-
1
-
-
0031711713
-
Mitochondrial dysfunction in Parkinson's disease
-
Mizuno Y, Yoshino H, Ikebe S-i, et al. Mitochondrial dysfunction in Parkinson's disease. Ann Neurol 1998;44(suppl 1):S99-S109.
-
(1998)
Ann Neurol
, vol.44
, Issue.SUPPL. 1
-
-
Mizuno, Y.1
Yoshino, H.2
Ikebe, S.-I.3
-
2
-
-
0022503139
-
Studies on the neurotoxicity of 1-methyl-4-phenyl-1,2,5,6- tetrahydropiridine: Inhibition of NAD-linked substrate oxidation by its metabolite 1-methyl-4-pyridinium
-
Vyas I, Heikkila RE, Nicklas WJ. Studies on the neurotoxicity of 1-methyl-4-phenyl-1,2,5,6-tetrahydropiridine: inhibition of NAD-linked substrate oxidation by its metabolite 1-methyl-4-pyridinium. J Neurochem 1986;46:1501-1507.
-
(1986)
J Neurochem
, vol.46
, pp. 1501-1507
-
-
Vyas, I.1
Heikkila, R.E.2
Nicklas, W.J.3
-
3
-
-
0027379322
-
Mitochondrial involvement in Parkinson's disease: The controversy continues
-
DiMauro S. Mitochondrial involvement in Parkinson's disease: The controversy continues. Neurology 1993;43:2170-2172.
-
(1993)
Neurology
, vol.43
, pp. 2170-2172
-
-
Dimauro, S.1
-
4
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente EM, Abou-Sleiman PM, Caputo V, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 2004;304:1158-1160.
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
-
5
-
-
0345490853
-
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
-
Abbas N, Lucking CB, Ricard S, et al. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. Hum Mol Genet 1999;8:567-574.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 567-574
-
-
Abbas, N.1
Lucking, C.B.2
Ricard, S.3
-
6
-
-
25444474703
-
Mitochondria take center stage in aging and neurodegeneration
-
Beal MF. Mitochondria take center stage in aging and neurodegeneration. Ann Neurol 2005;58:495-505.
-
(2005)
Ann Neurol
, vol.58
, pp. 495-505
-
-
Beal, M.F.1
-
7
-
-
23644436319
-
Disorders of nuclear-mitochondrial intergenomic signaling
-
Spinazzola A, Zeviani M. Disorders of nuclear-mitochondrial intergenomic signaling. Gene 2005;354:162-168.
-
(2005)
Gene
, vol.354
, pp. 162-168
-
-
Spinazzola, A.1
Zeviani, M.2
-
8
-
-
23644449234
-
Consequences of mutations in human DNA polymerase gamma
-
Longley MJ, Bienstock RJ, Copeland WC. Consequences of mutations in human DNA polymerase gamma. Gene 2005;18:125-131.
-
(2005)
Gene
, vol.18
, pp. 125-131
-
-
Longley, M.J.1
Bienstock, R.J.2
Copeland, W.C.3
-
9
-
-
4544273256
-
Parkinsonism, premature menopause, and mitochondrial DNA polymerase mutations: Clinical and molecular genetic study
-
Luoma P, Melberg A, Rinne JO, et al. Parkinsonism, premature menopause, and mitochondrial DNA polymerase mutations: clinical and molecular genetic study. Lancet 2004;364:875-882.
-
(2004)
Lancet
, vol.364
, pp. 875-882
-
-
Luoma, P.1
Melberg, A.2
Rinne, J.O.3
-
10
-
-
0029875973
-
Cytochemistry and immunocytochemistry of mitochondria in tissue sections
-
Sciacco M, Bonilla E. Cytochemistry and immunocytochemistry of mitochondria in tissue sections. Meth Enzymol 1996;264:509-521.
-
(1996)
Meth Enzymol
, vol.264
, pp. 509-521
-
-
Sciacco, M.1
Bonilla, E.2
-
11
-
-
0023429777
-
Cytochrome c oxidase deficiency in Leigh syndrome
-
DiMauro S, Servidei S, Zeviani M, et al. Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol 1987;22:498-506.
-
(1987)
Ann Neurol
, vol.22
, pp. 498-506
-
-
DiMauro, S.1
Servidei, S.2
Zeviani, M.3
-
13
-
-
0346025687
-
ND5 is a hotspot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy
-
Nishigaki Y, Marti RA, Hirano M. ND5 is a hotspot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy. Hum Mol Genet 2004;13:91-101.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 91-101
-
-
Nishigaki, Y.1
Marti, R.A.2
Hirano, M.3
-
14
-
-
0042922454
-
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ
-
Filosto M, Mancuso M, Nishigaki Y, et al. Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ. Arch Neurol 2003;60:1279-1284.
-
(2003)
Arch Neurol
, vol.60
, pp. 1279-1284
-
-
Filosto, M.1
Mancuso, M.2
Nishigaki, Y.3
-
15
-
-
12144288681
-
Fatal infantile neuromuscular presentation of glycogen storage disease type IV
-
Tay SKH, Akman HO, Chung WK, et al. Fatal infantile neuromuscular presentation of glycogen storage disease type IV. Neuromusc Disord 2004;14:253-260.
-
(2004)
Neuromusc Disord
, vol.14
, pp. 253-260
-
-
Tay, S.K.H.1
Akman, H.O.2
Chung, W.K.3
-
16
-
-
23944456723
-
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome
-
Luoma PT, Luo N, Loscher WN, et al. Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome. Hum Mol Genet 2005;14:1907-1920.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1907-1920
-
-
Luoma, P.T.1
Luo, N.2
Loscher, W.N.3
-
17
-
-
0033925871
-
Anxiety disorders and depressive disorders preceding Parkinson's disease: A case-control study
-
Shiba M, Bower JH, Maraganore DM, et al. Anxiety disorders and depressive disorders preceding Parkinson's disease: a case-control study. Movement Disord 2000;15:669-677.
-
(2000)
Movement Disord
, vol.15
, pp. 669-677
-
-
Shiba, M.1
Bower, J.H.2
Maraganore, D.M.3
-
18
-
-
0032899012
-
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with Parkinsonism/MELAS overlap syndrome
-
De Coo IFM, Renier WO, Ruitenbeek W, et al. A 4-base pair deletion in the mitochondrial cytochrome b gene associated with Parkinsonism/MELAS overlap syndrome. Ann Neurol 1999;45:130-133.
-
(1999)
Ann Neurol
, vol.45
, pp. 130-133
-
-
De Coo, I.F.M.1
Renier, W.O.2
Ruitenbeek, W.3
-
19
-
-
0033768121
-
A novel mitochondrial 12S rRNA point mutation in Parkinsonism, deafness and neuropathy
-
Thyagarajan D, Bressman S, Bruno C, et al. A novel mitochondrial 12S rRNA point mutation in Parkinsonism, deafness and neuropathy. Ann Neurol 2000;48:730-736.
-
(2000)
Ann Neurol
, vol.48
, pp. 730-736
-
-
Thyagarajan, D.1
Bressman, S.2
Bruno, C.3
-
20
-
-
3543017697
-
A novel POLG mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism
-
Mancuso M, Filosto M, Oh SJ, DiMauro S. A novel POLG mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism. Arch Neurol 2004;61:1777-1779.
-
(2004)
Arch Neurol
, vol.61
, pp. 1777-1779
-
-
Mancuso, M.1
Filosto, M.2
Oh, S.J.3
DiMauro, S.4
|