-
1
-
-
0031614624
-
Alzheimer disease
-
Smith MA. Alzheimer disease. Int Rev Neurobiol 1998;42:1-54.
-
(1998)
Int Rev Neurobiol
, vol.42
, pp. 1-54
-
-
Smith, M.A.1
-
2
-
-
0022414054
-
Diagnosis of Alzheimer's disease
-
Khachaturian Z. Diagnosis of Alzheimer's disease. Arch Neurol 1985;42:1097-105.
-
(1985)
Arch Neurol
, vol.42
, pp. 1097-1105
-
-
Khachaturian, Z.1
-
3
-
-
0027139556
-
Genetic heterogeneity of gene defects responsible for familial Alzheimer's disease
-
Tanzi RE, Gaston S, Bush A, et al. Genetic heterogeneity of gene defects responsible for familial Alzheimer's disease. Genetics 1994;91:255-63.
-
(1994)
Genetics
, vol.91
, pp. 255-263
-
-
Tanzi, R.E.1
Gaston, S.2
Bush, A.3
-
5
-
-
0030731562
-
Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease
-
Lehmann DJ, Johnsin C, Smith AD. Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset confirmed Alzheimer's disease. Hum Mol Genet 1997;6:1933-6.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1933-1936
-
-
Lehmann, D.J.1
Johnsin, C.2
Smith, A.D.3
-
7
-
-
0018924532
-
The cholinergenic system in old age and Alzheimer's disease
-
Perry EK. The cholinergenic system in old age and Alzheimer's disease. Age Ageing 1980;9:1-8.
-
(1980)
Age Ageing
, vol.9
, pp. 1-8
-
-
Perry, E.K.1
-
8
-
-
0000613740
-
Butyrylcholinesterase (BchE) alters the aggregation state of Aβ amyloid
-
Barber K, Mesulam M, Kraft G, Klein W. Butyrylcholinesterase (BchE) alters the aggregation state of Aβ amyloid. Soc Neurosci Abstr 1996;22:1172.
-
(1996)
Soc Neurosci Abstr
, vol.22
, pp. 1172
-
-
Barber, K.1
Mesulam, M.2
Kraft, G.3
Klein, W.4
-
9
-
-
0026695539
-
DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites
-
Bartels CF, Jensen FS, Lockridge O, et al. DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites. Am J Hum Genet 1992;50:1086-103.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1086-1103
-
-
Bartels, C.F.1
Jensen, F.S.2
Lockridge, O.3
-
10
-
-
0343401614
-
Butyrylcholinesterase K variant (BCHE K): Association with late-onset Alzheimer's disease
-
Sandbrink R, Gasperina A, Zerfass R, et al. Butyrylcholinesterase K variant (BCHE K): association with late-onset Alzheimer's disease. Neurobiol Aging 1998;19:S69A.
-
(1998)
Neurobiol Aging
, vol.19
-
-
Sandbrink, R.1
Gasperina, A.2
Zerfass, R.3
-
11
-
-
0033020325
-
Further evidence for a synergistic association between APOE ε4 and BCHE-K in confirmed Alzheimer's disease
-
Wiebusch H, Poirier J, Sévigny P, Schappert K. Further evidence for a synergistic association between APOE ε4 and BCHE-K in confirmed Alzheimer's disease. Hum Genet 1999;104:158-63.
-
(1999)
Hum Genet
, vol.104
, pp. 158-163
-
-
Wiebusch, H.1
Poirier, J.2
Sévigny, P.3
Schappert, K.4
-
12
-
-
7144262433
-
Analysis of the butyryl-cholinesterase gene and nearby chromosome 3 markers in Alzheimer's disease
-
Brindle N, Song Y, Rogaeva E, et al. Analysis of the butyryl-cholinesterase gene and nearby chromosome 3 markers in Alzheimer's disease. Hum Mol Genet 1998;7:933-5.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 933-935
-
-
Brindle, N.1
Song, Y.2
Rogaeva, E.3
-
13
-
-
0032547037
-
The butyrylcholinesterase gene is neither independently nor synergistically associated with late-onset AD in clinic- And community-based populations
-
Crawford F, Fallin D, Suo A, et al. The butyrylcholinesterase gene is neither independently nor synergistically associated with late-onset AD in clinic- and community-based populations. Neurosci Lett 1998;249:115-18.
-
(1998)
Neurosci Lett
, vol.249
, pp. 115-118
-
-
Crawford, F.1
Fallin, D.2
Suo, A.3
-
14
-
-
22444452691
-
The butyrylcholinesterase K variant is not associated with Alzheimer's disease
-
Helbeque N, Cottel D, Hermant X, Guez D, Amouyel P. The butyrylcholinesterase K variant is not associated with Alzheimer's disease. Alz Rep 1998;1:309-13.
-
(1998)
Alz Rep
, vol.1
, pp. 309-313
-
-
Helbeque, N.1
Cottel, D.2
Hermant, X.3
Guez, D.4
Amouyel, P.5
-
15
-
-
0032568899
-
Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients
-
Hiltunen M, Mannermaa A, Helisalmi S, et al. Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients. Neurosci Lett 1998;250:68-71.
-
(1998)
Neurosci Lett
, vol.250
, pp. 68-71
-
-
Hiltunen, M.1
Mannermaa, A.2
Helisalmi, S.3
-
16
-
-
0031757256
-
The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease
-
Kehoe PG, Williams H, Holmans P, et al. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. J Med Genet 1998;35:1034-5.
-
(1998)
J Med Genet
, vol.35
, pp. 1034-1035
-
-
Kehoe, P.G.1
Williams, H.2
Holmans, P.3
-
17
-
-
0021324274
-
On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population
-
Evans RT, Wardell J. On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population. J Med Genet 1984;21:99-102.
-
(1984)
J Med Genet
, vol.21
, pp. 99-102
-
-
Evans, R.T.1
Wardell, J.2
-
18
-
-
0022256704
-
Plasma cholinesterase variants. Family studies of the E1k gene
-
Whittaker M, Britten JJ. Plasma cholinesterase variants. Family studies of the E1k gene. Hum Hered 1985;35:364-8.
-
(1985)
Hum Hered
, vol.35
, pp. 364-368
-
-
Whittaker, M.1
Britten, J.J.2
-
19
-
-
0031052829
-
Ethnic differences in the frequency distribution of serum cholinesterase activity
-
Hosseini J, Firuzian F, Feely J. Ethnic differences in the frequency distribution of serum cholinesterase activity. Ir J Med Sci 1997;166:10-20.
-
(1997)
Ir J Med Sci
, vol.166
, pp. 10-20
-
-
Hosseini, J.1
Firuzian, F.2
Feely, J.3
-
21
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA work group under the auspices of the Department of Health and Human Services task force of Alzheimer's disease
-
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA work group under the auspices of the Department of Health and Human Services task force of Alzheimer's disease. Neurology 1984;34:939-44.
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
22
-
-
0016823810
-
Mini-Mental State. A practical method for grading the cognitive state of patients for the clinician
-
Folstein MF, Folstein SE, McHugh PR. Mini-Mental State. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 1975;12:189-98.
-
(1975)
J Psychiatr Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
23
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;13:1215.
-
(1988)
Nucleic Acids Res
, vol.13
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
24
-
-
0030030131
-
Detection of the plasma cholinesterase K variant by PCR using an amplification-created restriction site
-
Jensen FS, Nielsen LR, Schwartz M. Detection of the plasma cholinesterase K variant by PCR using an amplification-created restriction site. Hum Hered 1996;46: 26-31.
-
(1996)
Hum Hered
, vol.46
, pp. 26-31
-
-
Jensen, F.S.1
Nielsen, L.R.2
Schwartz, M.3
-
26
-
-
0032840053
-
Cathepsin D gene exon 2 polymorphism and sporadic Alzheimer's disease
-
McIlroy SP, Dynan KB, McGleenon BM, Lawson JT, Passmore AP. Cathepsin D gene exon 2 polymorphism and sporadic Alzheimer's disease. Neurosci Lett 1999;273:140-1.
-
(1999)
Neurosci Lett
, vol.273
, pp. 140-141
-
-
McIlroy, S.P.1
Dynan, K.B.2
McGleenon, B.M.3
Lawson, J.T.4
Passmore, A.P.5
-
27
-
-
0033574382
-
Risk of Alzheimer's disease is associated with a very low density lipoprotein receptor genotype in Northern Ireland
-
McIlroy SP, Vahidassr MD, Savage DA, Patterson CC, Lawson JT, Passmore AP. Risk of Alzheimer's disease is associated with a very low density lipoprotein receptor genotype in Northern Ireland. Am J Med Genet 1999;88: 140-4.
-
(1999)
Am J Med Genet
, vol.88
, pp. 140-144
-
-
McIlroy, S.P.1
Vahidassr, M.D.2
Savage, D.A.3
Patterson, C.C.4
Lawson, J.T.5
Passmore, A.P.6
-
28
-
-
0030006546
-
Alzheimer's disease: Interaction of apolipoprotein E genotype, family history of dementia, gender, education, ethnicity and age of onset
-
Duara R, Barker WW, Lopez-Alberola R, et al. Alzheimer's disease: interaction of apolipoprotein E genotype, family history of dementia, gender, education, ethnicity and age of onset. Neurology 1996;46:1575-9.
-
(1996)
Neurology
, vol.46
, pp. 1575-1579
-
-
Duara, R.1
Barker, W.W.2
Lopez-Alberola, R.3
-
29
-
-
17744410836
-
APOE-4 and age of onset of Alzheimer's disease: The NIMH genetics initiative
-
Blacker D, Haines JL, Rodes L, et al. APOE-4 and age of onset of Alzheimer's disease: the NIMH genetics initiative. Neurology 1997;48:139-47.
-
(1997)
Neurology
, vol.48
, pp. 139-147
-
-
Blacker, D.1
Haines, J.L.2
Rodes, L.3
-
30
-
-
0029561222
-
Apolipoprotein E (APOE) allele frequencies in late onset sporadic Alzheimer's disease (AD), mixed dementia and vascular dementia: Lack of association of epsilon 4 allele with AD in Italian octogenarian patients
-
Scacchi R, De Bernardini L, Mantuano E, Donini LM, Vilardo T, Corbo RM. Apolipoprotein E (APOE) allele frequencies in late onset sporadic Alzheimer's disease (AD), mixed dementia and vascular dementia: lack of association of epsilon 4 allele with AD in Italian octogenarian patients. Neurosci Lett 1995;210:231-4.
-
(1995)
Neurosci Lett
, vol.210
, pp. 231-234
-
-
Scacchi, R.1
De Bernardini, L.2
Mantuano, E.3
Donini, L.M.4
Vilardo, T.5
Corbo, R.M.6
|