-
2
-
-
36749037338
-
Mitochondrial dysfunction in neurodegenerative disorders
-
Baron M., Kudin A.P., and Kunz W.S. Mitochondrial dysfunction in neurodegenerative disorders. Biochem. Soc. Trans. 35 (2007) 1228-1231
-
(2007)
Biochem. Soc. Trans.
, vol.35
, pp. 1228-1231
-
-
Baron, M.1
Kudin, A.P.2
Kunz, W.S.3
-
3
-
-
0035852868
-
Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation
-
Bataillard M., Chatzoglou E., Rumbach L., Sternberg D., Tournade A., Lafort P., Jardel C., Maisonobe T., and Lombes A. Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation. Neurology 56 (2001) 405-407
-
(2001)
Neurology
, vol.56
, pp. 405-407
-
-
Bataillard, M.1
Chatzoglou, E.2
Rumbach, L.3
Sternberg, D.4
Tournade, A.5
Lafort, P.6
Jardel, C.7
Maisonobe, T.8
Lombes, A.9
-
4
-
-
0030612186
-
Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures
-
Bengzon J., Kokaia Z., Elmer E., Nanobashvili A., Kokaia M., and Lindvall O. Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures. Proc. Natl. Acad. Sci. U. S. A. 94 (1977) 10432-10437
-
(1977)
Proc. Natl. Acad. Sci. U. S. A.
, vol.94
, pp. 10432-10437
-
-
Bengzon, J.1
Kokaia, Z.2
Elmer, E.3
Nanobashvili, A.4
Kokaia, M.5
Lindvall, O.6
-
5
-
-
0032526986
-
Changes in mitochondrial function resulting from synaptic activity in the rat hippocampal slice
-
Bindokas V.P., Lee C.C., Colmers W.F., and Miller R.J. Changes in mitochondrial function resulting from synaptic activity in the rat hippocampal slice. J. Neurosci. 18 (1998) 4570-4587
-
(1998)
J. Neurosci.
, vol.18
, pp. 4570-4587
-
-
Bindokas, V.P.1
Lee, C.C.2
Colmers, W.F.3
Miller, R.J.4
-
6
-
-
0345035513
-
Cellular pathology of hilar neurons in Ammon's horn sclerosis
-
Blümcke I., Zuschratter W., Schewe J.C., Suter B., Lie A.A., Riederer B.M., Meier B., Schramm J., Elger C.E., and Wiestler O.D. Cellular pathology of hilar neurons in Ammon's horn sclerosis. J. Comp. Neurol. 414 (1999) 437-453
-
(1999)
J. Comp. Neurol.
, vol.414
, pp. 437-453
-
-
Blümcke, I.1
Zuschratter, W.2
Schewe, J.C.3
Suter, B.4
Lie, A.A.5
Riederer, B.M.6
Meier, B.7
Schramm, J.8
Elger, C.E.9
Wiestler, O.D.10
-
7
-
-
0032773120
-
A calcium signalling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency
-
Brini M., Pinton P., King M.P., Davidson M., Schon E.A., and Rizutto R. A calcium signalling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency. Nat. Med. 5 (1999) 951-954
-
(1999)
Nat. Med.
, vol.5
, pp. 951-954
-
-
Brini, M.1
Pinton, P.2
King, M.P.3
Davidson, M.4
Schon, E.A.5
Rizutto, R.6
-
8
-
-
0034904756
-
Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families
-
Brown M.D., Zhadanov S., Allen J.C., Hosseini S., Newman N.J., Atamonov V.V., Mikhailovskaya I.E., Sukernik R.I., and Wallace D.C. Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families. Hum. Genet. 109 (2001) 33-39
-
(2001)
Hum. Genet.
, vol.109
, pp. 33-39
-
-
Brown, M.D.1
Zhadanov, S.2
Allen, J.C.3
Hosseini, S.4
Newman, N.J.5
Atamonov, V.V.6
Mikhailovskaya, I.E.7
Sukernik, R.I.8
Wallace, D.C.9
-
9
-
-
0034308254
-
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes
-
Campos Y., Lorenzo G., Martin M.A., Torregrosa A., del Hoyo P., Rubio J.C., Garcia A., and Arenas J. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes. Neuromuscul. Disord. 10 (2000) 493-496
-
(2000)
Neuromuscul. Disord.
, vol.10
, pp. 493-496
-
-
Campos, Y.1
Lorenzo, G.2
Martin, M.A.3
Torregrosa, A.4
del Hoyo, P.5
Rubio, J.C.6
Garcia, A.7
Arenas, J.8
-
10
-
-
0035933047
-
Epileptic phenotypes associated with mitochondrial disorders
-
Canafoglia L., Franceschetti S., Antozzi C., Carrara F., Farina L., Granata T., Lamantea E., Savoiardo M., Uziel G., Villani F., Zeviani M., and Avanzini G. Epileptic phenotypes associated with mitochondrial disorders. Neurology 56 (2001) 1340-1346
-
(2001)
Neurology
, vol.56
, pp. 1340-1346
-
-
Canafoglia, L.1
Franceschetti, S.2
Antozzi, C.3
Carrara, F.4
Farina, L.5
Granata, T.6
Lamantea, E.7
Savoiardo, M.8
Uziel, G.9
Villani, F.10
Zeviani, M.11
Avanzini, G.12
-
11
-
-
57649171115
-
Mitochondrial approaches for neuroprotection
-
Chaturvedi R.K., and Beal M.F. Mitochondrial approaches for neuroprotection. Ann. N. Y. Acad. Sci. 1147 (2008) 395-412
-
(2008)
Ann. N. Y. Acad. Sci.
, vol.1147
, pp. 395-412
-
-
Chaturvedi, R.K.1
Beal, M.F.2
-
12
-
-
0032811737
-
Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy
-
Cock H., and Schapira A.H.V. Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy. Epilepsia 40 Suppl. 3 (1999) 33-40
-
(1999)
Epilepsia
, vol.40
, Issue.SUPPL. 3
, pp. 33-40
-
-
Cock, H.1
Schapira, A.H.V.2
-
13
-
-
0032899012
-
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome
-
De Coo I.F., Renier W.O., Ruitenbeek W., Ter Laak H.J., Bakker M., Schägger H., Van Oost B.A., and Smeets H.J. A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome. Ann. Neurol. 45 (1999) 130-133
-
(1999)
Ann. Neurol.
, vol.45
, pp. 130-133
-
-
De Coo, I.F.1
Renier, W.O.2
Ruitenbeek, W.3
Ter Laak, H.J.4
Bakker, M.5
Schägger, H.6
Van Oost, B.A.7
Smeets, H.J.8
-
14
-
-
0027166021
-
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome
-
De Vries D.D., van Engelen B.G., Gabrels F.J., Ruitenbeek W., and van Oost B.A. A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome. Ann. Neurol. 34 (1993) 410-412
-
(1993)
Ann. Neurol.
, vol.34
, pp. 410-412
-
-
De Vries, D.D.1
van Engelen, B.G.2
Gabrels, F.J.3
Ruitenbeek, W.4
van Oost, B.A.5
-
15
-
-
0032620538
-
Mitochondrial genes for generalized epilepsies
-
DiMauro S., Kulikova R., Tanji K., Bonilla E., and Hirano M. Mitochondrial genes for generalized epilepsies. Adv. Neurol. 79 (1999) 411-419
-
(1999)
Adv. Neurol.
, vol.79
, pp. 411-419
-
-
DiMauro, S.1
Kulikova, R.2
Tanji, K.3
Bonilla, E.4
Hirano, M.5
-
16
-
-
0034660457
-
Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease
-
Ferrante R.J., Andreassen O.A., Jenkins B.G., Dedeoglu A., Kuemmerle S., Kubilus J.K., Kaddurah-Daouk R., Hersch S.M., and Beal M.F. Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease. J. Neurosci. 15 (2000) 4389-4397
-
(2000)
J. Neurosci.
, vol.15
, pp. 4389-4397
-
-
Ferrante, R.J.1
Andreassen, O.A.2
Jenkins, B.G.3
Dedeoglu, A.4
Kuemmerle, S.5
Kubilus, J.K.6
Kaddurah-Daouk, R.7
Hersch, S.M.8
Beal, M.F.9
-
17
-
-
0034090292
-
Free radical production correlates with cell death in an in vitro model of epilepsy
-
Frantseva M.V., Velazquez J.L., Hwang P.A., and Carlen P.L. Free radical production correlates with cell death in an in vitro model of epilepsy. Eur. J. Neurosci. 12 (2000) 1431-1439
-
(2000)
Eur. J. Neurosci.
, vol.12
, pp. 1431-1439
-
-
Frantseva, M.V.1
Velazquez, J.L.2
Hwang, P.A.3
Carlen, P.L.4
-
18
-
-
0025666322
-
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Goto Y., Nonaka I., and Horai S. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348 (1990) 651-653
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
19
-
-
0026004614
-
A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
-
Goto Y., Nonaka I., and Horai S. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Biochim. Biophys. Acta 1097 (1991) 238-240
-
(1991)
Biochim. Biophys. Acta
, vol.1097
, pp. 238-240
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
20
-
-
0027935355
-
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
-
Goto Y., Tsugane K., Tanabe Y., Nonaka I., and Horai S. A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Biochem. Biophys. Res. Commun. 202 (1994) 1624-1630
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.202
, pp. 1624-1630
-
-
Goto, Y.1
Tsugane, K.2
Tanabe, Y.3
Nonaka, I.4
Horai, S.5
-
21
-
-
0031727452
-
MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity
-
Hanna M.G., Nelson I.P., Morgan-Hughes J.A., and Wood N.W. MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity. J. Neurol. Neurosurg. Psychiatry 65 (1998) 512-517
-
(1998)
J. Neurol. Neurosurg. Psychiatry
, vol.65
, pp. 512-517
-
-
Hanna, M.G.1
Nelson, I.P.2
Morgan-Hughes, J.A.3
Wood, N.W.4
-
22
-
-
0028143961
-
Hippocampal neuronal loss and regional hypometabolism in temporal lobe epilepsy
-
Henry T.R., Babb T.L., Engel Jr. J., Mazziotta J.C., Phelps M.E., and Crandall P.H. Hippocampal neuronal loss and regional hypometabolism in temporal lobe epilepsy. Ann. Neurol. 36 (1994) 925-927
-
(1994)
Ann. Neurol.
, vol.36
, pp. 925-927
-
-
Henry, T.R.1
Babb, T.L.2
Engel Jr., J.3
Mazziotta, J.C.4
Phelps, M.E.5
Crandall, P.H.6
-
23
-
-
67649718862
-
Mitochondrial diseases
-
Engel J., and Pedley T.A. (Eds), Lippincott Williams & Wilkins, Philadelphia
-
Hirano M., Kunz W.S., and DiMauro S. Mitochondrial diseases. In: Engel J., and Pedley T.A. (Eds). Epilepsy - A comprehensive textbook III (2008), Lippincott Williams & Wilkins, Philadelphia 2621-2630
-
(2008)
Epilepsy - A comprehensive textbook
, vol.III
, pp. 2621-2630
-
-
Hirano, M.1
Kunz, W.S.2
DiMauro, S.3
-
24
-
-
0032755006
-
In vivo development of brain phosphocreatine in normal and creatine-treated rabbit pups
-
Holtzman D., Khait I., Mulkern R., Allred E., Rand T., Jensen F., and Kraft R. In vivo development of brain phosphocreatine in normal and creatine-treated rabbit pups. J. Neurochem. 73 (1999) 2477-2484
-
(1999)
J. Neurochem.
, vol.73
, pp. 2477-2484
-
-
Holtzman, D.1
Khait, I.2
Mulkern, R.3
Allred, E.4
Rand, T.5
Jensen, F.6
Kraft, R.7
-
25
-
-
15644370475
-
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene
-
Jaksch M., Klopstock T., Kurlemann G., Dörner M., Hofmann S., Kleinle S., Hegemann S., Weissert M., Müller-Höcker J., Pongratz D., and Gerbitz K.D. Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene. Ann. Neurol. 44 (1998) 635-640
-
(1998)
Ann. Neurol.
, vol.44
, pp. 635-640
-
-
Jaksch, M.1
Klopstock, T.2
Kurlemann, G.3
Dörner, M.4
Hofmann, S.5
Kleinle, S.6
Hegemann, S.7
Weissert, M.8
Müller-Höcker, J.9
Pongratz, D.10
Gerbitz, K.D.11
-
26
-
-
48249143179
-
The ketogenic diet increases mitochondrial glutathione levels
-
Jarrett S.G., Milder J.B., Liang L.P., and Patel M. The ketogenic diet increases mitochondrial glutathione levels. J. Neurochem. 106 (2008) 1044-1051
-
(2008)
J. Neurochem.
, vol.106
, pp. 1044-1051
-
-
Jarrett, S.G.1
Milder, J.B.2
Liang, L.P.3
Patel, M.4
-
27
-
-
0038664183
-
Coupling of neuronal activity and mitochondrial metabolism as revealed by NAD(P)H fluorescence signals in organotypic hippocampal slice cultures of the rat
-
Kann O., Schuchmann S., Buchheim K., and Heinemann U. Coupling of neuronal activity and mitochondrial metabolism as revealed by NAD(P)H fluorescence signals in organotypic hippocampal slice cultures of the rat. Neuroscience 119 (2003) 87-100
-
(2003)
Neuroscience
, vol.119
, pp. 87-100
-
-
Kann, O.1
Schuchmann, S.2
Buchheim, K.3
Heinemann, U.4
-
28
-
-
26044454554
-
Metabolic dysfunction during neuronal activation in the ex vivo hippocampus from chronic epileptic rats and humans
-
Kann O., Kovacs R., Njunting M., Behrens C.J., Otahal J., Lehmann T.N., Gabriel S., and Heinemann U. Metabolic dysfunction during neuronal activation in the ex vivo hippocampus from chronic epileptic rats and humans. Brain 128 (2005) 2396-2407
-
(2005)
Brain
, vol.128
, pp. 2396-2407
-
-
Kann, O.1
Kovacs, R.2
Njunting, M.3
Behrens, C.J.4
Otahal, J.5
Lehmann, T.N.6
Gabriel, S.7
Heinemann, U.8
-
29
-
-
0033051815
-
Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis
-
Klivenyi P., Ferrante R.J., Matthews R.T., Bogdanov M.B., Klein A.M., Andreassen O.A., Mueller G., Wermer M., Kaddurah-Daouk R., and Beal M.F. Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis. Nat. Med. 5 (1999) 347-350
-
(1999)
Nat. Med.
, vol.5
, pp. 347-350
-
-
Klivenyi, P.1
Ferrante, R.J.2
Matthews, R.T.3
Bogdanov, M.B.4
Klein, A.M.5
Andreassen, O.A.6
Mueller, G.7
Wermer, M.8
Kaddurah-Daouk, R.9
Beal, M.F.10
-
30
-
-
0036900547
-
Free radical-mediated cell damage after experimental status epilepticus in hippocampal slice cultures
-
Kovacs R., Schuchmann S., Gabriel S., Kann O., Kardos J., and Heinemann U. Free radical-mediated cell damage after experimental status epilepticus in hippocampal slice cultures. J. Neurophysiol. 88 (2002) 2909-2918
-
(2002)
J. Neurophysiol.
, vol.88
, pp. 2909-2918
-
-
Kovacs, R.1
Schuchmann, S.2
Gabriel, S.3
Kann, O.4
Kardos, J.5
Heinemann, U.6
-
31
-
-
0036455133
-
Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus
-
Kudin A.P., Kudina T.A., Seyfried J., Vielhaber S., Beck H., Elger C.E., and Kunz W.S. Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus. Eur. J. Neurosci. 15 (2002) 1105-1114
-
(2002)
Eur. J. Neurosci.
, vol.15
, pp. 1105-1114
-
-
Kudin, A.P.1
Kudina, T.A.2
Seyfried, J.3
Vielhaber, S.4
Beck, H.5
Elger, C.E.6
Kunz, W.S.7
-
32
-
-
1042301416
-
Characterization of superoxide-producing sites in isolated brain mitochondria
-
Kudin A.P., Bimpong-Buta N.Y., Vielhaber S., Elger C.E., and Kunz W.S. Characterization of superoxide-producing sites in isolated brain mitochondria. J. Biol. Chem. 279 (2004) 4127-4135
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 4127-4135
-
-
Kudin, A.P.1
Bimpong-Buta, N.Y.2
Vielhaber, S.3
Elger, C.E.4
Kunz, W.S.5
-
33
-
-
10644267593
-
The mechanism of neuroprotection by topiramate in an animal model of epilepsy
-
Kudin A.P., Debska-Vielhaber G., Vielhaber S., Elger C.E., and Kunz W.S. The mechanism of neuroprotection by topiramate in an animal model of epilepsy. Epilepsia 45 (2004) 1478-1487
-
(2004)
Epilepsia
, vol.45
, pp. 1478-1487
-
-
Kudin, A.P.1
Debska-Vielhaber, G.2
Vielhaber, S.3
Elger, C.E.4
Kunz, W.S.5
-
34
-
-
18044391656
-
Characterization of superoxide production sites in isolated rat brain and skeletal muscle mitochondria
-
Kudin A.P., Debska-Vielhaber G., and Kunz W.S. Characterization of superoxide production sites in isolated rat brain and skeletal muscle mitochondria. Biomed. Pharmacother. 59 (2005) 163-168
-
(2005)
Biomed. Pharmacother.
, vol.59
, pp. 163-168
-
-
Kudin, A.P.1
Debska-Vielhaber, G.2
Kunz, W.S.3
-
35
-
-
50949088772
-
Sites of generation of reactive oxygen species in homogenates of brain tissue determined with the use of respiratory substrates and inhibitors
-
Kudin A.P., Malinska D., and Kunz W.S. Sites of generation of reactive oxygen species in homogenates of brain tissue determined with the use of respiratory substrates and inhibitors. Biochim. Biophys. Acta 1777 (2008) 689-695
-
(2008)
Biochim. Biophys. Acta
, vol.1777
, pp. 689-695
-
-
Kudin, A.P.1
Malinska, D.2
Kunz, W.S.3
-
36
-
-
0036221686
-
The role of mitochondria in epileptogenesis
-
Kunz W.S. The role of mitochondria in epileptogenesis. Curr. Opin. Neurol. 15 (2002) 179-184
-
(2002)
Curr. Opin. Neurol.
, vol.15
, pp. 179-184
-
-
Kunz, W.S.1
-
37
-
-
0033135867
-
Altered mitochondrial oxidative phosphorylation in hippokampal slices of kainate-treated rats
-
Kunz W.S., Goussakov I.V., Beck H., and Elger C.E. Altered mitochondrial oxidative phosphorylation in hippokampal slices of kainate-treated rats. Brain Res. 826 (1999) 236-242
-
(1999)
Brain Res.
, vol.826
, pp. 236-242
-
-
Kunz, W.S.1
Goussakov, I.V.2
Beck, H.3
Elger, C.E.4
-
38
-
-
0033757831
-
Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy
-
Kunz W.S., Kudin A.P., Vielhaber S., Blümcke I., Zuschratter W., Schramm J., Beck H., and Elger C.E. Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy. Ann. Neurol. 48 (2000) 766-773
-
(2000)
Ann. Neurol.
, vol.48
, pp. 766-773
-
-
Kunz, W.S.1
Kudin, A.P.2
Vielhaber, S.3
Blümcke, I.4
Zuschratter, W.5
Schramm, J.6
Beck, H.7
Elger, C.E.8
-
39
-
-
13044305983
-
Release of caspase-9 from mitochondria during neuronal apoptosis and cerebral ischemia
-
Krajewski S., Krajewska M., Ellerby L.M., Welsh K., Xie Z., Deveraux Q.L., Salvesen G.S., Bredesen D.E., Rosenthal R.E., Fiskum G., and Reed J.C. Release of caspase-9 from mitochondria during neuronal apoptosis and cerebral ischemia. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 5752-5757
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 5752-5757
-
-
Krajewski, S.1
Krajewska, M.2
Ellerby, L.M.3
Welsh, K.4
Xie, Z.5
Deveraux, Q.L.6
Salvesen, G.S.7
Bredesen, D.E.8
Rosenthal, R.E.9
Fiskum, G.10
Reed, J.C.11
-
40
-
-
0034669186
-
Mitochondrial superoxide production in kainate-induced hippocampal damage
-
Liang L.P., Ho Y.S., and Patel M. Mitochondrial superoxide production in kainate-induced hippocampal damage. Neuroscience 101 (2000) 563-570
-
(2000)
Neuroscience
, vol.101
, pp. 563-570
-
-
Liang, L.P.1
Ho, Y.S.2
Patel, M.3
-
41
-
-
2942596452
-
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome
-
Mancuso M., Filosto M., Mootha V.K., Rocchi A., Pistolesi S., Murri L., DiMauro S., and Siciliano G. A novel mitochondrial tRNAPhe mutation causes MERRF syndrome. Neurology 62 (2004) 2119-2121
-
(2004)
Neurology
, vol.62
, pp. 2119-2121
-
-
Mancuso, M.1
Filosto, M.2
Mootha, V.K.3
Rocchi, A.4
Pistolesi, S.5
Murri, L.6
DiMauro, S.7
Siciliano, G.8
-
42
-
-
0029046428
-
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene
-
Manfredi G., Schon E.A., Moraes C.T., Bonilla E., Berry G.T., Sladky J.T., and DiMauro S. A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene. Neuromuscul. Disord. 5 (1995) 391-398
-
(1995)
Neuromuscul. Disord.
, vol.5
, pp. 391-398
-
-
Manfredi, G.1
Schon, E.A.2
Moraes, C.T.3
Bonilla, E.4
Berry, G.T.5
Sladky, J.T.6
DiMauro, S.7
-
43
-
-
0029919367
-
Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy
-
Manfredi G., Schon E.A., Bonilla E., Moraes C.T., Shanske S., and DiMauro S. Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy. Hum. Mutat. 7 (1996) 158-163
-
(1996)
Hum. Mutat.
, vol.7
, pp. 158-163
-
-
Manfredi, G.1
Schon, E.A.2
Bonilla, E.3
Moraes, C.T.4
Shanske, S.5
DiMauro, S.6
-
44
-
-
0013950709
-
Epilepsy and the temporal lobes. A clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes
-
Margerison J.H., and Corsellis J.A. Epilepsy and the temporal lobes. A clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes. Brain 89 (1966) 499-530
-
(1966)
Brain
, vol.89
, pp. 499-530
-
-
Margerison, J.H.1
Corsellis, J.A.2
-
45
-
-
0027527126
-
Excitotoxicity and selective neuronal loss in epilepsy
-
Meldrum B.S. Excitotoxicity and selective neuronal loss in epilepsy. Brain Pathol. 3 (1993) 405-412
-
(1993)
Brain Pathol.
, vol.3
, pp. 405-412
-
-
Meldrum, B.S.1
-
46
-
-
0027145131
-
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
-
Moraes C.T., Ciacci F., Bonilla E., Jansen C., Hirano M., Rao N., Lovelace R.E., Rowland L.P., Schon E.A., and DiMauro S. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?. J. Clin. Invest. 92 (1993) 2906-2915
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 2906-2915
-
-
Moraes, C.T.1
Ciacci, F.2
Bonilla, E.3
Jansen, C.4
Hirano, M.5
Rao, N.6
Lovelace, R.E.7
Rowland, L.P.8
Schon, E.A.9
DiMauro, S.10
-
47
-
-
0027715020
-
A new point mutation associated with mitochondrial encephalomyopathy
-
Morten K.J., Cooper J.M., Brown G.K., Lake B.D., Pike D., and Poulton J. A new point mutation associated with mitochondrial encephalomyopathy. Hum. Mol. Genet. 2 (1993) 2081-2087
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2081-2087
-
-
Morten, K.J.1
Cooper, J.M.2
Brown, G.K.3
Lake, B.D.4
Pike, D.5
Poulton, J.6
-
48
-
-
14844312924
-
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF
-
Naini A.B., Lu J., Kaufmann P., Bernstein R.A., Mancuso M., Bonilla E., Hirano M., and DiMauro S. Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF. Arch. Neurol. 62 (2005) 473-476
-
(2005)
Arch. Neurol.
, vol.62
, pp. 473-476
-
-
Naini, A.B.1
Lu, J.2
Kaufmann, P.3
Bernstein, R.A.4
Mancuso, M.5
Bonilla, E.6
Hirano, M.7
DiMauro, S.8
-
49
-
-
2142705756
-
POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
-
Naviaux R.K., and Nguyen K.V. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann. Neurol. 55 (2004) 706-712
-
(2004)
Ann. Neurol.
, vol.55
, pp. 706-712
-
-
Naviaux, R.K.1
Nguyen, K.V.2
-
50
-
-
0042026576
-
A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndrome
-
Nishigaki Y., Tadesse S., Bonilla E., Shungu D., Hersh S., Keats B.J., Berlin C.I., Goldberg M.F., Vockley J., DiMauro S., and Hirano M. A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndrome. Neuromuscul. Disord. 13 (2003) 334-340
-
(2003)
Neuromuscul. Disord.
, vol.13
, pp. 334-340
-
-
Nishigaki, Y.1
Tadesse, S.2
Bonilla, E.3
Shungu, D.4
Hersh, S.5
Keats, B.J.6
Berlin, C.I.7
Goldberg, M.F.8
Vockley, J.9
DiMauro, S.10
Hirano, M.11
-
51
-
-
0029822865
-
The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
-
Nishino I., Komatsu M., Kodama S., Horai S., Nonaka I., and Goto Y. The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS). Muscle Nerve 19 (1996) 1603-1604
-
(1996)
Muscle Nerve
, vol.19
, pp. 1603-1604
-
-
Nishino, I.1
Komatsu, M.2
Kodama, S.3
Horai, S.4
Nonaka, I.5
Goto, Y.6
-
52
-
-
0031034339
-
Hippocampal atrophy is not a major determinant of regional hypometabolism in temporal lobe epilepsy
-
O'Brien T.J., Newton M.R., Cook M.J., Berlangieri S.U., Kilpatrick C., Morris K., and Berkovic S.F. Hippocampal atrophy is not a major determinant of regional hypometabolism in temporal lobe epilepsy. Epilepsia 38 (1997) 74-80
-
(1997)
Epilepsia
, vol.38
, pp. 74-80
-
-
O'Brien, T.J.1
Newton, M.R.2
Cook, M.J.3
Berlangieri, S.U.4
Kilpatrick, C.5
Morris, K.6
Berkovic, S.F.7
-
53
-
-
20144388281
-
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation
-
Pulkes T., Liolitsa D., Eunson L.H., Rose M., Nelson I.P., Rahman S., Poulton J., Marchington D.R., Landon D.N., Debono A.G., Morgan-Hughes J.A., and Hanna M.G. New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation. Neuromuscul. Disord. 15 (2005) 364-371
-
(2005)
Neuromuscul. Disord.
, vol.15
, pp. 364-371
-
-
Pulkes, T.1
Liolitsa, D.2
Eunson, L.H.3
Rose, M.4
Nelson, I.P.5
Rahman, S.6
Poulton, J.7
Marchington, D.R.8
Landon, D.N.9
Debono, A.G.10
Morgan-Hughes, J.A.11
Hanna, M.G.12
-
54
-
-
0034747856
-
An mtDNA mutation, 14453G->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome
-
Ravn K., Wibrand F., Hansen F.J., Horn N., Rosenberg T., and Schwartz M. An mtDNA mutation, 14453G->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome. Eur. J. Hum. Genet. 9 (2001) 805-809
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 805-809
-
-
Ravn, K.1
Wibrand, F.2
Hansen, F.J.3
Horn, N.4
Rosenberg, T.5
Schwartz, M.6
-
55
-
-
0024343409
-
Vascular involvement in mitochondrial myopathy
-
Sakuta R., and Nonaka I. Vascular involvement in mitochondrial myopathy. Ann. Neurol. 25 (1989) 594-601
-
(1989)
Ann. Neurol.
, vol.25
, pp. 594-601
-
-
Sakuta, R.1
Nonaka, I.2
-
56
-
-
0028786838
-
A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy
-
Santorelli F.M., Mak S.C., Vazquez-Acevedo M., Gonzlez-Halphen D., and DiMauro S. A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy. Biochem. Biophys. Res. Commun. 216 (1995) 835-840
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.216
, pp. 835-840
-
-
Santorelli, F.M.1
Mak, S.C.2
Vazquez-Acevedo, M.3
Gonzlez-Halphen, D.4
DiMauro, S.5
-
57
-
-
0031577593
-
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS
-
Santorelli F.M., Tanji K., Kulikova R., Shanske S., Vilarinho L., Hays A.P., and DiMauro S. Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS. Biochem. Biophys. Res. Commun. 238 (1997) 326-328
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.238
, pp. 326-328
-
-
Santorelli, F.M.1
Tanji, K.2
Kulikova, R.3
Shanske, S.4
Vilarinho, L.5
Hays, A.P.6
DiMauro, S.7
-
58
-
-
9144268527
-
Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells
-
Santra S., Gilkerson R.W., Davidson M., and Schon E.A. Ketogenic treatment reduces deleted mitochondrial DNAs in cultured human cells. Ann. Neurol. 56 (2004) 662-669
-
(2004)
Ann. Neurol.
, vol.56
, pp. 662-669
-
-
Santra, S.1
Gilkerson, R.W.2
Davidson, M.3
Schon, E.A.4
-
59
-
-
0028030728
-
A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
-
Sato W., Hayasaka K., Shoji Y., Takahashi T., Takada G., Saito M., Fukawa O., and Wachi E. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Biochem. Mol. Biol. Int. 33 (1994) 1055-1061
-
(1994)
Biochem. Mol. Biol. Int.
, vol.33
, pp. 1055-1061
-
-
Sato, W.1
Hayasaka, K.2
Shoji, Y.3
Takahashi, T.4
Takada, G.5
Saito, M.6
Fukawa, O.7
Wachi, E.8
-
60
-
-
0039699870
-
New insights in the metabolic consequences of large scale mtDNA deletions: a quantitative analysis of biochemical, morphological and genetic findings in human skeletal muscle
-
Schröder R., Vielhaber S., Wiedemann F.R., Kornblum C., Papassotiropoulos A., Broich P., Zierz S., Elger C.E., Reichmann H., Seibel P., Klockgether T., and Kunz W.S. New insights in the metabolic consequences of large scale mtDNA deletions: a quantitative analysis of biochemical, morphological and genetic findings in human skeletal muscle. J. Neuropath. Exp. Neurol. 59 (2000) 353-360
-
(2000)
J. Neuropath. Exp. Neurol.
, vol.59
, pp. 353-360
-
-
Schröder, R.1
Vielhaber, S.2
Wiedemann, F.R.3
Kornblum, C.4
Papassotiropoulos, A.5
Broich, P.6
Zierz, S.7
Elger, C.E.8
Reichmann, H.9
Seibel, P.10
Klockgether, T.11
Kunz, W.S.12
-
62
-
-
0031784401
-
Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation
-
Schuelke M., Bakker M., Stoltenburg G., Sperner J., and von Moers A. Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation. Ann. Neurol. 44 (1998) 700-704
-
(1998)
Ann. Neurol.
, vol.44
, pp. 700-704
-
-
Schuelke, M.1
Bakker, M.2
Stoltenburg, G.3
Sperner, J.4
von Moers, A.5
-
63
-
-
0025368281
-
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
-
Shoffner J.M., Lott M.T., Lezza A.M., Seibel P., Ballinger S.W., and Wallace D.C. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell 61 (1990) 931-937
-
(1990)
Cell
, vol.61
, pp. 931-937
-
-
Shoffner, J.M.1
Lott, M.T.2
Lezza, A.M.3
Seibel, P.4
Ballinger, S.W.5
Wallace, D.C.6
-
64
-
-
0029765443
-
Role of uncoupled and non-coupled oxidations in maintenance of safely low levels of oxygen and its one-electron reductants
-
Skulachev V.P. Role of uncoupled and non-coupled oxidations in maintenance of safely low levels of oxygen and its one-electron reductants. Q. Rev. Biophys. 29 (1996) 169-202
-
(1996)
Q. Rev. Biophys.
, vol.29
, pp. 169-202
-
-
Skulachev, V.P.1
-
65
-
-
0032860832
-
A novel mutation in the mitochondrial DNA transfer ribonucleic acid Asp gene in a child with myoclonic epilepsy and psychomotor regression
-
Shtilbans A., El-Schahawi M., Malkin E., Shanske S., Musumeci O., and DiMauro S. A novel mutation in the mitochondrial DNA transfer ribonucleic acid Asp gene in a child with myoclonic epilepsy and psychomotor regression. J. Child Neurol. 14 (1999) 610-613
-
(1999)
J. Child Neurol.
, vol.14
, pp. 610-613
-
-
Shtilbans, A.1
El-Schahawi, M.2
Malkin, E.3
Shanske, S.4
Musumeci, O.5
DiMauro, S.6
-
66
-
-
0034521771
-
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome
-
Shtilbans A., Shanske S., Goodman S., Sue C.M., Bruno C., Johnson T.L., Lava N.S., Waheed N., and DiMauro S. G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome. J. Child Neurol. 15 (2000) 759-761
-
(2000)
J. Child Neurol.
, vol.15
, pp. 759-761
-
-
Shtilbans, A.1
Shanske, S.2
Goodman, S.3
Sue, C.M.4
Bruno, C.5
Johnson, T.L.6
Lava, N.S.7
Waheed, N.8
DiMauro, S.9
-
67
-
-
0033767740
-
Dietary supplement creatine protects against traumatic brain injury
-
Sullivan P.G., Geiger J.D., Mattson M.P., and Scheff S.W. Dietary supplement creatine protects against traumatic brain injury. Ann. Neurol. 48 (2000) 723-729
-
(2000)
Ann. Neurol.
, vol.48
, pp. 723-729
-
-
Sullivan, P.G.1
Geiger, J.D.2
Mattson, M.P.3
Scheff, S.W.4
-
68
-
-
0030898772
-
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease
-
Suomalainen A., Majander A., Wallin M., et al. Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease. Neurology 48 (1997) 1244-1253
-
(1997)
Neurology
, vol.48
, pp. 1244-1253
-
-
Suomalainen, A.1
Majander, A.2
Wallin, M.3
-
69
-
-
0026660498
-
Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy
-
Taniike M., Fukushima H., Yanagihara I., Tsukamoto H., Tanaka J., Fujimura H., Nagai T., Sano T., Yamaoka K., and Inui K. Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy. Biochem. Biophys. Res. Commun. 186 (1992) 47-53
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.186
, pp. 47-53
-
-
Taniike, M.1
Fukushima, H.2
Yanagihara, I.3
Tsukamoto, H.4
Tanaka, J.5
Fujimura, H.6
Nagai, T.7
Sano, T.8
Yamaoka, K.9
Inui, K.10
-
70
-
-
0030891028
-
Mitochondrial involvement in post-tetanic potentiation of synaptic transmission
-
Tang Y.G., and Zucker R.S. Mitochondrial involvement in post-tetanic potentiation of synaptic transmission. Neuron 18 (1997) 483-491
-
(1997)
Neuron
, vol.18
, pp. 483-491
-
-
Tang, Y.G.1
Zucker, R.S.2
-
71
-
-
0029787365
-
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA
-
Taylor R.W., Chinnery P.F., Haldane F., Morris A.A., Bindoff L.A., Wilson J., and Turnbull D.M. MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA. Ann. Neurol. 40 (1996) 459-462
-
(1996)
Ann. Neurol.
, vol.40
, pp. 459-462
-
-
Taylor, R.W.1
Chinnery, P.F.2
Haldane, F.3
Morris, A.A.4
Bindoff, L.A.5
Wilson, J.6
Turnbull, D.M.7
-
72
-
-
0034955881
-
Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene
-
Taylor R.W., Singh-Kler R., Hayes C.M., Smith P.E., and Turnbull D.M. Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. Ann. Neurol. 50 (2001) 104-107
-
(2001)
Ann. Neurol.
, vol.50
, pp. 104-107
-
-
Taylor, R.W.1
Singh-Kler, R.2
Hayes, C.M.3
Smith, P.E.4
Turnbull, D.M.5
-
73
-
-
1942505923
-
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene
-
Taylor R.W., Schaefer A.M., McDonnell M.T., Petty R.K., Thomas A.M., Blakely E.L., Hayes C.M., McFarland R., and Turnbull D.M. Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene. Neurology 62 (2004) 1420-1423
-
(2004)
Neurology
, vol.62
, pp. 1420-1423
-
-
Taylor, R.W.1
Schaefer, A.M.2
McDonnell, M.T.3
Petty, R.K.4
Thomas, A.M.5
Blakely, E.L.6
Hayes, C.M.7
McFarland, R.8
Turnbull, D.M.9
-
74
-
-
0032924716
-
A novel mutation (8342G->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus
-
Tiranti V., Carrara F., Confalonieri P., Mora M., Maffei R.M., Lamantea E., and Zeviani M. A novel mutation (8342G->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus. Neuromuscul. Disord. 9 (1999) 66-71
-
(1999)
Neuromuscul. Disord.
, vol.9
, pp. 66-71
-
-
Tiranti, V.1
Carrara, F.2
Confalonieri, P.3
Mora, M.4
Maffei, R.M.5
Lamantea, E.6
Zeviani, M.7
-
76
-
-
0032538410
-
Mitochondrial toxin 3-nitropropionic acid evokes seizures in mice
-
Urbanska E.M., Blaszczak P., Saran T., Kleinrok Z., and Turski W.A. Mitochondrial toxin 3-nitropropionic acid evokes seizures in mice. Eur. J. Pharmacol. 359 (1998) 55-58
-
(1998)
Eur. J. Pharmacol.
, vol.359
, pp. 55-58
-
-
Urbanska, E.M.1
Blaszczak, P.2
Saran, T.3
Kleinrok, Z.4
Turski, W.A.5
-
77
-
-
0034943967
-
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
-
Van Goethem G., Dermaut B., Lofgren A., et al. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Nat. Genet. 28 (2001) 211-212
-
(2001)
Nat. Genet.
, vol.28
, pp. 211-212
-
-
Van Goethem, G.1
Dermaut, B.2
Lofgren, A.3
-
78
-
-
0036667980
-
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene
-
Varlamov D.A., Kudin A.P., Vielhaber S., Schröder R., Sassen R., Becker A., Kunz D., Haug D., Rebstock J., Heils A., Elger C.E., and Kunz W.S. Metabolic consequences of a novel missense mutation of the mtDNA CO I gene. Hum. Mol. Genet. 11 (2002) 1797-1805
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1797-1805
-
-
Varlamov, D.A.1
Kudin, A.P.2
Vielhaber, S.3
Schröder, R.4
Sassen, R.5
Becker, A.6
Kunz, D.7
Haug, D.8
Rebstock, J.9
Heils, A.10
Elger, C.E.11
Kunz, W.S.12
-
79
-
-
20244379388
-
Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy
-
Vielhaber S., von Oertzen J.H., Kudin A.P., Schoenfeld A., Menzel C., Biersack H.J., Kral T., Elger C.E., and Kunz W.S. Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy. Epilepsia 44 (2003) 193-199
-
(2003)
Epilepsia
, vol.44
, pp. 193-199
-
-
Vielhaber, S.1
von Oertzen, J.H.2
Kudin, A.P.3
Schoenfeld, A.4
Menzel, C.5
Biersack, H.J.6
Kral, T.7
Elger, C.E.8
Kunz, W.S.9
-
80
-
-
1642504396
-
Hippocampal N-acetyl aspartate levels do not mirror neuronal cell densities in creatine-supplemented epileptic rats
-
Vielhaber S., Kudin A.P., Kudina T.A., Stiller D., Scheich H., Schoenfeld A., Feistner H., Heinze H.J., Elger C.E., and Kunz W.S. Hippocampal N-acetyl aspartate levels do not mirror neuronal cell densities in creatine-supplemented epileptic rats. Eur. J. Neurosci. 18 (2003) 2292-22300
-
(2003)
Eur. J. Neurosci.
, vol.18
, pp. 2292-22300
-
-
Vielhaber, S.1
Kudin, A.P.2
Kudina, T.A.3
Stiller, D.4
Scheich, H.5
Schoenfeld, A.6
Feistner, H.7
Heinze, H.J.8
Elger, C.E.9
Kunz, W.S.10
-
81
-
-
37549060366
-
Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy
-
Vielhaber S., Niessen H.G., Debska-Vielhaber G., Kudin A.P., Wellmer J., Kaufmann J., Schönfeld M.A., Fendrich R., Willker W., Leibfritz D., Schramm J., Elger C.E., Heinze H.J., and Kunz W.S. Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy. Epilepsia 49 (2008) 40-50
-
(2008)
Epilepsia
, vol.49
, pp. 40-50
-
-
Vielhaber, S.1
Niessen, H.G.2
Debska-Vielhaber, G.3
Kudin, A.P.4
Wellmer, J.5
Kaufmann, J.6
Schönfeld, M.A.7
Fendrich, R.8
Willker, W.9
Leibfritz, D.10
Schramm, J.11
Elger, C.E.12
Heinze, H.J.13
Kunz, W.S.14
-
82
-
-
33644840446
-
Antiepileptic drugs and neuroprotection: current status and future roles
-
Willmore L.J. Antiepileptic drugs and neuroprotection: current status and future roles. Epilepsy Behav. 7 Suppl 3 (2005) S25-S28
-
(2005)
Epilepsy Behav.
, vol.7
, Issue.SUPPL. 3
-
-
Willmore, L.J.1
-
83
-
-
16844382687
-
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations
-
Winterthun S., Ferrari G., He L., et al. Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations. Neurology 64 (2005) 1204-1208
-
(2005)
Neurology
, vol.64
, pp. 1204-1208
-
-
Winterthun, S.1
Ferrari, G.2
He, L.3
-
84
-
-
0029968360
-
Preventive effect of melatonin against cyanide-induced seizures and lipid peroxidation in mice
-
Yamamoto H., and Tang H.W. Preventive effect of melatonin against cyanide-induced seizures and lipid peroxidation in mice. Neurosci. Lett. 207 (1996) 89-92
-
(1996)
Neurosci. Lett.
, vol.207
, pp. 89-92
-
-
Yamamoto, H.1
Tang, H.W.2
-
85
-
-
0027865639
-
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene
-
Zeviani M., Muntoni F., Savarese N., Serra G., Tiranti V., Carrara F., Mariotti C., and DiDonato S. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene. Eur. J. Hum. Genet. 1 (1993) 80-87
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 80-87
-
-
Zeviani, M.1
Muntoni, F.2
Savarese, N.3
Serra, G.4
Tiranti, V.5
Carrara, F.6
Mariotti, C.7
DiDonato, S.8
-
86
-
-
52649145996
-
Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma
-
Zsurka G., Baron M., Stewart J.D., Kornblum C., Bös M., Sassen R., Taylor R.W., Elger C.E., Chinnery P.F., and Kunz W.S. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma. J. Neuropathol. Exp. Neurol. 67 (2008) 857-866
-
(2008)
J. Neuropathol. Exp. Neurol.
, vol.67
, pp. 857-866
-
-
Zsurka, G.1
Baron, M.2
Stewart, J.D.3
Kornblum, C.4
Bös, M.5
Sassen, R.6
Taylor, R.W.7
Elger, C.E.8
Chinnery, P.F.9
Kunz, W.S.10
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