-
1
-
-
0034233474
-
Oxidative processes in Alzheimer's disease: The role of Aβ-metal interactions
-
Lynch T, Cherny RA, Bush AI: Oxidative processes in Alzheimer's disease: The role of Aβ-metal interactions. Exp Gerontol 2000;35:445-451.
-
(2000)
Exp Gerontol
, vol.35
, pp. 445-451
-
-
Lynch, T.1
Cherny, R.A.2
Bush, A.I.3
-
2
-
-
0030885482
-
Iron accumulation in Alzheimer d isease is a source of redox-generated free radicals
-
Smith MA, Harris PLR, Sayre LM, Perry G: Iron accumulation in Alzheimer d isease is a source of redox-generated free radicals. Proc Natl Acad Sci USA 1997;94:9866-9868.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 9866-9868
-
-
Smith, M.A.1
Harris, P.L.R.2
Sayre, L.M.3
Perry, G.4
-
4
-
-
0031467468
-
Association of transferrin C2 allele with late-onset Alzheimer's disease
-
Namekata K, Imagawa M, Terashi A, Ohta S, Oyama F, Ihara Y: Association of transferrin C2 allele with late-onset Alzheimer's disease. Hum Genet 1997;101:126-129.
-
(1997)
Hum Genet
, vol.101
, pp. 126-129
-
-
Namekata, K.1
Imagawa, M.2
Terashi, A.3
Ohta, S.4
Oyama, F.5
Ihara, Y.6
-
5
-
-
0035958815
-
Transferrin C2 variant does not confer a risk for Alzheimer's disease in Koreans
-
Kim KW, Jhoo JH, Lee JH, Lee DY, Lee KU, Youn JY, Woo JI: Transferrin C2 variant does not confer a risk for Alzheimer's disease in Koreans. Neurosci Lett 2001;308:45-48.
-
(2001)
Neurosci Lett
, vol.308
, pp. 45-48
-
-
Kim, K.W.1
Jhoo, J.H.2
Lee, J.H.3
Lee, D.Y.4
Lee, K.U.5
Youn, J.Y.6
Woo, J.I.7
-
6
-
-
0037016591
-
Transferrin gene polymorphism in Alzheimer's disease and dementia with Lewy bodies in humans
-
Hussain RI, Ballard CG, Edwarson JA, Morris CM: Transferrin gene polymorphism in Alzheimer's disease and dementia with Lewy bodies in humans. Neurosci Lett 2002;317:13-16.
-
(2002)
Neurosci Lett
, vol.317
, pp. 13-16
-
-
Hussain, R.I.1
Ballard, C.G.2
Edwarson, J.A.3
Morris, C.M.4
-
7
-
-
0035474950
-
Recent advances in disorders of iron metabolism: Mutations, mechanisms and modifiers
-
Roy CN, Andrews NC: Recent advances in disorders of iron metabolism: Mutations, mechanisms and modifiers. Hum Mol Genet 2001;10:2181-2186.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2181-2186
-
-
Roy, C.N.1
Andrews, N.C.2
-
8
-
-
0034949432
-
Hereditary hemochromatosis since discovery of the HFE gene
-
Lyon E, Frank E: Hereditary hemochromatosis since discovery of the HFE gene. Clin Chem 2001;47:1147-1156.
-
(2001)
Clin Chem
, vol.47
, pp. 1147-1156
-
-
Lyon, E.1
Frank, E.2
-
9
-
-
0034964682
-
The hemochromatosis gene affects the age of onset of sporadic Alzheimer's disease
-
Sampietro M, Caputo L, Casatta A, Meregalli M, Pellagatti A, Tagliabue J, Annoni G, Vergani C: The hemochromatosis gene affects the age of onset of sporadic Alzheimer's disease. Neurobiol Aging 2001;22:563-568.
-
(2001)
Neurobiol Aging
, vol.22
, pp. 563-568
-
-
Sampietro, M.1
Caputo, L.2
Casatta, A.3
Meregalli, M.4
Pellagatti, A.5
Tagliabue, J.6
Annoni, G.7
Vergani, C.8
-
10
-
-
0021271971
-
Clinical diagnosis of Alzheimer disease: Report of the NINCDS-ADRDA Work Group under the auspices of the Department of Health and Human Services Task Force on Alzheimer Disease
-
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM: Clinical diagnosis of Alzheimer disease: Report of the NINCDS-ADRDA Work Group under the auspices of the Department of Health and Human Services Task Force on Alzheimer Disease. Neurology 1984;24:939-944.
-
(1984)
Neurology
, vol.24
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
11
-
-
17044442568
-
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
-
Sánchez M, Bruguera M, Bosch J, Rodés J, Ballesta F, Oliva R: Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls. J Hepatol 1998;29:725-728.
-
(1998)
J Hepatol
, vol.29
, pp. 725-728
-
-
Sánchez, M.1
Bruguera, M.2
Bosch, J.3
Rodés, J.4
Ballesta, F.5
Oliva, R.6
-
12
-
-
0034601251
-
Are hereditary hemochromatosis mutations involved in Alzheimer disease?
-
Moalem S, Percy ME, Andrews DF, Kruck TPA, Wong S, Dalton AJ, Mehta P, Fedor B, Warren AC: Are hereditary hemochromatosis mutations involved in Alzheimer disease? Am J Med Genet 2000;93:58-66.
-
(2000)
Am J Med Genet
, vol.93
, pp. 58-66
-
-
Moalem, S.1
Percy, M.E.2
Andrews, D.F.3
Kruck, T.P.A.4
Wong, S.5
Dalton, A.J.6
Mehta, P.7
Fedor, B.8
Warren, A.C.9
-
13
-
-
0033954735
-
Differential oxidation of apolipoprotein E isoforms and interaction with phospholipids
-
Jolivalt C, Leininger-Muller B, Bertrand P, Herber R, Christen Y, Siest G: Differential oxidation of apolipoprotein E isoforms and interaction with phospholipids. Free Radic Biol Med 2000;28:129-140.
-
(2000)
Free Radic Biol Med
, vol.28
, pp. 129-140
-
-
Jolivalt, C.1
Leininger-Muller, B.2
Bertrand, P.3
Herber, R.4
Christen, Y.5
Siest, G.6
-
14
-
-
0034720842
-
Apolipoprotein E allele-dependent antioxidant activity in brains with Alzheimer's disease
-
Tamaoka A, Miyatake R, Matsuno S, Ishii K, Nagase S, Sahara N, Ono S, Mori H, Wakabayashi K, Tsuji S, Takahashi H, Shoji S: Apolipoprotein E allele-dependent antioxidant activity in brains with Alzheimer's disease. Neurology 2000;54:2319-2321.
-
(2000)
Neurology
, vol.54
, pp. 2319-2321
-
-
Tamaoka, A.1
Miyatake, R.2
Matsuno, S.3
Ishii, K.4
Nagase, S.5
Sahara, N.6
Ono, S.7
Mori, H.8
Wakabayashi, K.9
Tsuji, S.10
Takahashi, H.11
Shoji, S.12
-
15
-
-
0037016321
-
Apolipoprotein E modulates Alzheimer's Aβ (1-42)-induced oxidative damage to synaptosomes in an allele-specific manner
-
Lauderback CM, Kanski J, Hackett JM, Maeda N, Kindy MS, Butterfield DA: Apolipoprotein E modulates Alzheimer's Aβ (1-42)-induced oxidative damage to synaptosomes in an allele-specific manner. Brain Res 2002;924:90-97.
-
(2002)
Brain Res
, vol.924
, pp. 90-97
-
-
Lauderback, C.M.1
Kanski, J.2
Hackett, J.M.3
Maeda, N.4
Kindy, M.S.5
Butterfield, D.A.6
|