-
1
-
-
36248985106
-
Update on the genetics of Parkinson's disease
-
T. Gasser Update on the genetics of Parkinson's disease Mov. Disord. 22 Suppl. 17 2007 S343 S350
-
(2007)
Mov. Disord.
, vol.22
, Issue.SUPPL. 17
-
-
Gasser, T.1
-
2
-
-
0028298816
-
Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome
-
A.S. Najim al-Din, A. Wriekat, A. Mubaidin, M. Dasouki, and M. Hiari Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome Acta Neurol. Scand. 89 1994 347 352
-
(1994)
Acta Neurol. Scand.
, vol.89
, pp. 347-352
-
-
Najim Al-Din, A.S.1
Wriekat, A.2
Mubaidin, A.3
Dasouki, M.4
Hiari, M.5
-
3
-
-
33749133430
-
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
-
A. Ramirez, A. Heimbach, J. Gründemann, B. Stiller, D. Hampshire, L.P. Cid, I. Goebel, A.F. Mubaidin, A.L. Wriekat, and J. Roeper Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase Nat. Genet. 38 2006 1184 1191
-
(2006)
Nat. Genet.
, vol.38
, pp. 1184-1191
-
-
Ramirez, A.1
Heimbach, A.2
Gründemann, J.3
Stiller, B.4
Hampshire, D.5
Cid, L.P.6
Goebel, I.7
Mubaidin, A.F.8
Wriekat, A.L.9
Roeper, J.10
-
4
-
-
34248182509
-
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
-
A. Di Fonzo, H.F. Chien, M. Socal, S. Giraudo, C. Tassorelli, G. Iliceto, G. Fabbrini, R. Marconi, E. Fincati, and G. Abbruzzese ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease Neurology 68 2007 1557 1562
-
(2007)
Neurology
, vol.68
, pp. 1557-1562
-
-
Di Fonzo, A.1
Chien, H.F.2
Socal, M.3
Giraudo, S.4
Tassorelli, C.5
Iliceto, G.6
Fabbrini, G.7
Marconi, R.8
Fincati, E.9
Abbruzzese, G.10
-
5
-
-
42049103656
-
PARK9-linked parkinsonism in eastern Asia: Mutation detection in ATP13A2 and clinical phenotype
-
Y.P. Ning, K. Kanai, H. Tomiyama, Y. Li, M. Funayama, H. Yoshino, S. Sato, M. Asahina, S. Kuwabara, and A. Takeda PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype Neurology 70 2008 1491 1493
-
(2008)
Neurology
, vol.70
, pp. 1491-1493
-
-
Ning, Y.P.1
Kanai, K.2
Tomiyama, H.3
Li, Y.4
Funayama, M.5
Yoshino, H.6
Sato, S.7
Asahina, M.8
Kuwabara, S.9
Takeda, A.10
-
6
-
-
77953512439
-
Early-onset l-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
-
C. Paisán-Ruiz, R. Guevara, M. Federoff, H. Hanagasi, F. Sina, E. Elahi, S.A. Schneider, P. Schwingenschuh, N. Bajaj, and M. Emre Early-onset l-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations Mov. Disord. 25 2010 1791 1800
-
(2010)
Mov. Disord.
, vol.25
, pp. 1791-1800
-
-
Paisán-Ruiz, C.1
Guevara, R.2
Federoff, M.3
Hanagasi, H.4
Sina, F.5
Elahi, E.6
Schneider, S.A.7
Schwingenschuh, P.8
Bajaj, N.9
Emre, M.10
-
7
-
-
79951557128
-
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability
-
L. Santoro, G.J. Breedveld, F. Manganelli, R. Iodice, and C. Pisciotta Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability Neurogenetics 12 2011 33 39
-
(2011)
Neurogenetics
, vol.12
, pp. 33-39
-
-
Santoro, L.1
Breedveld, G.J.2
Manganelli, F.3
Iodice, R.4
Pisciotta, C.5
-
8
-
-
79551474118
-
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frame-shift mutation
-
D. Crosiers, B. Ceulemans, B. Meeus, K. Nuytemans, P. Pals, C. Van Broeckhoven, P. Cras, and J. Theuns Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frame-shift mutation Parkinsonism Relat. Disord. 17 2011 135 138
-
(2011)
Parkinsonism Relat. Disord.
, vol.17
, pp. 135-138
-
-
Crosiers, D.1
Ceulemans, B.2
Meeus, B.3
Nuytemans, K.4
Pals, P.5
Van Broeckhoven, C.6
Cras, P.7
Theuns, J.8
-
9
-
-
63149090431
-
Parkinson's disease: From monogenic forms to genetic susceptibility factors
-
S. Lesage, and A. Brice Parkinson's disease: from monogenic forms to genetic susceptibility factors Hum. Mol. Genet. 18 2009 R48 R59
-
(2009)
Hum. Mol. Genet.
, vol.18
-
-
Lesage, S.1
Brice, A.2
-
10
-
-
84867741659
-
Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants
-
J.P. Covy, E.A. Waxman, and B.I. Giasson Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants J. Neurosci. Res. 90 2012 2306 2316
-
(2012)
J. Neurosci. Res.
, vol.90
, pp. 2306-2316
-
-
Covy, J.P.1
Waxman, E.A.2
Giasson, B.I.3
-
11
-
-
84862189804
-
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
-
B. Dehay, A. Ramirez, M. Martinez-Vicente, C. Perier, M.H. Canron, E. Doudnikoff, A. Vital, M. Vila, C. Klein, and E.C. Bezard Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration Proc. Natl. Acad. Sci. USA 109 2012 9611 9616
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 9611-9616
-
-
Dehay, B.1
Ramirez, A.2
Martinez-Vicente, M.3
Perier, C.4
Canron, M.H.5
Doudnikoff, E.6
Vital, A.7
Vila, M.8
Klein, C.9
Bezard, E.C.10
-
12
-
-
84863091947
-
Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism
-
A. Podhajska, A. Musso, A. Trancikova, K. Stafa, R. Moser, S. Sonnay, L. Glauser, and D.J. Moore Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism PLoS ONE 7 2012 e39942
-
(2012)
PLoS ONE
, vol.7
, pp. 39942
-
-
Podhajska, A.1
Musso, A.2
Trancikova, A.3
Stafa, K.4
Moser, R.5
Sonnay, S.6
Glauser, L.7
Moore, D.J.8
-
13
-
-
84859246513
-
PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity
-
D. Ramonet, A. Podhajska, K. Stafa, S. Sonnay, A. Trancikova, E. Tsika, O. Pletnikova, J.C. Troncoso, L. Glauser, and D.J. Moore PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity Hum. Mol. Genet. 21 2012 1725 1743
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1725-1743
-
-
Ramonet, D.1
Podhajska, A.2
Stafa, K.3
Sonnay, S.4
Trancikova, A.5
Tsika, E.6
Pletnikova, O.7
Troncoso, J.C.8
Glauser, L.9
Moore, D.J.10
-
14
-
-
84865064424
-
Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity
-
M. Usenovic, A.L. Knight, A. Ray, V. Wong, K.R. Brown, G.A. Caldwell, K.A. Caldwell, I. Stagljar, and D. Krainc Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity Hum. Mol. Genet. 21 2012 3785 3794
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 3785-3794
-
-
Usenovic, M.1
Knight, A.L.2
Ray, A.3
Wong, V.4
Brown, K.R.5
Caldwell, G.A.6
Caldwell, K.A.7
Stagljar, I.8
Krainc, D.9
-
15
-
-
0034666116
-
Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons
-
M. Koike, H. Nakanishi, P. Saftig, J. Ezaki, K. Isahara, Y. Ohsawa, W. Schulz-Schaeffer, T. Watanabe, S. Waguri, and S. Kametaka Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons J. Neurosci. 20 2000 6898 6906
-
(2000)
J. Neurosci.
, vol.20
, pp. 6898-6906
-
-
Koike, M.1
Nakanishi, H.2
Saftig, P.3
Ezaki, J.4
Isahara, K.5
Ohsawa, Y.6
Schulz-Schaeffer, W.7
Watanabe, T.8
Waguri, S.9
Kametaka, S.10
-
16
-
-
34249715911
-
Generation of medaka gene knockout models by target-selected mutagenesis
-
Y. Taniguchi, S. Takeda, M. Furutani-Seiki, Y. Kamei, T. Todo, T. Sasado, T. Deguchi, H. Kondoh, J. Mudde, and M. Yamazoe Generation of medaka gene knockout models by target-selected mutagenesis Genome Biol. 7 2006 R116
-
(2006)
Genome Biol.
, vol.7
, pp. 116
-
-
Taniguchi, Y.1
Takeda, S.2
Furutani-Seiki, M.3
Kamei, Y.4
Todo, T.5
Sasado, T.6
Deguchi, T.7
Kondoh, H.8
Mudde, J.9
Yamazoe, M.10
-
17
-
-
70349443396
-
A chemical neurotoxin, MPTP induces Parkinson's disease like phenotype, movement disorders and persistent loss of dopamine neurons in medaka fish
-
H. Matsui, Y. Taniguchi, H. Inoue, K. Uemura, S. Takeda, and R. Takahashi A chemical neurotoxin, MPTP induces Parkinson's disease like phenotype, movement disorders and persistent loss of dopamine neurons in medaka fish Neurosci. Res. 65 2009 263 271
-
(2009)
Neurosci. Res.
, vol.65
, pp. 263-271
-
-
Matsui, H.1
Taniguchi, Y.2
Inoue, H.3
Uemura, K.4
Takeda, S.5
Takahashi, R.6
-
18
-
-
77956568458
-
Proteasome inhibition in medaka brain induces the features of Parkinson's disease
-
H. Matsui, H. Ito, Y. Taniguchi, H. Inoue, S. Takeda, and R. Takahashi Proteasome inhibition in medaka brain induces the features of Parkinson's disease J. Neurochem. 115 2010 178 187
-
(2010)
J. Neurochem.
, vol.115
, pp. 178-187
-
-
Matsui, H.1
Ito, H.2
Taniguchi, Y.3
Inoue, H.4
Takeda, S.5
Takahashi, R.6
-
19
-
-
0026539541
-
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)
-
D.N. Palmer, I.M. Fearnley, J.E. Walker, N.A. Hall, B.D. Lake, L.S. Wolfe, M. Haltia, R.D. Martinus, and R.D. Jolly Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease) Am. J. Med. Genet. 42 1992 561 567
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 561-567
-
-
Palmer, D.N.1
Fearnley, I.M.2
Walker, J.E.3
Hall, N.A.4
Lake, B.D.5
Wolfe, L.S.6
Haltia, M.7
Martinus, R.D.8
Jolly, R.D.9
-
20
-
-
2442541217
-
Mutation of the glycosylated asparagine residue 286 in human CLN2 protein results in loss of enzymatic activity
-
K. Tsiakas, R. Steinfeld, S. Storch, J. Ezaki, Z. Lukacs, E. Kominami, A. Kohlschütter, K. Ullrich, and T. Braulke Mutation of the glycosylated asparagine residue 286 in human CLN2 protein results in loss of enzymatic activity Glycobiology 14 2004 1C 5C
-
(2004)
Glycobiology
, vol.14
-
-
Tsiakas, K.1
Steinfeld, R.2
Storch, S.3
Ezaki, J.4
Lukacs, Z.5
Kominami, E.6
Kohlschütter, A.7
Ullrich, K.8
Braulke, T.9
-
21
-
-
0027224115
-
Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis
-
J. Tyynelä, D.N. Palmer, M. Baumann, and M. Haltia Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis FEBS Lett. 330 1993 8 12
-
(1993)
FEBS Lett.
, vol.330
, pp. 8-12
-
-
Tyynelä, J.1
Palmer, D.N.2
Baumann, M.3
Haltia, M.4
-
22
-
-
0030882856
-
Alpha-synuclein in Lewy bodies
-
M.G. Spillantini, M.L. Schmidt, V.M. Lee, J.Q. Trojanowski, R. Jakes, and M. Goedert Alpha-synuclein in Lewy bodies Nature 388 1997 839 840
-
(1997)
Nature
, vol.388
, pp. 839-840
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
23
-
-
0041589248
-
Alpha-synuclein is degraded by both autophagy and the proteasome
-
J.L. Webb, B. Ravikumar, J. Atkins, J.N. Skepper, and D.C. Rubinsztein Alpha-synuclein is degraded by both autophagy and the proteasome J. Biol. Chem. 278 2003 25009 25013
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 25009-25013
-
-
Webb, J.L.1
Ravikumar, B.2
Atkins, J.3
Skepper, J.N.4
Rubinsztein, D.C.5
-
24
-
-
58149314211
-
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
-
D. Narendra, A. Tanaka, D.F. Suen, and R.J. Youle Parkin is recruited selectively to impaired mitochondria and promotes their autophagy J. Cell Biol. 183 2008 795 803
-
(2008)
J. Cell Biol.
, vol.183
, pp. 795-803
-
-
Narendra, D.1
Tanaka, A.2
Suen, D.F.3
Youle, R.J.4
-
25
-
-
80051949129
-
Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein
-
J. Tan, T. Zhang, L. Jiang, J. Chi, D. Hu, Q. Pan, D. Wang, and Z. Zhang Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein J. Biol. Chem. 286 2011 29654 29662
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 29654-29662
-
-
Tan, J.1
Zhang, T.2
Jiang, L.3
Chi, J.4
Hu, D.5
Pan, Q.6
Wang, D.7
Zhang, Z.8
-
26
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
E. Sidransky, M.A. Nalls, J.O. Aasly, J. Aharon-Peretz, G. Annesi, E.R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, and A. Brice Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease N. Engl. J. Med. 361 2009 1651 1661
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1651-1661
-
-
Sidransky, E.1
Nalls, M.A.2
Aasly, J.O.3
Aharon-Peretz, J.4
Annesi, G.5
Barbosa, E.R.6
Bar-Shira, A.7
Berg, D.8
Bras, J.9
Brice, A.10
-
27
-
-
84858403126
-
Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity
-
M. Usenovic, E. Tresse, J.R. Mazzulli, J.P. Taylor, and D. Krainc Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity J. Neurosci. 32 2012 4240 4246
-
(2012)
J. Neurosci.
, vol.32
, pp. 4240-4246
-
-
Usenovic, M.1
Tresse, E.2
Mazzulli, J.R.3
Taylor, J.P.4
Krainc, D.5
-
28
-
-
33745079623
-
Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis
-
E. Siintola, S. Partanen, P. Strömme, A. Haapanen, M. Haltia, J. Maehlen, A.E. Lehesjoki, and J. Tyynelä Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis Brain 129 2006 1438 1445
-
(2006)
Brain
, vol.129
, pp. 1438-1445
-
-
Siintola, E.1
Partanen, S.2
Strömme, P.3
Haapanen, A.4
Haltia, M.5
Maehlen, J.6
Lehesjoki, A.E.7
Tyynelä, J.8
-
29
-
-
59249093607
-
Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10)
-
K. Fritchie, E. Siintola, D. Armao, A.E. Lehesjoki, T. Marino, C. Powell, M. Tennison, J.M. Booker, S. Koch, and S. Partanen Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10) Acta Neuropathol. 117 2009 201 208
-
(2009)
Acta Neuropathol.
, vol.117
, pp. 201-208
-
-
Fritchie, K.1
Siintola, E.2
Armao, D.3
Lehesjoki, A.E.4
Marino, T.5
Powell, C.6
Tennison, M.7
Booker, J.M.8
Koch, S.9
Partanen, S.10
-
30
-
-
33646871344
-
Cathepsin D deficiency is associated with a human neurodegenerative disorder
-
R. Steinfeld, K. Reinhardt, K. Schreiber, M. Hillebrand, R. Kraetzner, W. Bruck, P. Saftig, and J. Gartner Cathepsin D deficiency is associated with a human neurodegenerative disorder Am. J. Hum. Genet. 78 2006 988 998
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 988-998
-
-
Steinfeld, R.1
Reinhardt, K.2
Schreiber, K.3
Hillebrand, M.4
Kraetzner, R.5
Bruck, W.6
Saftig, P.7
Gartner, J.8
-
31
-
-
0020331661
-
Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: Motor neuron disease phenotype
-
K. Jellinger, A.P. Anzil, D. Seemann, and H. Bernheimer Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: motor neuron disease phenotype Clin. Neuropathol. 1 1982 31 44
-
(1982)
Clin. Neuropathol.
, vol.1
, pp. 31-44
-
-
Jellinger, K.1
Anzil, A.P.2
Seemann, D.3
Bernheimer, H.4
-
32
-
-
0026510492
-
Fabry's disease without angiokeratomas showing unusual eccrine gland vacuolation
-
M.A. Idoate, F.J. Pardo-Mindan, and C. Gonzalez Alamillo Fabry's disease without angiokeratomas showing unusual eccrine gland vacuolation J. Pathol. 167 1992 65 68
-
(1992)
J. Pathol.
, vol.167
, pp. 65-68
-
-
Idoate, M.A.1
Pardo-Mindan, F.J.2
Gonzalez Alamillo, C.3
-
33
-
-
74249113845
-
Loss of PINK1 in medaka fish (Oryzias latipes) causes late-onset decrease in spontaneous movement
-
H. Matsui, Y. Taniguchi, H. Inoue, Y. Kobayashi, Y. Sakaki, A. Toyoda, K. Uemura, D. Kobayashi, S. Takeda, and R. Takahashi Loss of PINK1 in medaka fish (Oryzias latipes) causes late-onset decrease in spontaneous movement Neurosci. Res. 66 2010 151 161
-
(2010)
Neurosci. Res.
, vol.66
, pp. 151-161
-
-
Matsui, H.1
Taniguchi, Y.2
Inoue, H.3
Kobayashi, Y.4
Sakaki, Y.5
Toyoda, A.6
Uemura, K.7
Kobayashi, D.8
Takeda, S.9
Takahashi, R.10
-
34
-
-
78149239653
-
Ammonium chloride and tunicamycin are novel toxins for dopaminergic neurons and induce Parkinson's disease-like phenotypes in medaka fish
-
H. Matsui, H. Ito, Y. Taniguchi, S. Takeda, and R. Takahashi Ammonium chloride and tunicamycin are novel toxins for dopaminergic neurons and induce Parkinson's disease-like phenotypes in medaka fish J. Neurochem. 115 2010 1150 1160
-
(2010)
J. Neurochem.
, vol.115
, pp. 1150-1160
-
-
Matsui, H.1
Ito, H.2
Taniguchi, Y.3
Takeda, S.4
Takahashi, R.5
-
35
-
-
84870495284
-
The zebrafish homologue of Parkinson's disease ATP13A2 is essential for embryonic survival
-
T. Lopes da Fonseca, A. Correia, W. Hasselaar, H.C. van der Linde, R. Willemsen, and T.F. Outeiro The zebrafish homologue of Parkinson's disease ATP13A2 is essential for embryonic survival Brain Res. Bull. 90 2013 118 126
-
(2013)
Brain Res. Bull.
, vol.90
, pp. 118-126
-
-
Lopes Da Fonseca, T.1
Correia, A.2
Hasselaar, W.3
Van Der Linde, H.C.4
Willemsen, R.5
Outeiro, T.F.6
-
36
-
-
0037208510
-
The molecular mechanisms of dopamine toxicity
-
A. Barzilai, D. Daily, R. Zilkha-Falb, I. Ziv, D. Offen, E. Melamed, and A. Shirvan The molecular mechanisms of dopamine toxicity Adv. Neurol. 91 2003 73 82
-
(2003)
Adv. Neurol.
, vol.91
, pp. 73-82
-
-
Barzilai, A.1
Daily, D.2
Zilkha-Falb, R.3
Ziv, I.4
Offen, D.5
Melamed, E.6
Shirvan, A.7
-
37
-
-
84861476741
-
Dopamine induced neurodegeneration in a PINK1 model of Parkinson's disease
-
S. Gandhi, A. Vaarmann, Z. Yao, M.R. Duchen, N.W. Wood, and A.Y. Abramov Dopamine induced neurodegeneration in a PINK1 model of Parkinson's disease PLoS ONE 7 2012 e37564
-
(2012)
PLoS ONE
, vol.7
, pp. 37564
-
-
Gandhi, S.1
Vaarmann, A.2
Yao, Z.3
Duchen, M.R.4
Wood, N.W.5
Abramov, A.Y.6
-
38
-
-
0034993599
-
Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: Contribution to the apoptotic theory in Parkinson's disease
-
D. Blum, S. Torch, N. Lambeng, M. Nissou, A.L. Benabid, R. Sadoul, and J.M. Verna Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease Prog. Neurobiol. 65 2001 135 172
-
(2001)
Prog. Neurobiol.
, vol.65
, pp. 135-172
-
-
Blum, D.1
Torch, S.2
Lambeng, N.3
Nissou, M.4
Benabid, A.L.5
Sadoul, R.6
Verna, J.M.7
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