-
1
-
-
0036209085
-
The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service
-
Hughes AJ Daniel SE Ben Shlomo Y Lees AJ The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service Brain 125 pt 4 2002 861 870
-
(2002)
Brain
, vol.125
, Issue.pt 4
, pp. 861-870
-
-
Hughes, AJ1
Daniel, SE2
Ben Shlomo, Y3
Lees, AJ4
-
3
-
-
14844300111
-
Nonlinear progression of Parkinson disease as determined by serial positron emission tomographic imaging of striatal fluorodopa F 18 activity
-
Hilker R Schweitzer K Coburger S Nonlinear progression of Parkinson disease as determined by serial positron emission tomographic imaging of striatal fluorodopa F 18 activity Arch Neurol 62 2005 378 382
-
(2005)
Arch Neurol
, vol.62
, pp. 378-382
-
-
Hilker, R1
Schweitzer, K2
Coburger, S3
-
4
-
-
85120186852
-
-
Gowers WR Diseases of the nervous system 1888 Chapman London
-
(1888)
-
-
Gowers, WR1
-
5
-
-
0028060492
-
Increased risk of Parkinson's disease in parents and siblings of patients
-
Payami H Larsen K Bernard S Nutt J Increased risk of Parkinson's disease in parents and siblings of patients Ann Neurol 36 1994 659 661
-
(1994)
Ann Neurol
, vol.36
, pp. 659-661
-
-
Payami, H1
Larsen, K2
Bernard, S3
Nutt, J4
-
7
-
-
0029005009
-
Increased risk of Parkinson's disease in relatives of patients
-
Vieregge P Heberlein I Increased risk of Parkinson's disease in relatives of patients Ann Neurol 3 1995 685
-
(1995)
Ann Neurol
, vol.3
, pp. 685
-
-
Vieregge, P1
Heberlein, I2
-
8
-
-
0030031344
-
Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy
-
De Michele G Filla A Volpe G Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy Mov Disord 11 1996 17 23
-
(1996)
Mov Disord
, vol.11
, pp. 17-23
-
-
De Michele, G1
Filla, A2
Volpe, G3
-
9
-
-
0030056696
-
Risk of Parkinson's disease among first-degree relatives: a community-based study
-
Marder K Tang MX Mejia H Risk of Parkinson's disease among first-degree relatives: a community-based study Neurology 47 1996 155 160
-
(1996)
Neurology
, vol.47
, pp. 155-160
-
-
Marder, K1
Tang, MX2
Mejia, H3
-
10
-
-
0031670136
-
Genetics of Parkinson's disease
-
Gasser T Genetics of Parkinson's disease Ann Neurol 44 3 suppl 1 1998 S53 S57
-
(1998)
Ann Neurol
, vol.44
, Issue.3 suppl 1
, pp. S53-S57
-
-
Gasser, T1
-
11
-
-
0033608187
-
Parkinson disease in twins: an etiologic study
-
Tanner CM Ottman R Goldman SM Parkinson disease in twins: an etiologic study JAMA 281 1999 341 346
-
(1999)
JAMA
, vol.281
, pp. 341-346
-
-
Tanner, CM1
Ottman, R2
Goldman, SM3
-
12
-
-
0032913951
-
The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins
-
Piccini P Burn DJ Ceravolo R Maraganore D Brooks DJ The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins Ann Neurol 45 1999 577 582
-
(1999)
Ann Neurol
, vol.45
, pp. 577-582
-
-
Piccini, P1
Burn, DJ2
Ceravolo, R3
Maraganore, D4
Brooks, DJ5
-
13
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH Lavedan C Leroy E Mutation in the alpha-synuclein gene identified in families with Parkinson's disease Science 276 1997 2045 2047
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, MH1
Lavedan, C2
Leroy, E3
-
14
-
-
0031990490
-
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
-
Kruger R Kuhn W Muller T Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease Nature Genet 18 1998 106 108
-
(1998)
Nature Genet
, vol.18
, pp. 106-108
-
-
Kruger, R1
Kuhn, W2
Muller, T3
-
15
-
-
0242300619
-
Alpha-synuclein locus triplication causes Parkinson's disease
-
Singleton AB Farrer M Johnson J Alpha-synuclein locus triplication causes Parkinson's disease Science 302 2003 841
-
(2003)
Science
, vol.302
, pp. 841
-
-
Singleton, AB1
Farrer, M2
Johnson, J3
-
16
-
-
10744227740
-
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications
-
Farrer M Kachergus J Forno L Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications Ann Neurol 55 2004 174 179
-
(2004)
Ann Neurol
, vol.55
, pp. 174-179
-
-
Farrer, M1
Kachergus, J2
Forno, L3
-
17
-
-
10744230149
-
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia
-
Zarranz JJ Alegre J Gomez-Esteban JC The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia Ann Neurol 55 2004 164 173
-
(2004)
Ann Neurol
, vol.55
, pp. 164-173
-
-
Zarranz, JJ1
Alegre, J2
Gomez-Esteban, JC3
-
19
-
-
0034077041
-
Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system
-
Abeliovich A Schmitz Y Farinas I Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system Neuron 25 2000 239 252
-
(2000)
Neuron
, vol.25
, pp. 239-252
-
-
Abeliovich, A1
Schmitz, Y2
Farinas, I3
-
20
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders
-
Masliah E Rockenstein E Veinbergs I Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders Science 287 2000 1265 1269
-
(2000)
Science
, vol.287
, pp. 1265-1269
-
-
Masliah, E1
Rockenstein, E2
Veinbergs, I3
-
21
-
-
0034704752
-
A Drosophila model of Parkinson's disease
-
Feany MB Bender WW A Drosophila model of Parkinson's disease Nature 404 2000 394 398
-
(2000)
Nature
, vol.404
, pp. 394-398
-
-
Feany, MB1
Bender, WW2
-
22
-
-
0037118259
-
Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein
-
Giasson BI Duda JE Quinn SM Zhang B Trojanowski JQ Lee VM Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein Neuron 34 2002 521 533
-
(2002)
Neuron
, vol.34
, pp. 521-533
-
-
Giasson, BI1
Duda, JE2
Quinn, SM3
Zhang, B4
Trojanowski, JQ5
Lee, VM6
-
23
-
-
0036550101
-
Parkinson-like neurodegeneration induced by targeted overexpression of alpha-synuclein in the nigrostriatal system
-
Kirik D Rosenblad C Burger C Parkinson-like neurodegeneration induced by targeted overexpression of alpha-synuclein in the nigrostriatal system J Neurosci 22 2002 2780 2791
-
(2002)
J Neurosci
, vol.22
, pp. 2780-2791
-
-
Kirik, D1
Rosenblad, C2
Burger, C3
-
24
-
-
0034681163
-
Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy
-
Conway KA Lee SJ Rochet JC Ding TT Williamson RE Lansbury PT Jr Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy Proc Natl Acad Sci USA 97 2000 571 576
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 571-576
-
-
Conway, KA1
Lee, SJ2
Rochet, JC3
Ding, TT4
Williamson, RE5
Lansbury, PT6
-
25
-
-
0035834360
-
Kinetic stabilization of the alpha-synuclein protofibril by a dopamine-alpha-synuclein adduct
-
Conway KA Rochet JC Bieganski RM Lansbury PT Jr Kinetic stabilization of the alpha-synuclein protofibril by a dopamine-alpha-synuclein adduct Science 294 2001 1346 1349
-
(2001)
Science
, vol.294
, pp. 1346-1349
-
-
Conway, KA1
Rochet, JC2
Bieganski, RM3
Lansbury, PT4
-
26
-
-
0034326816
-
Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity
-
Tabrizi SJ Orth M Wilkinson JM Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity Hum Mol Genet 9 2000 2683 2689
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2683-2689
-
-
Tabrizi, SJ1
Orth, M2
Wilkinson, JM3
-
27
-
-
20444416315
-
Alpha-synuclein phosphorylation enhances eosinophilic cytoplasmic inclusion formation in SH-SY5Y cells
-
Smith WW Margolis RL Li X Alpha-synuclein phosphorylation enhances eosinophilic cytoplasmic inclusion formation in SH-SY5Y cells J Neurosci 25 2005 5544 5552
-
(2005)
J Neurosci
, vol.25
, pp. 5544-5552
-
-
Smith, WW1
Margolis, RL2
Li, X3
-
28
-
-
2242472974
-
Phosphorylated alpha-synuclein is ubiquitinated in alpha-synucleinopathy lesions
-
Hasegawa M Fujiwara H Nonaka T Phosphorylated alpha-synuclein is ubiquitinated in alpha-synucleinopathy lesions J Biol Chem 277 2002 49071 49076
-
(2002)
J Biol Chem
, vol.277
, pp. 49071-49076
-
-
Hasegawa, M1
Fujiwara, H2
Nonaka, T3
-
29
-
-
17844406856
-
Alpha-synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease
-
Chen L Feany MB Alpha-synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease Nature Neurosci 8 2005 657 663
-
(2005)
Nature Neurosci
, vol.8
, pp. 657-663
-
-
Chen, L1
Feany, MB2
-
30
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T Asakawa S Hattori N Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism Nature 392 1998 605 608
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T1
Asakawa, S2
Hattori, N3
-
31
-
-
0015590978
-
Paralysis agitans of early onset with marked diurnal fluctuation of symptoms
-
Yamamura Y Sobue I Ando K Iida M Yanagi T Paralysis agitans of early onset with marked diurnal fluctuation of symptoms Neurology 23 1973 239 244
-
(1973)
Neurology
, vol.23
, pp. 239-244
-
-
Yamamura, Y1
Sobue, I2
Ando, K3
Iida, M4
Yanagi, T5
-
32
-
-
0028198309
-
Familial juvenile parkinsonism: clinical and pathologic study in a family
-
Takahashi H Ohama E Suzuki S Familial juvenile parkinsonism: clinical and pathologic study in a family Neurology 44 3 pt 1 1994 437 441
-
(1994)
Neurology
, vol.44
, Issue.3 pt 1
, pp. 437-441
-
-
Takahashi, H1
Ohama, E2
Suzuki, S3
-
33
-
-
16944362288
-
Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2–27
-
Matsumine H Saito M Shimoda-Matsubayashi S Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2–27 Am J Hum Genet 60 1997 588 596
-
(1997)
Am J Hum Genet
, vol.60
, pp. 588-596
-
-
Matsumine, H1
Saito, M2
Shimoda-Matsubayashi, S3
-
34
-
-
18244412384
-
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals
-
Hattori N Kitada T Matsumine H Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals Ann Neurol 44 1998 935 941
-
(1998)
Ann Neurol
, vol.44
, pp. 935-941
-
-
Hattori, N1
Kitada, T2
Matsumine, H3
-
35
-
-
0345490853
-
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
-
Abbas N Lucking CB Ricard S A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease Hum Mol Genet 8 1999 567 574
-
(1999)
Hum Mol Genet
, vol.8
, pp. 567-574
-
-
Abbas, N1
Lucking, CB2
Ricard, S3
-
36
-
-
0034848395
-
Lewy bodies and parkinsonism in families with parkin mutations
-
Farrer M Chan P Chen R Lewy bodies and parkinsonism in families with parkin mutations Ann Neurol 50 2001 293 300
-
(2001)
Ann Neurol
, vol.50
, pp. 293-300
-
-
Farrer, M1
Chan, P2
Chen, R3
-
37
-
-
18444398035
-
Complex relationship between Parkin mutations and Parkinson disease
-
West A Periquet M Lincoln S Complex relationship between Parkin mutations and Parkinson disease Am J Med Genet 114 2002 584 591
-
(2002)
Am J Med Genet
, vol.114
, pp. 584-591
-
-
West, A1
Periquet, M2
Lincoln, S3
-
38
-
-
0033933048
-
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
-
Shimura H Hattori N Kubo S Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase Nature Genet 25 2000 302 305
-
(2000)
Nature Genet
, vol.25
, pp. 302-305
-
-
Shimura, H1
Hattori, N2
Kubo, S3
-
39
-
-
0034700158
-
Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1
-
Zhang Y Gao J Chung KK Huang H Dawson VL Dawson TM Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1 Proc Natl Acad Sci USA 97 2000 13354 13359
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 13354-13359
-
-
Zhang, Y1
Gao, J2
Chung, KK3
Huang, H4
Dawson, VL5
Dawson, TM6
-
40
-
-
0035967883
-
An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin
-
Imai Y Soda M Inoue H Hattori N Mizuno Y Takahashi R An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin Cell 105 2001 891 902
-
(2001)
Cell
, vol.105
, pp. 891-902
-
-
Imai, Y1
Soda, M2
Inoue, H3
Hattori, N4
Mizuno, Y5
Takahashi, R6
-
41
-
-
10644281090
-
Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an alpha-synuclein rat model of Parkinson's disease
-
Lo BC Schneider BL Bauer M Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an alpha-synuclein rat model of Parkinson's disease Proc Natl Acad Sci USA 101 2004 17510 17515
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 17510-17515
-
-
Lo, BC1
Schneider, BL2
Bauer, M3
-
42
-
-
0141891953
-
Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons
-
Goldberg MS Fleming SM Palacino JJ Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons J Biol Chem 278 2003 43628 43635
-
(2003)
J Biol Chem
, vol.278
, pp. 43628-43635
-
-
Goldberg, MS1
Fleming, SM2
Palacino, JJ3
-
43
-
-
2442481789
-
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
-
Palacino JJ Sagi D Goldberg MS Mitochondrial dysfunction and oxidative damage in parkin-deficient mice J Biol Chem 279 2004 18614 18622
-
(2004)
J Biol Chem
, vol.279
, pp. 18614-18622
-
-
Palacino, JJ1
Sagi, D2
Goldberg, MS3
-
45
-
-
0037338634
-
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death
-
Darios F Corti O Lucking CB Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death Hum Mol Genet 12 2003 517 526
-
(2003)
Hum Mol Genet
, vol.12
, pp. 517-526
-
-
Darios, F1
Corti, O2
Lucking, CB3
-
46
-
-
4544326057
-
Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations
-
Muftuoglu M Elibol B Dalmizrak O Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations Mov Dis 19 2004 544 548
-
(2004)
Mov Dis
, vol.19
, pp. 544-548
-
-
Muftuoglu, M1
Elibol, B2
Dalmizrak, O3
-
47
-
-
2542534741
-
S-nitrosylation of parkin regulates ubiquitination and compromises parkin's protective function
-
Chung KK Thomas B Li X S-nitrosylation of parkin regulates ubiquitination and compromises parkin's protective function Science 304 2004 1328 1331
-
(2004)
Science
, vol.304
, pp. 1328-1331
-
-
Chung, KK1
Thomas, B2
Li, X3
-
48
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy E Boyer R Auburger G The ubiquitin pathway in Parkinson's disease Nature 395 1998 451 452
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E1
Boyer, R2
Auburger, G3
-
49
-
-
0033597972
-
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
-
Harhangi BS Farrer MJ Lincoln S The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease Neurosci Lett 270 1999 1 4
-
(1999)
Neurosci Lett
, vol.270
, pp. 1-4
-
-
Harhangi, BS1
Farrer, MJ2
Lincoln, S3
-
50
-
-
0033525009
-
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease
-
Lincoln S Vaughan J Wood N Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease Neuroreport 10 1999 427 429
-
(1999)
Neuroreport
, vol.10
, pp. 427-429
-
-
Lincoln, S1
Vaughan, J2
Wood, N3
-
51
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente EM Abou-Sleiman PM Caputo V Hereditary early-onset Parkinson's disease caused by mutations in PINK1 Science 304 2004 1158 1160
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, EM1
Abou-Sleiman, PM2
Caputo, V3
-
52
-
-
0035958558
-
Growth-suppressive effects of BPOZ and EGR2, two genes involved in the PTEN signaling pathway
-
Unoki M Nakamura Y Growth-suppressive effects of BPOZ and EGR2, two genes involved in the PTEN signaling pathway Oncogene 20 2001 4457 4465
-
(2001)
Oncogene
, vol.20
, pp. 4457-4465
-
-
Unoki, M1
Nakamura, Y2
-
53
-
-
4444274910
-
PINK1 mutations are associated with sporadic early-onset parkinsonism
-
Valente EM Salvi S Ialongo T PINK1 mutations are associated with sporadic early-onset parkinsonism Ann Neurol 56 2004 336 341
-
(2004)
Ann Neurol
, vol.56
, pp. 336-341
-
-
Valente, EM1
Salvi, S2
Ialongo, T3
-
54
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
Hatano Y Li Y Sato K Novel PINK1 mutations in early-onset parkinsonism Ann Neurol 56 2004 424 427
-
(2004)
Ann Neurol
, vol.56
, pp. 424-427
-
-
Hatano, Y1
Li, Y2
Sato, K3
-
56
-
-
0034614490
-
Signaling—2000 and beyond
-
Hunter T Signaling—2000 and beyond Cell 100 2000 113 127
-
(2000)
Cell
, vol.100
, pp. 113-127
-
-
Hunter, T1
-
57
-
-
0036097364
-
The origins of protein phosphorylation
-
Cohen P The origins of protein phosphorylation Nature Cell Biol 4 2002 E127 E130
-
(2002)
Nature Cell Biol
, vol.4
, pp. E127-E130
-
-
Cohen, P1
-
59
-
-
0028853625
-
Mammalian cytochrome-c oxidase: characterization of enzyme and immunological detection of subunits in tissue extracts and whole cells
-
Capaldi RA Marusich MF Taanman JW Mammalian cytochrome-c oxidase: characterization of enzyme and immunological detection of subunits in tissue extracts and whole cells Methods Enzymol 260 1995 117 132
-
(1995)
Methods Enzymol
, vol.260
, pp. 117-132
-
-
Capaldi, RA1
Marusich, MF2
Taanman, JW3
-
60
-
-
0029984584
-
Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia
-
Taanman JW Burton MD Marusich MF Kennaway NG Capaldi RA Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia Biochim Biophys Acta 1315 1996 199 207
-
(1996)
Biochim Biophys Acta
, vol.1315
, pp. 199-207
-
-
Taanman, JW1
Burton, MD2
Marusich, MF3
Kennaway, NG4
Capaldi, RA5
-
61
-
-
0038034950
-
Analysis of steady-state protein phosphorylation in mitochondria using a novel fluorescent phosphosensor dye
-
Schulenberg B Aggeler R Beechem JM Capaldi RA Patton WF Analysis of steady-state protein phosphorylation in mitochondria using a novel fluorescent phosphosensor dye J Biol Chem 278 2003 27251 27255
-
(2003)
J Biol Chem
, vol.278
, pp. 27251-27255
-
-
Schulenberg, B1
Aggeler, R2
Beechem, JM3
Capaldi, RA4
Patton, WF5
-
62
-
-
2942726285
-
The phosphorylation of subunits of complex I from bovine heart mitochondria
-
Chen R Fearnley IM Peak-Chew SY Walker JE The phosphorylation of subunits of complex I from bovine heart mitochondria J Biol Chem 279 2004 26036 26045
-
(2004)
J Biol Chem
, vol.279
, pp. 26036-26045
-
-
Chen, R1
Fearnley, IM2
Peak-Chew, SY3
Walker, JE4
-
63
-
-
4444286595
-
Focused proteomics: monoclonal antibody-based isolation of the oxidative phosphorylation machinery and detection of phosphoproteins using a fluorescent phosphoprotein gel stain
-
Murray J Marusich MF Capaldi RA Aggeler R Focused proteomics: monoclonal antibody-based isolation of the oxidative phosphorylation machinery and detection of phosphoproteins using a fluorescent phosphoprotein gel stain Electrophoresis 25 2004 2520 2525
-
(2004)
Electrophoresis
, vol.25
, pp. 2520-2525
-
-
Murray, J1
Marusich, MF2
Capaldi, RA3
Aggeler, R4
-
64
-
-
4444305698
-
Characterization of dynamic and steady-state protein phosphorylation using a fluorescent phosphoprotein gel stain and mass spectrometry
-
Schulenberg B Goodman TN Aggeler R Capaldi RA Patton WF Characterization of dynamic and steady-state protein phosphorylation using a fluorescent phosphoprotein gel stain and mass spectrometry Electrophoresis 25 2004 2526 2532
-
(2004)
Electrophoresis
, vol.25
, pp. 2526-2532
-
-
Schulenberg, B1
Goodman, TN2
Aggeler, R3
Capaldi, RA4
Patton, WF5
-
65
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
-
Di Fonzo A Rohe CF Ferreira J A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Lancet 365 2005 412 415
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A1
Rohe, CF2
Ferreira, J3
-
66
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols WC Pankratz N Hernandez D Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease Lancet 365 2005 410 412
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, WC1
Pankratz, N2
Hernandez, D3
-
67
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
-
Kachergus J Mata IF Hulihan M Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations Am J Hum Genet 76 2005 672 680
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-680
-
-
Kachergus, J1
Mata, IF2
Hulihan, M3
-
68
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks WP Abou-Sleiman PM Gandhi S A common LRRK2 mutation in idiopathic Parkinson's disease Lancet 365 2005 415 416
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, WP1
Abou-Sleiman, PM2
Gandhi, S3
-
69
-
-
20444414834
-
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
-
Deng H Le W Guo Y Hunter CB Xie W Jankovic J Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation Ann Neurol 57 2005 933 934
-
(2005)
Ann Neurol
, vol.57
, pp. 933-934
-
-
Deng, H1
Le, W2
Guo, Y3
Hunter, CB4
Xie, W5
Jankovic, J6
-
70
-
-
24644486896
-
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
-
Zabetian CP Samii A Mosley AD A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations Neurology 65 2005 741 744
-
(2005)
Neurology
, vol.65
, pp. 741-744
-
-
Zabetian, CP1
Samii, A2
Mosley, AD3
-
71
-
-
24644474856
-
The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases
-
Hernandez D Paisan RC Crawley A The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases Neurosci Lett 389 2005 137 139
-
(2005)
Neurosci Lett
, vol.389
, pp. 137-139
-
-
Hernandez, D1
Paisan, RC2
Crawley, A3
-
72
-
-
25144468286
-
LRRK2 mutations are not common in Alzheimer's disease
-
Toft M Sando SB Melquist S LRRK2 mutations are not common in Alzheimer's disease Mech Ageing Dev 126 2005 1201 1205
-
(2005)
Mech Ageing Dev
, vol.126
, pp. 1201-1205
-
-
Toft, M1
Sando, SB2
Melquist, S3
-
73
-
-
26444613397
-
Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation
-
Kay DM Kramer P Higgins D Zabetian CP Payami H Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation Mov Disord 20 2005 1077 1078
-
(2005)
Mov Disord
, vol.20
, pp. 1077-1078
-
-
Kay, DM1
Kramer, P2
Higgins, D3
Zabetian, CP4
Payami, H5
-
74
-
-
28544434193
-
PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation
-
Adams JR van Netten H Schulzer M PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation Brain 128 pt 12 2005 2777 2785
-
(2005)
Brain
, vol.128
, Issue.pt 12
, pp. 2777-2785
-
-
Adams, JR1
van Netten, H2
Schulzer, M3
-
75
-
-
0036196860
-
A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
-
Funayama M Hasegawa K Kowa H Saito M Tsuji S Obata F A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1 Ann Neurol 51 2002 296 301
-
(2002)
Ann Neurol
, vol.51
, pp. 296-301
-
-
Funayama, M1
Hasegawa, K2
Kowa, H3
Saito, M4
Tsuji, S5
Obata, F6
-
76
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Wszolek ZK Pfeiffer RF Tsuboi Y Autosomal dominant parkinsonism associated with variable synuclein and tau pathology Neurology 62 2004 1619 1622
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, ZK1
Pfeiffer, RF2
Tsuboi, Y3
-
77
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich A Biskup S Leitner P Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology Neuron 44 2004 601 607
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A1
Biskup, S2
Leitner, P3
-
78
-
-
23844546218
-
Pathophysiology, pleiotrophy and paradigm shifts: genetic lessons from Parkinson's disease
-
Ross OA Farrer MJ Pathophysiology, pleiotrophy and paradigm shifts: genetic lessons from Parkinson's disease Biochem Soc Trans 33 pt 4 2005 586 590
-
(2005)
Biochem Soc Trans
, vol.33
, Issue.pt 4
, pp. 586-590
-
-
Ross, OA1
Farrer, MJ2
-
79
-
-
0035575585
-
Rho family proteins: coordinating cell responses
-
Ridley AJ Rho family proteins: coordinating cell responses Trends Cell Biol 11 2001 471 477
-
(2001)
Trends Cell Biol
, vol.11
, pp. 471-477
-
-
Ridley, AJ1
-
80
-
-
0035860983
-
Complete genomic screen in Parkinson disease: evidence for multiple genes
-
Scott WK Nance MA Watts RL Complete genomic screen in Parkinson disease: evidence for multiple genes JAMA 286 2001 2239 2244
-
(2001)
JAMA
, vol.286
, pp. 2239-2244
-
-
Scott, WK1
Nance, MA2
Watts, RL3
-
81
-
-
0035949797
-
Genome-wide scan for Parkinson's disease: the GenePD Study
-
DeStefano AL Golbe LI Mark MH Genome-wide scan for Parkinson's disease: the GenePD Study Neurology 57 2001 1124 1126
-
(2001)
Neurology
, vol.57
, pp. 1124-1126
-
-
DeStefano, AL1
Golbe, LI2
Mark, MH3
-
82
-
-
0035880458
-
alpha-Synuclein gene haplotypes are associated with Parkinson's disease
-
Farrer M Maraganore DM Lockhart P alpha-Synuclein gene haplotypes are associated with Parkinson's disease Hum Mol Genet 10 2001 1847 1851
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1847-1851
-
-
Farrer, M1
Maraganore, DM2
Lockhart, P3
-
83
-
-
0037426704
-
Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability
-
Tan EK Tan C Shen H Alpha synuclein promoter and risk of Parkinson's disease: microsatellite and allelic size variability Neurosci Lett 336 2003 70 72
-
(2003)
Neurosci Lett
, vol.336
, pp. 70-72
-
-
Tan, EK1
Tan, C2
Shen, H3
-
84
-
-
0037108727
-
Functional association of the parkin gene promoter with idiopathic Parkinson's disease
-
West AB Maraganore D Crook J Functional association of the parkin gene promoter with idiopathic Parkinson's disease Hum Mol Genet 11 2002 2787 2792
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2787-2792
-
-
West, AB1
Maraganore, D2
Crook, J3
-
85
-
-
0036830525
-
A susceptibility gene for late-onset idiopathic Parkinson's disease
-
Hicks AA Petursson H Jonsson T A susceptibility gene for late-onset idiopathic Parkinson's disease Ann Neurol 52 2002 549 555
-
(2002)
Ann Neurol
, vol.52
, pp. 549-555
-
-
Hicks, AA1
Petursson, H2
Jonsson, T3
-
86
-
-
0022976146
-
Early onset Parkinson's disease in Saskatchewan—environmental considerations for etiology
-
Rajput AH Uitti RJ Stern W Laverty W Early onset Parkinson's disease in Saskatchewan—environmental considerations for etiology Can J Neurol Sci 13 1986 312 316
-
(1986)
Can J Neurol Sci
, vol.13
, pp. 312-316
-
-
Rajput, AH1
Uitti, RJ2
Stern, W3
Laverty, W4
-
87
-
-
0023933697
-
Neurological disorders and services in Saskatchewan—a report based on provincial health care records
-
Rajput AH Uitti RJ Rajput AH Neurological disorders and services in Saskatchewan—a report based on provincial health care records Neuroepidemiology 7 1988 145 151
-
(1988)
Neuroepidemiology
, vol.7
, pp. 145-151
-
-
Rajput, AH1
Uitti, RJ2
Rajput, AH3
-
88
-
-
0035885824
-
Risk factors for Parkinson's disease I In Indian patients
-
Behari M Srivastava Ak Das RR Pandey RM Risk factors for Parkinson's disease I In Indian patients J Neurol Sci 190 2001 49 55
-
(2001)
J Neurol Sci
, vol.190
, pp. 49-55
-
-
Behari, M1
Srivastava, Ak2
Das, RR3
Pandey, RM4
-
89
-
-
0025936440
-
Parkinson's disease and exposure to rural environmental factors: a population based case-control study
-
Semchuk KM Love EJ Lee RG Parkinson's disease and exposure to rural environmental factors: a population based case-control study Can J Neurol Sci 18 1991 279 286
-
(1991)
Can J Neurol Sci
, vol.18
, pp. 279-286
-
-
Semchuk, KM1
Love, EJ2
Lee, RG3
-
90
-
-
0023097950
-
Ecogenetics of Parkinson's disease: prevalence and environmental aspects in rural areas
-
Barbeau A Roy M Bernier G Campanella G Paris S Ecogenetics of Parkinson's disease: prevalence and environmental aspects in rural areas Can J Neurol Sci 14 1987 36 41
-
(1987)
Can J Neurol Sci
, vol.14
, pp. 36-41
-
-
Barbeau, A1
Roy, M2
Bernier, G3
Campanella, G4
Paris, S5
-
92
-
-
0032924712
-
Nutritional and occupational factors influencing the risk of Parkinson's disease: a case-control study in southeastern Sweden
-
Fall PA Fredrikson M Axelson O Granerus AK Nutritional and occupational factors influencing the risk of Parkinson's disease: a case-control study in southeastern Sweden Mov Disord 14 1999 28 37
-
(1999)
Mov Disord
, vol.14
, pp. 28-37
-
-
Fall, PA1
Fredrikson, M2
Axelson, O3
Granerus, AK4
-
93
-
-
0026711037
-
Parkinson's disease and exposure to agricultural work and pesticide chemicals
-
Semchuk KM Love EJ Lee RG Parkinson's disease and exposure to agricultural work and pesticide chemicals Neurology 42 1992 1328 1335
-
(1992)
Neurology
, vol.42
, pp. 1328-1335
-
-
Semchuk, KM1
Love, EJ2
Lee, RG3
-
94
-
-
0030012558
-
Possible environmental, occupational, and other etiologic factors for Parkinson's disease: a case-control study in Germany
-
Seidler A Hellenbrand W Robra BP Possible environmental, occupational, and other etiologic factors for Parkinson's disease: a case-control study in Germany Neurology 46 1996 1275 1284
-
(1996)
Neurology
, vol.46
, pp. 1275-1284
-
-
Seidler, A1
Hellenbrand, W2
Robra, BP3
-
96
-
-
0022349344
-
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxicity in mice is enhanced by pretreatment with diethyldithiocarbamate
-
Corsini GU Pintus S Chiueh CC Weiss JF Kopin IJ 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxicity in mice is enhanced by pretreatment with diethyldithiocarbamate Eur J Pharmacol 119 1985 127 128
-
(1985)
Eur J Pharmacol
, vol.119
, pp. 127-128
-
-
Corsini, GU1
Pintus, S2
Chiueh, CC3
Weiss, JF4
Kopin, IJ5
-
97
-
-
0029937494
-
Epidemiology of Parkinson's disease
-
Tanner CM Goldman SM Epidemiology of Parkinson's disease Neurol Clin 14 1996 317 335
-
(1996)
Neurol Clin
, vol.14
, pp. 317-335
-
-
Tanner, CM1
Goldman, SM2
-
99
-
-
0242667144
-
Immunohistochemical changes in the mouse striatum induced by the pyrethroid insecticide permethrin
-
Pittman JT Dodd CA Klein BG Immunohistochemical changes in the mouse striatum induced by the pyrethroid insecticide permethrin Int J Toxicol 22 2003 359 370
-
(2003)
Int J Toxicol
, vol.22
, pp. 359-370
-
-
Pittman, JT1
Dodd, CA2
Klein, BG3
-
100
-
-
0036777423
-
Selective effects of insecticides on nigrostriatal dopaminergic nerve pathways
-
Bloomquist JR Barlow RL Gillette JS Li W Kirby ML Selective effects of insecticides on nigrostriatal dopaminergic nerve pathways Neurotoxicology 23 2002 537 544
-
(2002)
Neurotoxicology
, vol.23
, pp. 537-544
-
-
Bloomquist, JR1
Barlow, RL2
Gillette, JS3
Li, W4
Kirby, ML5
-
101
-
-
29244478874
-
Deltamethrin, a pyrethroid insecticide, is a potent inducer for the activity-dependent gene expression of BDNF in neurons
-
Imamura L Yasuda M Kuramitsu K Hara D Tabuchi A Tsuda M Deltamethrin, a pyrethroid insecticide, is a potent inducer for the activity-dependent gene expression of BDNF in neurons J Pharmacol Exp Ther 316 2006 136 143
-
(2006)
J Pharmacol Exp Ther
, vol.316
, pp. 136-143
-
-
Imamura, L1
Yasuda, M2
Kuramitsu, K3
Hara, D4
Tabuchi, A5
Tsuda, M6
-
103
-
-
0037127197
-
The herbicide paraquat causes up-regulation and aggregation of alpha-synuclein in mice: paraquat and alpha-synuclein
-
Manning-Bog AB McCormack AL Li J Uversky VN Fink AL Di Monte DA The herbicide paraquat causes up-regulation and aggregation of alpha-synuclein in mice: paraquat and alpha-synuclein J Biol Chem 277 2002 1641 1644
-
(2002)
J Biol Chem
, vol.277
, pp. 1641-1644
-
-
Manning-Bog, AB1
McCormack, AL2
Li, J3
Uversky, VN4
Fink, AL5
Di Monte, DA6
-
104
-
-
9144275011
-
Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe
-
Champy P Hoglinger GU Feger J Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe J Neurochem 88 2004 63 69
-
(2004)
J Neurochem
, vol.88
, pp. 63-69
-
-
Champy, P1
Hoglinger, GU2
Feger, J3
-
105
-
-
0027504297
-
Advances in our understanding of the mechanisms of the neurotoxicity of MPTP and related compounds
-
Tipton KF Singer TP Advances in our understanding of the mechanisms of the neurotoxicity of MPTP and related compounds J Neurochem 61 1993 1191 1206
-
(1993)
J Neurochem
, vol.61
, pp. 1191-1206
-
-
Tipton, KF1
Singer, TP2
-
106
-
-
0027249375
-
Progression after chronic manganese exposure
-
Huang CC Lu CS Chu NS Progression after chronic manganese exposure Neurology 43 1993 1479 1483
-
(1993)
Neurology
, vol.43
, pp. 1479-1483
-
-
Huang, CC1
Lu, CS2
Chu, NS3
-
107
-
-
0000928960
-
Manganese poisoning
-
Mena I Manganese poisoning Vinken PJ Bruyn GW Handbook of clinical neurology. Vol 36. Intoxications of the nervous system. Part I 1979 North Holland Publishing Amsterdam 217 237
-
(1979)
, pp. 217-237
-
-
Mena, I1
-
108
-
-
21144447013
-
Searching for a relationship between manganese and welding and Parkinson's disease
-
Jankovic J Searching for a relationship between manganese and welding and Parkinson's disease Neurology 64 2005 2021 2028
-
(2005)
Neurology
, vol.64
, pp. 2021-2028
-
-
Jankovic, J1
-
109
-
-
0023002764
-
Cigarette smoking and Parkinson's disease
-
Baron JA Cigarette smoking and Parkinson's disease Neurology 36 1986 1490 1496
-
(1986)
Neurology
, vol.36
, pp. 1490-1496
-
-
Baron, JA1
-
110
-
-
0034950069
-
Prospective study of caffeine consumption and risk of Parkinson's disease in men and women
-
Ascherio A Zhang SM Hernan MA Prospective study of caffeine consumption and risk of Parkinson's disease in men and women Ann Neurol 50 2001 56 63
-
(2001)
Ann Neurol
, vol.50
, pp. 56-63
-
-
Ascherio, A1
Zhang, SM2
Hernan, MA3
-
111
-
-
0023789193
-
Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains
-
McGeer PL Itagaki S Boyes BE McGeer EG Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains Neurology 38 1988 1285 1291
-
(1988)
Neurology
, vol.38
, pp. 1285-1291
-
-
McGeer, PL1
Itagaki, S2
Boyes, BE3
McGeer, EG4
-
112
-
-
0028364696
-
Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson's disease
-
Boka G Anglade P Wallach D Javoy-Agid F Agid Y Hirsch EC Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson's disease Neurosci Lett 172 1994 151 154
-
(1994)
Neurosci Lett
, vol.172
, pp. 151-154
-
-
Boka, G1
Anglade, P2
Wallach, D3
Javoy-Agid, F4
Agid, Y5
Hirsch, EC6
-
113
-
-
0033121299
-
FcepsilonRII/CD23 is expressed in Parkinson's disease and induces, in vitro, production of nitric oxide and tumor necrosis factor-alpha in glial cells
-
Hunot S Dugas N Faucheux B FcepsilonRII/CD23 is expressed in Parkinson's disease and induces, in vitro, production of nitric oxide and tumor necrosis factor-alpha in glial cells J Neurosci 19 1999 3440 3447
-
(1999)
J Neurosci
, vol.19
, pp. 3440-3447
-
-
Hunot, S1
Dugas, N2
Faucheux, B3
-
114
-
-
0029811901
-
Arthritis and anti-inflammatory agents as possible protective factors for Alzheimer's disease: a review of 17 epidemiologic studies
-
McGeer PL Schulzer M McGeer EG Arthritis and anti-inflammatory agents as possible protective factors for Alzheimer's disease: a review of 17 epidemiologic studies Neurology 47 1996 425 432
-
(1996)
Neurology
, vol.47
, pp. 425-432
-
-
McGeer, PL1
Schulzer, M2
McGeer, EG3
-
115
-
-
0035936004
-
Nonsteroidal antiinflammatory drugs and the risk of Alzheimer's disease
-
in t’ Veld BA Ruitenberg A Hofman A Nonsteroidal antiinflammatory drugs and the risk of Alzheimer's disease N Engl J Med 345 2001 1515 1521
-
(2001)
N Engl J Med
, vol.345
, pp. 1515-1521
-
-
in t’ Veld, BA1
Ruitenberg, A2
Hofman, A3
-
116
-
-
0041653249
-
Nonsteroidal anti-inflammatory drugs and the risk of Parkinson disease
-
Chen H Zhang SM Hernan MA Schwarzschild MA Nonsteroidal anti-inflammatory drugs and the risk of Parkinson disease Arch Neurol 60 2003 1059 1064
-
(2003)
Arch Neurol
, vol.60
, pp. 1059-1064
-
-
Chen, H1
Zhang, SM2
Hernan, MA3
Schwarzschild, MA4
-
117
-
-
0005443101
-
Mitochondrial complex I deficiency in Parkinson's disease
-
Schapira AHV Cooper JM Dexter D Mitochondrial complex I deficiency in Parkinson's disease Ann Neurol 26 1989 122 123
-
(1989)
Ann Neurol
, vol.26
, pp. 122-123
-
-
Schapira, AHV1
Cooper, JM2
Dexter, D3
-
119
-
-
0027995435
-
Complex I, iron, and ferritin in Parkinson's disease substantia nigra
-
Mann VM Cooper JM Daniel SE Complex I, iron, and ferritin in Parkinson's disease substantia nigra Ann Neurol 36 1994 876 881
-
(1994)
Ann Neurol
, vol.36
, pp. 876-881
-
-
Mann, VM1
Cooper, JM2
Daniel, SE3
-
120
-
-
0025640845
-
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
-
Schapira AH Mann VM Cooper JM Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease J Neurochem 55 1990 2142 2145
-
(1990)
J Neurochem
, vol.55
, pp. 2142-2145
-
-
Schapira, AH1
Mann, VM2
Cooper, JM3
-
121
-
-
0028274216
-
Evidence for mitochondrial dysfunction in Parkinson's disease—a critical appraisal
-
Schapira AH Evidence for mitochondrial dysfunction in Parkinson's disease—a critical appraisal Mov Disord 9 1994 125 138
-
(1994)
Mov Disord
, vol.9
, pp. 125-138
-
-
Schapira, AH1
-
122
-
-
0028170328
-
A 31P magnetic resonance spectroscopy study of mitochondrial function in skeletal muscle of patients with Parkinson's disease
-
Taylor DJ Krige D Barnes PR A 31P magnetic resonance spectroscopy study of mitochondrial function in skeletal muscle of patients with Parkinson's disease J Neurol Sci 125 1994 77 81
-
(1994)
J Neurol Sci
, vol.125
, pp. 77-81
-
-
Taylor, DJ1
Krige, D2
Barnes, PR3
-
123
-
-
0029396976
-
Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle
-
Penn AM Roberts T Hodder J Allen PS Zhu G Martin WR Generalized mitochondrial dysfunction in Parkinson's disease detected by magnetic resonance spectroscopy of muscle Neurology 45 1995 2097 2099
-
(1995)
Neurology
, vol.45
, pp. 2097-2099
-
-
Penn, AM1
Roberts, T2
Hodder, J3
Allen, PS4
Zhu, G5
Martin, WR6
-
124
-
-
0024848034
-
Abnormalities of the electron transport chain in idiopathic Parkinson's disease
-
Parker WD Jr Boyson SJ Parks JK Abnormalities of the electron transport chain in idiopathic Parkinson's disease Ann Neurol 26 1989 719 723
-
(1989)
Ann Neurol
, vol.26
, pp. 719-723
-
-
Parker, WD1
Boyson, SJ2
Parks, JK3
-
125
-
-
0026484964
-
Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group
-
Krige D Carroll MT Cooper JM Marsden CD Schapira AH Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group Ann Neurol 32 1992 782 788
-
(1992)
Ann Neurol
, vol.32
, pp. 782-788
-
-
Krige, D1
Carroll, MT2
Cooper, JM3
Marsden, CD4
Schapira, AH5
-
126
-
-
0029050583
-
Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease
-
Haas RH Nasirian F Nakano K Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease Ann Neurol 37 1995 714 722
-
(1995)
Ann Neurol
, vol.37
, pp. 714-722
-
-
Haas, RH1
Nasirian, F2
Nakano, K3
-
128
-
-
0025010120
-
Mitochondrial DNA analysis in Parkinson's disease
-
Schapira AH Holt IJ Sweeney M Mitochondrial DNA analysis in Parkinson's disease Mov Disord 5 1990 294 297
-
(1990)
Mov Disord
, vol.5
, pp. 294-297
-
-
Schapira, AH1
Holt, IJ2
Sweeney, M3
-
129
-
-
0025863393
-
Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease
-
Ozawa T Tanaka M Ino H Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease Biochem Biophys Res Commun 176 1991 938 946
-
(1991)
Biochem Biophys Res Commun
, vol.176
, pp. 938-946
-
-
Ozawa, T1
Tanaka, M2
Ino, H3
-
130
-
-
0028854722
-
Point mutations of mitochondrial genome in Parkinson's disease
-
Ikebe S Tanaka M Ozawa T Point mutations of mitochondrial genome in Parkinson's disease Brain Res Mol Brain Res 28 1995 281 295
-
(1995)
Brain Res Mol Brain Res
, vol.28
, pp. 281-295
-
-
Ikebe, S1
Tanaka, M2
Ozawa, T3
-
131
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
Shoffner JM Brown MD Torroni A Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients Genomics 17 1993 171 184
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, JM1
Brown, MD2
Torroni, A3
-
135
-
-
0036297660
-
Sequence analysis of the entire mitochondrial genome in Parkinson's disease
-
Vives-Bauza C Andreu AL Manfredi G Sequence analysis of the entire mitochondrial genome in Parkinson's disease Biochem Biophys Res Commun 290 2002 1593 1601
-
(2002)
Biochem Biophys Res Commun
, vol.290
, pp. 1593-1601
-
-
Vives-Bauza, C1
Andreu, AL2
Manfredi, G3
-
136
-
-
0037385480
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
-
van der Walt JM Nicodemus KK Martin ER Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease Am J Hum Genet 72 2003 804 811
-
(2003)
Am J Hum Genet
, vol.72
, pp. 804-811
-
-
van der Walt, JM1
Nicodemus, KK2
Martin, ER3
-
137
-
-
20144389920
-
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD
-
Pyle A Foltynie T Tiangyou W Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD Ann Neurol 57 2005 564 567
-
(2005)
Ann Neurol
, vol.57
, pp. 564-567
-
-
Pyle, A1
Foltynie, T2
Tiangyou, W3
-
138
-
-
0037380725
-
mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish
-
Ross OA McCormack R Maxwell LD mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish Exp Gerontol 38 2003 397 405
-
(2003)
Exp Gerontol
, vol.38
, pp. 397-405
-
-
Ross, OA1
McCormack, R2
Maxwell, LD3
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