-
1
-
-
0030015934
-
Clinical analysis of 17 patients in 12 Japanese families with autosomal- recessive type juvenile parkinsonism
-
Ishikawa A, Tsuji S. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism. Neurology. 1996;47(1):160-166. (Pubitemid 26243878)
-
(1996)
Neurology
, vol.47
, Issue.1
, pp. 160-166
-
-
Ishikawa, A.1
Tsuji, S.2
-
2
-
-
16944362288
-
Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27
-
Matsumine H, Saito M, Shimoda-Matsubayashi S, et al. Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27. Am J Hum Genet. 1997;60(3):588-596. (Pubitemid 27097607)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.3
, pp. 588-596
-
-
Matsumine, H.1
Saito, M.2
Shimoda-Matsubayashi, S.3
Tanaka, H.4
Ishikawa, A.5
Nakagawa-Hattori, Y.6
Yokochi, M.7
Kobayashi, T.8
Igarashi, S.9
Takano, H.10
Sanpei, K.11
Koike, R.12
Mori, H.13
Kondo, T.14
Mizutani, Y.15
Schaffer, A.A.16
Yamamura, Y.17
Nakamura, S.18
Kuzuhara, S.19
Tsuji, S.20
Mizuno, Y.21
more..
-
3
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
DOI 10.1038/33416
-
Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 1998;392(6676):605-608. (Pubitemid 28207717)
-
(1998)
Nature
, vol.392
, Issue.6676
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
4
-
-
0036787533
-
Progression of nigrostriatal dysfunction in a parkin kindred: An [18F]dopa PET and clinical study
-
Khan NL, Brooks DJ, Pavese N, et al. Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study. Brain. 2002;125(pt 10):2248-2256.
-
(2002)
Brain
, vol.125
, Issue.PART 10
, pp. 2248-2256
-
-
Khan, N.L.1
Brooks, D.J.2
Pavese, N.3
-
5
-
-
0038662544
-
Parkin disease: A phenotypic study of a large case series
-
DOI 10.1093/brain/awg142
-
Khan NL, Graham E, Critchley P, et al. Parkin disease: a phenotypic study of a large case series. Brain. 2003;126(pt 6):1279-1292. (Pubitemid 36644375)
-
(2003)
Brain
, vol.126
, Issue.6
, pp. 1279-1292
-
-
Khan, N.L.1
Graham, E.2
Critchley, P.3
Schrag, A.E.4
Wood, N.W.5
Lees, A.J.6
Bhatia, K.P.7
Quinn, N.8
-
6
-
-
20344400149
-
Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years
-
DOI 10.1002/mds.20335
-
Khan NL, Horta W, Eunson L, et al. Parkin disease in a Brazilian kindred: manifesting heterozygotes and clinical follow-up over 10 years. Mov Disord. 2005;20(4):479-484. (Pubitemid 40779024)
-
(2005)
Movement Disorders
, vol.20
, Issue.4
, pp. 479-484
-
-
Khan, N.L.1
Horta, W.2
Eunson, L.3
Graham, E.4
Johnson, J.O.5
Chang, S.6
Davis, M.7
Singleton, A.8
Wood, N.W.9
Lees, A.J.10
-
7
-
-
1842475898
-
Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease
-
Khan NL, Katzenschlager R, Watt H, et al. Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease. Neurology. 2004;62(7):1224-1226. (Pubitemid 38456528)
-
(2004)
Neurology
, vol.62
, Issue.7
, pp. 1224-1226
-
-
Khan, N.L.1
Katzenschlager, R.2
Watt, H.3
Bhatia, K.P.4
Wood, N.W.5
Quinn, N.6
Lees, A.J.7
-
8
-
-
0042415580
-
European Consortium on Genetic Susceptibility in Parkinson's Disease. How much phenotypic variation can be attributed to parkin genotype?
-
French Parkinson's Disease Genetics Study Group
-
Lohmann E, Periquet M, Bonifati V, et al French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. How much phenotypic variation can be attributed to parkin genotype? Ann Neurol. 2003;54(2):176-185.
-
(2003)
Ann Neurol
, vol.54
, Issue.2
, pp. 176-185
-
-
Lohmann, E.1
Periquet, M.2
Bonifati, V.3
-
9
-
-
83255187845
-
Phenotype analysis in patients with early onset Parkinson's disease with and without parkin mutations
-
Kim HJ, Kim HJ, Lee JY, et al. Phenotype analysis in patients with early onset Parkinson's disease with and without parkin mutations. J Neurol. 2011;258(12):2260-2267.
-
(2011)
J Neurol
, vol.258
, Issue.12
, pp. 2260-2267
-
-
Kim, H.J.1
Kim, H.J.2
Lee, J.Y.3
-
10
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
DOI 10.1056/NEJM200005253422103
-
Lücking CB, Dürr A, Bonifati V, et al French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Association between early-onset Parkinson's disease and mutations in the parkin gene. N Engl J Med. 2000;342(21):1560-1567. (Pubitemid 30340501)
-
(2000)
New England Journal of Medicine
, vol.342
, Issue.21
, pp. 1560-1567
-
-
Lucking, C.B.1
Durr, A.2
Bonifati, V.3
Vaughan, J.4
De Michele, G.5
Gasser, T.6
Harhangi, B.S.7
Meco, G.8
Denefle, P.9
Wood, N.W.10
Agid, Y.11
Brice, A.12
Nicholl, D.13
Breteler, M.M.B.14
Oostra, B.A.15
De Mari, M.16
Marconi, R.17
Filla, A.18
Bonnet, A.-M.19
Broussolle, E.20
Pollak, P.21
Rascol, O.22
Rosier, M.23
Arnould, I.24
more..
-
11
-
-
0033933192
-
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
-
DOI 10.1002/1531-8249(200007)48:1<65::AID-AN
-
Klein C, Pramstaller PP, Kis B, et al. Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype. Ann Neurol. 2000;48(1):65-71. (Pubitemid 30432432)
-
(2000)
Annals of Neurology
, vol.48
, Issue.1
, pp. 65-71
-
-
Klein, C.1
Pramstaller, P.P.2
Bernhard, K.3
Page, C.C.4
Kann, M.5
Leung, J.6
Woodward, H.7
Castellan, C.C.8
Scherer, M.9
Vieregge, P.10
Breakefield, X.O.11
Kramer, P.L.12
Ozelius, L.J.13
-
12
-
-
18444419131
-
Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families [1]
-
Nichols WC, Pankratz N, Uniacke SK, et al. Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families. J Med Genet. 2002;39(7):489-492. (Pubitemid 34787742)
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.7
, pp. 489-492
-
-
Nichols, W.C.1
Pankratz, N.2
Uniacke, S.K.3
Pauciulo, M.W.4
Halter, C.5
Rudolph, A.6
Conneally, P.M.7
Foroud, T.8
Carter, J.9
Camicioli, R.10
Wojcieszek, J.11
Fernandez, M.12
Hubble, J.13
Rajput, A.14
Panisset, M.15
Mendis, T.16
Grimes, D.A.17
Serrano, R.C.18
Reich, S.19
Hauser, R.20
Sanchez-Ramos, J.21
Zesiewicz, T.22
Pfeiffer, R.23
Friedman, J.24
Fernandez, H.25
Shults, C.26
Seeberger, L.27
O'Brien, C.28
Pahwa, R.29
Elmer, L.30
Jennings, D.31
Marek, K.32
Truong, D.33
Pathak, M.34
Rodnitzyk, R.35
Kurlan, R.36
Tuite, P.37
Aminoff, M.38
Marder, K.39
Lewitt, P.40
Koller, W.41
Martin, W.42
Jankovic, J.43
Bertoni, J.44
Factor, S.45
Walker, F.46
Jung, K.U.47
Stacy, M.48
Simon, D.49
Blindauer, K.50
Manyam, B.51
Nieves, A.52
Velickovic, M.53
Gordon, M.F.54
Leehey, M.55
Gordon, P.56
Rao, J.57
Dalvi, A.58
Racette, B.59
Sethi, K.60
Sudarsky, L.61
Saunders, P.R.62
Simuni, T.63
Dewey, R.64
Hermanowicz, N.65
Feigin, A.66
Calabresse, V.67
Sutton, J.68
Ajax, T.69
Podakalny, G.D.70
Suchowersky, O.71
Uitti, R.72
Shulman, L.73
more..
-
13
-
-
67649383293
-
Identification of a novel Zn2+-binding domain in the autosomal recessive juvenile Parkinson-related E3 ligase parkin
-
Hristova VA, Beasley SA, Rylett RJ, Shaw GS. Identification of a novel Zn2+-binding domain in the autosomal recessive juvenile Parkinson-related E3 ligase parkin. J Biol Chem. 2009;284(22):14978-14986.
-
(2009)
J Biol Chem
, vol.284
, Issue.22
, pp. 14978-14986
-
-
Hristova, V.A.1
Beasley, S.A.2
Rylett, R.J.3
Shaw, G.S.4
-
14
-
-
68949209958
-
Cell death pathways in Parkinson's disease: Role of mitochondria
-
Yao Z, Wood NW. Cell death pathways in Parkinson's disease: role of mitochondria. Antioxid Redox Signal. 2009;11(9):2135-2149.
-
(2009)
Antioxid Redox Signal
, vol.11
, Issue.9
, pp. 2135-2149
-
-
Yao, Z.1
Wood, N.W.2
-
15
-
-
79952693640
-
Mitophagy and Parkinson's disease: The PINK1-parkin link
-
Deas E, Wood NW, Plun-Favreau H. Mitophagy and Parkinson's disease: the PINK1-parkin link. Biochim Biophys Acta. 2011;1813(4):623-633.
-
(2011)
Biochim Biophys Acta
, vol.1813
, Issue.4
, pp. 623-633
-
-
Deas, E.1
Wood, N.W.2
Plun-Favreau, H.3
-
16
-
-
0032144334
-
Clinical, pathologic and genetic studies on autosomal recessive early- onset parkinsonism with diurnal fluctuation
-
DOI 10.1016/S1353-8020(98)00015-7, PII S1353802098000157
-
Yamamura Y, Kuzuhara S, Kondo K, et al. Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation. Parkinsonism Relat Disord. 1998;4(2):65-72. (Pubitemid 28525352)
-
(1998)
Parkinsonism and Related Disorders
, vol.4
, Issue.2
, pp. 65-72
-
-
Yamamura, Y.1
Kuzuhara, S.2
Kondo, K.3
Yanagi, T.4
Uchida, M.5
Matsumine, H.6
Mizuno, Y.7
-
17
-
-
0031721141
-
Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
-
Mori H, Kondo T, Yokochi M, et al. Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q. Neurology. 1998;51(3):890-892. (Pubitemid 28449284)
-
(1998)
Neurology
, vol.51
, Issue.3
, pp. 890-892
-
-
Mori, H.1
Kondo, T.2
Yokochi, M.3
Matsumine, H.4
Nakagawa-Hattori, Y.5
Miyake, T.6
Suda, K.7
Mizuno, Y.8
-
18
-
-
0033814671
-
An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene
-
Hayashi S, Wakabayashi K, Ishikawa A, et al. An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene. Mov Disord. 2000;15(5):884-888.
-
(2000)
Mov Disord
, vol.15
, Issue.5
, pp. 884-888
-
-
Hayashi, S.1
Wakabayashi, K.2
Ishikawa, A.3
-
19
-
-
0035957112
-
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
-
van de Warrenburg BPC, Lammens M, Lücking CB, et al. Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations. Neurology. 2001;56(4):555-557. (Pubitemid 32172889)
-
(2001)
Neurology
, vol.56
, Issue.4
, pp. 555-557
-
-
Van De, W.B.P.C.1
Lammens, M.2
Lucking, C.B.3
Denefle, P.4
Wesseling, P.5
Booij, J.6
Praamstra, P.7
Quinn, N.8
Brice, A.9
Horstink, M.W.I.M.10
-
20
-
-
0034848395
-
Lewy bodies and parkinsonism in families with parkin mutations
-
DOI 10.1002/ana.1132
-
Farrer M, Chan P, Chen R, et al. Lewy bodies and parkinsonism in families with parkin mutations. Ann Neurol. 2001;50(3):293-300. (Pubitemid 32848731)
-
(2001)
Annals of Neurology
, vol.50
, Issue.3
, pp. 293-300
-
-
Farrer, M.1
Chan, P.2
Chen, R.3
Tan, L.4
Lincoln, S.5
Hernandez, D.6
Forno, L.7
Gwinn-Hardy, K.8
Petrucelli, L.9
Hussey, J.10
Singleton, A.11
Tanner, C.12
Hardy, J.13
Langston, J.W.14
-
21
-
-
0037356814
-
Genotype-phenotype correlation: Familial Parkinson disease
-
DOI 10.1046/j.1440-1789.2003.00476.x
-
Mori H, Hattori N, Mizuno Y. Genotype-phenotype correlation: familial Parkinson disease. Neuropathology. 2003;23(1):90-94. (Pubitemid 36406793)
-
(2003)
Neuropathology
, vol.23
, Issue.1
, pp. 90-94
-
-
Mori, H.1
Hattori, N.2
Mizuno, Y.3
-
22
-
-
0038699003
-
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
-
DOI 10.1016/S1353-8020(03)00016-6
-
Gouider-Khouja N, Larnaout A, Amouri R, et al. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family: clinical, genetic and pathological study. Parkinsonism Relat Disord. 2003;9(5):247-251. (Pubitemid 36627689)
-
(2003)
Parkinsonism and Related Disorders
, vol.9
, Issue.5
, pp. 247-251
-
-
Gouider-Khouja, N.1
Larnaout, A.2
Amouri, R.3
Sfar, S.4
Belal, S.5
Ben, H.C.6
Ben, H.M.7
Hattori, N.8
Mizuno, Y.9
Hentati, F.10
-
23
-
-
4143125488
-
Parkin-positive autosomal recessive juvenile parkinsonism with alpha-synuclein-positive inclusions
-
Sasaki S, Shirata A, Yamane K, Iwata M. Parkin-positive autosomal recessive juvenile Parkinsonism with alpha-synuclein-positive inclusions. Neurology. 2004;63(4):678-682. (Pubitemid 39100825)
-
(2004)
Neurology
, vol.63
, Issue.4
, pp. 678-682
-
-
Sasaki, S.1
Shirata, A.2
Yamane, K.3
Iwata, M.4
-
24
-
-
24644462201
-
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
-
DOI 10.1002/ana.20587
-
Pramstaller PP, Schlossmacher MG, Jacques TS, et al. Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers. Ann Neurol. 2005;58(3):411-422. (Pubitemid 41266627)
-
(2005)
Annals of Neurology
, vol.58
, Issue.3
, pp. 411-422
-
-
Pramstaller, P.P.1
Schlossmacher, M.G.2
Jacques, T.S.3
Scaravilli, F.4
Eskelson, C.5
Pepivani, I.6
Hedrich, K.7
Adel, S.8
Gonzales-McNeal, M.9
Hilker, R.10
Kramer, P.L.11
Klein, C.12
-
25
-
-
27844538840
-
Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2
-
DOI 10.1002/mds.20594
-
Orimo S, Amino T, Yokochi M, et al. Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2. Mov Disord. 2005;20(10):1350-1353. (Pubitemid 41645912)
-
(2005)
Movement Disorders
, vol.20
, Issue.10
, pp. 1350-1353
-
-
Orimo, S.1
Amino, T.2
Yokochi, M.3
Kojo, T.4
Uchihara, T.5
Takahashi, A.6
Wakabayashi, K.7
Takahashi, H.8
Hattori, N.9
Mizuno, Y.10
-
26
-
-
84877736149
-
A novel PARK2 mutation in a Peruvian family: Clinical and pathological characteristics
-
Torres L CM, Mata I, Mazzetti PE, et al. A novel PARK2 mutation in a Peruvian family: clinical and pathological characteristics. Mov Disord. 2011;26(suppl 2):S311-S312.
-
(2011)
Mov Disord
, vol.26
, Issue.SUPPL. 2
-
-
Torres, L.C.M.1
Mata, I.2
Mazzetti, P.E.3
-
27
-
-
84875495333
-
Lewy body pathology in a patient with a homozygous parkin deletion
-
doi:10.1002/mds.25346
-
Miyakawa S, Ogino M, Funabe S, et al. Lewy body pathology in a patient with a homozygous parkin deletion. Mov Disord. doi:10.1002/mds.25346.
-
Mov Disord
-
-
Miyakawa, S.1
Ogino, M.2
Funabe, S.3
-
28
-
-
10344260246
-
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: Clinicopathological correlations
-
DOI 10.1093/brain/awh303
-
Ozawa T, Paviour D, Quinn NP, et al. The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations. Brain. 2004;127(pt 12):2657-2671. (Pubitemid 39627375)
-
(2004)
Brain
, vol.127
, Issue.12
, pp. 2657-2671
-
-
Ozawa, T.1
Paviour, D.2
Quinn, N.P.3
Josephs, K.A.4
Sangha, H.5
Kilford, L.6
Healy, D.G.7
Wood, N.W.8
Lees, A.J.9
Holton, J.L.10
Revesz, T.11
-
29
-
-
33144489150
-
Diagnosis and management of dementia with Lewy bodies: Third report of the DLB consortium
-
DOI 10.1212/01.wnl.0000187889.17253.b1, PII 0000611420051227000008
-
McKeith IG, Dickson DW, Lowe J, et al Consortium on DLB. Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology. 2005;65(12):1863-1872. (Pubitemid 43970103)
-
(2005)
Neurology
, vol.65
, Issue.12
, pp. 1863-1872
-
-
McKeith, I.G.1
Dickson, D.W.2
Lowe, J.3
Emre, M.4
O'Brien, J.T.5
Feldman, H.6
Cummings, J.7
Duda, J.E.8
Lippa, C.9
Perry, E.K.10
Aarsland, D.11
Arai, H.12
Ballard, C.G.13
Boeve, B.14
Burn, D.J.15
Costa, D.16
Del, S.T.17
Dubois, B.18
Galasko, D.19
Gauthier, S.20
Goetz, C.G.21
Gomez-Tortosa, E.22
Halliday, G.23
Hansen, L.A.24
Hardy, J.25
Iwatsubo, T.26
Kalaria, R.N.27
Kaufer, D.28
Kenny, R.A.29
Korczyn, A.30
Kosaka, K.31
Lee, V.M.Y.32
Lees, A.33
Litvan, I.34
Londos, E.35
Lopez, O.L.36
Minoshima, S.37
Mizuno, Y.38
Molina, J.A.39
Mukaetova-Ladinska, E.B.40
Pasquier, F.41
Perry, R.H.42
Schulz, J.B.43
Trojanowski, J.Q.44
Yamada, M.45
more..
-
30
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson's disease
-
DOI 10.1016/S0197-4580(02)00065-9, PII S0197458002000659
-
Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging. 2003;24(2):197-211. (Pubitemid 36007810)
-
(2003)
Neurobiology of Aging
, vol.24
, Issue.2
, pp. 197-211
-
-
Braak, H.1
Del, T.K.2
Rub, U.3
De Vos, R.A.I.4
Jansen, S.E.N.H.5
Braak, E.6
-
31
-
-
84903504678
-
Substantia nigra and locus coeruleus
-
Paxinos G, Juergen KM, eds. 2nd ed. London, England: Elsevier Academic Press
-
Halliday G. Substantia nigra and locus coeruleus. In: Paxinos G, Juergen KM, eds. The Human Nervous System. 2nd ed. London, England: Elsevier Academic Press; 2004:449-463.
-
(2004)
The Human Nervous System
, pp. 449-463
-
-
Halliday, G.1
-
32
-
-
0028935631
-
Cell counts in the substantia nigra: A comparison of single section counts and disector counts in patients with Parkinson's disease and in controls
-
Ma SY, Collan Y, Röyttä M, Rinne JO, Rinne UK. Cell counts in the substantia nigra: a comparison of single section counts and disector counts in patients with Parkinson's disease and in controls. Neuropathol Appl Neurobiol. 1995;21(1):10-17.
-
(1995)
Neuropathol Appl Neurobiol
, vol.21
, Issue.1
, pp. 10-17
-
-
Ma, S.Y.1
Collan, Y.2
Röyttä, M.3
Rinne, J.O.4
Rinne, U.K.5
-
33
-
-
70450224253
-
Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease
-
Ahlskog JE. Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease. Parkinsonism Relat Disord. 2009;15(10):721-727.
-
(2009)
Parkinsonism Relat Disord
, vol.15
, Issue.10
, pp. 721-727
-
-
Ahlskog, J.E.1
-
34
-
-
84856964851
-
Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations
-
Paisán-Ruiz C, Li A, Schneider SA, et al. Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations. Neurobiol Aging. 2012;33(4):814-823.
-
(2012)
Neurobiol Aging
, vol.33
, Issue.4
, pp. 814-823
-
-
Paisán-Ruiz, C.1
Li, A.2
Schneider, S.A.3
-
35
-
-
77950855127
-
PINK1-linked parkinsonism is associated with Lewy body pathology
-
Samaranch L, Lorenzo-Betancor O, Arbelo JM, et al. PINK1-linked parkinsonism is associated with Lewy body pathology. Brain. 2010;133(pt 4):1128-1142.
-
(2010)
Brain
, vol.133
, Issue.PART 4
, pp. 1128-1142
-
-
Samaranch, L.1
Lorenzo-Betancor, O.2
Arbelo, J.M.3
-
37
-
-
84862689309
-
The neuropathology of genetic Parkinson's disease
-
Poulopoulos M, Levy OA, Alcalay RN. The neuropathology of genetic Parkinson's disease. Mov Disord. 2012;27(7):831-842.
-
(2012)
Mov Disord
, vol.27
, Issue.7
, pp. 831-842
-
-
Poulopoulos, M.1
Levy, O.A.2
Alcalay, R.N.3
-
38
-
-
0023898945
-
The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
-
Gibb WRG, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry. 1988;51(6):745-752.
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, Issue.6
, pp. 745-752
-
-
Gibb, W.R.G.1
Lees, A.J.2
-
39
-
-
0025954066
-
Ageing and Parkinson's disease: Substantia nigra regional selectivity
-
Fearnley JM, Lees AJ. Ageing and Parkinson's disease: substantia nigra regional selectivity. Brain. 1991;114(pt 5):2283-2301.
-
(1991)
Brain
, vol.114
, Issue.PART 5
, pp. 2283-2301
-
-
Fearnley, J.M.1
Lees, A.J.2
-
40
-
-
0034864630
-
Alpha-synuclein pathology is highly dependent on the case selection
-
DOI 10.1046/j.0305-1846.2001.00342.x
-
Parkkinen L, Soininen H, Laakso M, Alafuzoff I. Alpha-synuclein pathology is highly dependent on the case selection. Neuropathol Appl Neurobiol. 2001;27(4):314-325. (Pubitemid 32758618)
-
(2001)
Neuropathology and Applied Neurobiology
, vol.27
, Issue.4
, pp. 314-325
-
-
Parkkinen, L.1
Soininen, H.2
Laakso, M.3
Alafuzoff, I.4
-
41
-
-
68249141880
-
Lewy body pathology in normal elderly subjects
-
Markesbery WR, Jicha GA, Liu H, Schmitt FA. Lewy body pathology in normal elderly subjects. J Neuropathol Exp Neurol. 2009;68(7):816-822.
-
(2009)
J Neuropathol Exp Neurol
, vol.68
, Issue.7
, pp. 816-822
-
-
Markesbery, W.R.1
Jicha, G.A.2
Liu, H.3
Schmitt, F.A.4
-
42
-
-
24144470504
-
Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin
-
DOI 10.1093/hmg/ddi292
-
Sriram SR, Li X, Ko HS, et al. Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin. Hum Mol Genet. 2005;14(17):2571-2586. (Pubitemid 41236069)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.17
, pp. 2571-2586
-
-
Sriram, S.R.1
Li, X.2
Ko, H.S.3
Chung, K.K.K.4
Wong, E.5
Lim, K.L.6
Dawson, V.L.7
Dawson, T.M.8
-
43
-
-
0344011981
-
RING finger 1 mutations in Parkin produce altered localization of the protein
-
DOI 10.1093/hmg/ddg328
-
Cookson MR, Lockhart PJ, McLendon C, O'Farrell C, Schlossmacher M, Farrer MJ. RING finger 1mutations in Parkin produce altered localization of the protein. Hum Mol Genet. 2003;12(22):2957-2965. (Pubitemid 37442024)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.22
, pp. 2957-2965
-
-
Cookson, M.R.1
Lockhart, P.J.2
McLendon, C.3
O'Farrell, C.4
Schlossmacher, M.5
Farrer, M.J.6
-
44
-
-
34250372427
-
Deciphering the role of heterozygous mutations in genes associated with parkinsonism
-
DOI 10.1016/S1474-4422(07)70174-6, PII S1474442207701746
-
Klein C, Lohmann-Hedrich K, Rogaeva E, Schlossmacher MG, Lang AE. Deciphering the role of heterozygous mutations in genes associated with parkinsonism. Lancet Neurol. 2007;6(7):652-662. (Pubitemid 46921058)
-
(2007)
Lancet Neurology
, vol.6
, Issue.7
, pp. 652-662
-
-
Klein, C.1
Lohmann-Hedrich, K.2
Rogaeva, E.3
Schlossmacher, M.G.4
Lang, A.E.5
|