-
1
-
-
0000116504
-
Pathological clues to the cause of Parkinson's disease
-
Marsden CD, Fahn S (eds). London, Butterworth-Heinemann
-
Gibb WRG, Lees AJ: Pathological clues to the cause of Parkinson's disease; in Marsden CD, Fahn S (eds): Movement Disorders 3. London, Butterworth-Heinemann, 1994, pp 144-166.
-
(1994)
Movement Disorders
, vol.3
, pp. 144-166
-
-
Gibb, W.R.G.1
Lees, A.J.2
-
2
-
-
0021829406
-
Permanent human parkinsonism due to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP): Seven cases
-
Ballard P, Tetrud JW, Langston JW: Permanent human parkinsonism due to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP): Seven cases. Neurology 1985;35:949-956.
-
(1985)
Neurology
, vol.35
, pp. 949-956
-
-
Ballard, P.1
Tetrud, J.W.2
Langston, J.W.3
-
3
-
-
0026704066
-
An introduction to the free radical hypothesis in Parkinson's disease
-
Olanow CW: An introduction to the free radical hypothesis in Parkinson's disease. Ann Neurol 1992;32:S2-S9.
-
(1992)
Ann Neurol
, vol.32
-
-
Olanow, C.W.1
-
4
-
-
2542507783
-
Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: Evidence for association of a DRD2 allele
-
Plante-Bordeneuve V, Taussig D, Thomas F, Said G, Wood NW, Marsden CD, Harding AE: Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: Evidence for association of a DRD2 allele. Neurology 1997; 48:1589-1593.
-
(1997)
Neurology
, vol.48
, pp. 1589-1593
-
-
Plante-Bordeneuve, V.1
Taussig, D.2
Thomas, F.3
Said, G.4
Wood, N.W.5
Marsden, C.D.6
Harding, A.E.7
-
5
-
-
0028124654
-
Genetic linkage studies in autosomal dominant Parkinsonism: Evaluation of seven candidate genes
-
Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO: Genetic linkage studies in autosomal dominant Parkinsonism: Evaluation of seven candidate genes. Ann Neurol 1994;36:387-396.
-
(1994)
Ann Neurol
, vol.36
, pp. 387-396
-
-
Gasser, T.1
Wszolek, Z.K.2
Trofatter, J.3
Ozelius, L.4
Uitti, R.J.5
Lee, C.S.6
Gusella, J.7
Pfeiffer, R.F.8
Calne, D.B.9
Breakefield, X.O.10
-
6
-
-
0031696267
-
Genetic risk factors in Parkinson's disease
-
Wood NW: Genetic risk factors in Parkinson's disease. Ann Neurol 1998;44:S58-S62.
-
(1998)
Ann Neurol
, vol.44
-
-
Wood, N.W.1
-
7
-
-
10544234193
-
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
-
Polymeropoulos MH, Higgins JJ, Golbe LI, Johnson WG, Ide SE, Iorio GD, Sanges G, Stenroos ES, Pho LT, Schaffer AA, Lazzarini AM, Nussbaum RL, Duvoisin RC: Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science 1996;274:1197-1199.
-
(1996)
Science
, vol.274
, pp. 1197-1199
-
-
Polymeropoulos, M.H.1
Higgins, J.J.2
Golbe, L.I.3
Johnson, W.G.4
Ide, S.E.5
Iorio, G.D.6
Sanges, G.7
Stenroos, E.S.8
Pho, L.T.9
Schaffer, A.A.10
Lazzarini, A.M.11
Nussbaum, R.L.12
Duvoisin, R.C.13
-
8
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Iorio GD, Golbe LI, Nussbaum RL: Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Iorio, G.D.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
9
-
-
0032499206
-
Putting the Parkin into Parkinson's
-
Nussbaum RL: Putting the Parkin into Parkinson's. Nature 1998;392:544-545.
-
(1998)
Nature
, vol.392
, pp. 544-545
-
-
Nussbaum, R.L.1
-
10
-
-
0032937416
-
Polymorphism in the Parkin gene in sporadic Parkinson's disease
-
Wang M, Hattori N, Mastumine H, Kobayashi T, Yoshino H, Morioka A, Kitada T, Asakawa S, Minoshima S, Shimizu N, Mizuno Y: Polymorphism in the Parkin Gene in sporadic Parkinson's disease. Ann Neurol 1999;45:655-658.
-
(1999)
Ann Neurol
, vol.45
, pp. 655-658
-
-
Wang, M.1
Hattori, N.2
Mastumine, H.3
Kobayashi, T.4
Yoshino, H.5
Morioka, A.6
Kitada, T.7
Asakawa, S.8
Minoshima, S.9
Shimizu, N.10
Mizuno, Y.11
-
11
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
-
Hughes AJ, Daniel SE, Kilford L, Lees AJ: 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
-
12
-
-
0028828141
-
A clinical and genetic study of familial cases of Parkinson's disease
-
Plante-Bordeneuve V, Taussig D, Thomas F, Ziegler M, Said G: A clinical and genetic study of familial cases of Parkinson's disease. J Neurol Sci 1995;133:164-172.
-
(1995)
J Neurol Sci
, vol.133
, pp. 164-172
-
-
Plante-Bordeneuve, V.1
Taussig, D.2
Thomas, F.3
Ziegler, M.4
Said, G.5
-
13
-
-
0015875307
-
Parkinson's disease-genetic analysis and evidence of a multifactorial etiology
-
Kondo K, Kurland LT, Schull WJ: Parkinson's disease-genetic analysis and evidence of a multifactorial etiology. Mayo Clin Proc 1973;48: 465-475.
-
(1973)
Mayo Clin Proc
, vol.48
, pp. 465-475
-
-
Kondo, K.1
Kurland, L.T.2
Schull, W.J.3
-
14
-
-
16944362288
-
Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25,2-27
-
Matsumine H, Saito M, Satoe SM, Tanaka H, Ishikawa A, Yuko NH, Yokochi M, Kobayashi T, Igarashi S, Takano H, Sanpei K, Koike R, Mori H, Kondo T, Mizutani Y, Schaffer AA, Yamamura Y, Nakamura S, Kuzuhara S, Tsuji S, Mizuno Y: Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25,2-27. Am J Hum Genet 1997;60:588-596.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 588-596
-
-
Matsumine, H.1
Saito, M.2
Satoe, S.M.3
Tanaka, H.4
Ishikawa, A.5
Yuko, N.H.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..
-
15
-
-
0032499264
-
Mutations in the Parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N: Mutations in the Parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-608.
-
(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
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
16
-
-
18244412384
-
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in Parkin gene in affected individuals
-
Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kohayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y: Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in Parkin gene in affected individuals. Ann Neurol 1998;44: 935-941.
-
(1998)
Ann Neurol
, vol.44
, pp. 935-941
-
-
Hattori, N.1
Kitada, T.2
Matsumine, H.3
Asakawa, S.4
Yamamura, Y.5
Yoshino, H.6
Kohayashi, T.7
Yokochi, M.8
Wang, M.9
Yoritaka, A.10
Kondo, T.11
Kuzuhara, S.12
Nakamura, S.13
Shimizu, N.14
Mizuno, Y.15
-
17
-
-
0032054801
-
A Microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2)
-
Matsumine H, Yamamura Y, Hattori N, Kobayashi T, Kitada T, Yoritaka A, Mizuno Y: A Microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2). Genomics 1998;49:143-146.
-
(1998)
Genomics
, vol.49
, pp. 143-146
-
-
Matsumine, H.1
Yamamura, Y.2
Hattori, N.3
Kobayashi, T.4
Kitada, T.5
Yoritaka, A.6
Mizuno, Y.7
-
18
-
-
0032575607
-
Point mutation (Thr240Arg and Ala311Stop) in Parkin gene
-
Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y: Point mutation (Thr240Arg and Ala311Stop) in Parkin gene. Biochem Biophys Res Comm 1998;249: 754-758.
-
(1998)
Biochem Biophys Res Comm
, vol.249
, pp. 754-758
-
-
Hattori, N.1
Matsumine, H.2
Asakawa, S.3
Kitada, T.4
Yoshino, H.5
Elibol, B.6
Brookes, A.J.7
Yamamura, Y.8
Kobayashi, T.9
Wang, M.10
Yoritaka, A.11
Minoshima, S.12
Shimizu, N.13
Mizuno, Y.14
-
19
-
-
0032564235
-
Homozygous deletions in Parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
-
Lucking CB, Abbas N, Durr A, Bonifati V, Bonnet AM, de Broucker T, De Michele G, Wood NW, Agid Y, Brice A: Homozygous deletions in Parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. Lancet 1998;352:1355-1356.
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
Abbas, N.2
Durr, A.3
Bonifati, V.4
Bonnet, A.M.5
De Broucker, T.6
De Michele, G.7
Wood, N.W.8
Agid, Y.9
Brice, A.10
-
20
-
-
0028889485
-
Statement on use of apolipoprotein E testing for Alzheimer's disease
-
American College of Medical Genetics/American Society of Human Genetics Working Group an ApoE and Alzheimer's Disease: Statement on use of apolipoprotein E testing for Alzheimer's disease. JAMA 1995;274: 1627-1629.
-
(1995)
JAMA
, vol.274
, pp. 1627-1629
-
-
-
21
-
-
0032916090
-
Positron emission tomography reveals strong genetic influence in Parkinson's disease
-
Golbe LI: Positron emission tomography reveals strong genetic influence in Parkinson's disease. Ann Neurol 1999;45:557-558.
-
(1999)
Ann Neurol
, vol.45
, pp. 557-558
-
-
Golbe, L.I.1
-
22
-
-
0032913951
-
The role of inheritance in sporadic Parkinson's disease: Evidence from a longitudinal study of dopaminergic function in twins
-
Piccini P, Burn DJ, Ceravolo R, Maraganore D, Brooks DJ: The role of inheritance in sporadic Parkinson's disease: Evidence from a longitudinal study of dopaminergic function in twins. Ann Neurol 1999;45:577-582.
-
(1999)
Ann Neurol
, vol.45
, pp. 577-582
-
-
Piccini, P.1
Burn, D.J.2
Ceravolo, R.3
Maraganore, D.4
Brooks, D.J.5
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