-
2
-
-
0027750939
-
Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes
-
(1993)
Brain
, vol.116
, pp. 1451-1463
-
-
Benecke, R.1
Strümper, P.2
Weiss, H.3
-
4
-
-
0030066069
-
Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients
-
(1996)
Am J Med Genet
, vol.61
, pp. 283-289
-
-
Brown, M.D.1
Shoffner, J.M.2
Kim, Y.L.3
Jun, A.S.4
Graham, B.H.5
Cabell, M.F.6
Gurley, D.S.7
Wallace, D.C.8
-
10
-
-
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
-
(1998)
Ann Neurol
, vol.44
, pp. 935-941
-
-
Hattori, N.1
Kitada, T.2
Matsumine, H.3
Asakawa, S.4
Yamamura, Y.5
Yoshino, H.6
Kobayashi, T.7
Yokochi, M.8
Wang, M.9
Yoritaka, A.10
Kondo, T.11
Kuzuhara, S.12
Nakamura, S.13
Shimizu, N.14
Mizuno, Y.15
-
11
-
-
0030813676
-
Population genetics and disease susceptibility: Characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1835-1846
-
-
Hofmann, S.1
Jaksch, M.2
Bezold, R.3
Mertens, S.4
Aholt, S.5
Paprotta, A.6
Gerbitz, K.D.7
-
14
-
-
0028316759
-
Unaltered aconitase activity, but decreased complex I activity in substantia nigra pars compacta of patients with Parkinson's disease
-
(1994)
Neurosci Lett
, vol.169
, pp. 126-128
-
-
Janetzky, B.1
Hauck, S.2
Youdim, M.B.3
Riederer, P.4
Jellinger, K.5
Pantucek, F.6
Zöchling, R.7
Boissl, K.W.8
Reichmann, H.9
-
15
-
-
0029965659
-
Investigations on the point mutation at position 5460 of the mtDNA in different neurodegenerative and neuromuscular diseases
-
(1996)
Eur Neurol
, vol.36
, pp. 149-153
-
-
Janetzky, B.1
Schmid, C.2
Bischof, F.3
Frölich, L.4
Gsell, W.5
Kalaria, R.N.6
Riederer, P.7
Reichmann, H.8
-
16
-
-
0030449566
-
Mitochondrial DNA polymorphism in substantia nigra
-
(1996)
J Neurol Sci
, vol.144
, pp. 204-211
-
-
Kapsa, R.M.1
Jean-Francois, M.J.2
Lertrit, P.3
Weng, S.4
Siregar, N.5
Ojaimi, J.6
Donnan, G.7
Masters, C.8
Byrne, E.9
-
18
-
-
0032008669
-
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
-
(1998)
Neurogenetics
, vol.1
, pp. 197-204
-
-
Kösel, S.1
Grasbon-Frodl, E.M.2
Mautsch, U.3
Egensperger, R.4
Von Eitzen, U.5
Frishman, D.6
Hofmann, S.7
Gerbitz, K.D.8
Mehraein, P.9
Graeber, M.B.10
-
29
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Anthanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duoisin, R.C.17
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
34
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.M.1
Brown, M.D.2
Torroni, A.3
Lott, M.T.4
Cabell, M.F.5
Mirra, S.S.6
Beal, M.F.7
Yang, C.C.8
Gearing, M.9
Salvo, R.10
Watts, R.L.11
Juncos, J.L.12
Hansen, L.A.13
Crain, B.J.14
Fayad, M.15
Reckford, C.L.16
Wallace, D.C.17
-
36
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
(1996)
Ann Neurol
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
Tuttle, J.B.4
Trimmer, P.A.5
Sheehan, J.P.6
Bennett J.P., Jr.7
Davis, R.E.8
Parker W.D., Jr.9
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