-
1
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force
-
McKhann G.et al. Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force. Neurology. 34:1984;939-944.
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
-
2
-
-
0030669036
-
The pathogenesis of senile plaques
-
Dickson D.W. The pathogenesis of senile plaques. J. Neuropathol. Exp. Neurol. 56:1997;321-339.
-
(1997)
J. Neuropathol. Exp. Neurol.
, vol.56
, pp. 321-339
-
-
Dickson, D.W.1
-
3
-
-
0028267440
-
Normal and abnormal biology of the β-amyloid precursor protein
-
Selkoe D.J. Normal and abnormal biology of the β-amyloid precursor protein. Annu. Rev. Neurosci. 17:1994;489-517.
-
(1994)
Annu. Rev. Neurosci.
, vol.17
, pp. 489-517
-
-
Selkoe, D.J.1
-
4
-
-
0031057837
-
Exploring the etiology of Alzheimer disease using molecular genetics
-
Lendon C.L.et al. Exploring the etiology of Alzheimer disease using molecular genetics. J. Am. Med. Assoc. 277:1997;825-831.
-
(1997)
J. Am. Med. Assoc.
, vol.277
, pp. 825-831
-
-
Lendon, C.L.1
-
6
-
-
0028650421
-
Calcium and neuronal injury in Alzheimer's disease. Contributions of beta-amyloid protein mismetabolism, free radicals, and metabolic compromise
-
Mattson M.P. Calcium and neuronal injury in Alzheimer's disease. Contributions of beta-amyloid protein mismetabolism, free radicals, and metabolic compromise. Ann. New York Acad. Sci. 747:1994;50-76.
-
(1994)
Ann. New York Acad. Sci.
, vol.747
, pp. 50-76
-
-
Mattson, M.P.1
-
7
-
-
0030922421
-
Presenilins: Genes for life and death
-
Haass C. Presenilins: genes for life and death. Neuron. 18:1997;687-690.
-
(1997)
Neuron
, vol.18
, pp. 687-690
-
-
Haass, C.1
-
8
-
-
0030823158
-
Effects of age, gender, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease - A meta-analysis
-
Farrer L.A.et al. Effects of age, gender, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease - a meta-analysis. J. Am. Med. Assoc. 278:1997;1345-1356.
-
(1997)
J. Am. Med. Assoc.
, vol.278
, pp. 1345-1356
-
-
Farrer, L.A.1
-
9
-
-
0031278270
-
Lack of apolipoprotein E dramatically reduces amyloid β-deposition
-
Bales K.R.et al. Lack of apolipoprotein E dramatically reduces amyloid β-deposition. Nat. Genet. 17:1997;263-264.
-
(1997)
Nat. Genet.
, vol.17
, pp. 263-264
-
-
Bales, K.R.1
-
10
-
-
0344472422
-
Polymorphism in the transcriptional regulatory region of apolipoprotein E gene associated with risk for dementia of the Alzheimer type
-
Bullido M.J.et al. Polymorphism in the transcriptional regulatory region of apolipoprotein E gene associated with risk for dementia of the Alzheimer type. Nat. Genet. 18:1998;67-71.
-
(1998)
Nat. Genet.
, vol.18
, pp. 67-71
-
-
Bullido, M.J.1
-
11
-
-
0030774535
-
The genetics of Alzheimer's disease
-
Rubinzstein D.C. The genetics of Alzheimer's disease. Progr. Neurobiol. 52:1997;447-454.
-
(1997)
Progr. Neurobiol.
, vol.52
, pp. 447-454
-
-
Rubinzstein, D.C.1
-
12
-
-
0030731562
-
Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease
-
Lehmann D.J.et al. Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease. Hum. Mol. Genet. 6:1997;1933-1936.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1933-1936
-
-
Lehmann, D.J.1
-
13
-
-
0030770726
-
Complete genomic screen in late onset familial Alzheimer disease - Evidence for a new locus on chromosome 12
-
Pericak-Vance M.A.et al. Complete genomic screen in late onset familial Alzheimer disease - evidence for a new locus on chromosome 12. J. Am. Med. Assoc. 278:1997;1237-1241.
-
(1997)
J. Am. Med. Assoc.
, vol.278
, pp. 1237-1241
-
-
Pericak-Vance, M.A.1
-
14
-
-
0030587520
-
Amyloid beta protein in plasma from patients with sporadic Alzheimer's disease
-
Tamaoka A.et al. Amyloid beta protein in plasma from patients with sporadic Alzheimer's disease. J. Neurol. Sci. 141:1996;65-68.
-
(1996)
J. Neurol. Sci.
, vol.141
, pp. 65-68
-
-
Tamaoka, A.1
-
15
-
-
16044373524
-
Secreted amyloid β-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
-
Scheuner D.et al. Secreted amyloid β-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. Nat. Med. 2:1996;864-870.
-
(1996)
Nat. Med.
, vol.2
, pp. 864-870
-
-
Scheuner, D.1
-
16
-
-
0029975660
-
Brain parenchymal and microvascular amyloid in Alzheimer's disease
-
Vinter H.V.et al. Brain parenchymal and microvascular amyloid in Alzheimer's disease. Brain Pathol. 6:1996;179-195.
-
(1996)
Brain Pathol.
, vol.6
, pp. 179-195
-
-
Vinter, H.V.1
-
17
-
-
0030614814
-
Apolipoprotein E ε4 and the risk of dementia with stroke
-
Slooter A.J.et al. Apolipoprotein E ε4 and the risk of dementia with stroke. J. Am. Med. Assoc. 277:1997;818-821.
-
(1997)
J. Am. Med. Assoc.
, vol.277
, pp. 818-821
-
-
Slooter, A.J.1
-
18
-
-
0029968149
-
The underlying molecular mechanisms of apolipoprotein E polymorphism: Relationship to lipid disorders, cardiovascular disease, and Alzheimer's disease
-
Contois J.H.et al. The underlying molecular mechanisms of apolipoprotein E polymorphism: relationship to lipid disorders, cardiovascular disease, and Alzheimer's disease. Clin. Lab. Med. 16:1996;105-123.
-
(1996)
Clin. Lab. Med.
, vol.16
, pp. 105-123
-
-
Contois, J.H.1
-
19
-
-
0026458371
-
Hormone therapy to prevent disease and prolong life in postmenopausal women
-
Grady D.et al. Hormone therapy to prevent disease and prolong life in postmenopausal women. Ann. Intern. Med. 117:1992;1016-1037.
-
(1992)
Ann. Intern. Med.
, vol.117
, pp. 1016-1037
-
-
Grady, D.1
-
20
-
-
0029810689
-
Estrogen reduces atherosclerotic lesion development in apolipoprotein E-deficient mice
-
Bourassa P.A.K.et al. Estrogen reduces atherosclerotic lesion development in apolipoprotein E-deficient mice. Proc. Natl. Acad. Sci. U. S. A. 93:1996;10022-10027.
-
(1996)
Proc. Natl. Acad. Sci. U. S. A.
, vol.93
, pp. 10022-10027
-
-
Bourassa, P.A.K.1
-
21
-
-
0031054674
-
Brain infarction and the clinical expression of Alzheimer disease
-
Snowdon D.A.et al. Brain infarction and the clinical expression of Alzheimer disease. J. Am. Med. Assoc. 277:1997;813-817.
-
(1997)
J. Am. Med. Assoc.
, vol.277
, pp. 813-817
-
-
Snowdon, D.A.1
-
22
-
-
9444268676
-
Clinical correlates of white matter findings on cranial magnetic resonance imaging of 3301 elderly people
-
Longstreth W.T.et al. Clinical correlates of white matter findings on cranial magnetic resonance imaging of 3301 elderly people. Stroke. 27:1996;1274-1282.
-
(1996)
Stroke
, vol.27
, pp. 1274-1282
-
-
Longstreth, W.T.1
-
23
-
-
0030479954
-
Presence and severity of cerebral white matter lesions and hypertension, its treatment, and its control
-
Liao D.et al. Presence and severity of cerebral white matter lesions and hypertension, its treatment, and its control. Stroke. 27:1996;2262-2270.
-
(1996)
Stroke
, vol.27
, pp. 2262-2270
-
-
Liao, D.1
-
24
-
-
0030250567
-
Inflammation and Alzheimer's disease pathogenesis
-
Rogers J.et al. Inflammation and Alzheimer's disease pathogenesis. Neurobiol. Aging. 17:1996;681-686.
-
(1996)
Neurobiol. Aging
, vol.17
, pp. 681-686
-
-
Rogers, J.1
-
25
-
-
0031012177
-
Microglia in neurodegenerative disorders: Emphasis on Alzheimer's disease
-
McRae A.et al. Microglia in neurodegenerative disorders: emphasis on Alzheimer's disease. Gerontology. 43:1997;95-108.
-
(1997)
Gerontology
, vol.43
, pp. 95-108
-
-
McRae, A.1
-
26
-
-
0030905730
-
HLA-DR antigens associated with major genetic risk for late-onset Alzheimer's disease
-
Curran M.et al. HLA-DR antigens associated with major genetic risk for late-onset Alzheimer's disease. Neuroreport. 8:1997;1467-1469.
-
(1997)
Neuroreport
, vol.8
, pp. 1467-1469
-
-
Curran, M.1
-
27
-
-
0030816559
-
Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease
-
Payami H.et al. Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease. Neurology. 49:1997;512-518.
-
(1997)
Neurology
, vol.49
, pp. 512-518
-
-
Payami, H.1
-
28
-
-
0029125857
-
Aging, energy, and oxidative stress in neurodegenerative diseases
-
Beal M.F. Aging, energy, and oxidative stress in neurodegenerative diseases. Ann. Neurol. 38:1995;357-366.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 357-366
-
-
Beal, M.F.1
-
29
-
-
0029896354
-
Mechanisms of neuronal degeneration in Alzheimer's disease
-
Yankner B.A. Mechanisms of neuronal degeneration in Alzheimer's disease. Neuron. 16:1996;921-932.
-
(1996)
Neuron
, vol.16
, pp. 921-932
-
-
Yankner, B.A.1
-
30
-
-
0028118846
-
Inhibition of PC12 cell redox activity is a specific, early indicator of the mechanism of beta-amyloid-mediated cell death
-
Shearman M.S.et al. Inhibition of PC12 cell redox activity is a specific, early indicator of the mechanism of beta-amyloid-mediated cell death. Proc. Natl. Acad. Sci. U. S. A. 91:1994;1470-1474.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 1470-1474
-
-
Shearman, M.S.1
-
31
-
-
0030016323
-
Increased risk of dementia in mothers of Alzheimer's disease cases: Evidence for maternal inheritance
-
Edland S.D.et al. Increased risk of dementia in mothers of Alzheimer's disease cases: evidence for maternal inheritance. Neurology. 47:1996;254-256.
-
(1996)
Neurology
, vol.47
, pp. 254-256
-
-
Edland, S.D.1
-
32
-
-
0027178571
-
A comparison of familial and sporadic Alzheimer's disease
-
Duara R.et al. A comparison of familial and sporadic Alzheimer's disease. Neurology. 43:1993;1377-1384.
-
(1993)
Neurology
, vol.43
, pp. 1377-1384
-
-
Duara, R.1
-
33
-
-
0029091194
-
A mitochondrial DNA clone is associated with increased risk for Alzheimer disease
-
Hutchin T., Cortipassi G. A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Proc. Natl. Acad. Sci. U. S. A. 92:1995;6892-6895.
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 6892-6895
-
-
Hutchin, T.1
Cortipassi, G.2
-
34
-
-
0344965836
-
Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer's disease
-
Davis R.E.et al. Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer's disease. Proc. Natl. Acad. Sci. U. S. A. 91:1993;1470-1474.
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 1470-1474
-
-
Davis, R.E.1
-
35
-
-
0345397192
-
No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant
-
Wragg M.A.et al. No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant. Neurosci. Lett. 201:1996;509-512.
-
(1996)
Neurosci. Lett.
, vol.201
, pp. 509-512
-
-
Wragg, M.A.1
-
36
-
-
0030943678
-
A controlled trial of selegiline, α-tocopherol, or both as treatment for Alzheimer's disease. The Alzheimer's Disease Comparative Study
-
Sano M.et al. A controlled trial of selegiline, α-tocopherol, or both as treatment for Alzheimer's disease. The Alzheimer's Disease Comparative Study. New Engl. J. Med. 336:1997;1245-1247.
-
(1997)
New Engl. J. Med.
, vol.336
, pp. 1245-1247
-
-
Sano, M.1
-
37
-
-
0029844205
-
Human apolipoprotein E: The Alzheimer's disease connection
-
Weisgraber K.H., Mahley R.W. Human apolipoprotein E: the Alzheimer's disease connection. FASEB J. 10:1996;1485-1494.
-
(1996)
FASEB J.
, vol.10
, pp. 1485-1494
-
-
Weisgraber, K.H.1
Mahley, R.W.2
-
38
-
-
16044373524
-
Secreted amyloid-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
-
Scheuner D.et al. Secreted amyloid-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. Nat. Med. 2:1996;864-870.
-
(1996)
Nat. Med.
, vol.2
, pp. 864-870
-
-
Scheuner, D.1
-
39
-
-
9844261165
-
A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A42(43)
-
Eckman C.B.et al. A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A42(43). Hum. Mol. Genet. 6:1997;2087-2089.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2087-2089
-
-
Eckman, C.B.1
|