-
1
-
-
33745919520
-
Epidemiology of Parkinson's disease
-
10.1016/S1474-4422(06)70471-9
-
L.M.L. de Lau, and M.M.B. Breteler Epidemiology of Parkinson's disease Lancet Neurol. 5 2006 525 535 10.1016/S1474-4422(06)70471-9
-
(2006)
Lancet Neurol.
, vol.5
, pp. 525-535
-
-
De Lau, L.M.L.1
Breteler, M.M.B.2
-
2
-
-
68649110032
-
Mendelian forms of Parkinson's disease
-
10.1016/j.bbadis.2008.12.007
-
T. Gasser Mendelian forms of Parkinson's disease Biochim. Biophys. Acta 1792 2009 587 596 10.1016/j.bbadis.2008.12.007
-
(2009)
Biochim. Biophys. Acta
, vol.1792
, pp. 587-596
-
-
Gasser, T.1
-
3
-
-
84898864538
-
Recent advances in Parkinson's disease genetics
-
10.1007/s00415-013-7003-2
-
S. Lubbe, and H.R. Morris Recent advances in Parkinson's disease genetics J. Neurol. 2013 10.1007/s00415-013-7003-2
-
(2013)
J. Neurol.
-
-
Lubbe, S.1
Morris, H.R.2
-
4
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
10.1038/33416
-
T. Kitada, S. Asakawa, N. Hattori, H. Matsumine, Y. Yamamura, and S. Minoshima et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism Nature 392 1998 605 608 10.1038/33416
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
-
5
-
-
0242363670
-
Molecular pathways of neurodegeneration in Parkinson's disease
-
10.1126/science.1087753
-
T.M. Dawson Molecular pathways of neurodegeneration in Parkinson's disease Science 302 2003 819 822 10.1126/science.1087753
-
(2003)
Science
, vol.302
, pp. 819-822
-
-
Dawson, T.M.1
-
6
-
-
4444370179
-
How does parkin ligate ubiquitin to Parkinson's disease?
-
10.1038/sj.embor.7400188
-
P.J. Kahle, and C. Haass How does parkin ligate ubiquitin to Parkinson's disease? EMBO Rep. 5 2004 681 685 10.1038/sj.embor.7400188
-
(2004)
EMBO Rep.
, vol.5
, pp. 681-685
-
-
Kahle, P.J.1
Haass, C.2
-
7
-
-
0037386532
-
Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
-
10.1073/pnas.0737556100
-
J.C. Greene, A.J. Whitworth, I. Kuo, L.A. Andrews, M.B. Feany, and L.J. Pallanck Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants Proc. Natl. Acad. Sci. U. S. A. 100 2003 4078 4083 10.1073/pnas.0737556100
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 4078-4083
-
-
Greene, J.C.1
Whitworth, A.J.2
Kuo, I.3
Andrews, L.A.4
Feany, M.B.5
Pallanck, L.J.6
-
8
-
-
2442481789
-
Mitochondrial dysfunction and oxidative damage in parkin-deficient mice
-
10.1074/jbc.M401135200
-
J.J. Palacino Mitochondrial dysfunction and oxidative damage in parkin-deficient mice J. Biol. Chem. 279 2004 18614 18622 10.1074/jbc.M401135200
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 18614-18622
-
-
Palacino, J.J.1
-
9
-
-
77958535699
-
Mutant parkin impairs mitochondrial function and morphology in human fibroblasts
-
10.1371/journal.pone.0012962
-
A. Grünewald, L. Voges, A. Rakovic, M. Kasten, H. Vandebona, and C. Hemmelmann et al. Mutant parkin impairs mitochondrial function and morphology in human fibroblasts PLoS One 5 2010 e12962 10.1371/journal.pone.0012962
-
(2010)
PLoS One
, vol.5
, pp. 12962
-
-
Grünewald, A.1
Voges, L.2
Rakovic, A.3
Kasten, M.4
Vandebona, H.5
Hemmelmann, C.6
-
10
-
-
33846288002
-
Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6
-
10.1016/j.nbd.2006.10.007
-
H.-H. Hoepken, S. Gispert, B. Morales, O. Wingerter, D. Del Turco, and A. Mülsch et al. Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6 Neurobiol. Dis. 25 2007 401 411 10.1016/j.nbd.2006.10.007
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 401-411
-
-
Hoepken, H.-H.1
Gispert, S.2
Morales, B.3
Wingerter, O.4
Del Turco, D.5
Mülsch, A.6
-
11
-
-
57749100375
-
Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts
-
10.1002/ana.21492
-
H. Mortiboys, K.J. Thomas, W.J.H. Koopman, S. Klaffke, P. Abou-Sleiman, and S. Olpin et al. Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts Ann. Neurol. 64 2008 555 565 10.1002/ana.21492
-
(2008)
Ann. Neurol.
, vol.64
, pp. 555-565
-
-
Mortiboys, H.1
Thomas, K.J.2
Koopman, W.J.H.3
Klaffke, S.4
Abou-Sleiman, P.5
Olpin, S.6
-
12
-
-
79958245892
-
Mitochondrial defect and PGC-1α dysfunction in parkin-associated familial Parkinson's disease
-
10.1016/j.bbadis.2010.12.022
-
C. Pacelli, D. De Rasmo, A. Signorile, I. Grattagliano, G. di Tullio, and A. D'Orazio et al. Mitochondrial defect and PGC-1α dysfunction in parkin-associated familial Parkinson's disease Biochim. Biophys. Acta 2011 1812 1041 1053 10.1016/j.bbadis.2010.12.022
-
(1812)
Biochim. Biophys. Acta
, vol.2011
, pp. 1041-1053
-
-
Pacelli, C.1
De Rasmo, D.2
Signorile, A.3
Grattagliano, I.4
Di Tullio, G.5
D'Orazio, A.6
-
13
-
-
0033373674
-
Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease
-
10.1111/j.1749-6632.1999.tb07870.x
-
F.R. Wiedemann, K. Winkler, H. Lins, C.-W. Wallesch, and W.S. Kunz Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease Ann. N. Y. Acad. Sci. 893 1999 426 429 10.1111/j.1749-6632.1999.tb07870.x
-
(1999)
Ann. N. Y. Acad. Sci.
, vol.893
, pp. 426-429
-
-
Wiedemann, F.R.1
Winkler, K.2
Lins, H.3
Wallesch, C.-W.4
Kunz, W.S.5
-
14
-
-
84868149042
-
Primary skin fibroblasts as a model of Parkinson's disease
-
10.1007/s12035-012-8245-1
-
G. Auburger, M. Klinkenberg, J. Drost, K. Marcus, B. Morales-Gordo, and W.S. Kunz et al. Primary skin fibroblasts as a model of Parkinson's disease Mol. Neurobiol. 46 2012 20 27 10.1007/s12035-012-8245-1
-
(2012)
Mol. Neurobiol.
, vol.46
, pp. 20-27
-
-
Auburger, G.1
Klinkenberg, M.2
Drost, J.3
Marcus, K.4
Morales-Gordo, B.5
Kunz, W.S.6
-
15
-
-
4544326057
-
Mitochondrial complex i and IV activities in leukocytes from patients with parkin mutations
-
10.1002/mds.10695
-
M. Müftüoglu, B. Elibol, O. Dalmizrak, A. Ercan, G. Kulaksiz, and H. Ogüs et al. Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutations Mov. Disord. Off. J. Mov. Disord. Soc. 19 2004 544 548 10.1002/mds.10695
-
(2004)
Mov. Disord. Off. J. Mov. Disord. Soc.
, vol.19
, pp. 544-548
-
-
Müftüoglu, M.1
Elibol, B.2
Dalmizrak, O.3
Ercan, A.4
Kulaksiz, G.5
Ogüs, H.6
-
16
-
-
0023898945
-
The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
-
10.1136/jnnp.51.6.745
-
W.R. Gibb, and A.J. Lees The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease J. Neurol. Neurosurg. Psychiatry 51 1988 745 752 10.1136/jnnp.51.6.745
-
(1988)
J. Neurol. Neurosurg. Psychiatry
, vol.51
, pp. 745-752
-
-
Gibb, W.R.1
Lees, A.J.2
-
17
-
-
58349114656
-
Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease
-
10.1016/j.parkreldis.2008.04.005
-
S. Bardien, R. Keyser, Y. Yako, D. Lombard, and J. Carr Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease Parkinsonism Relat. Disord. 15 2009 116 121 10.1016/j.parkreldis.2008. 04.005
-
(2009)
Parkinsonism Relat. Disord.
, vol.15
, pp. 116-121
-
-
Bardien, S.1
Keyser, R.2
Yako, Y.3
Lombard, D.4
Carr, J.5
-
18
-
-
84655166928
-
Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population
-
10.1016/j.parkreldis.2011.09.022
-
W.L. Haylett, R.J. Keyser, M.C. du Plessis, C. van der Merwe, J. Blanckenberg, and D. Lombard et al. Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population Parkinsonism Relat. Disord. 18 2012 89 92 10.1016/j.parkreldis.2011.09.022
-
(2012)
Parkinsonism Relat. Disord.
, vol.18
, pp. 89-92
-
-
Haylett, W.L.1
Keyser, R.J.2
Du Plessis, M.C.3
Van Der Merwe, C.4
Blanckenberg, J.5
Lombard, D.6
-
19
-
-
77954660828
-
Analysis of exon dosage using MLPA in South African Parkinson's disease patients
-
10.1007/s10048-009-0229-6
-
R.J. Keyser, D. Lombard, R. Veikondis, J. Carr, and S. Bardien Analysis of exon dosage using MLPA in South African Parkinson's disease patients Neurogenetics 11 2010 305 312 10.1007/s10048-009-0229-6
-
(2010)
Neurogenetics
, vol.11
, pp. 305-312
-
-
Keyser, R.J.1
Lombard, D.2
Veikondis, R.3
Carr, J.4
Bardien, S.5
-
20
-
-
84899960429
-
-
J.P. (S version), D.B. (up to 2007), S.D. (up to 2002), D.S. (up to 2005), E. authors, R-core, nlme: Linear and Nonlinear Mixed Effects Models, 2013
-
J.P. (S version), D.B. (up to 2007), S.D. (up to 2002), D.S. (up to 2005), E. authors, R-core, nlme: Linear and Nonlinear Mixed Effects Models, 2013.
-
-
-
-
21
-
-
69449103790
-
Parkin deficiency disrupts calcium homeostasis by modulating phospholipase C signalling
-
10.1111/j.1742-4658.2009.07201.x
-
A. Sandebring, N. Dehvari, M. Perez-Manso, K.J. Thomas, E. Karpilovski, and M.R. Cookson et al. Parkin deficiency disrupts calcium homeostasis by modulating phospholipase C signalling FEBS J. 276 2009 5041 5052 10.1111/j.1742-4658.2009.07201.x
-
(2009)
FEBS J.
, vol.276
, pp. 5041-5052
-
-
Sandebring, A.1
Dehvari, N.2
Perez-Manso, M.3
Thomas, K.J.4
Karpilovski, E.5
Cookson, M.R.6
-
22
-
-
68549136513
-
Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology
-
10.1016/j.expneurol.2009.05.027
-
A. Grünewald, M.E. Gegg, J.-W. Taanman, R.H. King, N. Kock, and C. Klein et al. Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology Exp. Neurol. 219 2009 266 273 10.1016/j.expneurol.2009.05.027
-
(2009)
Exp. Neurol.
, vol.219
, pp. 266-273
-
-
Grünewald, A.1
Gegg, M.E.2
Taanman, J.-W.3
King, R.H.4
Kock, N.5
Klein, C.6
-
23
-
-
33747884623
-
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
-
10.1093/brain/awl126
-
K. Verhoeven, K.G. Claeys, S. Züchner, J.M. Schröder, J. Weis, and C. Ceuterick et al. MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2 Brain J. Neurol. 129 2006 2093 2102 10.1093/brain/awl126
-
(2006)
Brain J. Neurol.
, vol.129
, pp. 2093-2102
-
-
Verhoeven, K.1
Claeys, K.G.2
Züchner, S.3
Schröder, J.M.4
Weis, J.5
Ceuterick, C.6
-
24
-
-
70350434308
-
Mitochondrial pathology in muscle of a patient with a novel parkin mutation
-
H.A. Hanagasi, P. Serdaroglu, M. Ozansoy, N. Basak, H. Tasli, and M. Emre Mitochondrial pathology in muscle of a patient with a novel parkin mutation Int. J. Neurosci. 119 2009 1572 1583
-
(2009)
Int. J. Neurosci.
, vol.119
, pp. 1572-1583
-
-
Hanagasi, H.A.1
Serdaroglu, P.2
Ozansoy, M.3
Basak, N.4
Tasli, H.5
Emre, M.6
-
25
-
-
84867031150
-
Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue
-
10.1186/1756-6606-5-35
-
Y. Imaizumi, Y. Okada, W. Akamatsu, M. Koike, N. Kuzumaki, and H. Hayakawa et al. Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue Mol. Brain 5 2012 35 10.1186/1756-6606-5-35
-
(2012)
Mol. Brain
, vol.5
, pp. 35
-
-
Imaizumi, Y.1
Okada, Y.2
Akamatsu, W.3
Koike, M.4
Kuzumaki, N.5
Hayakawa, H.6
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