-
1
-
-
0031814491
-
Mitochondrial DNA and diseases of the nervous system. The spectrum
-
Di Mauro S, Schon EA. Mitochondrial DNA and diseases of the nervous system. The spectrum. Neuroscientist 1997; 4:53-63.
-
(1997)
Neuroscientist
, vol.4
, pp. 53-63
-
-
Di Mauro, S.1
Schon, E.A.2
-
2
-
-
0022503139
-
Studies on the neurotoxicity of 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine: 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-tetrahydropyridine: inhibition of NAD-linked substrate oxidation by its metabolite, 1-methyl-4-pyridinium. J Neurochem 1986;46:1501-7.
-
(1986)
J Neurochem
, vol.46
, pp. 1501-1507
-
-
Vyas, I.1
Heikkila, R.E.2
Nicklas, W.J.3
-
3
-
-
0024390719
-
Mitochondrial complex I deficiency in Parkinson's disease
-
Schapira AHV, Cooper JM, Dexter D, et al. Mitochondrial complex I deficiency in Parkinson's disease. Lancet 1989;i: 1269.
-
(1989)
Lancet
, vol.1
, pp. 1269
-
-
Schapira, A.H.V.1
Cooper, J.M.2
Dexter, D.3
-
4
-
-
0029071520
-
Role of mitochondria in etiology and pathogenesis of Parkinson's disease
-
Mizumo Y, Ikebe S, Hattori N, et al. Role of mitochondria in etiology and pathogenesis of Parkinson's disease. Biochim Biophys Acta 1995;1271:265-74.
-
(1995)
Biochim Biophys Acta
, vol.1271
, pp. 265-274
-
-
Mizumo, Y.1
Ikebe, S.2
Hattori, N.3
-
5
-
-
0025285735
-
Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
-
Truong DD, Harding AE, Scaravilli F, et al. Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies. Mov Disord 1990;5:109-17.
-
(1990)
Mov Disord
, vol.5
, pp. 109-117
-
-
Truong, D.D.1
Harding, A.E.2
Scaravilli, F.3
-
6
-
-
0030297454
-
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: A report of two families and two sporadic cases with unusual clinical and neuropathological features
-
Chalmers RAI, Brockington M, Howard RS, et al. Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features. J Neurol Sci 1996;143:41-5.
-
(1996)
J Neurol Sci
, vol.143
, pp. 41-45
-
-
Chalmers, R.A.I.1
Brockington, M.2
Howard, R.S.3
-
7
-
-
0032008669
-
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
-
Kosel S, Grasbon-Frodl EM, Mautsch U, et al. Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease. Neurogenetics 1998;1:197-204.
-
(1998)
Neurogenetics
, vol.1
, pp. 197-204
-
-
Kosel, S.1
Grasbon-Frodl, E.M.2
Mautsch, U.3
-
8
-
-
0032937713
-
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease
-
Grasbon-Frodl EM, Kosel S, Sprinzl M, et al. Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease. Neurogenetics 1999;2: 121-7.
-
(1999)
Neurogenetics
, vol.2
, pp. 121-127
-
-
Grasbon-Frodl, E.M.1
Kosel, S.2
Sprinzl, M.3
-
9
-
-
0032830133
-
The relationship of plasma catecholamine and lactate during anaerobic threshold exercise in mitochondrial myopathies
-
Siciliano G, Renna M, Manca ML, et al. The relationship of plasma catecholamine and lactate during anaerobic threshold exercise in mitochondrial myopathies. Neuromuscul Disord 1999;9:411-16.
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 411-416
-
-
Siciliano, G.1
Renna, M.2
Manca, M.L.3
-
10
-
-
0030868775
-
Mitochondrial DNA mutations in multiple symmetric lipomatosis
-
Klopstock T, Naumann M, Seibel P, et al. Mitochondrial DNA mutations in multiple symmetric lipomatosis. Mol Cell Biochem 1997;174:271-5.
-
(1997)
Mol Cell Biochem
, vol.174
, pp. 271-275
-
-
Klopstock, T.1
Naumann, M.2
Seibel, P.3
-
11
-
-
0024601360
-
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
-
Zeviani M, Servidei S, Gellera C, et al. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature 1989;339:309-11.
-
(1989)
Nature
, vol.339
, pp. 309-311
-
-
Zeviani, M.1
Servidei, S.2
Gellera, C.3
-
12
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-7.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
-
13
-
-
0032564235
-
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
-
Lucking CB, Abbas N, Durr A, et al. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. Lancet 1998;352:1355-6.
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
Abbas, N.2
Durr, A.3
-
14
-
-
0029840825
-
Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brain
-
Schnopp NM, Kosel S, Egensperger R, et al. Regional heterogeneity of mtDNA heteroplasmy in parkinsonian brain. Clin Neuropathol 1996;15:348-52.
-
(1996)
Clin Neuropathol
, vol.15
, pp. 348-352
-
-
Schnopp, N.M.1
Kosel, S.2
Egensperger, R.3
-
15
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
Swerdlow RH, Parks JK, Miller SW, et al. Origin and functional consequences of the complex I defect in Parkinson's disease. Ann Neurol 1996;40:663-71.
-
(1996)
Ann Neurol
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
-
16
-
-
0030931581
-
The common deletion is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction
-
Kosel S, Egensperger R, Schnopp NM, et al. The common deletion is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction Mov Disord 1997;12:639-15.
-
(1997)
Mov Disord
, vol.12
, pp. 639-715
-
-
Kosel, S.1
Egensperger, R.2
Schnopp, N.M.3
|