.77
, pp. 628-637
-
-
Calero, M.1
Pawlik, M.2
Soto, C.3
-
49
-
-
0035140013
-
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients
-
Levy E, Sastre M, Kumar A, et al. Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients. J Neuropathol Exp Neurol 2001;60:94-104
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 94-104
-
-
Levy, E.1
Sastre, M.2
Kumar, A.3
-
50
-
-
0034718576
-
A polymorphism in the cystatin C gene is a novel risk factor for late-onset Alzheimer's disease
-
Crawford FC, Freeman MJ, Schinka JA, et al. A polymorphism in the cystatin C gene is a novel risk factor for late-onset Alzheimer's disease. Neurology 2000;55:763-68
-
(2000)
Neurology
, vol.55
, pp. 763-768
-
-
Crawford, F.C.1
Freeman, M.J.2
Schinka, J.A.3
-
51
-
-
0028893380
-
Familial cerebral amyloid angiopathy (British type) with nonneuritic amyloid plaque-formation may be due to a novel amyloid protein
-
Ghiso J, Plant GT, Revesz T, Wisniewski T, Frangione B. Familial cerebral amyloid angiopathy (British type) with nonneuritic amyloid plaque-formation may be due to a novel amyloid protein. J Neurol Sci 1995;129:74-75
-
(1995)
J Neurol Sci
, vol.129
, pp. 74-75
-
-
Ghiso, J.1
Plant, G.T.2
Revesz, T.3
Wisniewski, T.4
Frangione, B.5
-
52
-
-
0030075631
-
Leptomeningeal amyloid and variant transthyretins
-
Benson MD. Leptomeningeal amyloid and variant transthyretins. Am J Pathol 1996;148:351-54
-
(1996)
Am J Pathol
, vol.148
, pp. 351-354
-
-
Benson, M.D.1
-
53
-
-
0033621165
-
Amyloid diseases: Abnormal protein aggregation in neurodegeneration
-
Koo EH, Lansbury PT, Kelly JW. Amyloid diseases: Abnormal protein aggregation in neurodegeneration. Proc Natl Acad Sci U S A 1999;96:9989-90
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 9989-9990
-
-
Koo, E.H.1
Lansbury, P.T.2
Kelly, J.W.3
-
54
-
-
0029730803
-
Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)
-
Garzuly F, Vidal R, Wisniewski T, Brittig F, Budka H. Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly). Neurology 1996;47:1562-67
-
(1996)
Neurology
, vol.47
, pp. 1562-1567
-
-
Garzuly, F.1
Vidal, R.2
Wisniewski, T.3
Brittig, F.4
Budka, H.5
-
55
-
-
0031055128
-
Transthyretin amyloidosis: A new mutation associated with dementia
-
Petersen RB, Goren H, Cohen M, et al. Transthyretin amyloidosis: A new mutation associated with dementia. Ann Neurol 1997;41:307-13
-
(1997)
Ann Neurol
, vol.41
, pp. 307-313
-
-
Petersen, R.B.1
Goren, H.2
Cohen, M.3
-
56
-
-
0030040173
-
Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G)
-
Vidal R, Garzuly F, Budka H, et al. Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G). Am J Pathol 1996;148:361-66
-
(1996)
Am J Pathol
, vol.148
, pp. 361-366
-
-
Vidal, R.1
Garzuly, F.2
Budka, H.3
-
57
-
-
0032012657
-
Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide
-
Kiuru S. Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide. Amyloid: Int J Exp Clin Invest 1998;5:55-66
-
(1998)
Amyloid: Int J Exp Clin Invest
, vol.5
, pp. 55-66
-
-
Kiuru, S.1
-
58
-
-
0025296194
-
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin
-
Haltia M, Ghiso J, Prelli F, et al. Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Am J Pathol 1990;136:1223-28
-
(1990)
Am J Pathol
, vol.136
, pp. 1223-1228
-
-
Haltia, M.1
Ghiso, J.2
Prelli, F.3
-
59
-
-
0025647488
-
Mutation in gelsolin gene in Finnish hereditary amyloidosis
-
Levy E, Haltia M, Fernandez-Madrid I, et al. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med 1990;172:1865-67
-
(1990)
J Exp Med
, vol.172
, pp. 1865-1867
-
-
Levy, E.1
Haltia, M.2
Fernandez-Madrid, I.3
-
60
-
-
0025637651
-
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type
-
Ghiso J, Haltia M, Prelli F, Novello J, Frangione B. Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type. Biochem J 1990;272:827-30
-
(1990)
Biochem J
, vol.272
, pp. 827-830
-
-
Ghiso, J.1
Haltia, M.2
Prelli, F.3
Novello, J.4
Frangione, B.5
-
61
-
-
0028263333
-
Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides
-
Maury CP, Nurmiaho-Lassila EL, Rossi H. Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides. Lab Invest 1994;70:558-64
-
(1994)
Lab Invest
, vol.70
, pp. 558-564
-
-
Maury, C.P.1
Nurmiaho-Lassila, E.L.2
Rossi, H.3
-
62
-
-
0033028206
-
Gelsolin-related spinal and cerebral amyloid angiopathy
-
Kiuru S, Salonen O, Haltia M. Gelsolin-related spinal and cerebral amyloid angiopathy. Ann Neurol 1999;45:305-11
-
(1999)
Ann Neurol
, vol.45
, pp. 305-311
-
-
Kiuru, S.1
Salonen, O.2
Haltia, M.3
-
63
-
-
0035902194
-
Shattuck lecture-neurodegenerative diseases and prions
-
Prusiner SB. Shattuck lecture-neurodegenerative diseases and prions. N Engl J Med 2001;344:1516-26
-
(2001)
N Engl J Med
, vol.344
, pp. 1516-1526
-
-
Prusiner, S.B.1
-
64
-
-
13344295093
-
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: The phenotype of the stop codon 145 mutation in PRNP
-
Ghetti B, Piccardo P, Spillantini MG, et al. Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: The phenotype of the stop codon 145 mutation in PRNP. Proc Natl Acad Sci U S A 1996;93:744-48
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 744-748
-
-
Ghetti, B.1
Piccardo, P.2
Spillantini, M.G.3
-
65
-
-
0034100159
-
Familial British dementia with amyloid angiopathy: Early clinical, neuropsychological and imaging findings
-
Mead S, James-Galton M, Revesz T, et al. Familial British dementia with amyloid angiopathy: Early clinical, neuropsychological and imaging findings. Brain 2000;123(Pt 5):975-91
-
(2000)
Brain
, vol.123
, Issue.PART 5
, pp. 975-991
-
-
Mead, S.1
James-Galton, M.2
Revesz, T.3
-
66
-
-
0025316704
-
Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation
-
Plant GT, Revesz T, Barnard RO, Harding AE, Gautier-Smith PC. Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation. Brain 1990;113:721-47
-
(1990)
Brain
, vol.113
, pp. 721-747
-
-
Plant, G.T.1
Revesz, T.2
Barnard, R.O.3
Harding, A.E.4
Gautier-Smith, P.C.5
-
67
-
-
0033600228
-
A stop-codon mutation in the BRI gene associated with familial British dementia
-
Vidal R, Frangione B, Rostagno A, et al. A stop-codon mutation in the BRI gene associated with familial British dementia. Nature 1999;399:776-81
-
(1999)
Nature
, vol.399
, pp. 776-781
-
-
Vidal, R.1
Frangione, B.2
Rostagno, A.3
-
68
-
-
0034712749
-
A decamer duplication in the 3′ region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred
-
Vidal R, Revesz T, Rostagno A, et al. A decamer duplication in the 3′ region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred. Proc Natl Acad Sci U S A 2000;97:4920-25
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 4920-4925
-
-
Vidal, R.1
Revesz, T.2
Rostagno, A.3
-
69
-
-
0033352083
-
Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia
-
Kim SH, Wang R, Gordon DJ, et al. Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia. Nat Neurosci 1999;2:984-88
-
(1999)
Nat Neurosci
, vol.2
, pp. 984-988
-
-
Kim, S.H.1
Wang, R.2
Gordon, D.J.3
-
70
-
-
0035941310
-
Systemic amyloid deposits in familial British dementia
-
Ghiso J, Holton J, Miravalle L, et al. Systemic amyloid deposits in familial British dementia. J Biol Chem 2001;276:43909-14
-
(2001)
J Biol Chem
, vol.276
, pp. 43909-43914
-
-
Ghiso, J.1
Holton, J.2
Miravalle, L.3
-
71
-
-
0347298759
-
Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease
-
Rostagno A, Revesz T, Lashley T, et al. Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease. J Biol Chem 2002;277:49782-90
-
(2002)
J Biol Chem
, vol.277
, pp. 49782-49790
-
-
Rostagno, A.1
Revesz, T.2
Lashley, T.3
-
72
-
-
0037038820
-
Vascular disorder in Alzheimer's disease: Role in pathogenesis of dementia and therapeutic targets
-
Zlokovic BV. Vascular disorder in Alzheimer's disease: Role in pathogenesis of dementia and therapeutic targets. Adv Drug Deliv Rev 2002;54:1553-59
-
(2002)
Adv Drug Deliv Rev
, vol.54
, pp. 1553-1559
-
-
Zlokovic, B.V.1
-
73
-
-
0030949335
-
Alzheimer's soluble amyloid beta is a normal component of human urine
-
Ghiso J, Calero M, Matsubara E, et al. Alzheimer's soluble amyloid beta is a normal component of human urine. FEBS Lett 1997;408:105-8
-
(1997)
FEBS Lett
, vol.408
, pp. 105-108
-
-
Ghiso, J.1
Calero, M.2
Matsubara, E.3
-
74
-
-
0029661424
-
Analysis of heterogeneous A4 peptides in human cerebrospinal fluid and blood by a newly developed sensitive Western blot assay
-
Ida N, Hartmann T, Pantel J, et al. Analysis of heterogeneous A4 peptides in human cerebrospinal fluid and blood by a newly developed sensitive Western blot assay. J Biol Chem 1996;271:22908-14
-
(1996)
J Biol Chem
, vol.271
, pp. 22908-22914
-
-
Ida, N.1
Hartmann, T.2
Pantel, J.3
-
75
-
-
0026753096
-
Beta amyloid is focally deposited within the outer basement membrane in the amyloid angiopathy of Alzheimer's disease. An immunoelectron microscopic study
-
Yamaguchi H, Yamazaki T, Lemere CA, Frosch MP, Selkoe DJ. Beta amyloid is focally deposited within the outer basement membrane in the amyloid angiopathy of Alzheimer's disease. An immunoelectron microscopic study. Am J Pathol 1992;141:249-59
-
(1992)
Am J Pathol
, vol.141
, pp. 249-259
-
-
Yamaguchi, H.1
Yamazaki, T.2
Lemere, C.A.3
Frosch, M.P.4
Selkoe, D.J.5
-
76
-
-
8944228919
-
High levels of circulating beta-amyloid peptide do not cause cerebral beta-amyloidosis in transgenic mice
-
Fukuchi K, Ho L, Younkin SG, et al. High levels of circulating beta-amyloid peptide do not cause cerebral beta-amyloidosis in transgenic mice. Am J Pathol 1996;149:219-27
-
(1996)
Am J Pathol
, vol.149
, pp. 219-227
-
-
Fukuchi, K.1
Ho, L.2
Younkin, S.G.3
-
77
-
-
0028171110
-
Non-fibrillar beta-amyloid protein is associated with smooth muscle cells of vessel walls in Alzheimer disease
-
Frackowiak J, Zoltowska A, Wisniewski HM. Non-fibrillar beta-amyloid protein is associated with smooth muscle cells of vessel walls in Alzheimer disease. J Neuropathol Exp Neurol 1994;53:637-45
-
(1994)
J Neuropathol Exp Neurol
, vol.53
, pp. 637-645
-
-
Frackowiak, J.1
Zoltowska, A.2
Wisniewski, H.M.3
-
78
-
-
0030024170
-
Production and increased detection of amyloid beta protein and amyloidogenic fragments in brain microvessels, meningeal vessels and choroid plexus in Alzheimer's disease
-
Kalaria RN. Premkumar DR, Pax AB, Cohen DL, Lieberburg I. Production and increased detection of amyloid beta protein and amyloidogenic fragments in brain microvessels, meningeal vessels and choroid plexus in Alzheimer's disease. Brain Res Mol Brain Res 1996;35:58-68
-
(1996)
Brain Res Mol Brain Res
, vol.35
, pp. 58-68
-
-
Kalaria, R.N.1
Premkumar, D.R.2
Pax, A.B.3
Cohen, D.L.4
Lieberburg, I.5
-
80
-
-
0031679480
-
Cerebral amyloid angiopathy - Amyloid beta accumulates in putative interstitial fluid drainage pathways in Alzheimer's disease
-
Weller RO, Massey A, Newman TA, Hutchings M, Kuo YM, Roher AE. Cerebral amyloid angiopathy-Amyloid beta accumulates in putative interstitial fluid drainage pathways in Alzheimer's disease. Am J Pathol 1998;153:725-33
-
(1998)
Am J Pathol
, vol.153
, pp. 725-733
-
-
Weller, R.O.1
Massey, A.2
Newman, T.A.3
Hutchings, M.4
Kuo, Y.M.5
Roher, A.E.6
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