-
4
-
-
0032573083
-
Pathogenic implications of mutations in the tau gene in pallidoponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13103-13107
-
-
Clark, L.1
Poorkaj, P.2
Wszolek, Z.3
Geschwind, D.4
Nasreddine, Z.5
Miller, B.6
Li, D.7
Payami, H.8
Awert, F.9
Markopoulou, K.10
Andreadis, A.11
D'souza, I.12
Lee, V.13
Trojanowski, J.14
Zhukareva, V.15
Bird, T.16
Schellenberg, G.17
Wilhelmsen, K.18
-
7
-
-
0030831959
-
Neurodegenerative diseases with cytoskeletal pathology: A biochemical classification
-
(1997)
Ann. Neurol.
, vol.42
, pp. 541-544
-
-
Dickson, D.1
-
10
-
-
0005601103
-
Co-occurrence of two amyloid proteins in a patient with familial amyloidosis, Finnish type
-
K. Iqbal, D. McLachlan, B. Winblad and H. Wisniewski, eds., John Wiley & Sons Ltd, New York
-
(1991)
Alzheimer's disease: Basic mechanisms, diagnosis and therapeutic strategies
, pp. 255-264
-
-
Frangione, B.1
Haltia, M.2
Levy, E.3
Ghiso, J.4
Kiuru, S.5
Prelli, F.6
-
11
-
-
13344295093
-
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: The phenotype of the stop codon 145 mutation in PRNP
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 744-748
-
-
Ghetti, B.1
Piccardo, P.2
Spillantini, M.G.3
Ichimiya, Y.4
Porro, M.5
Perini, F.6
Kitamoto, T.7
Tateishi, J.8
Seiler, C.9
Frangione, B.10
Bugiani, O.11
Giaccone, G.12
Prelli, F.13
Goedert, M.14
Dlouhy, S.R.15
Tagliavini, F.16
-
19
-
-
0026879650
-
Presenile dementia and cerebral hemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene
-
(1992)
Nature Genet.
, vol.1
, pp. 218-221
-
-
Hendriks, L.1
Van Duijin, C.M.2
Cras, P.3
Cruts, M.4
Van Hul, W.5
Van Harskamp, F.6
Warren, A.7
McInnis, M.8
Antonarakis, S.E.9
Martin, J.J.10
Hofman, A.11
Van Broeckhoven, C.12
-
20
-
-
0031866882
-
Cerebral infarcts in patients with autopsy-proven Alzheimer's disease: CERAD, part XVIII. Consortium to establish a registry for Alzheimer's disease
-
(1998)
Neurology
, vol.51
, pp. 159-162
-
-
Heyman, A.1
Fillenbaum, G.G.2
Welsh-Bohmer, K.A.3
Gearing, M.4
Mirra, S.S.5
Mohs, R.C.6
Peterson, B.L.7
Pieper, C.F.8
-
23
-
-
0026733343
-
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 998-1014
-
-
Kamino, K.1
Orr, H.T.2
Payami, H.3
Wijsman, E.M.4
Alonso, M.A.5
Pulst, S.M.6
Anderson, L.7
O'Dahl, S.8
Nemens, E.9
White, J.A.10
Sadovnick, A.D.11
Ball, M.J.12
Kelly, J.13
Warren, A.14
McInnis, M.15
Antonarakis, S.A.16
Korenberg, J.R.17
Sharma, V.18
Kukull, W.19
Larson, E.20
Heston, L.L.21
Martin, G.M.22
Bird, T.23
Schellemberg, G.24
more..
-
26
-
-
0025296269
-
Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type
-
(1990)
Science
, vol.248
, pp. 124-1126
-
-
Levy, E.1
Carman, M.2
Fernandez-Madrid, I.3
Power, M.4
Lieberburg, I.5
Van Duinen, S.6
Bots, G.7
Luyendijk, W.8
Frangione, B.9
-
32
-
-
0025966199
-
Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): Relation of the amyloid protein to variant gelsolin
-
(1990)
Biochem. Biophys. Acta
, vol.1096
, pp. 84-86
-
-
Maury, C.1
Baumann, M.2
-
33
-
-
0034100159
-
Familial British dementia with amyloid angiopathy: Early clinical, neuropsychological and imaging findings
-
(2000)
Brain
, vol.123
, pp. 975-986
-
-
Mead, S.1
James-Galton, M.2
Révész, T.3
Doshi, R.B.4
Harwood, G.5
Pan, E.L.6
Ghiso, J.7
Frangione, B.8
Plant, G.9
-
34
-
-
0014640130
-
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms
-
(1969)
Ann. Clin. Res.
, vol.1
, pp. 314-324
-
-
Meretoja, J.1
-
37
-
-
0031055128
-
Transthyretin amyloidosis: A new mutation associated with dementia
-
(1997)
Ann. Neurol.
, vol.41
, pp. 307-313
-
-
Petersen, R.1
Goren, H.2
Cohen, M.3
Richardson, S.4
Tresser, N.5
Lynn, A.6
Gali, M.7
Estes, M.8
Gambetti, P.9
-
44
-
-
0033536163
-
Immunization with amyloid-beta attenuates Alzheimer-disease-like pathology in the PDAPP mouse
-
(1999)
Nature
, vol.400
, pp. 173-177
-
-
Schenk, D.1
Barbour, R.2
Dunn, W.3
Gordon, G.4
Grajeda, H.5
Guido, T.6
Hu, K.7
Huang, J.8
Johnson-Wood, K.9
Khan, K.10
Kholodenko, D.11
Lee, M.12
Liao, Z.13
Lieberburg, I.14
Motter, R.15
Mutter, L.16
Soriano, F.17
Shopp, G.18
Vasquez, N.19
Vandevert, C.20
Walker, S.21
Wogulis, M.22
Yednock, T.23
Games, D.24
Seubert, P.25
more..
-
45
-
-
0027953616
-
Structure determination of extracellular fragments of amyloid proteins involved in Alzheimer's disease and Dutch-type hereditary cerebral hemorrhage with amyloidosis
-
(1994)
Eur. J. Biochem.
, vol.219
, pp. 237-239
-
-
Sorimachi, K.1
Craik, D.2
-
51
-
-
0002329070
-
A new APP mutation related to hereditary cerebral hemorrhage
-
(1999)
Alzh. Reports
, vol.2
-
-
Tagliavini, F.1
Rossi, G.2
Padovani, A.3
Magoni, M.4
Andora, G.5
Sgarzi, M.6
Bizzi, A.7
Savoiardo, M.8
Carella, F.9
Morbin, M.10
Giaccone, G.11
Bugiani, O.12
-
55
-
-
0030040173
-
Meningocerebrovascular amyloidosis associated with a novel Transthyretin mis-sense mutation at codon 18 (TTRD18G)
-
(1996)
Am. J. Pathol.
, vol.148
, pp. 361-366
-
-
Vidal, R.1
Garzuly, F.2
Budka, H.3
Lalowski, M.4
Linke, R.5
Brittig, F.6
Frangione, B.7
Wisniewski, T.8
-
57
-
-
0034712749
-
A decamer duplication in the 3' region of the BR1 gene originates a new amyloid peptide that is associated with dementia in a Danish kindred
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 4920-4925
-
-
Vidal, R.1
Révész, T.2
Rostagno, A.3
Kim, E.4
Holton, J.5
Bek, T.6
Bojsen-Møller, M.7
Braendgaard, H.8
Plant, G.9
Ghiso, J.10
Frangione, B.11
-
58
-
-
0023254674
-
Cerebral amyloid angiopathy: A critical review
-
(1987)
Stroke
, vol.18
, pp. 311-324
-
-
Vinters, H.1
-
60
-
-
0002451964
-
Nomenclature of amyloid fibril proteins
-
(1999)
Amyloid, Int. J. Exp. Clin. Invest.
, vol.6
, pp. 62-66
-
-
Westermark, P.1
Araki, S.2
Benson, M.3
Cohen, A.4
Frangione, B.5
Masters, C.6
Saraiva, M.7
Sipe, J.8
Husby, G.9
Kyle, R.10
Selkoe, D.11
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