-
1
-
-
0037164344
-
Genetics of haemochromatosis
-
Bomford A: Genetics of haemochromatosis. The Lancet 2002, 360(9346):1673-1681.
-
(2002)
The Lancet
, vol.360
, Issue.9346
, pp. 1673-1681
-
-
Bomford, A.1
-
2
-
-
28444449032
-
Clinical Aspects of hemochromatosis
-
O'Neil J, Powell L: Clinical Aspects of hemochromatosis. Semin Liver Dis 2005, 25(4):381-91.
-
(2005)
Semin Liver Dis
, vol.25
, Issue.4
, pp. 381-391
-
-
O'Neil, J.1
Powell, L.2
-
3
-
-
33644790930
-
The molecular genetics of haemochromatosis
-
Le Gac G, Ferec C: The molecular genetics of haemochromatosis. Eur J Hum Genet 2005, 13(11):1172-1185.
-
(2005)
Eur J Hum Genet
, vol.13
, Issue.11
, pp. 1172-1185
-
-
Le Gac, G.1
Ferec, C.2
-
4
-
-
20044366019
-
Oxidative Stress, Antioxidants and Neurodegenerative Diseases
-
Casetta I, Govoni V, Granieri E: Oxidative Stress, Antioxidants and Neurodegenerative Diseases. Curr Pharm Des 2005, 11(16):2033-52.
-
(2005)
Curr Pharm Des
, vol.11
, Issue.16
, pp. 2033-2052
-
-
Casetta, I.1
Govoni, V.2
Granieri, E.3
-
5
-
-
24644511602
-
Oxidative imbalance in Alzheimer's disease
-
Zhu X, Lee HG, Casadesus G, Avila J, Drew K, Perry G, Smith MA: Oxidative imbalance in Alzheimer's disease. Mol Neurobiol 2005, 31(1-3):205-17.
-
(2005)
Mol Neurobiol
, vol.31
, Issue.1-3
, pp. 205-217
-
-
Zhu, X.1
Lee, H.G.2
Casadesus, G.3
Avila, J.4
Drew, K.5
Perry, G.6
Smith, M.A.7
-
6
-
-
20944449836
-
Oxidative stress mechanisms and potential therapeutics in Alzheimer disease
-
Moreira PI, Siedlak SL, Aliev G, Zhu X, Cash AD, Smith MA, Perry G: Oxidative stress mechanisms and potential therapeutics in Alzheimer disease. J Neural Transm 2005, 112(7):921-32.
-
(2005)
J Neural Transm
, vol.112
, Issue.7
, pp. 921-932
-
-
Moreira, P.I.1
Siedlak, S.L.2
Aliev, G.3
Zhu, X.4
Cash, A.D.5
Smith, M.A.6
Perry, G.7
-
7
-
-
0041819578
-
Association of HFE mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with APOE
-
May 15
-
Pulliam JF, Jennings CD, Kryscio RJ, Davis DG, Wilson D, Montine TJ, Schmitt FA, Markesbery WR: Association of HFE mutations with neurodegeneration and oxidative stress in Alzheimer's disease and correlation with APOE. Am J Med Genet B Neuropsychiatr Genet 119(1)-48-53. 2003 May 15
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.119
, Issue.1
, pp. 48-53
-
-
Pulliam, J.F.1
Jennings, C.D.2
Kryscio, R.J.3
Davis, D.G.4
Wilson, D.5
Montine, T.J.6
Schmitt, F.A.7
Markesbery, W.R.8
-
8
-
-
3042654997
-
Does cellular iron dysregulation play a causative role in Parkinson's disease?
-
Kaur D, Andersen J: Does cellular iron dysregulation play a causative role in Parkinson's disease? Ageing Res Rev 2004, 3(3):327-43.
-
(2004)
Ageing Res Rev
, vol.3
, Issue.3
, pp. 327-343
-
-
Kaur, D.1
Andersen, J.2
-
9
-
-
0037378026
-
Oxidative stress in Parkinson's disease
-
Jenner P: Oxidative stress in Parkinson's disease. Ann Neurol 2003, 53(Suppl 3):S26-36.
-
(2003)
Ann Neurol
, vol.53
, Issue.SUPPL. 3
-
-
Jenner, P.1
-
10
-
-
0041696494
-
Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism
-
Dekker MC, Giesbergen PC, Njajou OT, van Swieten JC, Hofman A, Breteler MM, van Duijn CM: Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism. Neurosci Lett 2003, 348(2):117-9.
-
(2003)
Neurosci Lett
, vol.348
, Issue.2
, pp. 117-119
-
-
Dekker, M.C.1
Giesbergen, P.C.2
Njajou, O.T.3
van Swieten, J.C.4
Hofman, A.5
Breteler, M.M.6
van Duijn, C.M.7
-
11
-
-
0037135290
-
The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients
-
Buchanan DD, Silburn PA, Chalk JB, Le Couteur DG, Mellick GD: The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients. Neurosci Lett 2002, 327(2):91-4.
-
(2002)
Neurosci Lett
, vol.327
, Issue.2
, pp. 91-94
-
-
Buchanan, D.D.1
Silburn, P.A.2
Chalk, J.B.3
Le Couteur, D.G.4
Mellick, G.D.5
-
12
-
-
1542328195
-
Evaluation of HFE (hemochromatosis) mutations as genetic modifiers in sporadic AD and MCI
-
Berlin D, Chong G, Chertkow H, Bergman H, Phillips NA, Schipper HM: Evaluation of HFE (hemochromatosis) mutations as genetic modifiers in sporadic AD and MCI. Neurobiol Aging 2004, 25(4):465-74.
-
(2004)
Neurobiol Aging
, vol.25
, Issue.4
, pp. 465-474
-
-
Berlin, D.1
Chong, G.2
Chertkow, H.3
Bergman, H.4
Phillips, N.A.5
Schipper, H.M.6
-
13
-
-
0004235298
-
-
American Psychiatric Association: 4th revised edition Washington, DC
-
American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, 4th revised edition Washington, DC; 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
14
-
-
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, Katzman R, Price D, Stadlan EM: 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 1984, 34:939-944.
-
(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
-
15
-
-
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, 12:189-198.
-
(1975)
J Psychiatr Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
16
-
-
0027425211
-
The Clinical Dementia Rating (CDR): Current version and scoring rules
-
Morris JC: The Clinical Dementia Rating (CDR): Current version and scoring rules. Neurology 1993, 43:2412-2414.
-
(1993)
Neurology
, vol.43
, pp. 2412-2414
-
-
Morris, J.C.1
-
17
-
-
0032988610
-
Mild cognitive impairment: Clinical characterisation and outcome
-
Petersen RC, Smith GE, Waring SC, Ivnik RJ, Tangalos EG, Kokmen E: Mild cognitive impairment: clinical characterisation and outcome. Archives of Neurology 1999, 56:303-308.
-
(1999)
Archives of Neurology
, vol.56
, pp. 303-308
-
-
Petersen, R.C.1
Smith, G.E.2
Waring, S.C.3
Ivnik, R.J.4
Tangalos, E.G.5
Kokmen, E.6
-
18
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease. A clinico-pathological study of 100 cases
-
Hughes AJ, Daniel SE, Kilford L, Lees AJ: Accuracy of clinical diagnosis of idiopathic Parkinson's disease. A clinico-pathological study of 100 cases. JNNP 1992, 55:181-184.
-
(1992)
JNNP
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
19
-
-
0027327267
-
Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease
-
Saunders AM, Strittmatter WJ, Schmechel D, George-Hyslop PH, Pericak-Vance MA, Joo SH, Rosi BL, Gusella JF, Crapper-MacLachlan DR, Alberts MJ: Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. Neurology 1993, 43(8):1467-72.
-
(1993)
Neurology
, vol.43
, Issue.8
, pp. 1467-1472
-
-
Saunders, A.M.1
Strittmatter, W.J.2
Schmechel, D.3
George-Hyslop, P.H.4
Pericak-Vance, M.A.5
Joo, S.H.6
Rosi, B.L.7
Gusella, J.F.8
Crapper-MacLachlan, D.R.9
Alberts, M.J.10
-
20
-
-
0036306510
-
Association study between iron related genes polymorphisms and Parkinson's disease
-
Borie C, Gasparini F, Verpillat P, Bonnet AM, Agid Y, Hetet G, Brice A, Durr A, Grandchamp B: Association study between iron related genes polymorphisms and Parkinson's disease. J Neurol 2002, 249:801-804.
-
(2002)
J Neurol
, vol.249
, pp. 801-804
-
-
Borie, C.1
Gasparini, F.2
Verpillat, P.3
Bonnet, A.M.4
Agid, Y.5
Hetet, G.6
Brice, A.7
Durr, A.8
Grandchamp, B.9
-
21
-
-
0242500486
-
Association between the HFE mutations and unsuccessful ageing: A study in Alzheimer's disease patients from Northern Italy
-
Candore G, Licastro F, Chiappelli M, Franceschi C, Lio D, Rita Balistreri C, Piazza G, Colonna-Romano G, Grimaldi LM, Caruso C: Association between the HFE mutations and unsuccessful ageing: a study in Alzheimer's disease patients from Northern Italy. Mech Ageing Dev 2003, 124(4):525-8.
-
(2003)
Mech Ageing Dev
, vol.124
, Issue.4
, pp. 525-528
-
-
Candore, G.1
Licastro, F.2
Chiappelli, M.3
Franceschi, C.4
Lio, D.5
Rita Balistreri, C.6
Piazza, G.7
Colonna-Romano, G.8
Grimaldi, L.M.9
Caruso, C.10
-
22
-
-
0034601251
-
Are hereditary hemochromatosis mutations involved in Alzheimer disease?
-
Moalem S, Percy ME, Andrews DF, Kruck TP, Wong S, Dalton AJ, Mehta P, Fedor B, Warren AC: Are hereditary hemochromatosis mutations involved in Alzheimer disease? Am J Med Genet 2000, 93(1):58-66.
-
(2000)
Am J Med Genet
, vol.93
, Issue.1
, pp. 58-66
-
-
Moalem, S.1
Percy, M.E.2
Andrews, D.F.3
Kruck, T.P.4
Wong, S.5
Dalton, A.J.6
Mehta, P.7
Fedor, B.8
Warren, A.C.9
-
23
-
-
12244274984
-
Interaction of the H63D mutation in the hemochromatosis gene with the apolipoprotein E epsilon 4 allele modulates age at onset of Alzheimer's disease
-
Combarros O, Garcia-Roman M, Fontalba A, Fernandez-Luna JL, Llorca J, Infante J, Berciano J: Interaction of the H63D mutation in the hemochromatosis gene with the apolipoprotein E epsilon 4 allele modulates age at onset of Alzheimer's disease. Dement Geriatr Cogn Disord 2003, 15(3):151-4.
-
(2003)
Dement Geriatr Cogn Disord
, vol.15
, Issue.3
, pp. 151-154
-
-
Combarros, O.1
Garcia-Roman, M.2
Fontalba, A.3
Fernandez-Luna, J.L.4
Llorca, J.5
Infante, J.6
Berciano, J.7
-
24
-
-
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(4):563-8.
-
(2001)
Neurobiol Aging
, vol.22
, Issue.4
, 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
-
25
-
-
1942469548
-
Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease
-
Robson KJ, Lehmann DJ, Wimhurst VL, Livesey KJ, Combrinck M, Merryweather-Clarke AT, Warden DR, Smith AD: Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. J Med Genet 2004, 41(4):261-5.
-
(2004)
J Med Genet
, vol.41
, Issue.4
, pp. 261-265
-
-
Robson, K.J.1
Lehmann, D.J.2
Wimhurst, V.L.3
Livesey, K.J.4
Combrinck, M.5
Merryweather-Clarke, A.T.6
Warden, D.R.7
Smith, A.D.8
|