-
1
-
-
0001339107
-
Intracerebral haematomas: A clinical study of 40 surgical cases
-
1 Luyendijk W and Schoen JHR (1964). Intracerebral haematomas: a clinical study of 40 surgical cases. Psychiat Neurol Neurochir 67, 445-468
-
(1964)
Psychiat Neurol Neurochir
, vol.67
, pp. 445-468
-
-
Luyendijk, W.1
Schoen, J.H.R.2
-
2
-
-
0023892051
-
Hereditary cerebral hemorrage caused by cortical amyloid angiopathy
-
2 Luyendijk W, Bots GTAM, Vegter-van der Vlis M, Went LN and Frangione B (1988). Hereditary cerebral hemorrage caused by cortical amyloid angiopathy. J Neurol Sci 85, 267-280
-
(1988)
J Neurol Sci
, vol.85
, pp. 267-280
-
-
Luyendijk, W.1
Bots, G.T.A.M.2
Vegter-Van Der Vlis, M.3
Went, L.N.4
Frangione, B.5
-
3
-
-
0026639398
-
Comparison betwewen the Icelandic and Dutch forms of hereditary cerebral amyloid angiopathy
-
3 Haan J and Roos RAC (1992). Comparison betwewen the Icelandic and Dutch forms of hereditary cerebral amyloid angiopathy. Clin Neurol Neurosurg 94 (suppl), S82-S83
-
(1992)
Clin Neurol Neurosurg
, vol.94
, Issue.SUPPL.
-
-
Haan, J.1
Roos, R.A.C.2
-
4
-
-
0006876721
-
Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer's disease
-
4 Van Duinen SG, Castano EM, Prelli F, Bots GTAM, Luyendijk W and Frangione B (1987). Hereditary cerebral hemorrhage with amyloidosis in patients of Dutch origin is related to Alzheimer's disease. Proc Natl Acad USA 84, 5991-5994
-
(1987)
Proc Natl Acad USA
, vol.84
, pp. 5991-5994
-
-
Van Duinen, S.G.1
Castano, E.M.2
Prelli, F.3
Bots, G.T.A.M.4
Luyendijk, W.5
Frangione, B.6
-
5
-
-
0025369198
-
Amyloid β-protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)
-
5 Van Broeckhoven C, Haan J, Bakker E, Hardy JA, Vanhul W, Wehnert A, Vegter-van der Vlis M and Roos RAC (1990). Amyloid β-protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch). Science 248, 1120-1122
-
(1990)
Science
, vol.248
, pp. 1120-1122
-
-
Van Broeckhoven, C.1
Haan, J.2
Bakker, E.3
Hardy, J.A.4
Vanhul, W.5
Wehnert, A.6
Vegter-Van Der Vlis, M.7
Roos, R.A.C.8
-
6
-
-
0023177469
-
Hereditary cystatin C (gamma trace) amyloid angiopathy of the CNS causing cerebral hemorrhage
-
6 Jensson O, Gudmundsson G, Arnason A, Blondal H, Petursdottir I, Thorsteinsson L, Grubb A, Lofberg H, Cohen D and Frangione B (1987). Hereditary cystatin C (gamma trace) amyloid angiopathy of the CNS causing cerebral hemorrhage. Acta Neurol Scand 76, 102-114
-
(1987)
Acta Neurol Scand
, vol.76
, pp. 102-114
-
-
Jensson, O.1
Gudmundsson, G.2
Arnason, A.3
Blondal, H.4
Petursdottir, I.5
Thorsteinsson, L.6
Grubb, A.7
Lofberg, H.8
Cohen, D.9
Frangione, B.10
-
7
-
-
0024338979
-
The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20
-
7 Abrahamson M, Islam M,Q., Szpirer J, Szpirer C and Levan G (1989). The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20. Hum Genet 82, 223-226
-
(1989)
Hum Genet
, vol.82
, pp. 223-226
-
-
Abrahamson, M.1
Islam, M.2
Szpirer, J.3
Szpirer, C.4
Levan, G.5
-
8
-
-
0029927290
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II - A review of histopathological aspects
-
8 Maat-Schieman MLC, Van Duinen SG, Bornebroek M, Haan J and Roos RAC (1996). Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II - A review of histopathological aspects. Brain Pathology 6, 115-120
-
(1996)
Brain Pathology
, vol.6
, pp. 115-120
-
-
Maat-Schieman, M.L.C.1
Van Duinen, S.G.2
Bornebroek, M.3
Haan, J.4
Roos, R.A.C.5
-
9
-
-
0025939678
-
Codon 618 variant of Alzheimer's amyloid gene associated with inhereted cerebral hemorrhage
-
9 Fernandez-Madrid Y, Levy E, Marder K and Frangione B (1991). Codon 618 variant of Alzheimer's amyloid gene associated with inhereted cerebral hemorrhage. Ann Neurol 30, 730-733
-
(1991)
Ann Neurol
, vol.30
, pp. 730-733
-
-
Fernandez-Madrid, Y.1
Levy, E.2
Marder, K.3
Frangione, B.4
-
10
-
-
0025296269
-
Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type
-
10 Levy E, Carman MD, Fernandez-Madrid Y, Power MD, Lieberburg I, Van Duinen SG, Bots GTAM, Luyendijk W and Frangione B (1990). Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type. Science 248, 1124-1126
-
(1990)
Science
, vol.248
, pp. 1124-1126
-
-
Levy, E.1
Carman, M.D.2
Fernandez-Madrid, Y.3
Power, M.D.4
Lieberburg, I.5
Van Duinen, S.G.6
Bots, G.T.A.M.7
Luyendijk, W.8
Frangione, B.9
-
11
-
-
0025989981
-
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)
-
11 Bakker E, Van Broeckhoven C, Haan J, Voorhoeve E, Van Hul W, Levy E, Lieberburg I, Carman MD, Van Ommen GJB, Frangione B and Roos RAC (1991). DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type). Am J Hum Genet 49, 518-521
-
(1991)
Am J Hum Genet
, vol.49
, pp. 518-521
-
-
Bakker, E.1
Van Broeckhoven, C.2
Haan, J.3
Voorhoeve, E.4
Van Hul, W.5
Levy, E.6
Lieberburg, I.7
Carman, M.D.8
Van Ommen, G.J.B.9
Frangione, B.10
Roos, R.A.C.11
-
13
-
-
0025367646
-
Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Clinical and computed tomographic analysis of 24 cases
-
13 Haan J, Algra P and Roos RAC (1990). Hereditary cerebral hemorrhage with amyloidosis - Dutch type: clinical and computed tomographic analysis of 24 cases. Arch Neurol 47, 649-653
-
(1990)
Arch Neurol
, vol.47
, pp. 649-653
-
-
Haan, J.1
Algra, P.2
Roos, R.A.C.3
-
14
-
-
0029894227
-
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I - A review of the clinical, radiologic and genetic aspects
-
14 Bornebroek M, Haan J, Maat-Schieman MLC, Van Duinen SG and Roos RAC (1996). Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I - A review of the clinical, radiologic and genetic aspects. Brain Pathology 6, 111-114
-
(1996)
Brain Pathology
, vol.6
, pp. 111-114
-
-
Bornebroek, M.1
Haan, J.2
Maat-Schieman, M.L.C.3
Van Duinen, S.G.4
Roos, R.A.C.5
-
15
-
-
0029039146
-
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D): Clinicopathological studies
-
15 Wattendorf AR, Frangione B, Luyendijk W and Bots GTAM (1995). Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies. J Neurol Neurosurg Psychiatry 58, 699-705
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 699-705
-
-
Wattendorf, A.R.1
Frangione, B.2
Luyendijk, W.3
Bots, G.T.A.M.4
-
16
-
-
0031469486
-
Mortality from hereditary cerebral hemorrhage with amyloidosis - Dutch type: Impact of sex, year of birth and line of transmission
-
16 Westendorp R, Haan J, Bakker E, Timmers WF and Roos RAC (1997). Mortality from hereditary cerebral hemorrhage with amyloidosis - Dutch type: Impact of sex, year of birth and line of transmission. Brain 120, 2243-2249
-
(1997)
Brain
, vol.120
, pp. 2243-2249
-
-
Bornebroek, M.1
Westendorp, R.2
Haan, J.3
Bakker, E.4
Timmers, W.F.5
Roos, R.A.C.6
-
17
-
-
0029843412
-
Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Better correlation of cognitive deterioration with advancing age than with the number of focal lesions or white matter hyperintensities
-
17 Bornebroek M, van Buchem MA, Haan J, Brand J, Lanser JKB, Bruïne FT and Roos RAC (1996). Hereditary cerebral hemorrhage with amyloidosis - Dutch type: better correlation of cognitive deterioration with advancing age than with the number of focal lesions or white matter hyperintensities. Alz Dis Assoc Dis 10, 224-231
-
(1996)
Alz Dis Assoc Dis
, vol.10
, pp. 224-231
-
-
Bornebroek, M.1
Van Buchem, M.A.2
Haan, J.3
Brand, J.4
Lanser, J.K.B.5
Bruïne, F.T.6
Roos, R.A.C.7
-
18
-
-
0030064215
-
White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation
-
18 Bornebroek M, Haan J, van Buchem MA, Lanser JKB, de Vries-vd Weerd MAC, Zoetewey M and Roos RAC (1996). White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation. Arch Neurol 53, 43-48
-
(1996)
Arch Neurol
, vol.53
, pp. 43-48
-
-
Bornebroek, M.1
Haan, J.2
Van Buchem, M.A.3
Lanser, J.K.B.4
De Vries-vd Weerd, M.A.C.5
Zoetewey, M.6
Roos, R.A.C.7
-
19
-
-
0028272066
-
How does cerebrovascular disease cause dementia?
-
19 O'Brien MD (1994). How does cerebrovascular disease cause dementia? Dementia 5, 133-136
-
(1994)
Dementia
, vol.5
, pp. 133-136
-
-
O'Brien, M.D.1
-
20
-
-
0025048011
-
Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Magnetic resonance imaging of seven cases
-
20 Haan J, Roos RAC, Algra P, Lanser JKB, Bots GTAM and Vegter-van der Vlis M (1990). Hereditary cerebral hemorrhage with amyloidosis - Dutch type: Magnetic resonance imaging of seven cases. Brain 113, 1251-1267
-
(1990)
Brain
, vol.113
, pp. 1251-1267
-
-
Haan, J.1
Roos, R.A.C.2
Algra, P.3
Lanser, J.K.B.4
Bots, G.T.A.M.5
Vegter-Van Der Vlis, M.6
-
21
-
-
0028170271
-
The apolipoprotein E Î4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations
-
21 Haan J, Van Broeckhoven C, van Duijn CM, Voorhoeve E, Van Harskamp F, Van Swieten JC, Maat-Schieman MLC, Roos RAC and Bakker E (1994). The apolipoprotein E Î4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations. Ann Neurol 36, 434-437
-
(1994)
Ann Neurol
, vol.36
, pp. 434-437
-
-
Haan, J.1
Van Broeckhoven, C.2
Van Duijn, C.M.3
Voorhoeve, E.4
Van Harskamp, F.5
Van Swieten, J.C.6
Maat-Schieman, M.L.C.7
Roos, R.A.C.8
Bakker, E.9
-
22
-
-
0028878581
-
No protective effect of apolipoprotein E Î2 allele in Dutch hereditary cerebral amyloid angiopathy
-
22 Haan J, Roos RAC and Bakker E (1995). No protective effect of apolipoprotein E Î2 allele in Dutch hereditary cerebral amyloid angiopathy [letter]. Ann Neurol 37, 282
-
(1995)
Ann Neurol
, vol.37
, pp. 282
-
-
Haan, J.1
Roos, R.A.C.2
Bakker, E.3
-
23
-
-
0030919727
-
Dutch hereditary cerebral amyloid angiopathy: Structural lesions and APOE genotype
-
23 Bornebroek M, Haan J, Van Duinen SG, Maat-Schieman MLC, van Buchem MA, Bakker E, Van Broeckhoven C and Roos RAC (1997). Dutch hereditary cerebral amyloid angiopathy: structural lesions and APOE genotype. Ann Neurol 41, 695-698
-
(1997)
Ann Neurol
, vol.41
, pp. 695-698
-
-
Bornebroek, M.1
Haan, J.2
Van Duinen, S.G.3
Maat-Schieman, M.L.C.4
Van Buchem, M.A.5
Bakker, E.6
Van Broeckhoven, C.7
Roos, R.A.C.8
-
24
-
-
0030028429
-
Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease
-
24 Wragg M, Hutton M, Talbot C, Busfield F, Han SW, Lendon C, Clark RF, Morris JC, Edwards D, Goate A, Pfeiffer E, Crook R, Prihar G, Phillips H, Baker M, Hardy J, Rossor M, Houlden H, Karran E, Roberts G and Craddock N (1996). Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Lancet 347, 509-512
-
(1996)
Lancet
, vol.347
, pp. 509-512
-
-
Wragg, M.1
Hutton, M.2
Talbot, C.3
Busfield, F.4
Han, S.W.5
Lendon, C.6
Clark, R.F.7
Morris, J.C.8
Edwards, D.9
Goate, A.10
Pfeiffer, E.11
Crook, R.12
Prihar, G.13
Phillips, H.14
Baker, M.15
Hardy, J.16
Rossor, M.17
Houlden, H.18
Karran, E.19
Roberts, G.20
Craddock, N.21
more..
-
25
-
-
0030874252
-
Presenilin 1 polymorphism and hereditary cerebral hemorrhage with amyloidosis Dutch type
-
25 Bornebroek M, Haan J, Backhovens H, Deutz P, van Buchem MA, van den Broeck M, Bakker E, Roos RAC and Van Broeckhoven C (1997). Presenilin 1 polymorphism and hereditary cerebral hemorrhage with amyloidosis Dutch type. Ann Neurol 42, 108-110
-
(1997)
Ann Neurol
, vol.42
, pp. 108-110
-
-
Bornebroek, M.1
Haan, J.2
Backhovens, H.3
Deutz, P.4
Van Buchem, M.A.5
Van Den Broeck, M.6
Bakker, E.7
Roos, R.A.C.8
Van Broeckhoven, C.9
-
26
-
-
0029149611
-
Cortical tissue of patients with hereditary cerebral hemorrhage with amyloidosis (Dutch) contains various extracellular matrix deposits
-
26 Van Duinen SG, Maat-Schieman MLC, Bruyn JA, Haan J and Roos RAC (1995). Cortical tissue of patients with hereditary cerebral hemorrhage with amyloidosis (Dutch) contains various extracellular matrix deposits. Lab Invest 73, 183-189
-
(1995)
Lab Invest
, vol.73
, pp. 183-189
-
-
Van Duinen, S.G.1
Maat-Schieman, M.L.C.2
Bruyn, J.A.3
Haan, J.4
Roos, R.A.C.5
-
27
-
-
0026437675
-
Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch)
-
27 Maat-Schieman MLC, Van Duinen SG, Haan J and Roos RAC (1992). Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch). Acta Neuropathol 84, 674-679
-
(1992)
Acta Neuropathol
, vol.84
, pp. 674-679
-
-
Maat-Schieman, M.L.C.1
Van Duinen, S.G.2
Haan, J.3
Roos, R.A.C.4
-
28
-
-
0027980967
-
Microglia in diffuse plaques in hereditary cerebral hemorrhage with amyloidosis (Dutch). An immunohistochemical study
-
28 Maat-Schieman MLC, Rozemuller AJ, Van Duinen SG, Haan J, Eikelenboom P and Roos RAC (1994). Microglia in diffuse plaques in hereditary cerebral hemorrhage with amyloidosis (Dutch). An immunohistochemical study. J Neuropathol Exp Neurol 53, 483-491
-
(1994)
J Neuropathol Exp Neurol
, vol.53
, pp. 483-491
-
-
Maat-Schieman, M.L.C.1
Rozemuller, A.J.2
Van Duinen, S.G.3
Haan, J.4
Eikelenboom, P.5
Roos, R.A.C.6
-
29
-
-
0012510759
-
Amyloid plaque core protein in Alzheimer's disease and Down syndrome
-
29 Masters CL, Simms G, Weinman NA, Multhaup G and Beyreuther K (1985). Amyloid plaque core protein in Alzheimer's disease and Down syndrome. Proc Natl Acad Sci USA 82, 4245-4249
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 4245-4249
-
-
Masters, C.L.1
Simms, G.2
Weinman, N.A.3
Multhaup, G.4
Beyreuther, K.5
-
30
-
-
0025779179
-
Solution structures of β peptide and its constituent fragments: Relation to amyloid deposition
-
30 Barrow CJ and Zagorski MG (1991). Solution structures of β peptide and its constituent fragments: relation to amyloid deposition. Science 253, 179-181
-
(1991)
Science
, vol.253
, pp. 179-181
-
-
Barrow, C.J.1
Zagorski, M.G.2
-
31
-
-
0026595567
-
Assembly and aggregation properties of synthetic Alzheimer's A4/β amyloid peptides analogs
-
31 Burdick D, Soreghan B, Kwon M, Kosmoski J, Knauer M, Henschen A, Yates J, Cotman C and Glabe C (1992). Assembly and aggregation properties of synthetic Alzheimer's A4/β amyloid peptides analogs. J Biol Chem 267, 546-554
-
(1992)
J Biol Chem
, vol.267
, pp. 546-554
-
-
Burdick, D.1
Soreghan, B.2
Kwon, M.3
Kosmoski, J.4
Knauer, M.5
Henschen, A.6
Yates, J.7
Cotman, C.8
Glabe, C.9
-
32
-
-
0027258525
-
The carboxy terminus of β amyloid is critical for the seeding of amyloid formation: Implications for the pathogenesis of Alzheimer's disease
-
32 Jarrett JT, Berger EP and Lansbury PT (1993). The carboxy terminus of β amyloid is critical for the seeding of amyloid formation: Implications for the pathogenesis of Alzheimer's disease. Biochemistry 32, 4693-4697
-
(1993)
Biochemistry
, vol.32
, pp. 4693-4697
-
-
Jarrett, J.T.1
Berger, E.P.2
Lansbury, P.T.3
-
33
-
-
0028169925
-
Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: Evidence that an initially deposited species is A beta 42(43)
-
33 Iwatsubo T, Odaka A, Suzuki N, Mizusawa H, Nukina N and Ihara Y (1994). Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: evidence that an initially deposited species is A beta 42(43). Neuron 13, 45-53
-
(1994)
Neuron
, vol.13
, pp. 45-53
-
-
Iwatsubo, T.1
Odaka, A.2
Suzuki, N.3
Mizusawa, H.4
Nukina, N.5
Ihara, Y.6
-
34
-
-
0023105114
-
The precursor of Alzheimer's disease amyloid A4 protein resembles a cell surface receptor
-
34 Kang J, Lemaire H, Unterbeck A, Salbaum JM, Masters CL, Grzeschik K, Multhaup G, Beyreuther K and Muller-Hill B (1987). The precursor of Alzheimer's disease amyloid A4 protein resembles a cell surface receptor. Nature 325, 733-736
-
(1987)
Nature
, vol.325
, pp. 733-736
-
-
Kang, J.1
Lemaire, H.2
Unterbeck, A.3
Salbaum, J.M.4
Masters, C.L.5
Grzeschik, K.6
Multhaup, G.7
Beyreuther, K.8
Muller-Hill, B.9
-
35
-
-
0023109592
-
Amyloid β gene: cDNA, mRNA distribution, and genetic linkage near Alzheimer locus
-
35 Tanzi RE, Gusella JF, Watkins PC, Bruns GAP, St George-Hyslop P, Van Keuren ML, Patterson D, Pagan S, Kurnitt DM and Neve RL (1987). Amyloid β gene: cDNA, mRNA distribution, and genetic linkage near Alzheimer locus. Science 235, 880-884
-
(1987)
Science
, vol.235
, pp. 880-884
-
-
Tanzi, R.E.1
Gusella, J.F.2
Watkins, P.C.3
Bruns, G.A.P.4
St George-Hyslop, P.5
Van Keuren, M.L.6
Patterson, D.7
Pagan, S.8
Kurnitt, D.M.9
Neve, R.L.10
-
36
-
-
0025219026
-
Genomic organisation of the human amyloid β-protein precursor gene
-
36 Yoshikai S, Sasaki H, Doh-ura K, Furuya H and Sakaki Y (1990). Genomic organisation of the human amyloid β-protein precursor gene. Gene 87, 257-263
-
(1990)
Gene
, vol.87
, pp. 257-263
-
-
Yoshikai, S.1
Sasaki, H.2
Doh-Ura, K.3
Furuya, H.4
Sakaki, Y.5
-
37
-
-
0023870043
-
A new A4 amyloid mRNA contains a domain homologues to serine protease inhibitors
-
37 Ponte P, Gonzalez-DeWhitt P, Schilling J, Miller J, Hsu D, Greenberg B, Davis K, Wallace W, Lieberburg I, Fuller F and Cordell B (1988). A new A4 amyloid mRNA contains a domain homologues to serine protease inhibitors. Nature 331, 525-532
-
(1988)
Nature
, vol.331
, pp. 525-532
-
-
Ponte, P.1
Gonzalez-Dewhitt, P.2
Schilling, J.3
Miller, J.4
Hsu, D.5
Greenberg, B.6
Davis, K.7
Wallace, W.8
Lieberburg, I.9
Fuller, F.10
Cordell, B.11
-
38
-
-
0024463491
-
Protease nexin-II, a potent antichymotrypsin, shows identity to amyloid beta-protein precursor
-
38 Van Nostrand WE, Wagner SL, Suzuki M, Choi BH, Farrow JS, Geddes JW, Cotman CW and Cunnigham DD (1989). Protease nexin-II, a potent antichymotrypsin, shows identity to amyloid beta-protein precursor. Nature 341, 546-549
-
(1989)
Nature
, vol.341
, pp. 546-549
-
-
Van Nostrand, W.E.1
Wagner, S.L.2
Suzuki, M.3
Choi, B.H.4
Farrow, J.S.5
Geddes, J.W.6
Cotman, C.W.7
Cunnigham, D.D.8
-
39
-
-
0027517128
-
Protease nexin-2 / amyloid β protein precursor: A tight-binding inhibitor of coagulation factor IXa
-
39 Schmaier AH, Dahl LD, Rozemuller AJ, Roos RAC, Wagner SL, Chung R and Van Nostrand WE (1993). Protease nexin-2 / amyloid β protein precursor: a tight-binding inhibitor of coagulation factor IXa. J Clin Invest 92, 2540-2545
-
(1993)
J Clin Invest
, vol.92
, pp. 2540-2545
-
-
Schmaier, A.H.1
Dahl, L.D.2
Rozemuller, A.J.3
Roos, R.A.C.4
Wagner, S.L.5
Chung, R.6
Van Nostrand, W.E.7
-
40
-
-
0025365401
-
Platelet coagulation factor XIa-inhibitor, a form of Alzheimer amyloid precursor protein
-
40 Smith RP, Higuchi DA and Broze J (1990). Platelet coagulation factor XIa-inhibitor, a form of Alzheimer amyloid precursor protein. Science 248, 1126-1128
-
(1990)
Science
, vol.248
, pp. 1126-1128
-
-
Smith, R.P.1
Higuchi, D.A.2
Broze, J.3
-
41
-
-
0027052057
-
Potential role of protease nexin-2/amyloid β-protein precursor as a cerebral anticoagulant
-
41 Van Nostrand WE, Schmaier AH and Wagner SL (1992). Potential role of protease nexin-2/amyloid β-protein precursor as a cerebral anticoagulant. Ann N Y Acad Sci 674, 243-252
-
(1992)
Ann N Y Acad Sci
, vol.674
, pp. 243-252
-
-
Van Nostrand, W.E.1
Schmaier, A.H.2
Wagner, S.L.3
-
42
-
-
0025357613
-
Immunopurification and protease inhibitory properties of protease nexin-2/amyloid beta-protein precursor
-
42 Van Nostrand WE, Wagner SL, Farrow JS and Cunnigham DD (1990). Immunopurification and protease inhibitory properties of protease nexin-2/amyloid beta-protein precursor. J Biol Chem 265, 9591-9594
-
(1990)
J Biol Chem
, vol.265
, pp. 9591-9594
-
-
Van Nostrand, W.E.1
Wagner, S.L.2
Farrow, J.S.3
Cunnigham, D.D.4
-
43
-
-
0031933064
-
Binding of β precursor protein to coagulation factor XIa in patients with hereditary cerebral hemorrhage with amyloidosis Dutch type
-
43 Bornebroek M, von dem Borne PAKr, Haan J, Meijers JCM, Van Nostrand WE and Roos RAC (1998). Binding of β precursor protein to coagulation factor XIa in patients with hereditary cerebral hemorrhage with amyloidosis Dutch type. J Neurol 245, 111-115
-
(1998)
J Neurol
, vol.245
, pp. 111-115
-
-
Bornebroek, M.1
Von Dem Borne, P.A.Kr.2
Haan, J.3
Meijers, J.C.M.4
Van Nostrand, W.E.5
Roos, R.A.C.6
-
44
-
-
0026659436
-
Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis-Dutch type share a decrease in cerebrospinal fluid levels of amyloid β-protein precursor
-
44 Van Nostrand WE, Wagner SL, Haan J, Bakker E and Roos RAC (1992). Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis-Dutch type share a decrease in cerebrospinal fluid levels of amyloid β-protein precursor. Ann Neurol 32, 215-218
-
(1992)
Ann Neurol
, vol.32
, pp. 215-218
-
-
Van Nostrand, W.E.1
Wagner, S.L.2
Haan, J.3
Bakker, E.4
Roos, R.A.C.5
-
45
-
-
0025295039
-
Cleavage of amyloid β protein during constitutive processing of its precursor
-
45 Esch FS, Keim PS, Beattie EC, Blacher RW, Culwell AR, Olterdorf T, McClure D and Ward PJ (1990). Cleavage of amyloid β protein during constitutive processing of its precursor. Science 248, 122-1124
-
(1990)
Science
, vol.248
, pp. 122-1124
-
-
Esch, F.S.1
Keim, P.S.2
Beattie, E.C.3
Blacher, R.W.4
Culwell, A.R.5
Olterdorf, T.6
McClure, D.7
Ward, P.J.8
-
46
-
-
0028924248
-
Generation of amyloid β protein from its precursor is sequence specific
-
46 Citron M, Teplow DB and Selkoe DJ (1995). Generation of amyloid β protein from its precursor is sequence specific. Neuron 14, 661-670
-
(1995)
Neuron
, vol.14
, pp. 661-670
-
-
Citron, M.1
Teplow, D.B.2
Selkoe, D.J.3
-
47
-
-
0026879650
-
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene
-
47 Hendriks L, van Duijn CM, Cras P, Cruts M, Van Hul W, Van Harskamp F, Warren A, McInnes MG, Antonarakis SE, Martin JJ, Hofman A and Van Broeckhoven C (1992). Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene. Nature Genet 1, 218-221
-
(1992)
Nature Genet
, vol.1
, pp. 218-221
-
-
Hendriks, L.1
Van Duijn, C.M.2
Cras, P.3
Cruts, M.4
Van Hul, W.5
Van Harskamp, F.6
Warren, A.7
McInnes, M.G.8
Antonarakis, S.E.9
Martin, J.J.10
Hofman, A.11
Van Broeckhoven, C.12
-
48
-
-
0000171546
-
An Italian type of HCHWA
-
Abstract
-
48 Bugiani O, Padovani A, Magoni M, Andora G, Sgarzi M, Savoiardo A, Bizzi G, Giaccone G, Rossi G and Tagliavini F (1998). An Italian type of HCHWA. Neurobiol Aging S238 (Abstract)
-
(1998)
Neurobiol Aging
-
-
Bugiani, O.1
Padovani, A.2
Magoni, M.3
Andora, G.4
Sgarzi, M.5
Savoiardo, A.6
Bizzi, G.7
Giaccone, G.8
Rossi, G.9
Tagliavini, F.10
-
49
-
-
0026075602
-
Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene
-
49 Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J and Mullan M (1991). Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene. Nature 353, 844-846
-
(1991)
Nature
, vol.353
, pp. 844-846
-
-
Chartier-Harlin, M.C.1
Crawford, F.2
Houlden, H.3
Warren, A.4
Hughes, D.5
Fidani, L.6
Goate, A.7
Rossor, M.8
Roques, P.9
Hardy, J.10
Mullan, M.11
-
50
-
-
0025950987
-
A mutation in the amyloid precursor protein gene associated with hereditary Alzheimer's disease
-
50 Murrell J, Farlow M, Ghetti B and Benson MD (1991). A mutation in the amyloid precursor protein gene associated with hereditary Alzheimer's disease. Science 254, 97-99
-
(1991)
Science
, vol.254
, pp. 97-99
-
-
Murrell, J.1
Farlow, M.2
Ghetti, B.3
Benson, M.D.4
-
51
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
51 Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L, Mant R, Newton P, Rooke K, Roques P, Talbot C, Pericak-Vance MA, Roses A, Williamson R, Rossor M, Owen M and Hardy J (1991). Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349, 728-730
-
(1991)
Nature
, vol.349
, pp. 728-730
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.A.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
52
-
-
0026907151
-
A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid
-
52 Mullan M, Crawford F, Axelman K, Houlden H, Lilius L, Winblad B and Lannfelt L (1992). A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid. Nature Genet 1, 345-347
-
(1992)
Nature Genet
, vol.1
, pp. 345-347
-
-
Mullan, M.1
Crawford, F.2
Axelman, K.3
Houlden, H.4
Lilius, L.5
Winblad, B.6
Lannfelt, L.7
-
53
-
-
0031052381
-
Amyloid, presenilins and Alzheimer's disease
-
53 Hardy J (1997). Amyloid, presenilins and Alzheimer's disease. Trends Neurosci 20, 154-159
-
(1997)
Trends Neurosci
, vol.20
, pp. 154-159
-
-
Hardy, J.1
-
54
-
-
0026745610
-
Mutation of the β-amyloid precursor protein in familial Alzheimer's disease increases β-protein production
-
54 Citron M, Oltersdorf T, Haass C, McConlogue L, Hung AY, Seubert P, Vigo-Pelfrey C, Lieberburg I and Selkoe DJ (1992). Mutation of the β-amyloid precursor protein in familial Alzheimer's disease increases β-protein production. Nature 360, 672-674
-
(1992)
Nature
, vol.360
, pp. 672-674
-
-
Citron, M.1
Oltersdorf, T.2
Haass, C.3
McConlogue, L.4
Hung, A.Y.5
Seubert, P.6
Vigo-Pelfrey, C.7
Lieberburg, I.8
Selkoe, D.J.9
-
55
-
-
0028322017
-
An increased percentage of long amyloid β protein secreted by familial amyloid β protein precursor (βAPP717) mutants
-
55 Suzuki N, Cheung TT, Cai X, Odaka A, Otvos JrL, Eckman C, Golde TE and Younkin SG (1994). An increased percentage of long amyloid β protein secreted by familial amyloid β protein precursor (βAPP717) mutants. Science 264, 1336-1340
-
(1994)
Science
, vol.264
, pp. 1336-1340
-
-
Suzuki, N.1
Cheung, T.T.2
Cai, X.3
Odaka, A.4
Otvos L., Jr.5
Eckman, C.6
Golde, T.E.7
Younkin, S.G.8
-
56
-
-
0031742418
-
Flernisch and Dutch mutations in amyloid β precursor protein have different effects on amyloid β secretion
-
56 De Jonghe C, Zehr C, Yager D, Prada C, Younkin S, Hendriks L, Vanbroeckhoven C and Eckman C (1998). Flernisch and Dutch mutations in amyloid β precursor protein have different effects on amyloid β secretion. Neurobiol Dis 4, 281-286
-
(1998)
Neurobiol Dis
, vol.4
, pp. 281-286
-
-
De Jonghe, C.1
Zehr, C.2
Yager, D.3
Prada, C.4
Younkin, S.5
Hendriks, L.6
Vanbroeckhoven, C.7
Eckman, C.8
-
57
-
-
0029081010
-
Why do DNA testing? practical and ethical implications of new neurogenetic tests
-
57 Bird TD and Bennett RL (1995). Why do DNA testing? practical and ethical implications of new neurogenetic tests. Ann Neurol 38, 141-146
-
(1995)
Ann Neurol
, vol.38
, pp. 141-146
-
-
Bird, T.D.1
Bennett, R.L.2
-
58
-
-
0026469703
-
Understanding the low uptake of presymptomatic DNA-testing for Huntington's disease
-
58 Tibben A, Niermeijer MF, Roos RAC, Vegter-van der Vlis M, Frets PG, Van Ommen GJB, van de Kamp JJP and Verhage F (1992). Understanding the low uptake of presymptomatic DNA-testing for Huntington's disease. Lancet 340, 1416
-
(1992)
Lancet
, vol.340
, pp. 1416
-
-
Tibben, A.1
Niermeijer, M.F.2
Roos, R.A.C.3
Vegter-Van Der Vlis, M.4
Frets, P.G.5
Van Ommen, G.J.B.6
Van De Kamp, J.J.P.7
Verhage, F.8
|