-
1
-
-
0036845531
-
Dementia and Alzheimer disease incidence: A prospective cohort study
-
Kukull, W.A., Higdon, R., Bowen, J.D., McCormick, W.C. et al. (2002), ’Dementia and Alzheimer disease incidence: A prospective cohort study’, Arch. Neurol. Vol. 59, pp. 1737–1746.
-
(2002)
Arch. Neurol
, vol.59
, pp. 1737-1746
-
-
Kukull, W.A.1
Higdon, R.2
Bowen, J.D.3
McCormick, W.C.4
-
2
-
-
2342609768
-
State-specific projections through 2025 of Alzheimer disease preva-lence
-
Hebert, L.E., Scherr, P.A., Bienias, J.L., Bennett, D.A. et al. (2004), ‘State-specific projections through 2025 of Alzheimer disease preva-lence’, Neurology Vol. 62, p. 1645.
-
(2004)
Neurology
, vol.62
, pp. 1645
-
-
Hebert, L.E.1
Scherr, P.A.2
Bienias, J.L.3
Bennett, D.A.4
-
3
-
-
0026340592
-
Prevalence of Alzheimer’s disease and other dementias in an elderly urban population: Relationship with age sex, and education
-
Fratiglioni, L., Grut, M., Forsell, Y., Viitanen, M. et al. (1991), ‘Prevalence of Alzheimer’s disease and other dementias in an elderly urban population: Relationship with age sex, and education’, Neurology Vol. 41, pp. 1886–1892.
-
(1991)
Neurology
, vol.41
, pp. 1886-1892
-
-
Fratiglioni, L.1
Grut, M.2
Forsell, Y.3
Viitanen, M.4
-
4
-
-
0031695197
-
Projections of Alzheimer’s disease in the United States and the public health impact of delaying disease onset
-
Brookmeyer, R., Gray, S. and Kawas, C. (1998), ‘Projections of Alzheimer’s disease in the United States and the public health impact of delaying disease onset’, Am. J. Public Health Vol. 88, pp. 1337–1342.
-
(1998)
Am. J. Public Health
, vol.88
, pp. 1337-1342
-
-
Brookmeyer, R.1
Gray, S.2
Kawas, C.3
-
5
-
-
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 on Alzheimer’s Disease
-
McKhann, G., Drachman, D., Folstein, M. et al. (1984), ‘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 on Alzheimer’s Disease’, Neurology Vol. 34, pp. 939–944.
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
-
6
-
-
0037202852
-
The dementias
-
Ritchie, K. and Lovestone, S. (2002), ‘The dementias’, Lancet Vol. 360, pp. 1759–1766.
-
(2002)
Lancet
, vol.360
, pp. 1759-1766
-
-
Ritchie, K.1
Lovestone, S.2
-
7
-
-
37649001373
-
Maternal family history of Alzheimer’s disease predisposes to reduced brain glucose metabolism
-
Mosconi, L., Brys, M., Switalski, R., Mistur, R. et al. (2007), ‘Maternal family history of Alzheimer’s disease predisposes to reduced brain glucose metabolism’, Proc. Natl. Acad. Sci. USAVol. 104, pp. 19067–19072.
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 19067-19072
-
-
Mosconi, L.1
Brys, M.2
Switalski, R.3
Mistur, R.4
-
8
-
-
38149071577
-
Current and future uses of neuroimaging for cognitively impaired patients
-
Small, G.W., Bookheimer, S.Y., Thompson, P.M. et al. (2008), ‘Current and future uses of neuroimaging for cognitively impaired patients’, Lancet Neurol. Vol. 7, pp. 161–172.
-
(2008)
Lancet Neurol
, vol.7
, pp. 161-172
-
-
Small, G.W.1
Bookheimer, S.Y.2
Thompson, P.M.3
-
9
-
-
0001792170
-
Structural magnetic resonance imaging in the practical assessment of dementia: Beyond exclusion
-
Scheltens, P., Fox, N., Barkhof, F. and De Carli, C. (2002), ‘Structural magnetic resonance imaging in the practical assessment of dementia: Beyond exclusion’, Lancet Neurol. Vol. 1, pp. 13–21.
-
(2002)
Lancet Neurol
, vol.1
, pp. 13-21
-
-
Scheltens, P.1
Fox, N.2
Barkhof, F.3
de Carli, C.4
-
10
-
-
17844364259
-
Brain glucose metabolism in the early and specific diagnosis of Alzheimer’s disease
-
Mosconi, L. (2005), ‘Brain glucose metabolism in the early and specific diagnosis of Alzheimer’s disease’, Eur. J. Nucl. Med. Mol. Imaging Vol. 32, pp. 486–510.
-
(2005)
Eur. J. Nucl. Med. Mol. Imaging
, vol.32
, pp. 486-510
-
-
Mosconi, L.1
-
11
-
-
0036168618
-
Evaluating early dementia with and without assessment of regional cerebral metabolism by PET: A comparison of predicted costs and benefits
-
Silverman, D.H.S., Gambhir, S.S., Huang, H.W., Schwimmer, J. et al. (2002), ‘Evaluating early dementia with and without assessment of regional cerebral metabolism by PET: A comparison of predicted costs and benefits’, J. Nucl. Med. Vol. 43, pp. 253–266.
-
(2002)
J. Nucl. Med
, vol.43
, pp. 253-266
-
-
Silverman, D.H.S.1
Gambhir, S.S.2
Huang, H.W.3
Schwimmer, J.4
-
12
-
-
43549110738
-
Positron emission tom-ography imaging in dementia
-
Herholz, K., Carter, S.F. and Jones, M. (2007), ‘Positron emission tom-ography imaging in dementia’, Br. J. Radiol. Vol. 2, pp. 160–167.
-
(2007)
Br. J. Radiol
, vol.2
, pp. 160-167
-
-
Herholz, K.1
Carter, S.F.2
Jones, M.3
-
13
-
-
57649187117
-
Brain glucose hypo-metabolism and oxidative stress in preclinical Alzheimer’s disease
-
Mosconi, L., Pupi, A. and de Leon, M.J. (2009), ‘Brain glucose hypo-metabolism and oxidative stress in preclinical Alzheimer’s disease’, Ann. NY Acad. Sci. Vol. 1147, pp. 180–195.
-
(2009)
Ann. NY Acad. Sci
, vol.1147
, pp. 180-195
-
-
Mosconi, L.1
Pupi, A.2
de Leon, M.J.3
-
14
-
-
10744232413
-
Imaging brain amyloid in Alzheimer’s disease with Pittsburgh compound-B
-
Klunk, W.E., Engler, H., Nordberg, A., Yamming, W. et al. (2004), ‘Imaging brain amyloid in Alzheimer’s disease with Pittsburgh compound-B’, Ann. Neurol. Vol. 55, pp. 306–319.
-
(2004)
Ann. Neurol
, vol.55
, pp. 306-319
-
-
Klunk, W.E.1
Engler, H.2
Nordberg, A.3
Yamming, W.4
-
15
-
-
33750975078
-
Voxel –based analysis of PET amyloid ligand [11C]PIB uptake in Alzheimer disease
-
Kemppainen, N., Aalto, S., Wilson, I., Nagren, K. et al. (2006), ‘Voxel –based analysis of PET amyloid ligand [11C]PIB uptake in Alzheimer disease’, Neurology Vol. 67, pp. 1575–1580.
-
(2006)
Neurology
, vol.67
, pp. 1575-1580
-
-
Kemppainen, N.1
Aalto, S.2
Wilson, I.3
Nagren, K.4
-
16
-
-
35648932901
-
Beta – amyloid imaging and memory in non-demented individuals: Evidence for preclinical Alzheimer’s disease
-
Pike, K.E., Savage, G., Villemagne, V.L., Ng, S. et al. (2007), ‘Beta – amyloid imaging and memory in non-demented individuals: Evidence for preclinical Alzheimer’s disease’, Brain Vol. 130, pp. 2837–2844.
-
(2007)
Brain
, vol.130
, pp. 2837-2844
-
-
Pike, K.E.1
Savage, G.2
Villemagne, V.L.3
Ng, S.4
-
17
-
-
33747048954
-
[11C]PIB in a nondemented population: Potential antecedent marker of Alzheimer disease
-
Mintun, M.A.M., LaRossa, G.N., Sheline, Y.I.M., Dence, C.S.M. et al. (2006), ‘[11C]PIB in a nondemented population: Potential antecedent marker of Alzheimer disease’, Neurology Vol. 67, pp. 446–452.
-
(2006)
Neurology
, vol.67
, pp. 446-452
-
-
Mintun, M.A.M.1
Larossa, G.N.2
Sheline, Y.I.M.3
Dence, C.S.M.4
-
18
-
-
33644832047
-
Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid
-
Fagan, A.M., Mintun, M.A., Mach, R.H., Lee, S. et al. (2006), ‘Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid’, Ann. Neurol. Vol. 59, pp. 512–519.
-
(2006)
Ann. Neurol
, vol.59
, pp. 512-519
-
-
Fagan, A.M.1
Mintun, M.A.2
Mach, R.H.3
Lee, S.4
-
19
-
-
0035950188
-
New frontiers in Alzheimer’s disease genetics
-
Tanzi, R.E. and Bertram, L. (2001), ‘New frontiers in Alzheimer’s disease genetics’, Neuron Vol. 32, pp. 181–184.
-
(2001)
Neuron
, vol.32
, pp. 181-184
-
-
Tanzi, R.E.1
Bertram, L.2
-
20
-
-
0033968306
-
Molecular genetics of Alzheimer’s disease
-
St George–Hyslop, P. (2000), ‘Molecular genetics of Alzheimer’s disease’, Biol. Psychiatry Vol. 47, pp. 183–199.
-
(2000)
Biol. Psychiatry
, vol.47
, pp. 183-199
-
-
St George–Hyslop, P.1
-
21
-
-
0025908356
-
The consortium to establish a registry for Alzheimer’s disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer’s disease
-
Mirra, S.S., Heyman, A., McKeel, D., Sumi, S.M. et al. (1991), ‘The consortium to establish a registry for Alzheimer’s disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer’s disease’, Neurology Vol. 41, pp. 479–486.
-
(1991)
Neurology
, vol.41
, pp. 479-486
-
-
Mirra, S.S.1
Heyman, A.2
McKeel, D.3
Sumi, S.M.4
-
22
-
-
0032989712
-
Tangles and plaques in nondemen-ted aging and “preclinical” Alzheimer’s disease
-
Price, J.L. and Morris, J.C. (1999), ‘Tangles and plaques in nondemen-ted aging and “preclinical” Alzheimer’s disease’, Ann. Neurol. Vol. 45, pp. 358–368.
-
(1999)
Ann. Neurol
, vol.45
, pp. 358-368
-
-
Price, J.L.1
Morris, J.C.2
-
23
-
-
0031038918
-
Alzheimer’s disease: Genotypes, phenotype, and treatments
-
Selkoe, D.J. (1997), ‘Alzheimer’s disease: Genotypes, phenotype, and treatments’, Science Vol. 275, pp. 630–631.
-
(1997)
Science
, vol.275
, pp. 630-631
-
-
Selkoe, D.J.1
-
24
-
-
0032888131
-
Soluble amyloid beta peptide concentration as a predictor of synaptic change in Alzheimer’s disease
-
Lue, L.F., Kuo, Y.M., Roher, A.E., Brachova, L. et al. (1999), ‘Soluble amyloid beta peptide concentration as a predictor of synaptic change in Alzheimer’s disease’, Am. J. Pathol. Vol. 155, pp. 853–862.
-
(1999)
Am. J. Pathol
, vol.155
, pp. 853-862
-
-
Lue, L.F.1
Kuo, Y.M.2
Roher, A.E.3
Brachova, L.4
-
25
-
-
0024472693
-
Neurotoxicity of a fragment of the amyloid precursor associated with Alzheimer’s disease
-
Yankner, B.A., Davies, L.R., Fisher, S., Villa-Komaroff, L. et al. (1989), ‘Neurotoxicity of a fragment of the amyloid precursor associated with Alzheimer’s disease’, Science Vol. 245, pp. 417–420.
-
(1989)
Science
, vol.245
, pp. 417-420
-
-
Yankner, B.A.1
Davies, L.R.2
Fisher, S.3
Villa-Komaroff, L.4
-
26
-
-
0024990330
-
Neurotrophic and neurotoxic effects of amyloid beta protein: Reversal by tachykinin neuropeptides
-
Yankner, B.A., Duffy, L. and Kirschner, D. (1990), ‘Neurotrophic and neurotoxic effects of amyloid beta protein: Reversal by tachykinin neuropeptides’, Science Vol. 250, pp. 279–282.
-
(1990)
Science
, vol.250
, pp. 279-282
-
-
Yankner, B.A.1
Duffy, L.2
Kirschner, D.3
-
27
-
-
0031824782
-
Aging renders the brain vulnerable to amyloid beta-protein neurotoxicity
-
Geula, C., Wu, C.K., Saroff, D., Lorenzo, A. et al. (1998), ‘Aging renders the brain vulnerable to amyloid beta-protein neurotoxicity’, Nat. Med. Vol. 4, pp. 827–831.
-
(1998)
Nat. Med
, vol.4
, pp. 827-831
-
-
Geula, C.1
Wu, C.K.2
Saroff, D.3
Lorenzo, A.4
-
28
-
-
0028233494
-
Hydrogen per-oxide mediates amyloid [beta]protein toxicity
-
Behl, C., Davis, J., Lesley, R. and Schubert, D. (1994), ‘Hydrogen per-oxide mediates amyloid [beta]protein toxicity’, Cell Vol. 77, pp. 817–827.
-
(1994)
Cell
, vol.77
, pp. 817-827
-
-
Behl, C.1
Davis, J.2
Lesley, R.3
Schubert, D.4
-
29
-
-
0035950225
-
Clearing the brain’s amyloid cobwebs
-
Selkoe, D.J. (2001), ‘Clearing the brain’s amyloid cobwebs’, Neuron Vol. 32, pp. 177–180.
-
(2001)
Neuron
, vol.32
, pp. 177-180
-
-
Selkoe, D.J.1
-
30
-
-
0028796841
-
Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer’s disease
-
Kennedy, A.M., Frackowiak, R.S.J., Newman, S.K., Bloomfield, P.M. et al. (1995), ‘Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer’s disease’, Neurosci. Lett. Vol. 186, pp. 17–20.
-
(1995)
Neurosci. Lett
, vol.186
, pp. 17-20
-
-
Kennedy, A.M.1
Frackowiak, R.S.J.2
Newman, S.K.3
Bloomfield, P.M.4
-
31
-
-
33947261376
-
Hypometabolism exceeds atrophy in presymptomatic early-onset familial Alzheimer’s disease
-
Mosconi, L., Sorbi, S., de Leon, M.J., Nacmias, B. et al. (2006), ‘Hypometabolism exceeds atrophy in presymptomatic early-onset familial Alzheimer’s disease’, J. Nucl. Med. Vol. 47, pp. 1778–1786.
-
(2006)
J. Nucl. Med
, vol.47
, pp. 1778-1786
-
-
Mosconi, L.1
Sorbi, S.2
de Leon, M.J.3
Nacmias, B.4
-
32
-
-
34249984684
-
Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees
-
Klunk, W.E., Price, J.C., Mathis, C.A., Tsopelas, N.D. et al. (2007), ‘Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees’, J. Neurosci. Vol. 27, pp. 6174–6184.
-
(2007)
J. Neurosci
, vol.27
, pp. 6174-6184
-
-
Klunk, W.E.1
Price, J.C.2
Mathis, C.A.3
Tsopelas, N.D.4
-
33
-
-
46849093845
-
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer’s disease
-
Koivunen, J., Verkkoniemi, S., Aalto, S., Paetau, A. et al. (2008), ‘PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer’s disease’, Brain Vol. 131, pp. 1845–1853.
-
(2008)
Brain
, vol.131
, pp. 1845-1853
-
-
Koivunen, J.1
Verkkoniemi, S.2
Aalto, S.3
Paetau, A.4
-
34
-
-
42249109406
-
Carbon 11-labeled Pittsburgh compound B positron emission tomographic amyloid imaging in patients with APP locus duplication
-
Remes, A.M., Laru, L., Tuominen, H., Aalto, S. et al. (2008), ‘Carbon 11-labeled Pittsburgh compound B positron emission tomographic amyloid imaging in patients with APP locus duplication’, Arch. Neurol. Vol. 65, pp. 540–544.
-
(2008)
Arch. Neurol
, vol.65
, pp. 540-544
-
-
Remes, A.M.1
Laru, L.2
Tuominen, H.3
Aalto, S.4
-
35
-
-
62449330486
-
A reces-sive mutation in the APP gene with dominant-negative effect on amy-loidogenesis
-
Di Fede, G., Catania, M., Morbin, M., Rossi, G. et al. (2009), ‘A reces-sive mutation in the APP gene with dominant-negative effect on amy-loidogenesis’, Science Vol. 323, pp. 1473–1477.
-
(2009)
Science
, vol.323
, pp. 1473-1477
-
-
Di Fede, G.1
Catania, M.2
Morbin, M.3
Rossi, G.4
-
36
-
-
41749096713
-
A new amyloid B variant favoring oligomerization in Alzheimer’s-type dementia
-
Tomiyama, T., Nagata, T., Shimada, H., Teraoka, R. et al. (2008), ‘A new amyloid B variant favoring oligomerization in Alzheimer’s-type dementia’, Ann. Neurol. Vol. 63, pp. 377–387.
-
(2008)
Ann. Neurol
, vol.63
, pp. 377-387
-
-
Tomiyama, T.1
Nagata, T.2
Shimada, H.3
Teraoka, R.4
-
37
-
-
32244435907
-
Role of genes and environments for explaining Alzheimer disease
-
Gatz, M., Reynolds, C.A., Fratiglioni, L., Johansson, B. et al. (2006), ‘Role of genes and environments for explaining Alzheimer disease’, Arch. Gen. Psychiatry Vol. 63, pp. 168–174.
-
(2006)
Arch. Gen. Psychiatry
, vol.63
, pp. 168-174
-
-
Gatz, M.1
Reynolds, C.A.2
Fratiglioni, L.3
Johansson, B.4
-
38
-
-
18844479720
-
Heritability for Alzheimer’s disease: The study of dementia in Swedish twins
-
Gatz, M., Pedersen, N.L., Berg, S., Johansson, B. et al. (1997), ‘Heritability for Alzheimer’s disease: The study of dementia in Swedish twins’, J. Gerontol. A Biol. Sci. Med. Sci. Vol. 52, pp. 117–125.
-
(1997)
J. Gerontol. a Biol. Sci. Med. Sci
, vol.52
, pp. 117-125
-
-
Gatz, M.1
Pedersen, N.L.2
Berg, S.3
Johansson, B.4
-
39
-
-
0030047250
-
Alzheimer’s disease in Finnish twins
-
Raiha, I., Kaprio, J., Koskenvuo, M., Johansson, B. et al. (1996), ‘Alzheimer’s disease in Finnish twins’, Lancet Vol. 347, pp. 573–578
-
(1996)
Lancet
, vol.347
, pp. 573-578
-
-
Raiha, I.1
Kaprio, J.2
Koskenvuo, M.3
Johansson, B.4
-
40
-
-
0027407565
-
Apolipoprotein E: High-avidity binding to β-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease
-
Strittmatter, W.J., Saunders, A.M., Schmechel, D., Pericak-Vance, M. et al. (1993), ‘Apolipoprotein E: High-avidity binding to β-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease’, Proc. Natl. Acad. Sci. USAVol. 90, pp. 1977–1981.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 1977-1981
-
-
Strittmatter, W.J.1
Saunders, A.M.2
Schmechel, D.3
Pericak-Vance, M.4
-
41
-
-
0027365822
-
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease
-
Schmechel, D.E., Saunders, A.M., Strittmatter, W.J., Crain, B.J. et al. (1993), ‘Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease’, Proc. Natl. Acad. Sci. USAVol. 90, pp. 9649–9653.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 9649-9653
-
-
Schmechel, D.E.1
Saunders, A.M.2
Strittmatter, W.J.3
Crain, B.J.4
-
42
-
-
4243215848
-
Apolipoprotein E isoform-dependent amyloid deposition and neuritic degeneration in a mouse model of Alzheimer’s disease
-
Holtzman, D.M., Bales, K.R., Tenkova, T., Fagan, A.M. et al. (2000), ‘Apolipoprotein E isoform-dependent amyloid deposition and neuritic degeneration in a mouse model of Alzheimer’s disease’, Proc. Natl. Acad. Sci. USAVol. 97, pp. 2892–2897.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 2892-2897
-
-
Holtzman, D.M.1
Bales, K.R.2
Tenkova, T.3
Fagan, A.M.4
-
43
-
-
0034746840
-
Role of apoE/A interactions in the pathogen-esis of Alzheimer’s disease and cerebral amyloid angiopathy
-
Holtzman, D.M. (2001), ‘Role of apoE/A interactions in the pathogen-esis of Alzheimer’s disease and cerebral amyloid angiopathy’, J. Mol. Neurosci. Vol. 17, pp. 147–155.
-
(2001)
J. Mol. Neurosci
, vol.17
, pp. 147-155
-
-
Holtzman, D.M.1
-
44
-
-
4143063440
-
Apolipoprotein E dose-dependent modulation of beta-amyloid deposition in a transgenic mouse model of Alzheimer’s disease
-
DeMattos, R.B. (2004), ‘Apolipoprotein E dose-dependent modulation of beta-amyloid deposition in a transgenic mouse model of Alzheimer’s disease’, J. Mol. Neurosci. Vol. 23, pp. 255–262.
-
(2004)
J. Mol. Neurosci
, vol.23
, pp. 255-262
-
-
Demattos, R.B.1
-
45
-
-
23944526029
-
Amyloid mediates the association of apolipoprotein E e4 allele to cognitive function in older people
-
Bennet, D.A., Schneider, J.A., Wilson, R.S., Bienias, J.L. et al. (2005), ‘Amyloid mediates the association of apolipoprotein E e4 allele to cognitive function in older people’, J. Neurol. Neurosurg. Psych. Vol. 76, pp. 1194–1199.
-
(2005)
J. Neurol. Neurosurg. Psych
, vol.76
, pp. 1194-1199
-
-
Bennet, D.A.1
Schneider, J.A.2
Wilson, R.S.3
Bienias, J.L.4
-
46
-
-
0037345672
-
Expanding the association between the APOE gene and the risk of Alzheimer’s disease: Possible roles for APOE promoter polymorphisms and alterations in APOE transcription
-
Laws, S.M., Hone, E., Gandy, S. and Martins, R.N. (2003), ‘Expanding the association between the APOE gene and the risk of Alzheimer’s disease: Possible roles for APOE promoter polymorphisms and alterations in APOE transcription’. J. Neurochem. Vol. 84, pp. 1215–1236.
-
(2003)
J. Neurochem
, vol.84
, pp. 1215-1236
-
-
Laws, S.M.1
Hone, E.2
Gandy, S.3
Martins, R.N.4
-
47
-
-
15444344926
-
Hippocampal volumes in cognitively normal persons at genetic risk for Alzheimer’s disease
-
Reiman, E.M., Uecker, A., Caselli, R.J., Lewis, S. et al. (1998), ‘Hippocampal volumes in cognitively normal persons at genetic risk for Alzheimer’s disease’, Ann. Neurol. Vol. 44, pp. 288–291.
-
(1998)
Ann. Neurol
, vol.44
, pp. 288-291
-
-
Reiman, E.M.1
Uecker, A.2
Caselli, R.J.3
Lewis, S.4
-
48
-
-
0033544033
-
APOE–epsilon4 is associated with less frontal and more medial tem-poral lobe atrophy in AD
-
Geroldi, C., Pihlajamaki, M., Laakso, M.P., DeCarli, C. et al. (1999), ‘APOE–epsilon4 is associated with less frontal and more medial tem-poral lobe atrophy in AD’, Neurology Vol. 53, pp. 1825–1832.
-
(1999)
Neurology
, vol.53
, pp. 1825-1832
-
-
Geroldi, C.1
Pihlajamaki, M.2
Laakso, M.P.3
Decarli, C.4
-
49
-
-
0028950856
-
Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer disease
-
Small, G.W., Mazziotta, J.C., Collins, M.T., Baxter, L.R. et al. (1995), ‘Apolipoprotein E type 4 allele and cerebral glucose metabolism in relatives at risk for familial Alzheimer disease’, JAMA Vol. 273, pp. 942–947.
-
(1995)
JAMA
, vol.273
, pp. 942-947
-
-
Small, G.W.1
Mazziotta, J.C.2
Collins, M.T.3
Baxter, L.R.4
-
50
-
-
12944259210
-
Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer’s disease
-
Small, G.W., Ercoli, L.M., Silverman, D.H.S., Huang, S.C. et al. (2000), ‘Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer’s disease’, Proc. Natl. Acad. Sci. USA Vol. 97, pp. 6037–6042.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 6037-6042
-
-
Small, G.W.1
Ercoli, L.M.2
Silverman, D.H.S.3
Huang, S.C.4
-
51
-
-
0035853154
-
Declining brain activity in cognitively normal apolipoprotein E epsilon 4 heterozygotes: A foundation for using positron emission tomography to efficiently test treatments to prevent Alzheimer’s disease
-
Reiman, E.M., Caselli, R.J., Chen, K., Alexander, G.E. et al. (2001), ‘Declining brain activity in cognitively normal apolipoprotein E epsilon 4 heterozygotes: A foundation for using positron emission tomography to efficiently test treatments to prevent Alzheimer’s disease’, Proc. Natl. Acad. Sci. USAVol. 98, pp. 3334–3339.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 3334-3339
-
-
Reiman, E.M.1
Caselli, R.J.2
Chen, K.3
Alexander, G.E.4
-
52
-
-
0347719366
-
Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer’s dementia
-
Reiman, E.M., Chen, K., Alexander, G.E., Caselli, R.J. et al. (2004), ‘Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer’s dementia’, Proc. Natl. Acad. Sci. USA Vol. 101, pp. 284–289.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 284-289
-
-
Reiman, E.M.1
Chen, K.2
Alexander, G.E.3
Caselli, R.J.4
-
53
-
-
33846613222
-
The neuronal sortilin–related receptor SORL1 is genetically associated with Alzheimer disease
-
Rogaeva, E., Meng, Y., Lee, J.H., Gu, Y. et al. (2007), ‘The neuronal sortilin–related receptor SORL1 is genetically associated with Alzheimer disease’, Nat. Genet. Vol. 39, pp. 168–177.
-
(2007)
Nat. Genet
, vol.39
, pp. 168-177
-
-
Rogaeva, E.1
Meng, Y.2
Lee, J.H.3
Gu, Y.4
-
54
-
-
34247177933
-
The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort
-
Lee, J.H., Cheng, R., Schupf, N., Manly, J. et al. (2007), ‘The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort’, Arch. Neurol. Vol. 64, pp. 501–506.
-
(2007)
Arch. Neurol
, vol.64
, pp. 501-506
-
-
Lee, J.H.1
Cheng, R.2
Schupf, N.3
Manly, J.4
-
55
-
-
55149121151
-
Possible association between SORL1 and Alzheimer disease?
-
Lee, J.H., Shibata, N., Cheng, R. and Mayeux, R. (2008), ‘Possible association between SORL1 and Alzheimer disease?’, Dement. Geriatr. Cogn. Disord. Vol. 26, p. 482.
-
(2008)
Dement. Geriatr. Cogn. Disord
, vol.26
, pp. 482
-
-
Lee, J.H.1
Shibata, N.2
Cheng, R.3
Mayeux, R.4
-
56
-
-
37349015908
-
Association between SORL1 and Alzheimer disease in a genome-wide study
-
Meng, Y., Lee, J.H., Cheng, R. and Mayeux, R. (2007), ‘Association between SORL1 and Alzheimer disease in a genome-wide study’, Neuroreport Vol. 18, pp. 1761–1764.
-
(2007)
Neuroreport
, vol.18
, pp. 1761-1764
-
-
Meng, Y.1
Lee, J.H.2
Cheng, R.3
Mayeux, R.4
-
57
-
-
33748536734
-
LR11/SorLA expression is reduced in sporadic Alzheimer disease but not in familial Alzheimer disease
-
Dodson, S.E., Gearing, M., Lippa, C.F., Montine, T.J. et al. (2006), ‘LR11/SorLA expression is reduced in sporadic Alzheimer disease but not in familial Alzheimer disease’, J. Neuropathol. Exp. Neurol. Vol. 65, pp. 866–872.
-
(2006)
J. Neuropathol. Exp. Neurol
, vol.65
, pp. 866-872
-
-
Dodson, S.E.1
Gearing, M.2
Lippa, C.F.3
Montine, T.J.4
-
58
-
-
45249114641
-
Influence of SORL1 gene variants: Association with CSF amyloid-beta products in probable Alzheimer’s disease
-
Kolsch, H., Jessen, F., Wiltfang, J., Lewczuk, P. et al. (2008), ‘Influence of SORL1 gene variants: Association with CSF amyloid-beta products in probable Alzheimer’s disease’, Neurosci. Lett. Vol. 440, pp. 68–71.
-
(2008)
Neurosci. Lett
, vol.440
, pp. 68-71
-
-
Kolsch, H.1
Jessen, F.2
Wiltfang, J.3
Lewczuk, P.4
-
59
-
-
61449117869
-
Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease
-
Cuenco, K.T., Lunetta, K.L., Baldwin, C.T., McKee, A.C. et al. (2008), ‘Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease’, Arch. Neurol. Vol. 65, pp. 1640–1648.
-
(2008)
Arch. Neurol
, vol.65
, pp. 1640-1648
-
-
Cuenco, K.T.1
Lunetta, K.L.2
Baldwin, C.T.3
McKee, A.C.4
-
60
-
-
34249745769
-
GAB2 alleles modify Alzheimer’s risk in APOE e4 carriers
-
Reiman, E.M., Webster, J.A., Myers, A.J., Hardy, J. et al. (2007), ‘GAB2 alleles modify Alzheimer’s risk in APOE e4 carriers’, Neuron Vol. 54, pp. 713–720.
-
(2007)
Neuron
, vol.54
, pp. 713-720
-
-
Reiman, E.M.1
Webster, J.A.2
Myers, A.J.3
Hardy, J.4
-
61
-
-
64049116471
-
Common variation in GRB-associated binding protein 2 (GAB2) and increased risk for Alzheimer dementia
-
Sleegers, K., Bettens, K., Brouwers, N., Engelborghs, S. et al. (2008), ‘Common variation in GRB-associated binding protein 2 (GAB2) and increased risk for Alzheimer dementia’, Hum. Mutat. Vol. 29, pp. 338–344.
-
(2008)
Hum. Mutat
, vol.29
, pp. 338-344
-
-
Sleegers, K.1
Bettens, K.2
Brouwers, N.3
Engelborghs, S.4
-
62
-
-
0035849822
-
Essential role for Gab2 in the allergic response
-
Gu, H., Saito, K., Klaman, L.D., Fleming, T. et al. (2001), ‘Essential role for Gab2 in the allergic response’, Nature Vol. 412, pp. 186–190.
-
(2001)
Nature
, vol.412
, pp. 186-190
-
-
Gu, H.1
Saito, K.2
Klaman, L.D.3
Fleming, T.4
-
63
-
-
15744388308
-
Presenilin-dependent processing and nuclear function of gamma-protocadherins
-
Haas, I.G., Frank, M., Veron, N. and Kemler, R. (2005), ‘Presenilin-dependent processing and nuclear function of gamma-protocadherins’. J. Biol. Chem. Vol. 280, pp. 9313–9319.
-
(2005)
’. J. Biol. Chem
, vol.280
, pp. 9313-9319
-
-
Haas, I.G.1
Frank, M.2
Veron, N.3
Kemler, R.4
-
64
-
-
59149084048
-
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer’s disease
-
Carrasquillo, M.M., Zou, F., Pankratz, V.S., Wilcox, S.L. et al. (2009), ‘Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer’s disease’, Nat. Genet. Vol. 41, pp. 192–198.
-
(2009)
Nat. Genet
, vol.41
, pp. 192-198
-
-
Carrasquillo, M.M.1
Zou, F.2
Pankratz, V.S.3
Wilcox, S.L.4
-
65
-
-
33750334020
-
Common KIBRA alleles are associated with human memory performance
-
Papassotiropoulos, A., Stephan, D.A., Huentelman, M.J., Hoerndli, F.J. et al. (2006), ‘Common KIBRA alleles are associated with human memory performance’, Science Vol. 314, pp. 475–478.
-
(2006)
Science
, vol.314
, pp. 475-478
-
-
Papassotiropoulos, A.1
Stephan, D.A.2
Huentelman, M.J.3
Hoerndli, F.J.4
-
66
-
-
50249122340
-
KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment
-
Almeida, O.P., Schwab, S.G., Lautenschlager, N.T., Morar, B. et al. (2008), ‘KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment’, J. Cell. Mol. Med. Vol. 12, pp. 1672–1676.
-
(2008)
J. Cell. Mol. Med
, vol.12
, pp. 1672-1676
-
-
Almeida, O.P.1
Schwab, S.G.2
Lautenschlager, N.T.3
Morar, B.4
-
67
-
-
77951976812
-
Evidence for an association between KIBRA and late-onset Alzheimer’s disease
-
Epub ahead of print
-
Corneveaux, J.J., Liang, W.S., Reiman, E.M. et al. (2008), ‘Evidence for an association between KIBRA and late-onset Alzheimer’s disease’, Neurobiol. Aging doi:10.1016/jneurobiolaging2008.07. [Epub ahead of print]
-
(2008)
Neurobiol. Aging
-
-
Corneveaux, J.J.1
Liang, W.S.2
Reiman, E.M.3
-
68
-
-
57749099316
-
Age-dependent association of KIBRA genetic variation and Alzheimer’s disease risk
-
Aging
-
Rodriguez –Rodriguez, E., Infanti, J., Llorca, J., Mateo, I. et al. (2009), ‘Age-dependent association of KIBRA genetic variation and Alzheimer’s disease risk’, Neurobiol. Aging Vol. 30, pp. 322–324.
-
(2009)
Neurobiol
, vol.30
, pp. 322-324
-
-
Rodriguezrodriguez, –.E.1
Infanti, J.2
Llorca, J.3
Mateo, I.4
-
69
-
-
37149030873
-
Alzheimer’s disease: Advances in trafficking
-
Mayeux, R. and Hyslop, P.S. (2008), ‘Alzheimer’s disease: Advances in trafficking’, Lancet Neurol. Vol. 7, pp. 2–3.
-
(2008)
Lancet Neurol
, vol.7
, pp. 2-3
-
-
Mayeux, R.1
Hyslop, P.S.2
-
70
-
-
0030823158
-
Effects of age, sex, and ethnicity on the association between apolipo-protein E genotype and Alzheimer disease
-
Farrer, L.A., Cupples, L.A., Haines, J.L., Hyman, B. et al. (1997), ‘Effects of age, sex, and ethnicity on the association between apolipo-protein E genotype and Alzheimer disease’, JAMA Vol. 278, pp. 1349–1356.
-
(1997)
JAMA
, vol.278
, pp. 1349-1356
-
-
Farrer, L.A.1
Cupples, L.A.2
Haines, J.L.3
Hyman, B.4
-
71
-
-
0027931716
-
The consortium to establish a registry for Alzheimer’s disease (CERAD). Part VI. Family history assessment: A multicenter study of first degree relatives of Alzheimer’s disease probands and nondemented spouse controls
-
Silverman, J.M., Raiford, K., Edland, S., Fillenbaum, G. et al. (1994), ‘The consortium to establish a registry for Alzheimer’s disease (CERAD). Part VI. Family history assessment: A multicenter study of first degree relatives of Alzheimer’s disease probands and nondemented spouse controls’, Neurology Vol. 44, pp. 1253–1259.
-
(1994)
Neurology
, vol.44
, pp. 1253-1259
-
-
Silverman, J.M.1
Raiford, K.2
Edland, S.3
Fillenbaum, G.4
-
72
-
-
3442877311
-
Estimating risk curves for first-degree relatives of patients with Alzheimer’s disease: The REVEAL study
-
Cupples, L.A., Farrer, L.A., Sadovnik, A.D., Relkin, N. et al. (2004), ‘Estimating risk curves for first-degree relatives of patients with Alzheimer’s disease: The REVEAL study’, Genet. Med. Vol. 6, pp. 192–196.
-
(2004)
Genet. Med
, vol.6
, pp. 192-196
-
-
Cupples, L.A.1
Farrer, L.A.2
Sadovnik, A.D.3
Relkin, N.4
-
73
-
-
0037116658
-
Risk of dementia among white and African American relatives of patients with Alzheimer disease
-
Green, R.C., Cupples, L.A., Go, R., Benke, K.S. et al. (2002), ‘Risk of dementia among white and African American relatives of patients with Alzheimer disease’, JAMAVol. 287, pp. 329–336.
-
(2002)
Jamavol
, vol.287
, pp. 329-336
-
-
Green, R.C.1
Cupples, L.A.2
Go, R.3
Benke, K.S.4
-
74
-
-
18244409886
-
Variability of familial risk of Alzheimer disease across the late life span
-
Silverman, J.M., Ciresi, G., Smith, C.J., Marin, D.B. et al. (2005), ‘Variability of familial risk of Alzheimer disease across the late life span’, Arch. Gen. Psychiat. Vol. 62, pp. 565–573.
-
(2005)
Arch. Gen. Psychiat
, vol.62
, pp. 565-573
-
-
Silverman, J.M.1
Ciresi, G.2
Smith, C.J.3
Marin, D.B.4
-
75
-
-
40849111447
-
Conjugal Alzheimer disease
-
Jayadev, S., Steinbart, E.J., Chi, Y.Y., Kukull, W.A. et al. (2008), ‘Conjugal Alzheimer disease’, Arch. Neurol. Vol. 65, pp. 373–378.
-
(2008)
Arch. Neurol
, vol.65
, pp. 373-378
-
-
Jayadev, S.1
Steinbart, E.J.2
Chi, Y.Y.3
Kukull, W.A.4
-
76
-
-
0027220646
-
Conjugal Alzheimer’s disease: Is there an increased risk in offspring?
-
Bird, T.D., Nemens, E.J. and Kukull, W.A. (1993), ‘Conjugal Alzheimer’s disease: Is there an increased risk in offspring?’, Ann. Neurol. Vol. 34, pp. 396–399.
-
(1993)
Ann. Neurol
, vol.34
, pp. 396-399
-
-
Bird, T.D.1
Nemens, E.J.2
Kukull, W.A.3
-
77
-
-
0027178571
-
A comparison of familial and sporadic Alzheimer’s disease
-
Duara, R., Lopez-Alberola, R.F., Barker, W.W., Loewenstein, D.A. et al. (1993), ‘A comparison of familial and sporadic Alzheimer’s disease’, Neurology Vol. 43, pp. 1377–1384.
-
(1993)
Neurology
, vol.43
, pp. 1377-1384
-
-
Duara, R.1
Lopez-Alberola, R.F.2
Barker, W.W.3
Loewenstein, D.A.4
-
78
-
-
0030016323
-
Increased risk of dementia in mothers of Alzheimer’s disease cases: Evidence for maternal inheritance
-
Edland, S.D., Silverman, J.M., Peskind, E.R., Tsuang, D. et al. (1996), ‘Increased risk of dementia in mothers of Alzheimer’s disease cases: Evidence for maternal inheritance’, Neurology Vol. 47, pp. 254–256.
-
(1996)
Neurology
, vol.47
, pp. 254-256
-
-
Edland, S.D.1
Silverman, J.M.2
Peskind, E.R.3
Tsuang, D.4
-
79
-
-
0033588280
-
Genetic epidemiological study of maternal and paternal transmission of Alzheimer’s disease
-
Ehrenkrantz, D., Silverman, J.M., Smith, C.J., Tsuang, D. et al. (1999), ‘Genetic epidemiological study of maternal and paternal transmission of Alzheimer’s disease’. Am. J. Med. Genet. Vol. 88, pp. 378–382.
-
(1999)
Am. J. Med. Genet.
, vol.88
, pp. 378-382
-
-
Ehrenkrantz, D.1
Silverman, J.M.2
Smith, C.J.3
Tsuang, D.4
-
80
-
-
37149039011
-
Variability of age at onset in siblings with familial Alzheimer disease
-
Gomez –Tortosa, E., Barquero, M.S., Baron, M., Saint, H.J. et al. (2007), ‘Variability of age at onset in siblings with familial Alzheimer disease’. Arch. Neurol. Vol. 64, pp. 1743–1748.
-
(2007)
’. Arch. Neurol
, vol.64
, pp. 1743-1748
-
-
Gomez –Tortosa, E.1
Barquero, M.S.2
Baron, M.3
Saint, H.J.4
-
81
-
-
0021054024
-
Alzheimer’s disease: Genetic aspects and associated clinical dis-orders
-
Heyman, A., Wilkinson, W.E., Hurwitz, B.J., Schmechel, D. et al. (1983), ‘Alzheimer’s disease: Genetic aspects and associated clinical dis-orders’, Ann. Neurol. Vol. 14, pp. 507–515.
-
(1983)
Ann. Neurol
, vol.14
, pp. 507-515
-
-
Heyman, A.1
Wilkinson, W.E.2
Hurwitz, B.J.3
Schmechel, D.4
-
82
-
-
85108220376
-
Lifetime risk of dementia and Alzheimer’s disease: Estimates from the Framingham study
-
Seshadri, S., Wolf, P.A., Beiser, A., Au, R. et al. (1996), ‘Lifetime risk of dementia and Alzheimer’s disease: Estimates from the Framingham study’, Neurology Vol. 46, pp. 411–412.
-
(1996)
Neurology
, vol.46
, pp. 411-412
-
-
Seshadri, S.1
Wolf, P.A.2
Beiser, A.3
Au, R.4
-
83
-
-
0030006546
-
Alzheimer’s disease: Interaction of apolipoprotein E genotype, family history of dementia, gender, education, ethnicity, and age of onset
-
Duara, R., Barker, W.W., Lopez –Alberola, R., Loewenstein, D.A. et al. (1996), ‘Alzheimer’s disease: Interaction of apolipoprotein E genotype, family history of dementia, gender, education, ethnicity, and age of onset’, Neurology Vol. 46, pp. 1575–1579.
-
(1996)
Neurology
, vol.46
, pp. 1575-1579
-
-
Duara, R.1
Barker, W.W.2
Lopez –Alberola, R.3
Loewenstein, D.A.4
-
84
-
-
62149115284
-
Declining brain glucose metabolism in normal individuals with a maternal history of Alzheimer’s
-
Mosconi, L., Mistur, R., Glodzik, L., Brys, M. et al. (2009), ‘Declining brain glucose metabolism in normal individuals with a maternal history of Alzheimer’s’, Neurology Vol. 72, pp. 513–520.
-
(2009)
Neurology
, vol.72
, pp. 513-520
-
-
Mosconi, L.1
Mistur, R.2
Glodzik, L.3
Brys, M.4
-
85
-
-
0035845499
-
Prediction of cognitive decline in normal elderly subjects with 2-[18F]fluoro-2-deoxy-D-glucose/positron-emission tomography (FDG/PET)
-
de Leon, M.J., Convit, A., Wolf, O.T., Tarshish, C.Y. et al. (2001), ‘Prediction of cognitive decline in normal elderly subjects with 2-[18F]fluoro-2-deoxy-D-glucose/positron-emission tomography (FDG/PET)’, Proc. Natl. Acad. Sci. USAVol. 98, pp. 10966–10971.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 10966-10971
-
-
de Leon, M.J.1
Convit, A.2
Wolf, O.T.3
Tarshish, C.Y.4
-
86
-
-
38149006292
-
Hippocampal hypometabolism predicts cognitive decline from normal aging
-
Mosconi, L., De Santi, S., Li, J., Tsui, W.H. et al. (2008), ‘Hippocampal hypometabolism predicts cognitive decline from normal aging’, Neurobiol. Aging Vol. 29, pp. 676–692.
-
(2008)
Neurobiol. Aging
, vol.29
, pp. 676-692
-
-
Mosconi, L.1
de Santi, S.2
Li, J.3
Tsui, W.H.4
-
87
-
-
8544273687
-
Resourceful imprint-ing
-
Constancia, M., Kelsey, G. and Relk, W. (2004), ‘Resourceful imprint-ing’, Nature Vol. 432, pp. 53–57.
-
(2004)
Nature
, vol.432
, pp. 53-57
-
-
Constancia, M.1
Kelsey, G.2
Relk, W.3
-
88
-
-
0028086834
-
Mechanisms of genomic imprinting in mammals
-
Gold, J.D. and Pedersen, R.A. (1994), ‘Mechanisms of genomic imprinting in mammals’, Curr. Top. Dev. Biol. Vol. 29, pp. 227–280.
-
(1994)
Curr. Top. Dev. Biol
, vol.29
, pp. 227-280
-
-
Gold, J.D.1
Pedersen, R.A.2
-
89
-
-
0025958320
-
Genomic imprinting in mammalian development: A parental tug-of-war
-
Moore, T. and Haig, D. (1991), ‘Genomic imprinting in mammalian development: A parental tug-of-war’, Trends Genet. Vol. 7, pp. 45–49.
-
(1991)
Trends Genet
, vol.7
, pp. 45-49
-
-
Moore, T.1
Haig, D.2
-
90
-
-
3542991430
-
Differential chromosome sensitivity to 5-azacytidine in Alzheimer’s disease
-
Payao, S.L., Smith, M.D. and Bertolucci, P.H. (1998), ‘Differential chromosome sensitivity to 5-azacytidine in Alzheimer’s disease’, Gerontology Vol. 44, pp. 267–271.
-
(1998)
Gerontology
, vol.44
, pp. 267-271
-
-
Payao, S.L.1
Smith, M.D.2
Bertolucci, P.H.3
-
91
-
-
0037043838
-
Evidence for parent of origin effect in late-onset Alzheimer disease
-
Bassett, S.S., Avramopoulos, D. and Fallin, D. (2002), ‘Evidence for parent of origin effect in late-onset Alzheimer disease’, Am. J. Med. Genet. Vol. 114, pp. 679–686.
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 679-686
-
-
Bassett, S.S.1
Avramopoulos, D.2
Fallin, D.3
-
92
-
-
38549099255
-
Hormonal imprinting: Phylogeny, ontogeny, diseases and possible role in present-day human evolution
-
Csaba, G. (2008), ‘Hormonal imprinting: Phylogeny, ontogeny, diseases and possible role in present-day human evolution’, Cell Biochem. Funct. Vol. 26, pp. 1–10.
-
(2008)
Cell Biochem. Funct
, vol.26
, pp. 1-10
-
-
Csaba, G.1
-
93
-
-
35549001312
-
Genomic imprinting effects on brain development and function
-
Wilkinson, L.S., Davies, W. and Isles, A.R. (2007), ‘Genomic imprinting effects on brain development and function’, Nat. Rev. Neurosci. Vol. 8, pp. 832–843.
-
(2007)
Nat. Rev. Neurosci
, vol.8
, pp. 832-843
-
-
Wilkinson, L.S.1
Davies, W.2
Isles, A.R.3
-
94
-
-
20044386140
-
Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice
-
Davies, W., Isles, A., Smith, R., Karunadasa, D. et al. (2005), ‘Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice’, Nat. Genet. Vol. 37, pp. 625–629.
-
(2005)
Nat. Genet
, vol.37
, pp. 625-629
-
-
Davies, W.1
Isles, A.2
Smith, R.3
Karunadasa, D.4
-
95
-
-
33750347347
-
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
-
Lin, M.T. and Beal, M.F. (2006), ‘Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases’, Nature Vol. 443, pp. 787–795.
-
(2006)
Nature
, vol.443
, pp. 787-795
-
-
Lin, M.T.1
Beal, M.F.2
-
96
-
-
33745410626
-
Mitochondrial disease
-
Schapira, A.H. (2006), ‘Mitochondrial disease’, Lancet Vol. 368, pp. 70–82.
-
(2006)
Lancet
, vol.368
, pp. 70-82
-
-
Schapira, A.H.1
-
97
-
-
0028946289
-
Radical AGEing in Alzheimer’s disease
-
Smith, M.A., Sayre, L.M., Monnier, V.M. and Perry, G. (1995), ‘Radical AGEing in Alzheimer’s disease’, Trends Neurosci. Vol. 18, pp. 172–176.
-
(1995)
Trends Neurosci
, vol.18
, pp. 172-176
-
-
Smith, M.A.1
Sayre, L.M.2
Monnier, V.M.3
Perry, G.4
-
98
-
-
0028152717
-
Oxidative damage to mitochondrial DNA is increased in Alzheimer’s disease
-
Mecocci, P., MacGarvey, U. and Beal, M.F. (1994), ‘Oxidative damage to mitochondrial DNA is increased in Alzheimer’s disease’, Ann. Neurol. Vol. 36, pp. 747–750.
-
(1994)
Ann. Neurol
, vol.36
, pp. 747-750
-
-
Mecocci, P.1
Macgarvey, U.2
Beal, M.F.3
-
99
-
-
0025334082
-
Autopsy samples of Alzheimer’s cortex show increased peroxidation in vitro
-
Subbarao, K.V., Richardson, J.S. and Ang, L.C. (1990), ‘Autopsy samples of Alzheimer’s cortex show increased peroxidation in vitro’. J. Neurochem. Vol. 55, pp. 342–345.
-
(1990)
J. Neurochem
, vol.55
, pp. 342-345
-
-
Subbarao, K.V.1
Richardson, J.S.2
Ang, L.C.3
-
100
-
-
34648819814
-
Treating neuro degeneration by modifying mitochondria: Potential solutions to a “complex” problem
-
Swerdlow, R.H. (2007), ‘Treating neuro degeneration by modifying mitochondria: Potential solutions to a “complex” problem’, Antiox. Redox Signal. Vol. 9, pp. 1591–1604.
-
(2007)
Antiox. Redox Signal
, vol.9
, pp. 1591-1604
-
-
Swerdlow, R.H.1
-
101
-
-
0028110234
-
Cortical cyto-chrome oxidase activity is reduced in Alzheimer’s disease
-
Mutisya, E.M., Bowling, A.C. and Beal, M.F. (1994), ‘Cortical cyto-chrome oxidase activity is reduced in Alzheimer’s disease’, J.Neurochem. Vol. 63, pp. 2179–2184.
-
(1994)
J.Neurochem
, vol.63
, pp. 2179-2184
-
-
Mutisya, E.M.1
Bowling, A.C.2
Beal, M.F.3
-
102
-
-
0035341254
-
Mitochondrial abnormalities in Alzheimer’s disease
-
Hirai, K., Aliev, G., Nunomura, A., Fujioka, H. et al. (2001), ‘Mitochondrial abnormalities in Alzheimer’s disease’, J. Neurosci. Vol. 21, pp. 3017–3023.
-
(2001)
J. Neurosci.
, vol.21
, pp. 3017-3023
-
-
Hirai, K.1
Aliev, G.2
Nunomura, A.3
Fujioka, H.4
-
103
-
-
0035399655
-
Energy hypometa-bolism in posterior cingulate cortex of Alzheimer’s patients: Superficial laminar cytochrome oxidase associated with disease duration
-
Valla, J., Berndt, J.D. and Gonzales-Lima, F. (2001), ‘Energy hypometa-bolism in posterior cingulate cortex of Alzheimer’s patients: Superficial laminar cytochrome oxidase associated with disease duration’, J. Neurosci. Vol. 21, pp. 4923–4930.
-
(2001)
J. Neurosci.
, vol.21
, pp. 4923-4930
-
-
Valla, J.1
Berndt, J.D.2
Gonzales-Lima, F.3
-
104
-
-
0028023533
-
Functional alterations in Alzheimer’s disease: Selective loss of mitochondrial-encoded cyto-chrome oxidase mRNA in the hippocampal formation
-
Simonian, N.A. and Hyman, B.T. (1994), ‘Functional alterations in Alzheimer’s disease: Selective loss of mitochondrial-encoded cyto-chrome oxidase mRNA in the hippocampal formation’, J. Neuropathol. Exp. Neurol. Vol. 53, pp. 508–512.
-
(1994)
J. Neuropathol. Exp. Neurol
, vol.53
, pp. 508-512
-
-
Simonian, N.A.1
Hyman, B.T.2
-
105
-
-
0024561501
-
Cytochrome oxidase: An endogenous metabolic marker for neuronal activity
-
Wong-Riley, M.T.T. (1989), ‘Cytochrome oxidase: An endogenous metabolic marker for neuronal activity’, Trends Neurosci. Vol. 12, pp. 94–101.
-
(1989)
Trends Neurosci
, vol.12
, pp. 94-101
-
-
Wong-Riley, M.T.T.1
-
106
-
-
0026044467
-
Neuronal expression of nuclear and mitochondrial genes for cytochrome oxidase (CO) subunits analyzed by in situ hybridization: Comparison with CO activity and protein
-
Hevner, R.F. and Wong-Riley, M.T. (1991), ‘Neuronal expression of nuclear and mitochondrial genes for cytochrome oxidase (CO) subunits analyzed by in situ hybridization: Comparison with CO activity and protein’, J. Neurosci. Vol. 11, pp. 1942–1958.
-
(1991)
J. Neurosci.
, vol.11
, pp. 1942-1958
-
-
Hevner, R.F.1
Wong-Riley, M.T.2
-
107
-
-
0025024024
-
Cytochrome oxidase deficiency in Alzheimer’s disease
-
Parker, W.D., Jr, Filley, C.M. and Parks, J.K. (1990), ‘Cytochrome oxidase deficiency in Alzheimer’s disease’, Neurology Vol. 40, pp. 1302–1303.
-
(1990)
Neurology
, vol.40
, pp. 1302-1303
-
-
Parker, W.D.1
Filley, C.M.2
Parks, J.K.3
-
108
-
-
0028201012
-
Reduced platelet cytochrome c oxidase activity in Alzheimer’s disease
-
Parker, W.D., Jr, Mahr, N.J., Filley, C.M., Parks, J.K. et al. (1994), ‘Reduced platelet cytochrome c oxidase activity in Alzheimer’s disease’, Neurology Vol. 44, pp. 1086–1090.
-
(1994)
Neurology
, vol.44
, pp. 1086-1090
-
-
Parker, W.D.1
Mahr, N.J.2
Filley, C.M.3
Parks, J.K.4
-
109
-
-
0031036773
-
Decreased expression of nuclear and mitochondrial DNA-encoded genes of oxidative phosphorylation in association neocortex in Alzheimer disease
-
Chandrasekaran, K., Hatanpää, K., Rapoport, S.I. and Brady, D.R. (1997), ‘Decreased expression of nuclear and mitochondrial DNA-encoded genes of oxidative phosphorylation in association neocortex in Alzheimer disease’, Brain Res. Mol. Brain Res. Vol. 44, pp. 99–104.
-
(1997)
Brain Res. Mol. Brain Res
, vol.44
, pp. 99-104
-
-
Chandrasekaran, K.1
Hatanpää, K.2
Rapoport, S.I.3
Brady, D.R.4
-
110
-
-
0036231792
-
Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer’s disease
-
Bosetti, F., Brizzi, F., Barogi, S., Mancuso, M. et al. (2002), ‘Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer’s disease’, Neurobiol. Aging Vol. 23, pp. 371–376.
-
(2002)
Neurobiol. Aging
, vol.23
, pp. 371-376
-
-
Bosetti, F.1
Brizzi, F.2
Barogi, S.3
Mancuso, M.4
-
111
-
-
0348111546
-
Cytochrome c oxidase is decreased in Alzheimer’s disease platelets
-
Cardoso, S.M., Proenca, M.T., Santos, S. and de Oliveira, C.R. (2004), ‘Cytochrome c oxidase is decreased in Alzheimer’s disease platelets’, Neurobiol. Aging Vol. 25, pp. 105–110.
-
(2004)
Neurobiol. Aging
, vol.25
, pp. 105-110
-
-
Cardoso, S.M.1
Proenca, M.T.2
Santos, S.3
de Oliveira, C.R.4
-
112
-
-
33751406988
-
Impaired platelet mitochondrial activity in Alzheimer’s disease and mild cognitive impairment
-
Valla, J., Schneider, L., Niedzielko, T., Coon, K.D. et al. (2006), ‘Impaired platelet mitochondrial activity in Alzheimer’s disease and mild cognitive impairment’, Mitochondrion Vol. 6, pp. 323–330.
-
(2006)
Mitochondrion
, vol.6
, pp. 323-330
-
-
Valla, J.1
Schneider, L.2
Niedzielko, T.3
Coon, K.D.4
-
113
-
-
0031585485
-
Oxidative metabolism in cultured fibroblasts derived from sporadic Alzheimer’s disease (AD) patients
-
Curti, D., Rognoni, F., Gasparini, L., Cattaneo, A. et al. (1997), ‘Oxidative metabolism in cultured fibroblasts derived from sporadic Alzheimer’s disease (AD) patients’, Neurosci. Lett. Vol. 236, pp. 13–16.
-
(1997)
Neurosci. Lett
, vol.236
, pp. 13-16
-
-
Curti, D.1
Rognoni, F.2
Gasparini, L.3
Cattaneo, A.4
-
114
-
-
0026718966
-
Brain cytochrome oxidase in Alzheimer’s disease
-
Kish, S.J., Bergeron, C., Rajput, A.H., Dozic, S. et al. (1992), ‘Brain cytochrome oxidase in Alzheimer’s disease’, J. Neurochem. Vol. 59, pp. 776–779.
-
(1992)
J. Neurochem
, vol.59
, pp. 776-779
-
-
Kish, S.J.1
Bergeron, C.2
Rajput, A.H.3
Dozic, S.4
-
115
-
-
0017280471
-
The construction of viable nuclear-cytoplasmic hybrid cells by nuclear transplantation
-
Lucas, J.J. and Kates, J.R. (1976), ‘The construction of viable nuclear-cytoplasmic hybrid cells by nuclear transplantation’, Cell Vol. 7, pp. 397–405.
-
(1976)
Cell
, vol.7
, pp. 397-405
-
-
Lucas, J.J.1
Kates, J.R.2
-
116
-
-
3042806534
-
A “mitochondrial cascade hypothesis” for sporadic Alzheimer’s disease
-
Swerdlow, R.H. and Khan, S.M. (2004), ‘A “mitochondrial cascade hypothesis” for sporadic Alzheimer’s disease’, Med. Hypotheses Vol. 63, pp. 8–20.
-
(2004)
Med. Hypotheses
, vol.63
, pp. 8-20
-
-
Swerdlow, R.H.1
Khan, S.M.2
-
117
-
-
0030724118
-
Cybrids in Alzheimer’s disease: A cellular model of the disease?
-
Swerdlow, R.H., Parks, J.K., Cassarino, D.S., Maguire, D.J. et al. (1997), ‘Cybrids in Alzheimer’s disease: A cellular model of the disease?’, Neurology Vol. 49, pp. 918–925.
-
(1997)
Neurology
, vol.49
, pp. 918-925
-
-
Swerdlow, R.H.1
Parks, J.K.2
Cassarino, D.S.3
Maguire, D.J.4
-
118
-
-
0033866833
-
Alzheimer’s disease cybrids replicate beta-amyloid abnormalities through cell death pathways
-
Khan, S.M., Cassarino, D.S., Abramova, N.N., Keeney, P.M. et al. (2000), ‘Alzheimer’s disease cybrids replicate beta-amyloid abnormalities through cell death pathways’, Ann. Neurol. Vol. 48, pp. 148–155.
-
(2000)
Ann. Neurol
, vol.48
, pp. 148-155
-
-
Khan, S.M.1
Cassarino, D.S.2
Abramova, N.N.3
Keeney, P.M.4
-
119
-
-
0034102780
-
Abnormal mitochondrial morphology in sporadic Parkinson’s and Alzheimer’s disease cybrid cell lines
-
Trimmer, P.A., Swerdlow, R.H., Parks, J.K., Keeney, P.M. et al. (2000), ‘Abnormal mitochondrial morphology in sporadic Parkinson’s and Alzheimer’s disease cybrid cell lines’, Exp. Neurol. Vol. 162, pp. 37–50.
-
(2000)
Exp. Neurol
, vol.162
, pp. 37-50
-
-
Trimmer, P.A.1
Swerdlow, R.H.2
Parks, J.K.3
Keeney, P.M.4
-
120
-
-
3042513691
-
Mitochondria dysfunction of Alzheimer’s disease cybrids enhances Abeta toxicity
-
Cardoso, S.M., Santana, I., Swerdlow, R.H. and Oliveira, C.R. (2004), ‘Mitochondria dysfunction of Alzheimer’s disease cybrids enhances Abeta toxicity’, J. Neurochem. Vol. 89, pp. 1417–1426.
-
(2004)
J. Neurochem
, vol.89
, pp. 1417-1426
-
-
Cardoso, S.M.1
Santana, I.2
Swerdlow, R.H.3
Oliveira, C.R.4
-
121
-
-
3242668604
-
Alzheimer’s brains harbor somatic mtDNA controlregion mutations that suppress mito-chondrial transcription and replication
-
Coskun, P.E., Beal, M.F. and Wallace, D.C. (2004), ‘Alzheimer’s brains harbor somatic mtDNA controlregion mutations that suppress mito-chondrial transcription and replication’, Proc. Natl. Acad. Sci. USA Vol. 101, pp. 10726–10731.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 10726-10731
-
-
Coskun, P.E.1
Beal, M.F.2
Wallace, D.C.3
-
122
-
-
0035125774
-
Point mutations of the mtDNA control region in normal and neurode-generative human brains
-
Chinnery, P.F., Taylor, G.A., Howell, N., Brown, D.T. et al. (2001), ‘Point mutations of the mtDNA control region in normal and neurode-generative human brains’, Am. J. Hum. Genet. Vol. 68, pp. 529–532.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 529-532
-
-
Chinnery, P.F.1
Taylor, G.A.2
Howell, N.3
Brown, D.T.4
-
123
-
-
0027933135
-
Marked changes in mitochondrial DNA deletion levels in Alzheimer brains
-
Corral-Debrinski, M., Horton, T., Lott, M.T., Shoffner, J.M. et al. (1994), ‘Marked changes in mitochondrial DNA deletion levels in Alzheimer brains’, Genomics Vol. 23, pp. 471–476.
-
(1994)
Genomics
, vol.23
, pp. 471-476
-
-
Corral-Debrinski, M.1
Horton, T.2
Lott, M.T.3
Shoffner, J.M.4
-
124
-
-
0030811838
-
Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer’s and Parkinson’s diseases
-
Egensperger, R., Kosel, S., Schnopp, N.M., Mehraein, P. et al. (1997). ‘Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer’s and Parkinson’s diseases’, Neuropathol. Appl. Neurobiol. Vol. 23, pp. 315–321.
-
(1997)
Neuropathol. Appl. Neurobiol
, vol.23
, pp. 315-321
-
-
Egensperger, R.1
Kosel, S.2
Schnopp, N.M.3
Mehraein, P.4
-
125
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
Shoffner, J.M., Brown, M.D., Torroni, A., Lott, M.T. et al. (1993), ‘Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients’, Genomics Vol. 17, pp. 171–184.
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.M.1
Brown, M.D.2
Torroni, A.3
Lott, M.T.4
-
126
-
-
0028843809
-
No association found between Alzheimer’s disease and a mitochondrial tRNA glutamine gene variant
-
Wragg, M.A., Talbot, C.J., Morris, J.C., Lendon, C.L. et al. (1995), ‘No association found between Alzheimer’s disease and a mitochondrial tRNA glutamine gene variant’, Neurosci. Lett. Vol. 201, pp. 107–110.
-
(1995)
Neurosci. Lett
, vol.201
, pp. 107-110
-
-
Wragg, M.A.1
Talbot, C.J.2
Morris, J.C.3
Lendon, C.L.4
-
127
-
-
17744397107
-
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer’s disease
-
Carrieri, G., Bonafe, M., De Luca, M., Rose, G. et al. (2001), ‘Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer’s disease’, Hum. Genet. Vol. 108, pp. 194–198.
-
(2001)
Hum. Genet
, vol.108
, pp. 194-198
-
-
Carrieri, G.1
Bonafe, M.2
de Luca, M.3
Rose, G.4
-
128
-
-
3242707016
-
Analysis of European mitochondrial haplogroups with Alzheimer disease risk
-
van der Walt, J.M., Dementieva, Y.A., Martin, E.R., Scott, W.K. et al. (2004), ‘Analysis of European mitochondrial haplogroups with Alzheimer disease risk’, Neurosci. Lett. Vol. 365, pp. 28–32.
-
(2004)
Neurosci. Lett
, vol.365
, pp. 28-32
-
-
van der Walt, J.M.1
Dementieva, Y.A.2
Martin, E.R.3
Scott, W.K.4
-
129
-
-
0033516529
-
Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population
-
Chagnon, P., Gee, M., Filion, M., Robitaille, Y. et al. (1999), ‘Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population’, Am. J. Med.Genet. Vol. 85, pp. 20–30.
-
(1999)
Am. J. Med.Genet.
, vol.85
, pp. 20-30
-
-
Chagnon, P.1
Gee, M.2
Filion, M.3
Robitaille, Y.4
-
130
-
-
59849089676
-
Microsatellite repeat instability and neurological disease
-
Brouwer, J.R., Willemsen, R. and Oostra, B.A. (2009), ‘Microsatellite repeat instability and neurological disease’, Bioessays Vol. 31, pp. 71–83.
-
(2009)
Bioessays
, vol.31
, pp. 71-83
-
-
Brouwer, J.R.1
Willemsen, R.2
Oostra, B.A.3
-
131
-
-
0033033679
-
Age of onset in Huntington disease: Sex specific influence of apolipoprotein E genotype and normal CAG repeat length
-
Kehoe, J.P., Krawczak, M., Harper, P.S., Owen, M.J. et al. (1999), ‘Age of onset in Huntington disease: Sex specific influence of apolipoprotein E genotype and normal CAG repeat length’, J. Med. Genet. Vol. 36, pp. 108–111.
-
(1999)
J. Med. Genet
, vol.36
, pp. 108-111
-
-
Kehoe, J.P.1
Krawczak, M.2
Harper, P.S.3
Owen, M.J.4
-
132
-
-
2542583041
-
Fragile X mental retardation syndrome: From pathogenesis to diagnostic issue
-
Suppl. 1)
-
Mandel, J.L. and Biancalana, V. (2004), ‘Fragile X mental retardation syndrome: From pathogenesis to diagnostic issue’, Growth Horm. IGF Res. Vol. 14 (Suppl. 1), pp. 158–165.
-
(2004)
Growth Horm. IGF Res
, vol.14
, pp. 158-165
-
-
Mandel, J.L.1
Biancalana, V.2
-
133
-
-
57049116558
-
Predictors of progression in patients with Friedreich ataxia
-
La Pean, A., Jeffries, N., Grow, C., Ravina, B. et al. (2008), ‘Predictors of progression in patients with Friedreich ataxia’, Mov. Disord. Vol. 23, pp. 2026–2032.
-
(2008)
Mov. Disord
, vol.23
, pp. 2026-2032
-
-
la Pean, A.1
Jeffries, N.2
Grow, C.3
Ravina, B.4
-
134
-
-
54049141673
-
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients
-
Botta, A., Rinaldi, F., Catalli, C., Vergani, L. et al. (2009), ‘The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients’, J.Med. Genet. Vol. 45, pp. 639–646.
-
(2009)
J.Med. Genet
, vol.45
, pp. 639-646
-
-
Botta, A.1
Rinaldi, F.2
Catalli, C.3
Vergani, L.4
-
135
-
-
0032784090
-
Molecular genetic characterisation of frontotemporal dementia on chromosome 3
-
Ashworth, A., Lloyd, S., Brown, J., Gydesen, S. et al. (1999), ‘Molecular genetic characterisation of frontotemporal dementia on chromosome 3’, Dement. Geriatr. Cogn. Disord. Vol. 10, pp. 93–101.
-
(1999)
Dement. Geriatr. Cogn. Disord
, vol.10
, pp. 93-101
-
-
Ashworth, A.1
Lloyd, S.2
Brown, J.3
Gydesen, S.4
-
136
-
-
33748904800
-
Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease
-
Mackenzie, I.R., Butland, S.L., Devon, R.S., Dwosh, E. et al. (2006), ‘Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease’, BMC Neurol. Vol. 6, pp. 32–38.
-
(2006)
BMC Neurol
, vol.6
, pp. 32-38
-
-
Mackenzie, I.R.1
Butland, S.L.2
Devon, R.S.3
Dwosh, E.4
-
137
-
-
2542596183
-
Parkinson’s disease
-
Samii, A., Nutt, J.G. and Ransom, B.R. (2004), ‘Parkinson’s disease’, Lancet Vol. 363, pp. 1783–1793.
-
(2004)
Lancet
, vol.363
, pp. 1783-1793
-
-
Samii, A.1
Nutt, J.G.2
Ransom, B.R.3
-
138
-
-
57149109123
-
Movement disorders: Insights into mechanisms and hopes for treatment
-
Wider, C. and Wszolek, Z.K. (2009), ‘Movement disorders: Insights into mechanisms and hopes for treatment’, Lancet Neurol. Vol. 8, pp. 8 – 10.
-
(2009)
Lancet Neurol
, vol.8
, pp. 8-10
-
-
Wider, C.1
Wszolek, Z.K.2
-
139
-
-
68649108355
-
Mitochondrial dysfunction in the limelight of Parkinson’s disease pathogenesis
-
Banerjee, R., Starkov, A.A., Beal, M.F. and Thomas, B. (2008), ‘Mitochondrial dysfunction in the limelight of Parkinson’s disease pathogenesis’, Biochim. Biophys. Acta Vol. 1792, pp. 651–663.
-
(2008)
Biochim. Biophys. Acta
, vol.1792
, pp. 651-663
-
-
Banerjee, R.1
Starkov, A.A.2
Beal, M.F.3
Thomas, B.4
-
140
-
-
0035123216
-
Gender ratio differences between Parkinson’s disease patients and their affected relatives
-
Swerdlow, R.H., Parker, W.D., Currie, L.J., Bennett, J.P. et al. (2001), ‘Gender ratio differences between Parkinson’s disease patients and their affected relatives’, Parkinsonism Relat. Disord. Vol. 7, pp. 129–133.
-
(2001)
Parkinsonism Relat. Disord
, vol.7
, pp. 129-133
-
-
Swerdlow, R.H.1
Parker, W.D.2
Currie, L.J.3
Bennett, J.P.4
-
141
-
-
1842335744
-
Maternal inheritance in Parkinson’s disease
-
Wooten, G.F., Currie, L.J., Bennet, J.P., Harrison, M.B. et al. (1997), ‘Maternal inheritance in Parkinson’s disease’, Ann. Neurol. Vol. 41, pp. 265–268.
-
(1997)
Ann. Neurol
, vol.41
, pp. 265-268
-
-
Wooten, G.F.1
Currie, L.J.2
Bennet, J.P.3
Harrison, M.B.4
-
142
-
-
0037385480
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
-
van der Walt, J.M., Nicodemus, K.K., Martin, E.R., Scott, W.K. et al. (2003), ‘Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease’, Am. J. Hum. Genet. Vol. 72, pp. 804–811.
-
(2003)
Am. J. Hum. Genet
, vol.72
, pp. 804-811
-
-
van der Walt, J.M.1
Nicodemus, K.K.2
Martin, E.R.3
Scott, W.K.4
-
143
-
-
20144389920
-
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD
-
Pyle, A., Foltynie, T., Tiangyou, W., Lambert, C. et al. (2005), ‘Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD’, Ann. Neurol. Vol. 57, pp. 564–567.
-
(2005)
Ann. Neurol
, vol.57
, pp. 564-567
-
-
Pyle, A.1
Foltynie, T.2
Tiangyou, W.3
Lambert, C.4
-
144
-
-
2942750228
-
Mitochondrial DNA polymorphisms as risk factors for Parkinson’s disease and Parkinson’s disease dementia
-
Autere, J., Moilanen, J.S., Finnila, S., Soininen, H. et al. (2004), ‘Mitochondrial DNA polymorphisms as risk factors for Parkinson’s disease and Parkinson’s disease dementia’, Hum. Genet. Vol. 115, pp. 29–35.
-
(2004)
Hum. Genet
, vol.115
, pp. 29-35
-
-
Autere, J.1
Moilanen, J.S.2
Finnila, S.3
Soininen, H.4
-
145
-
-
0033794686
-
Mitochondrial ND1 sequence analysis and association of the T4216C mutation with Parkinson’s disease
-
Kirchner, S.C., Hallagan, S.E., Farin, F.M., Dilley, J. et al. (2000), ‘Mitochondrial ND1 sequence analysis and association of the T4216C mutation with Parkinson’s disease’, Neurotoxicology Vol. 21, pp. 441–445.
-
(2000)
Neurotoxicology
, vol.21
, pp. 441-445
-
-
Kirchner, S.C.1
Hallagan, S.E.2
Farin, F.M.3
Dilley, J.4
-
146
-
-
24044555258
-
Mitochondrial DNA polymorphisms and risk of Parkinson’s disease in Spanish population
-
Huerta, C., Castro, M.G., Coto, E., Blazquez, M. et al. (2005), ‘Mitochondrial DNA polymorphisms and risk of Parkinson’s disease in Spanish population’, J. Neurol. Sci. Vol. 236, pp. 49–54.
-
(2005)
J. Neurol. Sci
, vol.236
, pp. 49-54
-
-
Huerta, C.1
Castro, M.G.2
Coto, E.3
Blazquez, M.4
-
147
-
-
0033837202
-
Variability and validity of polymorphism association studies in Parkinson’s disease
-
Tan, E.K., Khajavi, M., Thornby, J.I., Nagamitsu, S. et al. (2000), ‘Variability and validity of polymorphism association studies in Parkinson’s disease’, Neurology Vol. 55, pp. 533–538.
-
(2000)
Neurology
, vol.55
, pp. 533-538
-
-
Tan, E.K.1
Khajavi, M.2
Thornby, J.I.3
Nagamitsu, S.4
-
148
-
-
0020680904
-
Chronic parkinsonism in humans due to a product of meperidine-analog syn-thesis
-
Langston, J.W., Ballard, P.A., Tetrud, J.W. and Irwin, I. (1983), ‘Chronic parkinsonism in humans due to a product of meperidine-analog syn-thesis’, Science Vol. 219, pp. 979–980.
-
(1983)
Science
, vol.219
, pp. 979-980
-
-
Langston, J.W.1
Ballard, P.A.2
Tetrud, J.W.3
Irwin, I.4
-
149
-
-
0033681149
-
Chronic systemic pesticide exposure reproduces features of Parkinson’s disease
-
Betarbet, R., Sherer, T.B., MacKenzie, G., Garcia-Osuna, M. et al. (2000), ‘Chronic systemic pesticide exposure reproduces features of Parkinson’s disease’, Nat. Neurosci. Vol. 3, pp. 1301–1306.
-
(2000)
Nat. Neurosci
, vol.3
, pp. 1301-1306
-
-
Betarbet, R.1
Sherer, T.B.2
Mackenzie, G.3
Garcia-Osuna, M.4
-
150
-
-
0024390719
-
Mitochondrial complex I deficiency in Parkinson’s disease
-
Schapira, A.H.V., Cooper, J.M., Dexter, D., Jenner, P. et al. (1989), ‘Mitochondrial complex I deficiency in Parkinson’s disease’, Lancet Vol. 1, p. 1269.
-
(1989)
Lancet
, vol.1
, pp. 1269
-
-
Schapira, A.H.V.1
Cooper, J.M.2
Dexter, D.3
Jenner, P.4
-
151
-
-
0024334283
-
Mitochondrial function in Parkinson’s disease
-
Bindoff, L.A., Birch-Machin, M., Cartlidge, N.E.F., Parker, W.D.J. et al. (1989), ‘Mitochondrial function in Parkinson’s disease’, Lancet Vol. 2, p. 49.
-
(1989)
Lancet
, vol.2
, pp. 49
-
-
Bindoff, L.A.1
Birch-Machin, M.2
Cartlidge, N.E.F.3
Parker, W.D.J.4
-
152
-
-
0024848034
-
Electron transport chain abnormalities in idiopathic Parkinson’s disease
-
Parker, W.D., Jr, Boyson, S.J. and Parks, J.K. (1989), ‘Electron transport chain abnormalities in idiopathic Parkinson’s disease’, Ann. Neurol. Vol. 26, pp. 719–723.
-
(1989)
Ann. Neurol
, vol.26
, pp. 719-723
-
-
Parker, W.D.1
Boyson, S.J.2
Parks, J.K.3
-
153
-
-
34250716407
-
Mitochondrial dysfunction in Parkinson’s disease
-
Schapira, A.H. (2007), ‘Mitochondrial dysfunction in Parkinson’s disease’, Cell Death Differ. Vol. 14, pp. 1261–1266.
-
(2007)
Cell Death Differ
, vol.14
, pp. 1261-1266
-
-
Schapira, A.H.1
-
154
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson’s disease
-
Swerdlow, R.H., Parks, J.K., Miller, S.W., Tuttle, J.B. et al. (1996), ‘Origin and functional consequences of the complex I defect in Parkinson’s disease’, Ann. Neurol. Vol. 40, pp. 663–671.
-
(1996)
Ann. Neurol
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
Tuttle, J.B.4
-
155
-
-
34347353834
-
Mitochondria in cybrids containing mtDNA from persons with mitochondriopathies
-
Swerdlow, R.H. (2007), ‘Mitochondria in cybrids containing mtDNA from persons with mitochondriopathies’, J. Neurosci. Res. Vol. 85, pp. 3416–3428.
-
(2007)
J. Neurosci. Res.
, vol.85
, pp. 3416-3428
-
-
Swerdlow, R.H.1
-
156
-
-
0031792679
-
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson’s disease family
-
Swerdlow, R.H., Parks, J.K., Davis, J.N., Cassarino, D.S. et al. (1998), ‘Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson’s disease family’, Ann. Neurol. Vol. 44, pp. 873–881.
-
(1998)
Ann. Neurol
, vol.44
, pp. 873-881
-
-
Swerdlow, R.H.1
Parks, J.K.2
Davis, J.N.3
Cassarino, D.S.4
-
157
-
-
33847716347
-
The clinical diagnosis and molecular genetics of Kearns –Sayre syndrome: A complex mitochondrial encephalomyopathy
-
Maceluch, J.A. and Niedziela, M.(2007), ‘The clinical diagnosis and molecular genetics of Kearns –Sayre syndrome: A complex mitochondrial encephalomyopathy’, Pediatr. Endocrinol. Rev. Vol. 4, pp. 117–137.
-
(2007)
Pediatr. Endocrinol. Rev
, vol.4
, pp. 117-137
-
-
Maceluch, J.A.1
Niedziela, M.2
-
159
-
-
0036372802
-
Clinical features and genetics of myoclonic epilepsy with ragged red fibers
-
DiMauro, S., Hirano, M., Kaufmann, P., Tanji, K. et al. (2002), ‘Clinical features and genetics of myoclonic epilepsy with ragged red fibers’, Adv. Neurol. Vol. 89, pp. 217–229.
-
(2002)
Adv. Neurol
, vol.89
, pp. 217-229
-
-
Dimauro, S.1
Hirano, M.2
Kaufmann, P.3
Tanji, K.4
-
160
-
-
0025267548
-
A new mitochondrial disease associated with mitochon-drial DNA heteroplasmy
-
Holt, I.J., Harding, A.E., Petty, R.K.H. and Morgan-Hughes, J.A. (1990), ‘A new mitochondrial disease associated with mitochon-drial DNA heteroplasmy’, Am. J. Hum. Genet. Vol. 46, pp. 428–433.
-
(1990)
Am. J. Hum. Genet
, vol.46
, pp. 428-433
-
-
Holt, I.J.1
Harding, A.E.2
Petty, R.K.H.3
Morgan-Hughes, J.A.4
-
161
-
-
33745870877
-
Leber’s hereditary optic neuropathy: A multifactorial disease
-
Yen, M.Y., Wang, A.G. and Wei, Y.H. (2006), ‘Leber’s hereditary optic neuropathy: A multifactorial disease’, Prog. Retin. Eye Res. Vol. 25, pp. 381–396.
-
(2006)
Prog. Retin. Eye Res
, vol.25
, pp. 381-396
-
-
Yen, M.Y.1
Wang, A.G.2
Wei, Y.H.3
-
162
-
-
0029979139
-
A novel mitochondrial DNA point mutation in the tRNAIle gene is associated with progressive external ophthalmoplegia
-
Silvestri, G., Servidei, S., Rana, M., Ricci, E. et al. (1996), ‘A novel mitochondrial DNA point mutation in the tRNAIle gene is associated with progressive external ophthalmoplegia’, Biochem. Biophys. Res. Comm. Vol. 220, pp. 623–627.
-
(1996)
Biochem. Biophys. Res. Comm
, vol.220
, pp. 623-627
-
-
Silvestri, G.1
Servidei, S.2
Rana, M.3
Ricci, E.4
-
163
-
-
65549148928
-
A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and-DQ status and autoantibody pattern
-
Hosszufalusi, N., Karcagi, V., Horvath, R., Palik, E. et al. (2009), ‘A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and-DQ status and autoantibody pattern’, Diabetes Metab. Res. Rev. Vol. 25, pp. 127–135.
-
(2009)
Diabetes Metab. Res. Rev.
, vol.25
, pp. 127-135
-
-
Hosszufalusi, N.1
Karcagi, V.2
Horvath, R.3
Palik, E.4
-
164
-
-
32044452016
-
Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy
-
Pal, D.K., Durner, M., Klotz, I., Dicker, E. et al. (2006), ‘Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy’, Brain Dev. Vol. 28, pp. 92–98.
-
(2006)
Brain Dev
, vol.28
, pp. 92-98
-
-
Pal, D.K.1
Durner, M.2
Klotz, I.3
Dicker, E.4
-
165
-
-
0031004189
-
Sex of parent transmission effect in Tourette’s syndrome: Evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect
-
Eapen, V., O’Neill, J., Gurling, H.M. and Robertson, M.M. (1997), ‘Sex of parent transmission effect in Tourette’s syndrome: Evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect’, Neurology Vol. 48, pp. 801–802.
-
(1997)
Neurology
, vol.48
, pp. 801-802
-
-
Eapen, V.1
O’Neill, J.2
Gurling, H.M.3
Robertson, M.M.4
-
166
-
-
49449111926
-
Mechanisms of imprinting of the Prader –Willi/Angelman region
-
Horsthemke, B. and Wagstaff, J. (2008), ‘Mechanisms of imprinting of the Prader –Willi/Angelman region’, Am. J. Med. Genet. Vol. 146, pp. 2041–2052.
-
(2008)
Am. J. Med. Genet.
, vol.146
, pp. 2041-2052
-
-
Horsthemke, B.1
Wagstaff, J.2
-
167
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook, E.H., Jr, Lindgren, V., Leventhal, B.L., Courchesne, R. et al. (1997), ‘Autism or atypical autism in maternally but not paternally derived proximal 15q duplication’, Am. J. Hum.Genet. Vol. 60, pp. 928–934.
-
(1997)
Am. J. Hum.Genet
, vol.60
, pp. 928-934
-
-
Cook, E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
-
168
-
-
0036487995
-
The role of mtDNA background in disease expression: A new primary LHON mutation associated with Western Eurasian hap-logroup
-
Brown, M.D., Starikovskaya, E., Derbeneva, O., Hosseini, S. et al. (2002), ‘The role of mtDNA background in disease expression: A new primary LHON mutation associated with Western Eurasian hap-logroup’, J. Hum. Genet. Vol. 110, pp. 130–138.
-
(2002)
J. Hum. Genet
, vol.110
, pp. 130-138
-
-
Brown, M.D.1
Starikovskaya, E.2
Derbeneva, O.3
Hosseini, S.4
-
169
-
-
0035949487
-
Presenilin, Notch, and the genesis and treatment of Alzheimer’s disease
-
Selkoe, D.J. (2001), ‘Presenilin, Notch, and the genesis and treatment of Alzheimer’s disease’, Proc. Natl. Acad. Sci. USA Vol. 98, pp. 11039–11041.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 11039-11041
-
-
Selkoe, D.J.1
-
170
-
-
0034604340
-
Alzheimer’s disease: Neurodevelopment converges with neurodegeneration
-
Bothwell, M. and Giniger, E. (2000), ‘Alzheimer’s disease: Neurodevelopment converges with neurodegeneration’, Cell Vol. 102, pp. 271–273.
-
(2000)
Cell
, vol.102
, pp. 271-273
-
-
Bothwell, M.1
Giniger, E.2
-
171
-
-
60549089207
-
APP binds DR6 to trigger axon pruning and neuron death via distinct caspases
-
Nikolaev, A., McLaughlin, T., O’Leary, D.D. and Tessier –Lavigne, M. (2009), ‘APP binds DR6 to trigger axon pruning and neuron death via distinct caspases’, Nature Vol. 457, pp. 981–989.
-
(2009)
Nature
, vol.457
, pp. 981-989
-
-
Nikolaev, A.1
McLaughlin, T.2
O’Leary, D.D.3
Tessier, –.4
|