-
1
-
-
0018608356
-
Chronic parkinsonism secondary to intravenous injection of meperidine analogues
-
Davis G.C., Williams A.C., Markey S.P., Ebert M.H., Caine E.D., Reichert C.M., Kopin I.J. Chronic parkinsonism secondary to intravenous injection of meperidine analogues. Psychiatry Res. 1979, 1:249-254.
-
(1979)
Psychiatry Res.
, vol.1
, pp. 249-254
-
-
Davis, G.C.1
Williams, A.C.2
Markey, S.P.3
Ebert, M.H.4
Caine, E.D.5
Reichert, C.M.6
Kopin, I.J.7
-
2
-
-
84884305932
-
Decreased mitochondrial DNA copy number in the hippocampus and peripheral blood during opiate addiction is mediated by autophagy and can be salvaged by melatonin
-
Feng Y.M., Jia Y.F., Su L.Y., Wang D., Lv L., Xu L., Yao Y.G. Decreased mitochondrial DNA copy number in the hippocampus and peripheral blood during opiate addiction is mediated by autophagy and can be salvaged by melatonin. Autophagy 2013, 9:1395-1406.
-
(2013)
Autophagy
, vol.9
, pp. 1395-1406
-
-
Feng, Y.M.1
Jia, Y.F.2
Su, L.Y.3
Wang, D.4
Lv, L.5
Xu, L.6
Yao, Y.G.7
-
3
-
-
20544461885
-
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians
-
Ghezzi D., Marelli C., Achilli A., Goldwurm S., Pezzoli G., Barone P., Pellecchia M.T., Stanzione P., Brusa L., Bentivoglio A.R., Bonuccelli U., Petrozzi L., Abbruzzese G., Marchese R., Cortelli P., Grimaldi D., Martinelli P., Ferrarese C., Garavaglia B., Sangiorgi S., Carelli V., Torroni A., Albanese A., Zeviani M. Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians. Eur. J. Hum. Genet. 2005, 13:748-752.
-
(2005)
Eur. J. Hum. Genet.
, vol.13
, pp. 748-752
-
-
Ghezzi, D.1
Marelli, C.2
Achilli, A.3
Goldwurm, S.4
Pezzoli, G.5
Barone, P.6
Pellecchia, M.T.7
Stanzione, P.8
Brusa, L.9
Bentivoglio, A.R.10
Bonuccelli, U.11
Petrozzi, L.12
Abbruzzese, G.13
Marchese, R.14
Cortelli, P.15
Grimaldi, D.16
Martinelli, P.17
Ferrarese, C.18
Garavaglia, B.19
Sangiorgi, S.20
Carelli, V.21
Torroni, A.22
Albanese, A.23
Zeviani, M.24
more..
-
4
-
-
84893842173
-
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy
-
Giordano C., Iommarini L., Giordano L., Maresca A., Pisano A., Valentino M.L., Caporali L., Liguori R., Deceglie S., Roberti M., Fanelli F., Fracasso F., Ross-Cisneros F.N., D'Adamo P., Hudson G., Pyle A., Yu-Wai-Man P., Chinnery P.F., Zeviani M., Salomao S.R., Berezovsky A., Belfort R., Ventura D.F., Moraes M., Moraes Filho M., Barboni P., Sadun F., De Negri A., Sadun A.A., Tancredi A., Mancini M., d'Amati G., Loguercio Polosa P., Cantatore P., Carelli V. Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. Brain 2014, 137(Pt 2):335-353.
-
(2014)
Brain
, vol.137
, pp. 335-353
-
-
Giordano, C.1
Iommarini, L.2
Giordano, L.3
Maresca, A.4
Pisano, A.5
Valentino, M.L.6
Caporali, L.7
Liguori, R.8
Deceglie, S.9
Roberti, M.10
Fanelli, F.11
Fracasso, F.12
Ross-Cisneros, F.N.13
D'Adamo, P.14
Hudson, G.15
Pyle, A.16
Yu-Wai-Man, P.17
Chinnery, P.F.18
Zeviani, M.19
Salomao, S.R.20
Berezovsky, A.21
Belfort, R.22
Ventura, D.F.23
Moraes, M.24
Moraes Filho, M.25
Barboni, P.26
Sadun, F.27
De Negri, A.28
Sadun, A.A.29
Tancredi, A.30
Mancini, M.31
d'Amati, G.32
Loguercio Polosa, P.33
Cantatore, P.34
Carelli, V.35
more..
-
5
-
-
84861211027
-
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy
-
Gomez-Duran A., Pacheu-Grau D., Martinez-Romero I., Lopez-Gallardo E., Lopez-Perez M.J., Montoya J., Ruiz-Pesini E. Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Bba-mol Basis Dis. 2012, 1822:1216-1222.
-
(2012)
Bba-mol Basis Dis.
, vol.1822
, pp. 1216-1222
-
-
Gomez-Duran, A.1
Pacheu-Grau, D.2
Martinez-Romero, I.3
Lopez-Gallardo, E.4
Lopez-Perez, M.J.5
Montoya, J.6
Ruiz-Pesini, E.7
-
6
-
-
84915795258
-
Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle
-
Grady J.P., Murphy J.L., Blakely E.L., Haller R.G., Taylor R.W., Turnbull D.M., Tuppen H.A.L. Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle. PLoS One 2014, 9:e114462.
-
(2014)
PLoS One
, vol.9
, pp. e114462
-
-
Grady, J.P.1
Murphy, J.L.2
Blakely, E.L.3
Haller, R.G.4
Taylor, R.W.5
Turnbull, D.M.6
Tuppen, H.A.L.7
-
7
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
Hatano Y., Li Y., Sato K., Asakawa S., Yamamura Y., Tomiyama H., Yoshino H., Asahina M., Kobayashi S., Hassin-Baer S., Lu C.S., Ng A.R., Rosales R.L., Shimizu N., Toda T., Mizuno Y., Hattori N. Novel PINK1 mutations in early-onset parkinsonism. Ann. Neurol. 2004, 56:424-427.
-
(2004)
Ann. Neurol.
, vol.56
, pp. 424-427
-
-
Hatano, Y.1
Li, Y.2
Sato, K.3
Asakawa, S.4
Yamamura, Y.5
Tomiyama, H.6
Yoshino, H.7
Asahina, M.8
Kobayashi, S.9
Hassin-Baer, S.10
Lu, C.S.11
Ng, A.R.12
Rosales, R.L.13
Shimizu, N.14
Toda, T.15
Mizuno, Y.16
Hattori, N.17
-
8
-
-
84901614656
-
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases
-
Hudson G., Gomez-Duran A., Wilson I.J., Chinnery P.F. Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. PLoS Genet. 2014, 10:e1004369.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004369
-
-
Hudson, G.1
Gomez-Duran, A.2
Wilson, I.J.3
Chinnery, P.F.4
-
9
-
-
84879484724
-
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
-
Hudson G., Nalls M., Evans J.R., Breen D.P., Winder-Rhodes S., Morrison K.E., Morris H.R., Williams-Gray C.H., Barker R.A., Singleton A.B., Hardy J., Wood N.E., Burn D.J., Chinnery P.F. Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease. Neurology 2013, 80:2042-2048.
-
(2013)
Neurology
, vol.80
, pp. 2042-2048
-
-
Hudson, G.1
Nalls, M.2
Evans, J.R.3
Breen, D.P.4
Winder-Rhodes, S.5
Morrison, K.E.6
Morris, H.R.7
Williams-Gray, C.H.8
Barker, R.A.9
Singleton, A.B.10
Hardy, J.11
Wood, N.E.12
Burn, D.J.13
Chinnery, P.F.14
-
10
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
-
Hughes A.J., Daniel S.E., Kilford L., Lees A.J. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psychiatry 1992, 55:181-184.
-
(1992)
J. Neurol. Neurosurg. Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
11
-
-
41549121974
-
Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background
-
Latsoudis H., Spanaki C., Chlouverakis G., Plaitakis A. Mitochondrial DNA polymorphisms and haplogroups in Parkinson's disease and control individuals with a similar genetic background. J. Hum. Genet. 2008, 53:349-356.
-
(2008)
J. Hum. Genet.
, vol.53
, pp. 349-356
-
-
Latsoudis, H.1
Spanaki, C.2
Chlouverakis, G.3
Plaitakis, A.4
-
12
-
-
0034214103
-
Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells
-
Lee H.C., Yin P.H., Lu C.Y., Chi C.W., Wei Y.H. Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells. Biochem. J. 2000, 348:425-432.
-
(2000)
Biochem. J.
, vol.348
, pp. 425-432
-
-
Lee, H.C.1
Yin, P.H.2
Lu, C.Y.3
Chi, C.W.4
Wei, Y.H.5
-
13
-
-
78149361243
-
Association between a common mitochondrial DNA D-loop polycytosine variant and alteration of mitochondrial copy number in human peripheral blood cells
-
Liou C.W., Lin T.K., Chen J.B., Tiao M.M., Weng S.W., Chen S.D., Chuang Y.C., Chuang J.H., Wang P.W. Association between a common mitochondrial DNA D-loop polycytosine variant and alteration of mitochondrial copy number in human peripheral blood cells. J. Med. Genet. 2010, 47:723-728.
-
(2010)
J. Med. Genet.
, vol.47
, pp. 723-728
-
-
Liou, C.W.1
Lin, T.K.2
Chen, J.B.3
Tiao, M.M.4
Weng, S.W.5
Chen, S.D.6
Chuang, Y.C.7
Chuang, J.H.8
Wang, P.W.9
-
14
-
-
41149114560
-
Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1)
-
Mills R.D., Sim C.H., Mok S.S., Mulhern T.D., Culvenor J.G., Cheng H.C. Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1). J. Neurochem. 2008, 105:18-33.
-
(2008)
J. Neurochem.
, vol.105
, pp. 18-33
-
-
Mills, R.D.1
Sim, C.H.2
Mok, S.S.3
Mulhern, T.D.4
Culvenor, J.G.5
Cheng, H.C.6
-
15
-
-
77956196141
-
Mitochondria dysfunction and neurodegenerative disorders: cause or consequence
-
Morais V.A., De Strooper B. Mitochondria dysfunction and neurodegenerative disorders: cause or consequence. J. Alzheimers Dis. 2010, 20:S255-S263.
-
(2010)
J. Alzheimers Dis.
, vol.20
, pp. S255-S263
-
-
Morais, V.A.1
De Strooper, B.2
-
16
-
-
84894291922
-
Alpha-Synuclein and mitochondrial dysfunction in Parkinson's disease
-
Mullin S., Schapira A. Alpha-Synuclein and mitochondrial dysfunction in Parkinson's disease. Mol. Neurobiol. 2013, 47:587-597.
-
(2013)
Mol. Neurobiol.
, vol.47
, pp. 587-597
-
-
Mullin, S.1
Schapira, A.2
-
17
-
-
18944374033
-
The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment
-
Nasreddine Z.S., Phillips N.A., Bedirian V., Charbonneau S., Whitehead V., Collin I., Cummings J.L., Chertkow H. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J. Am. Geriatr. Soc. 2005, 53:695-699.
-
(2005)
J. Am. Geriatr. Soc.
, vol.53
, pp. 695-699
-
-
Nasreddine, Z.S.1
Phillips, N.A.2
Bedirian, V.3
Charbonneau, S.4
Whitehead, V.5
Collin, I.6
Cummings, J.L.7
Chertkow, H.8
-
18
-
-
84907995146
-
Genetic impact on cognition and brain function in newly diagnosed Parkinson's disease: ICICLE-PD study
-
ICICLE-PD Study Group
-
Nombela C., Rowe J.B., Winder-Rhodes S.E., Hampshire A., Owen A.M., Breen D.P., Duncan G.W., Khoo T.K., Yarnall A.J., Firbank M.J., Chinnery P.F., Robbins T.W., O'Brien J.T., Brooks D.J., Burn D.J., Barker R.A. Genetic impact on cognition and brain function in newly diagnosed Parkinson's disease: ICICLE-PD study. Brain 2014, 137(Pt 10):2743-2758. ICICLE-PD Study Group.
-
(2014)
Brain
, vol.137
, pp. 2743-2758
-
-
Nombela, C.1
Rowe, J.B.2
Winder-Rhodes, S.E.3
Hampshire, A.4
Owen, A.M.5
Breen, D.P.6
Duncan, G.W.7
Khoo, T.K.8
Yarnall, A.J.9
Firbank, M.J.10
Chinnery, P.F.11
Robbins, T.W.12
O'Brien, J.T.13
Brooks, D.J.14
Burn, D.J.15
Barker, R.A.16
-
19
-
-
84901604919
-
Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease
-
Petersen M.H., Budtz-Jorgensen E., Sorensen S.A., Nielsen J.E., Hjermind L.E., Vinther-Jensen T., Nielsen S.M.B., Norremolle A. Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease. Mitochondrion 2014, 17:14-21.
-
(2014)
Mitochondrion
, vol.17
, pp. 14-21
-
-
Petersen, M.H.1
Budtz-Jorgensen, E.2
Sorensen, S.A.3
Nielsen, J.E.4
Hjermind, L.E.5
Vinther-Jensen, T.6
Nielsen, S.M.B.7
Norremolle, A.8
-
20
-
-
84879288527
-
The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons
-
Reeve A., Meagher M., Lax N., Simcox E., Hepplewhite P., Jaros E., Turnbull D. The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons. J. Neurosci. 2013, 33:10790-10801.
-
(2013)
J. Neurosci.
, vol.33
, pp. 10790-10801
-
-
Reeve, A.1
Meagher, M.2
Lax, N.3
Simcox, E.4
Hepplewhite, P.5
Jaros, E.6
Turnbull, D.7
-
21
-
-
84897879235
-
Mitochondrial DNA copy numbers in pyramidal neurons are decreased and mitochondrial biogenesis transcriptome signaling is disrupted in Alzheimer's disease hippocampi
-
Rice A.C., Keeney P.M., Algarzae N.K., Ladd A.C., Thomas R.R., Bennett J.P. Mitochondrial DNA copy numbers in pyramidal neurons are decreased and mitochondrial biogenesis transcriptome signaling is disrupted in Alzheimer's disease hippocampi. J. Alzheimers Dis. 2014, 40:319-330.
-
(2014)
J. Alzheimers Dis.
, vol.40
, pp. 319-330
-
-
Rice, A.C.1
Keeney, P.M.2
Algarzae, N.K.3
Ladd, A.C.4
Thomas, R.R.5
Bennett, J.P.6
-
22
-
-
0023037928
-
CAMDEX. A standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia
-
Roth M., Tym E., Mountjoy C.Q., Huppert F.A., Hendrie H., Verma S., Goddard R. CAMDEX. A standardised instrument for the diagnosis of mental disorder in the elderly with special reference to the early detection of dementia. Br. J. Psychiatry 1986, 149:698-709.
-
(1986)
Br. J. Psychiatry
, vol.149
, pp. 698-709
-
-
Roth, M.1
Tym, E.2
Mountjoy, C.Q.3
Huppert, F.A.4
Hendrie, H.5
Verma, S.6
Goddard, R.7
-
23
-
-
84877104879
-
Reduced mitochondrial DNA copy number in peripheral blood leukocytes increases the risk of soft tissue sarcoma
-
Xie H., Lev D., Gong Y.L., Wang S., Pollock R.E., Wu X.F., Gu J. Reduced mitochondrial DNA copy number in peripheral blood leukocytes increases the risk of soft tissue sarcoma. Carcinogenesis 2013, 34:1039-1043.
-
(2013)
Carcinogenesis
, vol.34
, pp. 1039-1043
-
-
Xie, H.1
Lev, D.2
Gong, Y.L.3
Wang, S.4
Pollock, R.E.5
Wu, X.F.6
Gu, J.7
-
24
-
-
84895770516
-
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD study
-
Yarnall A.J., Breen D.P., Duncan G.W., Khoo T.K., Coleman S.Y., Firbank M.J., Nombela C., Winder-Rhodes S., Evans J.R., Rowe J.B., Mollenhauer B., Kruse N., Hudson G., Chinnery P.F., O'Brien J.T., Robbins T.W., Wesnes K., Brooks D.J., Barker R.A., Burn D.J., Group I.-P.S. Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD study. Neurology 2014, 82:308-316.
-
(2014)
Neurology
, vol.82
, pp. 308-316
-
-
Yarnall, A.J.1
Breen, D.P.2
Duncan, G.W.3
Khoo, T.K.4
Coleman, S.Y.5
Firbank, M.J.6
Nombela, C.7
Winder-Rhodes, S.8
Evans, J.R.9
Rowe, J.B.10
Mollenhauer, B.11
Kruse, N.12
Hudson, G.13
Chinnery, P.F.14
O'Brien, J.T.15
Robbins, T.W.16
Wesnes, K.17
Brooks, D.J.18
Barker, R.A.19
Burn, D.J.20
Group, I.-P.S.21
more..
|