-
1
-
-
0014021742
-
Experimental transmission of a Kuru-like syndrome to chimpanzees
-
Gajdusek DC, Gibbs CJ, Jr, Alpers M (1966) Experimental transmission of a Kuru-like syndrome to chimpanzees. Nature 209(5025):794-796.
-
(1966)
Nature
, vol.209
, Issue.5025
, pp. 794-796
-
-
Gajdusek, D.C.1
Gibbs, C.J.2
Alpers, M.3
-
2
-
-
0020437641
-
An update on long-term in vivo and in vitro studies designed to identify a virus as the cause of amyotrophic lateral sclerosis, parkinsonism dementia, and Parkinson's disease
-
Gibbs CJ, Jr, Gajdusek DC (1982) An update on long-term in vivo and in vitro studies designed to identify a virus as the cause of amyotrophic lateral sclerosis, parkinsonism dementia, and Parkinson's disease. Adv Neurol 36:343-353.
-
(1982)
Adv Neurol
, vol.36
, pp. 343-353
-
-
Gibbs, C.J.1
Gajdusek, D.C.2
-
3
-
-
0014469501
-
Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy
-
Graham JG, Oppenheimer DR (1969) Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy. J Neurol Neurosurg Psychiatry 32(1):28-34.
-
(1969)
J Neurol Neurosurg Psychiatry
, vol.32
, Issue.1
, pp. 28-34
-
-
Graham, J.G.1
Oppenheimer, D.R.2
-
4
-
-
0024843373
-
Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)
-
Papp MI, Kahn JE, Lantos PL (1989) Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome). J Neurol Sci 94(1-3):79-100.
-
(1989)
J Neurol Sci
, vol.94
, Issue.1-3
, pp. 79-100
-
-
Papp, M.I.1
Kahn, J.E.2
Lantos, P.L.3
-
5
-
-
0032584686
-
Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies
-
Spillantini MG, et al. (1998) Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies. Neurosci Lett 251(3):205-208.
-
(1998)
Neurosci Lett
, vol.251
, Issue.3
, pp. 205-208
-
-
Spillantini, M.G.1
-
6
-
-
0031713491
-
Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble α-synuclein
-
Tu PH, et al. (1998) Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble α-synuclein. Ann Neurol 44(3):415-422.
-
(1998)
Ann Neurol
, vol.44
, Issue.3
, pp. 415-422
-
-
Tu, P.H.1
-
7
-
-
0032546895
-
α-Synuclein immunoreactivity in glial cytoplasmic inclusions in multiple systematrophy
-
Wakabayashi K, Yoshimoto M, Tsuji S, Takahashi H (1998) α-Synuclein immunoreactivity in glial cytoplasmic inclusions in multiple systematrophy. Neurosci Lett 249(2-3):180-182.
-
(1998)
Neurosci Lett
, vol.249
, Issue.2-3
, pp. 180-182
-
-
Wakabayashi, K.1
Yoshimoto, M.2
Tsuji, S.3
Takahashi, H.4
-
8
-
-
0030882856
-
Alpha-synuclein in Lewy bodies
-
Spillantini MG, et al. (1997) Alpha-synuclein in Lewy bodies. Nature 388(6645):839-840.
-
(1997)
Nature
, vol.388
, Issue.6645
, pp. 839-840
-
-
Spillantini, M.G.1
-
9
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, et al. (1997) Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 276(5321):2045-2047.
-
(1997)
Science
, vol.276
, Issue.5321
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
-
10
-
-
0033589692
-
Prevalence of progressive supranuclear palsy and multiple system atrophy: A cross-sectional study
-
Schrag A, Ben-Shlomo Y, Quinn NP (1999) Prevalence of progressive supranuclear palsy and multiple system atrophy: A cross-sectional study. Lancet 354(9192):1771-1775.
-
(1999)
Lancet
, vol.354
, Issue.9192
, pp. 1771-1775
-
-
Schrag, A.1
Ben-Shlomo, Y.2
Quinn, N.P.3
-
11
-
-
0030695277
-
Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990
-
Bower JH, Maraganore DM, McDonnell SK, Rocca WA (1997) Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990. Neurology 49(5):1284-1288.
-
(1997)
Neurology
, vol.49
, Issue.5
, pp. 1284-1288
-
-
Bower, J.H.1
Maraganore, D.M.2
McDonnell, S.K.3
Rocca, W.A.4
-
12
-
-
0033081705
-
Consensus statement on the diagnosis of multiple system atrophy
-
Gilman S, et al. (1999) Consensus statement on the diagnosis of multiple system atrophy. J Neurol Sci 163(1):94-98.
-
(1999)
J Neurol Sci
, vol.163
, Issue.1
, pp. 94-98
-
-
Gilman, S.1
-
13
-
-
84888349390
-
Transmission of multiple system atrophy prions to transgenic mice
-
Watts JC, et al. (2013) Transmission of multiple system atrophy prions to transgenic mice. Proc Natl Acad Sci USA 110(48):19555-19560.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, Issue.48
, pp. 19555-19560
-
-
Watts, J.C.1
-
14
-
-
84940969467
-
Propagation of prions causing synucleinopathies in cultured cells
-
Woerman AL, et al. (2015) Propagation of prions causing synucleinopathies in cultured cells. Proc Natl Acad Sci USA 112(35):E4949-E4958.
-
(2015)
Proc Natl Acad Sci USA
, vol.112
, Issue.35
, pp. E4949-E4958
-
-
Woerman, A.L.1
-
15
-
-
52449086856
-
Second consensus statement on the diagnosis of multiple system atrophy
-
Gilman S, et al. (2008) Second consensus statement on the diagnosis of multiple system atrophy. Neurology 71(9):670-676.
-
(2008)
Neurology
, vol.71
, Issue.9
, pp. 670-676
-
-
Gilman, S.1
-
16
-
-
0035215492
-
Multiple system atrophy: Pathophysiology and management
-
Wenning GK, Braune S (2001) Multiple system atrophy: Pathophysiology and management. CNS Drugs 15(11):839-852.
-
(2001)
CNS Drugs
, vol.15
, Issue.11
, pp. 839-852
-
-
Wenning, G.K.1
Braune, S.2
-
17
-
-
33750502211
-
MSA-C is the predominant clinical phenotype of MSA in Japan: Analysis of 142 patients with probable MSA
-
Yabe I, et al. (2006) MSA-C is the predominant clinical phenotype of MSA in Japan: Analysis of 142 patients with probable MSA. J Neurol Sci 249(2):115-121.
-
(2006)
J Neurol Sci
, vol.249
, Issue.2
, pp. 115-121
-
-
Yabe, I.1
-
18
-
-
34548182758
-
Features of probable multiple system atrophy patients identified among 4770 patients with parkinsonism enrolled in the multicentre registry of the German Competence Network on Parkinson's disease
-
Wüllner U, et al. (2007) Features of probable multiple system atrophy patients identified among 4770 patients with parkinsonism enrolled in the multicentre registry of the German Competence Network on Parkinson's disease. J Neural Transm 114(9):1161-1165.
-
(2007)
J Neural Transm
, vol.114
, Issue.9
, pp. 1161-1165
-
-
Wüllner, U.1
-
19
-
-
44949211482
-
Clinical outcomes of progressive supranuclear palsy and multiple system atrophy
-
O'Sullivan SS, et al. (2008) Clinical outcomes of progressive supranuclear palsy and multiple system atrophy. Brain 131(Pt 5):1362-1372.
-
(2008)
Brain
, vol.131
, pp. 1362-1372
-
-
O'Sullivan, S.S.1
-
20
-
-
77954104112
-
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: A mutation update
-
Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C (2010) Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: A mutation update. Hum Mutat 31(7):763-780.
-
(2010)
Hum Mutat
, vol.31
, Issue.7
, pp. 763-780
-
-
Nuytemans, K.1
Theuns, J.2
Cruts, M.3
Van Broeckhoven, C.4
-
21
-
-
67249139655
-
SNCA variants are associated with increased risk for multiple system atrophy
-
Scholz SW, et al. (2009) SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol 65(5):610-614.
-
(2009)
Ann Neurol
, vol.65
, Issue.5
, pp. 610-614
-
-
Scholz, S.W.1
-
22
-
-
84885461450
-
α-Synucleinopathy associated with G51D SNCA mutation: A link between Parkinson's disease and multiple system atrophy?
-
Kiely AP, et al. (2013) α-Synucleinopathy associated with G51D SNCA mutation: A link between Parkinson's disease and multiple system atrophy? Acta Neuropathol 125(5):753-769.
-
(2013)
Acta Neuropathol
, vol.125
, Issue.5
, pp. 753-769
-
-
Kiely, A.P.1
-
23
-
-
84878405578
-
G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome
-
Lesage S, et al., French Parkinson's Disease Genetics Study Group (2013) G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome. Ann Neurol 73(4):459-471.
-
(2013)
Ann Neurol
, vol.73
, Issue.4
, pp. 459-471
-
-
Lesage, S.1
-
24
-
-
84902118984
-
Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology
-
Pasanen P, et al. (2014) Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology. Neurobiol Aging 35(9):2180.e1-2180.e5.
-
(2014)
Neurobiol Aging
, vol.35
, Issue.9
, pp. 2180e1-2180e5
-
-
Pasanen, P.1
-
25
-
-
84880440278
-
Mutations in COQ2 in familial and sporadic multiple-system atrophy
-
Multiple-System Atrophy Research Collaboration (2013) Mutations in COQ2 in familial and sporadic multiple-system atrophy. N Engl J Med 369(3):233-244.
-
(2013)
N Engl J Med
, vol.369
, Issue.3
, pp. 233-244
-
-
-
26
-
-
1342347397
-
Interleukin-1A (-889) genetic polymorphism increases the risk of multiple system atrophy
-
Combarros O, Infante J, Llorca J, Berciano J (2003) Interleukin-1A (-889) genetic polymorphism increases the risk of multiple system atrophy. Mov Disord 18(11):1385-1386.
-
(2003)
Mov Disord
, vol.18
, Issue.11
, pp. 1385-1386
-
-
Combarros, O.1
Infante, J.2
Llorca, J.3
Berciano, J.4
-
27
-
-
10644256410
-
Interleukin-8, intercellular adhesion molecule-1 and tumour necrosis factor-alpha gene polymorphisms and the risk for multiple system atrophy
-
Infante J, Llorca J, Berciano J, Combarros O (2005) Interleukin-8, intercellular adhesion molecule-1 and tumour necrosis factor-alpha gene polymorphisms and the risk for multiple system atrophy. J Neurol Sci 228(1):11-13.
-
(2005)
J Neurol Sci
, vol.228
, Issue.1
, pp. 11-13
-
-
Infante, J.1
Llorca, J.2
Berciano, J.3
Combarros, O.4
-
28
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling GC, et al. (1995) Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 83(1):79-90.
-
(1995)
Cell
, vol.83
, Issue.1
, pp. 79-90
-
-
Telling, G.C.1
-
29
-
-
84904636970
-
Intramuscular injection of α-synuclein induces CNS α-synuclein pathology and a rapid-onset motor phenotype in transgenic mice
-
Sacino AN, et al. (2014) Intramuscular injection of α-synuclein induces CNS α-synuclein pathology and a rapid-onset motor phenotype in transgenic mice. Proc Natl Acad Sci USA 111(29):10732-10737.
-
(2014)
Proc Natl Acad Sci USA
, vol.111
, Issue.29
, pp. 10732-10737
-
-
Sacino, A.N.1
-
30
-
-
0037213933
-
Rapid prion neuroinvasion following tongue infection
-
Bartz JC, Kincaid AE, Bessen RA (2003) Rapid prion neuroinvasion following tongue infection. J Virol 77(1):583-591.
-
(2003)
J Virol
, vol.77
, Issue.1
, pp. 583-591
-
-
Bartz, J.C.1
Kincaid, A.E.2
Bessen, R.A.3
-
31
-
-
0017643758
-
Unconventional viruses and the origin and disappearance of kuru
-
Gajdusek DC (1977) Unconventional viruses and the origin and disappearance of kuru. Science 197(4307):943-960.
-
(1977)
Science
, vol.197
, Issue.4307
, pp. 943-960
-
-
Gajdusek, D.C.1
-
32
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner SB (1982) Novel proteinaceous infectious particles cause scrapie. Science 216(4542):136-144.
-
(1982)
Science
, vol.216
, Issue.4542
, pp. 136-144
-
-
Prusiner, S.B.1
-
33
-
-
84903265012
-
-
Yale Univ Press, New Haven, CT
-
Prusiner SB (2014) Madness and Memory (Yale Univ Press, New Haven, CT), p 344.
-
(2014)
Madness and Memory
, pp. 344
-
-
Prusiner, S.B.1
-
34
-
-
84937392013
-
Neurodegenerative diseases: Expanding the prion concept
-
Walker LC, Jucker M (2015) Neurodegenerative diseases: Expanding the prion concept. Annu Rev Neurosci 38:87-103.
-
(2015)
Annu Rev Neurosci
, vol.38
, pp. 87-103
-
-
Walker, L.C.1
Jucker, M.2
-
35
-
-
0021019026
-
Scrapie prions aggregate to form amyloid-like birefringent rods
-
Prusiner SB, et al. (1983) Scrapie prions aggregate to form amyloid-like birefringent rods. Cell 35(2 Pt 1):349-358.
-
(1983)
Cell
, vol.35
, Issue.2
, pp. 349-358
-
-
Prusiner, S.B.1
-
36
-
-
0029257497
-
The core Alzheimer's peptide NAC forms amyloid fibrils which seed and are seeded by beta-amyloid: Is NAC a common trigger or target in neurodegenerative disease?
-
Han H, Weinreb PH, Lansbury PT, Jr (1995) The core Alzheimer's peptide NAC forms amyloid fibrils which seed and are seeded by beta-amyloid: Is NAC a common trigger or target in neurodegenerative disease? Chem Biol 2(3):163-169.
-
(1995)
Chem Biol
, vol.2
, Issue.3
, pp. 163-169
-
-
Han, H.1
Weinreb, P.H.2
Lansbury, P.T.3
-
37
-
-
43249114934
-
Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease
-
Kordower JH, Chu Y, Hauser RA, Freeman TB, Olanow CW (2008) Lewy body-like pathology in long-term embryonic nigral transplants in Parkinson's disease. Nat Med 14(5):504-506.
-
(2008)
Nat Med
, vol.14
, Issue.5
, pp. 504-506
-
-
Kordower, J.H.1
Chu, Y.2
Hauser, R.A.3
Freeman, T.B.4
Olanow, C.W.5
-
38
-
-
43249110200
-
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
-
Li JY, et al. (2008) Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation. Nat Med 14(5):501-503.
-
(2008)
Nat Med
, vol.14
, Issue.5
, pp. 501-503
-
-
Li, J.Y.1
-
39
-
-
69149088365
-
Is Parkinson's disease a prion disorder?
-
Olanow CW, Prusiner SB (2009) Is Parkinson's disease a prion disorder? Proc Natl Acad Sci USA 106(31):12571-12572.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.31
, pp. 12571-12572
-
-
Olanow, C.W.1
Prusiner, S.B.2
-
40
-
-
84863433677
-
Prion-like acceleration of a synucleinopathy in a transgenic mouse model
-
Mougenot A-L, et al. (2012) Prion-like acceleration of a synucleinopathy in a transgenic mouse model. Neurobiol Aging 33(9):2225-2228.
-
(2012)
Neurobiol Aging
, vol.33
, Issue.9
, pp. 2225-2228
-
-
Mougenot, A.-L.1
-
41
-
-
84862609075
-
Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice
-
Luk KC, et al. (2012) Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice. J Exp Med 209(5):975-986.
-
(2012)
J Exp Med
, vol.209
, Issue.5
, pp. 975-986
-
-
Luk, K.C.1
-
42
-
-
84869109864
-
Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice
-
Luk KC, et al. (2012) Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice. Science 338(6109):949-953.
-
(2012)
Science
, vol.338
, Issue.6109
, pp. 949-953
-
-
Luk, K.C.1
-
43
-
-
84899896344
-
Amyloidogenic α-synuclein seeds do not invariably induce rapid, widespread pathology in mice
-
Sacino AN, et al. (2014) Amyloidogenic α-synuclein seeds do not invariably induce rapid, widespread pathology in mice. Acta Neuropathol 127(5):645-665.
-
(2014)
Acta Neuropathol
, vol.127
, Issue.5
, pp. 645-665
-
-
Sacino, A.N.1
-
44
-
-
84934983329
-
α-Synuclein strains cause distinct synucleinopathies after local and systemic administration
-
Peelaerts W, et al. (2015) α-Synuclein strains cause distinct synucleinopathies after local and systemic administration. Nature 522(7556):340-344.
-
(2015)
Nature
, vol.522
, Issue.7556
, pp. 340-344
-
-
Peelaerts, W.1
-
45
-
-
84897977607
-
Lewy body extracts from Parkinson disease brains trigger α-synuclein pathology and neurodegeneration in mice and monkeys
-
Recasens A, et al. (2014) Lewy body extracts from Parkinson disease brains trigger α-synuclein pathology and neurodegeneration in mice and monkeys. Ann Neurol 75(3):351-362.
-
(2014)
Ann Neurol
, vol.75
, Issue.3
, pp. 351-362
-
-
Recasens, A.1
-
46
-
-
84876057762
-
Prion-like spreading of pathological α-synuclein in brain
-
Masuda-Suzukake M, et al. (2013) Prion-like spreading of pathological α-synuclein in brain. Brain 136(Pt 4):1128-1138.
-
(2013)
Brain
, vol.136
, pp. 1128-1138
-
-
Masuda-Suzukake, M.1
-
47
-
-
0034602442
-
Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions
-
Giasson BI, et al. (2000) Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions. Science 290(5493):985-989.
-
(2000)
Science
, vol.290
, Issue.5493
, pp. 985-989
-
-
Giasson, B.I.1
-
48
-
-
0035854437
-
Ubiquitination of a new form of α-synuclein by parkin from human brain: Implications for Parkinson's disease
-
Shimura H, et al. (2001) Ubiquitination of a new form of α-synuclein by parkin from human brain: Implications for Parkinson's disease. Science 293(5528):263-269.
-
(2001)
Science
, vol.293
, Issue.5528
, pp. 263-269
-
-
Shimura, H.1
-
49
-
-
0036174010
-
Alpha-Synuclein is phosphorylated in synucleinopathy lesions
-
Fujiwara H, et al. (2002) alpha-Synuclein is phosphorylated in synucleinopathy lesions. Nat Cell Biol 4(2):160-164.
-
(2002)
Nat Cell Biol
, vol.4
, Issue.2
, pp. 160-164
-
-
Fujiwara, H.1
-
50
-
-
79960261026
-
Sumoylation inhibits α-synuclein aggregation and toxicity
-
Krumova P, et al. (2011) Sumoylation inhibits α-synuclein aggregation and toxicity. J Cell Biol 194(1):49-60.
-
(2011)
J Cell Biol
, vol.194
, Issue.1
, pp. 49-60
-
-
Krumova, P.1
-
51
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
Telling GC, et al. (1996) Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev 10(14):1736-1750.
-
(1996)
Genes Dev
, vol.10
, Issue.14
, pp. 1736-1750
-
-
Telling, G.C.1
-
52
-
-
84863561735
-
Identification of I137M and other mutations that modulate incubation periods for two human prion strains
-
Giles K, et al. (2012) Identification of I137M and other mutations that modulate incubation periods for two human prion strains. J Virol 86(11):6033-6041.
-
(2012)
J Virol
, vol.86
, Issue.11
, pp. 6033-6041
-
-
Giles, K.1
-
53
-
-
0017367439
-
Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery
-
Bernoulli C, et al. (1977) Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery. Lancet 1(8009):478-479.
-
(1977)
Lancet
, vol.1
, Issue.8009
, pp. 478-479
-
-
Bernoulli, C.1
-
54
-
-
0028285630
-
Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery
-
Gibbs CJ, Jr, et al. (1994) Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery. J Neurol Neurosurg Psychiatry 57(6):757-758.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, Issue.6
, pp. 757-758
-
-
Gibbs, C.J.1
-
55
-
-
0035174927
-
Transmission of scrapie by steel-surface-bound prions
-
Flechsig E, et al. (2001) Transmission of scrapie by steel-surface-bound prions. Mol Med 7(10):679-684.
-
(2001)
Mol Med
, vol.7
, Issue.10
, pp. 679-684
-
-
Flechsig, E.1
-
56
-
-
57149118018
-
Resistance of bovine spongiform encephalopathy (BSE) prions to inactivation
-
Giles K, et al. (2008) Resistance of bovine spongiform encephalopathy (BSE) prions to inactivation. PLoS Pathog 4(11):e1000206.
-
(2008)
PLoS Pathog
, vol.4
, Issue.11
, pp. e1000206
-
-
Giles, K.1
-
57
-
-
0014208039
-
Aromatic amino acids and modification of parkinsonism
-
Cotzias GC, Van Woert MH, Schiffer LM (1967) Aromatic amino acids and modification of parkinsonism. N Engl J Med 276(7):374-379.
-
(1967)
N Engl J Med
, vol.276
, Issue.7
, pp. 374-379
-
-
Cotzias, G.C.1
Van Woert, M.H.2
Schiffer, L.M.3
-
59
-
-
67349131839
-
Staging/typing of Lewy body related alpha-synuclein pathology: A study of the BrainNet Europe Consortium
-
Alafuzoff I, et al. (2009) Staging/typing of Lewy body related alpha-synuclein pathology: A study of the BrainNet Europe Consortium. Acta Neuropathol 117(6):635-652.
-
(2009)
Acta Neuropathol
, vol.117
, Issue.6
, pp. 635-652
-
-
Alafuzoff, I.1
-
60
-
-
0037118259
-
Neuronal α-synucleinopathy with severe movement disorder in mice expressing A53T human α-synuclein
-
Giasson BI, et al. (2002) Neuronal α-synucleinopathy with severe movement disorder in mice expressing A53T human α-synuclein. Neuron 34(4):521-533.
-
(2002)
Neuron
, vol.34
, Issue.4
, pp. 521-533
-
-
Giasson, B.I.1
-
61
-
-
0037109727
-
Synaptic vesicle depletion correlates with attenuated synaptic responses to prolonged repetitive stimulation in mice lacking alpha-synuclein
-
Cabin DE, et al. (2002) Synaptic vesicle depletion correlates with attenuated synaptic responses to prolonged repetitive stimulation in mice lacking alpha-synuclein. J Neurosci 22(20):8797-8807.
-
(2002)
J Neurosci
, vol.22
, Issue.20
, pp. 8797-8807
-
-
Cabin, D.E.1
-
62
-
-
77952478217
-
Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated alpha-synuclein gene mutations precede central nervous system changes
-
Kuo YM, et al. (2010) Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated alpha-synuclein gene mutations precede central nervous system changes. Hum Mol Genet 19(9):1633-1650.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.9
, pp. 1633-1650
-
-
Kuo, Y.M.1
-
63
-
-
0022530549
-
Linkage of prion protein and scrapie incubation time genes
-
Carlson GA, et al. (1986) Linkage of prion protein and scrapie incubation time genes. Cell 46(4):503-511.
-
(1986)
Cell
, vol.46
, Issue.4
, pp. 503-511
-
-
Carlson, G.A.1
|