-
1
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
Foster N.L., Wilhelmsen K., Sima A.A.F., Jones M.Z., D'Amato C.J., Gilman S., Participants C. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Ann. Neurol. 41:1997;706-715.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.F.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
Participants, C.7
-
2
-
-
0031951197
-
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
-
Gasser T., Muller-Myhsok B., Wszolek Z.K., Oehlmann R., Calne D.B., Bonifati V., Bereznai B., Fabrizio E., Vieregge P., Horstmann R.D. A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nat. Genet. 18:1998;262-265.
-
(1998)
Nat. Genet.
, vol.18
, pp. 262-265
-
-
Gasser, T.1
Muller-Myhsok, B.2
Wszolek, Z.K.3
Oehlmann, R.4
Calne, D.B.5
Bonifati, V.6
Bereznai, B.7
Fabrizio, E.8
Vieregge, P.9
Horstmann, R.D.10
-
3
-
-
0029806563
-
Clinical genetic analysis of Parkinson's disease in the Contursi kindred
-
Golbe L.I., Di Iorio G., Sanges G., Lazzarini A.M., La Sala S., Bonavita V., Duvoisin R.C. Clinical genetic analysis of Parkinson's disease in the Contursi kindred. Ann. Neurol. 40:1996;767-775.
-
(1996)
Ann. Neurol.
, vol.40
, pp. 767-775
-
-
Golbe, L.I.1
Di Iorio, G.2
Sanges, G.3
Lazzarini, A.M.4
La Sala, S.5
Bonavita, V.6
Duvoisin, R.C.7
-
4
-
-
0032574461
-
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism
-
Hardy J., Perez-Tur J., Baker M., Farrer M., Crook R., Hutton M., Johnson W.G., Gwinn K., Muenter M., Rocca W.A., Maraganore D. Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism. Am. J. Med. Genet. 81:1998;166-171.
-
(1998)
Am. J. Med. Genet.
, vol.81
, pp. 166-171
-
-
Hardy, J.1
Perez-Tur, J.2
Baker, M.3
Farrer, M.4
Crook, R.5
Hutton, M.6
Johnson, W.G.7
Gwinn, K.8
Muenter, M.9
Rocca, W.A.10
Maraganore, D.11
-
5
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
-
Hughes A.J., Daniel S.E., Kilford L., Lees A.J. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psychiatry. 55:1992;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
-
6
-
-
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. 392:1998;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
-
7
-
-
0031990490
-
Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
-
Kruger R., Kuhn W., Muller T., Woitalla D., Graeber M., Kosel S., Przuntek H., Epplen J.T., Schols L., Riess O. Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease. Nat. Genet. 18:1998;106-108.
-
(1998)
Nat. Genet.
, vol.18
, pp. 106-108
-
-
Kruger, R.1
Kuhn, W.2
Muller, T.3
Woitalla, D.4
Graeber, M.5
Kosel, S.6
Przuntek, H.7
Epplen, J.T.8
Schols, L.9
Riess, O.10
-
8
-
-
0029090839
-
A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation
-
Markopoulou K., Wszolek Z.K., Pfeiffer R.F. A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation. Ann. Neurol. 38:1995;373-378.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 373-378
-
-
Markopoulou, K.1
Wszolek, Z.K.2
Pfeiffer, R.F.3
-
9
-
-
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., Tanaka H., Ishikawa A., Nakagawa-Hattori Y., Yokochi M., Kobayashi T., Igarashi S. Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27. Am. J. Hum. Genet. 60:1997;588-596.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, 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
-
10
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance
-
O'Connell J., Weeks D. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance. Nat. Genet. 11:1995;402-408.
-
(1995)
Nat. Genet.
, vol.11
, pp. 402-408
-
-
O'Connell, J.1
Weeks, D.2
-
11
-
-
0028060492
-
Increased risk of Parkinson disease in parents and siblings of patients
-
Payami H., Larsen K., Bernard S., Nutt J. Increased risk of Parkinson disease in parents and siblings of patients. Ann. Neurol. 36:1994;659-661.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 659-661
-
-
Payami, H.1
Larsen, K.2
Bernard, S.3
Nutt, J.4
-
13
-
-
10544234193
-
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
-
Polymeropoulos M.H., Higgins J.J., Golbe L.I., Johnson W.G., Ide S.E., Di Lorio G., Sanges G., Stenroos E.S., Pho L.T., Schaffer A.A., Lazzzrini A.M., Nussbaum R.L., Duvoisin R.C. Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science. 274:1996;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
Di Lorio, G.6
Sanges, G.7
Stenroos, E.S.8
Pho, L.T.9
Schaffer, A.A.10
Lazzzrini, A.M.11
Nussbaum, R.L.12
Duvoisin, R.C.13
-
14
-
-
0030744876
-
Mutation in the α-Synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., Lavedan C., Leroy E., Ide S.E., Dehejia A., Dutra A., Pike B., Root H., Rubenstein J., Boyer R., Stenroos E.S., Chandrasekharappa S., Athanassiadou A., Papapetropoulos T., Johnson W.G., Lazzarini A.M., Duvoisin R.C., Di Lorio G., Golbe L.I., Nussbaum R.L. Mutation in the α-Synuclein gene identified in families with Parkinson's disease. Science. 276:1997;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
Di Lorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
15
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P., Bird T.D., Wijsman E., Nemens E., Garruto R.M., Anderson L., Andreadis A., Wiederholt W.C., Raskind M., Schellenberg G.D. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann. Neurol. 43:1998;815-825.
-
(1998)
Ann. Neurol.
, vol.43
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
Andreadis, A.7
Wiederholt, W.C.8
Raskind, M.9
Schellenberg, G.D.10
-
17
-
-
0028127866
-
Autosomal dominant Lewy body Parkinsonism in a four-generation family
-
Waters C.H., Miller C.A. Autosomal dominant Lewy body Parkinsonism in a four-generation family. Ann. Neurol. 35:1994;59-64.
-
(1994)
Ann. Neurol.
, vol.35
, pp. 59-64
-
-
Waters, C.H.1
Miller, C.A.2
-
19
-
-
0032477559
-
Analysis of the α-synuclein G209A mutation in familial Parkinson's disease
-
Zareparsi S., Kaye J., Camicioli R., Kramer P., Nutt J., Bird T., Litt M., Payami H. Analysis of the α-synuclein G209A mutation in familial Parkinson's disease. Lancet. 351:1998;37-38.
-
(1998)
Lancet
, vol.351
, pp. 37-38
-
-
Zareparsi, S.1
Kaye, J.2
Camicioli, R.3
Kramer, P.4
Nutt, J.5
Bird, T.6
Litt, M.7
Payami, H.8
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