-
1
-
-
0027486997
-
Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: Glutamine or arginine at position 191, for the respective A or B allozymes
-
Adkins, S., Gan, K. N., Mody, M., & La Du, B. N. (1993). Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: Glutamine or arginine at position 191, for the respective A or B allozymes. American Journal of Human Genetics, 52, 598-608.
-
(1993)
American Journal of Human Genetics
, vol.52
, pp. 598-608
-
-
Adkins, S.1
Gan, K.N.2
Mody, M.3
La Du, B.N.4
-
2
-
-
0032587920
-
Gln → Arg 191 polymorphism of paraoxonase and Parkinson's disease
-
Akhmedova, S., Anisimov, S., Yakimovsky, A., & Schwartz, E. (1999). Gln → Arg 191 polymorphism of paraoxonase and Parkinson's disease. Human Heredity, 49, 178-180.
-
(1999)
Human Heredity
, vol.49
, pp. 178-180
-
-
Akhmedova, S.1
Anisimov, S.2
Yakimovsky, A.3
Schwartz, E.4
-
3
-
-
0035283113
-
Paraoxonase 1 Met-Leu 54 polymorphism is associated with Parkinson's disease
-
Akhmedova, S. N., Yakimovsky, A. K., & Schwartz, E. I. (2001). Paraoxonase 1 Met-Leu 54 polymorphism is associated with Parkinson's disease. Journal of the Neurological Sciences, 184, 179-182.
-
(2001)
Journal of the Neurological Sciences
, vol.184
, pp. 179-182
-
-
Akhmedova, S.N.1
Yakimovsky, A.K.2
Schwartz, E.I.3
-
4
-
-
67349252457
-
Increase of uric acid and purine compounds in biological fluids of multiple sclerosis patients
-
Amorini, A. M., Petzold, A., Tavazzi, B., Eikelenboom, J., Keir, G., Belli, A., et al. (2009). Increase of uric acid and purine compounds in biological fluids of multiple sclerosis patients. Clinical Biochemistry, 42, 1001-1006.
-
(2009)
Clinical Biochemistry
, vol.42
, pp. 1001-1006
-
-
Amorini, A.M.1
Petzold, A.2
Tavazzi, B.3
Eikelenboom, J.4
Keir, G.5
Belli, A.6
-
5
-
-
27244450879
-
Elevated protein carbonylation in the brain white matter and gray matter of patients with multiple sclerosis
-
DOI 10.1002/jnr.20587
-
Bizzozero, O. A., DeJesus, G., Callahan, K., & Pastuszyn, A. (2005). Elevated protein carbonylation in the brain white matter and gray matter of patients with multiple sclerosis. Journal ofNeuroscience Research, 81 , 687-695. (Pubitemid 41532164)
-
(2005)
Journal of Neuroscience Research
, vol.81
, Issue.5
, pp. 687-695
-
-
Bizzozero, O.A.1
DeJesus, G.2
Callahan, K.3
Pastuszyn, A.4
-
6
-
-
0023143167
-
Confidence intervals
-
Bulpitt, C. J. (1987). Confidence intervals. Lancet, 1, 494-497.
-
(1987)
Lancet
, vol.1
, pp. 494-497
-
-
Bulpitt, C.J.1
-
7
-
-
0028934696
-
Changes in cerebrospinal fluid levels of malondialdehyde and glutathione reductase activity in multiple sclerosis
-
Calabrese, V., Raffaele, R., Cosentino, E., & Rizza, V. (1994). Changes in cerebrospinal fluid levels of malondialdehyde and glutathione reductase activity in multiple sclerosis. International Journal of Clinical Pharmacology Research, 14, 119-123.
-
(1994)
International Journal of Clinical Pharmacology Research
, vol.14
, pp. 119-123
-
-
Calabrese, V.1
Raffaele, R.2
Cosentino, E.3
Rizza, V.4
-
8
-
-
36749009738
-
Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke
-
Can Demirdöǧen, B., Türkanoǧlu, A., Bek, S., Sanisoǧlu, Y., Demirkaya, S., Vural, O., et al. (2008). Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke. Clinical Biochemistry, 41, 1-9.
-
(2008)
Clinical Biochemistry
, vol.41
, pp. 1-9
-
-
Can Demirdöǧen, B.1
Türkanoǧlu, A.2
Bek, S.3
Sanisoǧlu, Y.4
Demirkaya, S.5
Vural, O.6
-
9
-
-
0036651220
-
Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease
-
Carmine, A., Buervenich, S., Sydow, O., Anvret, M., & Olson, L. (2002). Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease. Movement Disorders, 17, 764-766.
-
(2002)
Movement Disorders
, vol.17
, pp. 764-766
-
-
Carmine, A.1
Buervenich, S.2
Sydow, O.3
Anvret, M.4
Olson, L.5
-
10
-
-
4344624315
-
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population
-
Clarimon, J., Eerola, J., Hellstrom, O., Tienari, P. J., & Singleton, A. (2004). Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population. Neuroscience Letters, 367, 168-170.
-
(2004)
Neuroscience Letters
, vol.367
, pp. 168-170
-
-
Clarimon, J.1
Eerola, J.2
Hellstrom, O.3
Tienari, P.J.4
Singleton, A.5
-
11
-
-
0035873230
-
Gene therapy to prevent organophosphate intoxication
-
Cowan, J., Sinton, C. M., Varley, A. W., Wians, F. H., Haley, R. W., & Munford, R. S. (2001). Gene therapy to prevent organophosphate intoxication. Toxicology and Applied Pharmacology, 173, 1-6.
-
(2001)
Toxicology and Applied Pharmacology
, vol.173
, pp. 1-6
-
-
Cowan, J.1
Sinton, C.M.2
Varley, A.W.3
Wians, F.H.4
Haley, R.W.5
Munford, R.S.6
-
12
-
-
18744364425
-
Paraoxonase 1 192/55 gene polymorphisms in Alzheimer's disease
-
Dantoine, T. F., Drouet, M., Debord, J., Merle, L., Cogne, M., & Charmes, J. P. (2002). Paraoxonase 1 192/55 gene polymorphisms in Alzheimer's disease. Annals of the New York Academy of Sciences, 977, 239-244.
-
(2002)
Annals of the New York Academy of Sciences
, vol.977
, pp. 239-244
-
-
Dantoine, T.F.1
Drouet, M.2
Debord, J.3
Merle, L.4
Cogne, M.5
Charmes, J.P.6
-
13
-
-
0032954775
-
Cerebrospinal fluid nitrate levels in patients with multiple sclerosis
-
DOI 10.1159/000007997
-
de Bustos, F., Navarro, J. A., de Andrés, C., Molina, J. A., Jiménez-Jiménez, F. J., Ortí-Pareja, M., et al. (1999). Cerebrospinal fluid nitrate levels in patients with multiple sclerosis. European Neurology, 41, 44-47. (Pubitemid 29043111)
-
(1999)
European Neurology
, vol.41
, Issue.1
, pp. 44-47
-
-
De Bustos, F.1
Navarro, J.A.2
De Andres, C.3
Molina, J.A.4
Jimenez-Jimenez, F.J.5
Orti-Pareja, M.6
Gasalla, T.7
Tallon-Barranco, A.8
Martinez-Salio, A.9
Arenas, J.10
-
14
-
-
59149100558
-
Interaction between PON1 and population density in amyotrophic lateral sclerosis
-
Diekstra, F. P., Beleza-Meireles, A., Leigh, N. P., Shaw, C. E., & Al-Chalabi, A. (2009). Interaction between PON1 and population density in amyotrophic lateral sclerosis. Neuroreport, 20, 186-190.
-
(2009)
Neuroreport
, vol.20
, pp. 186-190
-
-
Diekstra, F.P.1
Beleza-Meireles, A.2
Leigh, N.P.3
Shaw, C.E.4
Al-Chalabi, A.5
-
15
-
-
33947512180
-
Polymorphisms in the genes of cytochrome oxidase P450 2D6 (CYP2D6), paraoxonase 1 (PON1) and apolipoprotein e (APOE) as risk factors for Parkinson's disease
-
Duric, G., Svetel, M., Nikolaevic, S. I., Dragadevic, N., Gavrilovic, J., & Kostic, V. S. (2007). Polymorphisms in the genes of cytochrome oxidase P450 2D6 (CYP2D6), paraoxonase 1 (PON1) and apolipoprotein E (APOE) as risk factors for Parkinson's disease. Vojnosanitetski Pregled, 64, 25-30.
-
(2007)
Vojnosanitetski Pregled
, vol.64
, pp. 25-30
-
-
Duric, G.1
Svetel, M.2
Nikolaevic, S.I.3
Dragadevic, N.4
Gavrilovic, J.5
Kostic, V.S.6
-
16
-
-
1642513783
-
Genetics of multiple sclerosis
-
Dyment, D. A., Ebers, G. C., & Sadovnick, A. D. (2004). Genetics of multiple sclerosis. Lancet Neurology, 3, 104-110.
-
(2004)
Lancet Neurology
, vol.3
, pp. 104-110
-
-
Dyment, D.A.1
Ebers, G.C.2
Sadovnick, A.D.3
-
17
-
-
29644434198
-
Polymorphisms in the PON gene cluster are associated with Alzheimer disease
-
Erlich, P. M., Lunetta, K. L., Cupples, L. A., Huyck, M., Green, R. C., Baldwin, C. T., et al. (2006). Polymorphisms in the PON gene cluster are associated with Alzheimer disease. Human Molecular Genetics, 15, 77-85.
-
(2006)
Human Molecular Genetics
, vol.15
, pp. 77-85
-
-
Erlich, P.M.1
Lunetta, K.L.2
Cupples, L.A.3
Huyck, M.4
Green, R.C.5
Baldwin, C.T.6
-
18
-
-
28044438183
-
Increased levels of lipid hydroperoxydes in plasma of patients with multiple sclerosis: A relationship with paraoxonase activity
-
Ferretti, G., Bacchetti, T., Principi, F., Di Ludovico, F., Viti, B., Angeleri, V. A., et al. (2005). Increased levels of lipid hydroperoxydes in plasma of patients with multiple sclerosis: A relationship with paraoxonase activity. Multiple Sclerosis, 11, 677-682.
-
(2005)
Multiple Sclerosis
, vol.11
, pp. 677-682
-
-
Ferretti, G.1
Bacchetti, T.2
Principi, F.3
Di Ludovico, F.4
Viti, B.5
Angeleri, V.A.6
-
19
-
-
21544473194
-
Pesticides exposure and genetic polymorphism of paraoxonase in the susceptibility of Parkinson's disease
-
Fong, C. S., Cheng, C. W., & Wu, R. M. (2005). Pesticides exposure and genetic polymorphism of paraoxonase in the susceptibility of Parkinson's disease. Acta Neurologica (Taiwan), 14, 55-60.
-
(2005)
Acta Neurologica (Taiwan)
, vol.14
, pp. 55-60
-
-
Fong, C.S.1
Cheng, C.W.2
Wu, R.M.3
-
20
-
-
0036043065
-
Genetics of multiple sclerosis: Linkage and association studies
-
Giordano, M., D'Alfonso, S., & Momigliano-Richiardi, P. (2002). Genetics of multiple sclerosis: linkage and association studies. American Journal of Pharmacogenomics, 2, 37-58.
-
(2002)
American Journal of Pharmacogenomics
, vol.2
, pp. 37-58
-
-
Giordano, M.1
D'Alfonso, S.2
Momigliano-Richiardi, P.3
-
21
-
-
4644255312
-
Cerebrospinal fluid isoprostanes are not related to inflammatory activity in relapsing-remitting multiple sclerosis
-
Greco, A., Minghetti, L., Puopolo, M., Cannoni, S., Romano, S., Pozzilli, C., et al. (2004). Cerebrospinal fluid isoprostanes are not related to inflammatory activity in relapsing-remitting multiple sclerosis. Journal of the Neurological Sciences, 224, 23-27.
-
(2004)
Journal of the Neurological Sciences
, vol.224
, pp. 23-27
-
-
Greco, A.1
Minghetti, L.2
Puopolo, M.3
Cannoni, S.4
Romano, S.5
Pozzilli, C.6
-
22
-
-
34547814093
-
Paraoxonase 1 gene polymorphisms in patients with osteonecrosis of the femoral head with and without cerebral white matter lesions
-
Hadjigeorgiou, G. M., Malizos, K., Dardiotis, E., Aggelakis, K., Dardioti, M., Zibis, A., et al. (2007). Paraoxonase 1 gene polymorphisms in patients with osteonecrosis of the femoral head with and without cerebral white matter lesions. Journal of Orthopaedic Research, 25, 1087-1093.
-
(2007)
Journal of Orthopaedic Research
, vol.25
, pp. 1087-1093
-
-
Hadjigeorgiou, G.M.1
Malizos, K.2
Dardiotis, E.3
Aggelakis, K.4
Dardioti, M.5
Zibis, A.6
-
23
-
-
1542345607
-
Paraoxonase 1 gene polymorphisms and dementia in humans
-
Helbecque, N., Cottel, D., Codron, V., Berr, C., & Amouyel, P. (2004). Paraoxonase 1 gene polymorphisms and dementia in humans. Neuroscience Letters, 358, 41-44.
-
(2004)
Neuroscience Letters
, vol.358
, pp. 41-44
-
-
Helbecque, N.1
Cottel, D.2
Codron, V.3
Berr, C.4
Amouyel, P.5
-
24
-
-
33746511459
-
Human serum paraoxonase gene polymorphisms, Q192R and L55M, are not associated with the risk of cerebral infarction in Chinese Han population
-
Huang, Q., Liu, Y. H., Yang, Q. D., Xiao, B., Ge, L., Zhang, N., et al. (2006). Human serum paraoxonase gene polymorphisms, Q192R and L55M, are not associated with the risk of cerebral infarction in Chinese Han population. Neurological Research, 28, 549-554.
-
(2006)
Neurological Research
, vol.28
, pp. 549-554
-
-
Huang, Q.1
Liu, Y.H.2
Yang, Q.D.3
Xiao, B.4
Ge, L.5
Zhang, N.6
-
25
-
-
0027396833
-
The molecular basis of the human serum paraoxonase activity polymorphism
-
Humbert, R., Adler, D. A., Disteche, C. M., Hassett, C., Omiecinski, C. J., & Furlong, C. E. (1993). The molecular basis of the human serum paraoxonase activity polymorphism. Nature Genetics, 3, 73-76.
-
(1993)
Nature Genetics
, vol.3
, pp. 73-76
-
-
Humbert, R.1
Adler, D.A.2
Disteche, C.M.3
Hassett, C.4
Omiecinski, C.J.5
Furlong, C.E.6
-
26
-
-
0345020390
-
Cerebrospinal fluid levels of alpha-tocopherol in patients with multiple sclerosis
-
DOI 10.1016/S0304-3940(98)00370-X, PII S030439409800370X
-
Jiménez-Jiménez, F. J., de Bustos, F., Molina, J. A., de Andrés, C., Gasalla, T., Ortí-Pareja, M., et al. (1998). Cerebrospinal fluid levels of alpha-tocopherol in patients with multiple sclerosis. Neuroscience Letters, 249, 65-67. (Pubitemid 28308235)
-
(1998)
Neuroscience Letters
, vol.249
, Issue.1
, pp. 65-67
-
-
Jimenez-Jimenez, F.J.1
De Bustos, F.2
Molina, J.A.3
De Andres, C.4
Gasalla, T.5
Orti-Pareja, M.6
Zurdo, M.7
Porta, J.8
Castellano-Millan, F.9
Arenas, J.10
De Salamanca, R.E.11
-
27
-
-
33644810396
-
Advanced glycoxidation end products in patients with multiple sclerosis
-
Kalousová, M., Havrdová, E., Mrázová, K., Spacek, P., Braun, M., Uhrová, J., et al. (2005). Advanced glycoxidation end products in patients with multiple sclerosis. Prague Medical Report, 106, 167-174.
-
(2005)
Prague Medical Report
, vol.106
, pp. 167-174
-
-
Kalousová, M.1
Havrdová, E.2
Mrázová, K.3
Spacek, P.4
Braun, M.5
Uhrová, J.6
-
28
-
-
20044390760
-
No evidence of increased oxidative degradation of urate to allantoin in the CSF and serum of patients with multiple sclerosis
-
Kastenbauer, S., Kieseier, B. C., & Becker, B. F. (2005). No evidence of increased oxidative degradation of urate to allantoin in the CSF and serum of patients with multiple sclerosis. Journal of Neurology, 252, 611-612.
-
(2005)
Journal of Neurology
, vol.252
, pp. 611-612
-
-
Kastenbauer, S.1
Kieseier, B.C.2
Becker, B.F.3
-
29
-
-
0037382429
-
Paraoxonase 1 promoter and coding region polymorphisms in Parkinson's disease
-
Kelada, S. N., Costa-Mallén, P., Checkoway, H., Viernes, H. A., Farin, F. M., Smith-Weller, T., et al. (2003). Paraoxonase 1 promoter and coding region polymorphisms in Parkinson's disease. Journal of Neurology, Neurosurgery and Psychiatry, 74, 545-548.
-
(2003)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.74
, pp. 545-548
-
-
Kelada, S.N.1
Costa-Mallén, P.2
Checkoway, H.3
Viernes, H.A.4
Farin, F.M.5
Smith-Weller, T.6
-
30
-
-
0032576016
-
Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease
-
Kondo, I., & Yamamoto, M. (1998). Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease. Brain Research, 806, 271-273.
-
(1998)
Brain Research
, vol.806
, pp. 271-273
-
-
Kondo, I.1
Yamamoto, M.2
-
31
-
-
57149135486
-
Paraoxonase-1 55/192 genotypes in schizophrenic patients and their relatives in Turkish population
-
Kucukali, C. I., Aydin, M., Ozkok, E., Orhan, N., Cakir, U., Kilic, G., et al. (2008). Paraoxonase-1 55/192 genotypes in schizophrenic patients and their relatives in Turkish population. Psychiatric Genetics, 18, 289-294.
-
(2008)
Psychiatric Genetics
, vol.18
, pp. 289-294
-
-
Kucukali, C.I.1
Aydin, M.2
Ozkok, E.3
Orhan, N.4
Cakir, U.5
Kilic, G.6
-
32
-
-
0002557986
-
Human serum paraoxonase/arylesterase
-
W. Kalow (Ed.). New York: Pergamon Press
-
La Du, B. N. (1992). Human serum paraoxonase/arylesterase. In W. Kalow (Ed.), Pharmacogenetics of drugs metabolism (pp. 51-91). New York: Pergamon Press.
-
(1992)
Pharmacogenetics of Drugs Metabolism
, pp. 51-91
-
-
La Du, B.N.1
-
33
-
-
0026647212
-
Measurement of low molecular-weight antioxidants, uric acid, tyrosine and tryptophan in plaques and white matter from patients with multiple sclerosis
-
Langemann, H., Kabiersch, A., & Newcombe, J. (1992). Measurement of low molecular-weight antioxidants, uric acid, tyrosine and tryptophan in plaques and white matter from patients with multiple sclerosis. European Neurology, 32, 248-252.
-
(1992)
European Neurology
, vol.32
, pp. 248-252
-
-
Langemann, H.1
Kabiersch, A.2
Newcombe, J.3
-
34
-
-
40449106435
-
Polymorphisms at the paraoxonase 1 L55 M and Q192R loci affect the pathophysiology of Alzheimer's disease: Emphasis on the cholinergic system and beta-amyloid levels
-
Leduc, V., & Poirier, J. (2008). Polymorphisms at the paraoxonase 1 L55 M and Q192R loci affect the pathophysiology of Alzheimer's disease: Emphasis on the cholinergic system and beta-amyloid levels. Neurodegeneration Diseases, 5, 225-227.
-
(2008)
Neurodegeneration Diseases
, vol.5
, pp. 225-227
-
-
Leduc, V.1
Poirier, J.2
-
35
-
-
0026447497
-
The role of reactive oxygen species in the pathogenesis of multiple sclerosis
-
LeVine, S. M. (1992). The role of reactive oxygen species in the pathogenesis of multiple sclerosis. Medical Hypotheses, 39, 271-274.
-
(1992)
Medical Hypotheses
, vol.39
, pp. 271-274
-
-
Levine, S.M.1
-
36
-
-
0346095221
-
Paraoxonase gene polymorphisms, oxidative stress, and diseases
-
Li, H. L., Liu, D. P., & Liang, C. C. (2003). Paraoxonase gene polymorphisms, oxidative stress, and diseases. Journal of Molecular Medicine, 81, 766-779.
-
(2003)
Journal of Molecular Medicine
, vol.81
, pp. 766-779
-
-
Li, H.L.1
Liu, D.P.2
Liang, C.C.3
-
37
-
-
0036321308
-
The paraoxonase gene family and coronary heart disease
-
Mackness, B., Durrington, P. N., & Mackness, M. I. (2002). The paraoxonase gene family and coronary heart disease. Current Opinion in Lipidology, 13, 357-362.
-
(2002)
Current Opinion in Lipidology
, vol.13
, pp. 357-362
-
-
MacKness, B.1
Durrington, P.N.2
MacKness, M.I.3
-
38
-
-
0031859456
-
Serum paraoxonase (PON1) 55 and 192 polymorphism and paraoxonase activity and concentration in non-insulin dependent diabetes mellitus
-
Mackness, B., Mackness, M. I., Arrol, S., Turkie, W., Julier, K., Abuasha, B., et al. (1998). Serum paraoxonase (PON1) 55 and 192 polymorphism and paraoxonase activity and concentration in non-insulin dependent diabetes mellitus. Atherosclerosis, 139, 341-349.
-
(1998)
Atherosclerosis
, vol.139
, pp. 341-349
-
-
MacKness, B.1
MacKness, M.I.2
Arrol, S.3
Turkie, W.4
Julier, K.5
Abuasha, B.6
-
39
-
-
0029889417
-
Paraoxonase: Biochemistry, genetics and relationship to plasma lipoproteins
-
Mackness, M. I., Mackness, B., Durrington, P. N., Connelly, P. W., & Hegele, R. A. (1996). Paraoxonase: biochemistry, genetics and relationship to plasma lipoproteins. Current Opinion in Lipidology, 7, 69-76.
-
(1996)
Current Opinion in Lipidology
, vol.7
, pp. 69-76
-
-
MacKness, M.I.1
MacKness, B.2
Durrington, P.N.3
Connelly, P.W.4
Hegele, R.A.5
-
40
-
-
33847185147
-
Elevated cerebrospinal fluid F2-isoprostane levels indicating oxidative stress in healthy siblings of multiple sclerosis patients
-
Mattsson, N., Haghighi, S., Andersen, O., Yao, Y., Rosengren, L., Blennow, K., et al. (2007). Elevated cerebrospinal fluid F2-isoprostane levels indicating oxidative stress in healthy siblings of multiple sclerosis patients. Neuroscience Letters, 414, 233-236.
-
(2007)
Neuroscience Letters
, vol.414
, pp. 233-236
-
-
Mattsson, N.1
Haghighi, S.2
Andersen, O.3
Yao, Y.4
Rosengren, L.5
Blennow, K.6
-
41
-
-
0034955141
-
Recommended diagnostic criteria for multiple sclerosis guidelines from the International Panel on the Diagnosis of Multiple Sclerosis
-
McDonald, W. I., Compston, A., Edan, G., Goodkin, D., Härtung, H. P., Lublin, F. B., et al. (2001). Recommended diagnostic criteria for multiple sclerosis guidelines from the International Panel on the Diagnosis of Multiple Sclerosis. Annals of Neurology, 50, 121-127.
-
(2001)
Annals of Neurology
, vol.50
, pp. 121-127
-
-
McDonald, W.I.1
Compston, A.2
Edan, G.3
Goodkin, D.4
Härtung, H.P.5
Lublin, F.B.6
-
42
-
-
0028210146
-
Low density lipoprotein uptake by macrophages in multiple sclerosis plaques: Implications for pathogenesis
-
Newcombe, J., Li, H., & Cuzner, M. L. (1994). Low density lipoprotein uptake by macrophages in multiple sclerosis plaques: Implications for pathogenesis. Neuropathology and Applied Neurobiology, 20, 152-162.
-
(1994)
Neuropathology and Applied Neurobiology
, vol.20
, pp. 152-162
-
-
Newcombe, J.1
Li, H.2
Cuzner, M.L.3
-
44
-
-
42649124609
-
Environmental risk factors in multiple sclerosis
-
Pugliatti, M., Harbo, H. F., Holmøy, T., Kampman, M. T., Myhr, K. M., Riise, T., et al. (2008). Environmental risk factors in multiple sclerosis. Acta Neurologica Scandinavica Supplement, 188, 34-40.
-
(2008)
Acta Neurologica Scandinavica Supplement
, vol.188
, pp. 34-40
-
-
Pugliatti, M.1
Harbo, H.F.2
Holmøy, T.3
Kampman, M.T.4
Myhr, K.M.5
Riise, T.6
-
45
-
-
51649096593
-
The genetics of clinical outcome in multiple sclerosis
-
Ramagopalan, S. V., Deluca, G. C., Degenhardt, A., & Ebers, G. C. (2008). The genetics of clinical outcome in multiple sclerosis. Journal of Neuroimmunology, 201-202, 183-199.
-
(2008)
Journal of Neuroimmunology
, vol.201-202
, pp. 183-199
-
-
Ramagopalan, S.V.1
Deluca, G.C.2
Degenhardt, A.3
Ebers, G.C.4
-
46
-
-
0033941426
-
MRI cerebral white matter lesions and paraoxonase PON1 polymorphisms: Three-year follow-up of the austrian stroke prevention study
-
Schmidt, R., Schmidt, H., Fazekas, F., Kapeller, P., Roob, G., Lechner, A., et al. (2000). MRI cerebral white matter lesions and paraoxonase PON1 polymorphisms: Three-year follow-up of the austrian stroke prevention study. Arteriosclerosis, Thrombosis, and Vascular Biology, 20, 1811-1816.
-
(2000)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.20
, pp. 1811-1816
-
-
Schmidt, R.1
Schmidt, H.2
Fazekas, F.3
Kapeller, P.4
Roob, G.5
Lechner, A.6
-
47
-
-
40549084012
-
The paraoxonase gene polymorphism in stroke patients and lipid profile
-
Shin, B. S., Oh, S. Y., Kim, Y. S., & Kim, K. W. (2008). The paraoxonase gene polymorphism in stroke patients and lipid profile. Acta Neurologica Scandinavica, 117, 237-243.
-
(2008)
Acta Neurologica Scandinavica
, vol.117
, pp. 237-243
-
-
Shin, B.S.1
Oh, S.Y.2
Kim, Y.S.3
Kim, K.W.4
-
48
-
-
34249079947
-
Glyoxalase i A111E, paraoxonase 1 Q192R and L55M polymorphisms: Susceptibility factors of multiple sclerosis?
-
Sidoti, A., Antognelli, C., Rinaldi, C., D'Angelo, R., Dattola, V., Girlanda, P., et al. (2007). Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? Multiple Sclerosis, 13, 446-153.
-
(2007)
Multiple Sclerosis
, vol.13
, pp. 446-153
-
-
Sidoti, A.1
Antognelli, C.2
Rinaldi, C.3
D'Angelo, R.4
Dattola, V.5
Girlanda, P.6
-
49
-
-
0033792112
-
Paraoxonase polymorphisms, pesticide exposure and Parkinson's disease in a Caucasian population
-
Taylor, M. C., Le Couteur, D. G., Mekkick, G. D., & Board, P. G. (2000). Paraoxonase polymorphisms, pesticide exposure and Parkinson's disease in a Caucasian population. Journal of Neural Transmission, 107, 979-983.
-
(2000)
Journal of Neural Transmission
, vol.107
, pp. 979-983
-
-
Taylor, M.C.1
Le Couteur, D.G.2
Mekkick, G.D.3
Board, P.G.4
-
50
-
-
0026500136
-
Evidence for increased lipid peroxidation in multiple sclerosis
-
Toshniwal, P. K., & Zarling, E. J. (1992). Evidence for increased lipid peroxidation in multiple sclerosis. Neurochemical Research, 17, 205-207.
-
(1992)
Neurochemical Research
, vol.17
, pp. 205-207
-
-
Toshniwal, P.K.1
Zarling, E.J.2
-
51
-
-
0038168097
-
Paraoxonase 1 polymorphism Leu-Met55 is associated with cerebral infarction in Japanese population
-
Ueno, T., Shimazaki, E., Matsumoto, T., Watanabe, H., Tsunemi, A., Takahashi, Y., et al. (2003). Paraoxonase 1 polymorphism Leu-Met55 is associated with cerebral infarction in Japanese population. Medical Science Monitor, 9, CR208-212.
-
(2003)
Medical Science Monitor
, vol.9
-
-
Ueno, T.1
Shimazaki, E.2
Matsumoto, T.3
Watanabe, H.4
Tsunemi, A.5
Takahashi, Y.6
-
52
-
-
33745227281
-
NAD(P)H:quinone oxidoreductase 1 expression in multiple sclerosis lesions
-
DOI 10.1016/j.freeradbiomed.2006.04.013, PII S0891584906002565
-
van Horssen, J., Schreibelt, G., Bö, L., Montagne, L., Drukarch, B., van Muiswinkel, F. L., et al. (2006). NAD(P)H:quinone oxido-reductase 1 expression in multiple sclerosis lesions. Free Radical Biology and Medicine, 41, 311-317. (Pubitemid 43928505)
-
(2006)
Free Radical Biology and Medicine
, vol.41
, Issue.2
, pp. 311-317
-
-
Van Horssen, J.1
Schreibelt, G.2
Bo, L.3
Montagne, L.4
Drukarch, B.5
Van Muiswinkel, F.L.6
De Vries, H.E.7
-
53
-
-
56349160121
-
Severe oxidative damage in multiple sclerosis lesions coincides with enhanced antioxidant enzyme expression
-
van Horssen, J., Schreibelt, G., Drexhage, J., Hazes, T., Dijkstra, C. D., van der Valk, P., et al. (2008). Severe oxidative damage in multiple sclerosis lesions coincides with enhanced antioxidant enzyme expression. Free Radical Biology and Medicine, 45, 1729-1737.
-
(2008)
Free Radical Biology and Medicine
, vol.45
, pp. 1729-1737
-
-
Van Horssen, J.1
Schreibelt, G.2
Drexhage, J.3
Hazes, T.4
Dijkstra, C.D.5
Van Der Valk, P.6
-
54
-
-
0033677464
-
No association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a Chinese population
-
Wang, J., & Liu, Z. (2000). No association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a Chinese population. Movement Disorders, 15, 1265-1267.
-
(2000)
Movement Disorders
, vol.15
, pp. 1265-1267
-
-
Wang, J.1
Liu, Z.2
-
55
-
-
68249141410
-
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS
-
Wills, A. M., Cronin, S., Slowik, A., Kasperaviciute, D., Van Es, M. A., Morahan, J. M., et al. (2009). A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Neurology, 73, 16-24.
-
(2009)
Neurology
, vol.73
, pp. 16-24
-
-
Wills, A.M.1
Cronin, S.2
Slowik, A.3
Kasperaviciute, D.4
Van Es, M.A.5
Morahan, J.M.6
-
56
-
-
4744363276
-
Association of parao-xonase 1 gene polymorphisms with risk of Parkinson's disease: A meta-analysis
-
Zintzaras, E., & Hadjigeorgiou, G. M. (2004). Association of parao-xonase 1 gene polymorphisms with risk of Parkinson's disease: A meta-analysis. Journal of Human Genetics, 49, 474-481.
-
(2004)
Journal of Human Genetics
, vol.49
, pp. 474-481
-
-
Zintzaras, E.1
Hadjigeorgiou, G.M.2
-
57
-
-
0035056015
-
Genetic polymorphisms in older subjects with vascular or Alzheimer's dementia
-
DOI 10.1034/j.1600-0404.2001.103005304.x
-
Zuliani, G., Ble', A., Zanca, R., Munari, M. R., Zurlo, A., Vavalle, C., et al. (2001). Genetic polymorphisms in older subjects with vascular or Alzheimer's dementia. Acta Neurologica Scandinavica, 103, 304-308. (Pubitemid 32368006)
-
(2001)
Acta Neurologica Scandinavica
, vol.103
, Issue.5
, pp. 304-308
-
-
Zuliani, G.1
Ble, A.2
Zanca, R.3
Munari, M.R.4
Zurlo, A.5
Vavalle, C.6
Atti, A.R.7
Fellin, R.8
|