-
2
-
-
84878768010
-
Low frequency of α-synuclein mutations in familial Parkinson's disease
-
in press
-
Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T (1997): Low frequency of α-synuclein mutations in familial Parkinson's disease. Ann Neurol (in press).
-
(1997)
Ann Neurol
-
-
Farrer, M.1
Wavrant-De Vrieze, F.2
Crook, R.3
Boles, L.4
Perez-Tur, J.5
Hardy, J.6
Johnson, W.G.7
Steele, J.8
Maraganore, D.9
Gwinn, K.10
Lynch, T.11
-
3
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus
-
in press
-
Foster NL, Wilhelmsen K, Sima AAF, Jones MZ, D'Amato C, Gilman S and the Participants of the Chromosome 17-related Dementia Conference (1997): Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus. Ann Neurol (in press).
-
(1997)
Ann Neurol
-
-
Wilhelmsen K, F.N.L.1
Sima, A.A.F.2
Jones, M.Z.3
D'Amato, C.4
Gilman, S.5
-
4
-
-
0031577202
-
Genetic complexity and Parkinson's disease
-
Gasser T, Müller-Myshok B, Wszolek ZK, Dürr A, Vaughan JR, Bonifati V, Meco G, Bereznai B, Oehlmann R, Agid Y, Brice A, Wood N, and the European Consortium on Genetic Susceptibility in Parkinson's disease (1997): Genetic complexity and Parkinson's disease. Science 277:388-389.
-
(1997)
Science
, vol.277
, pp. 388-389
-
-
Gasser, T.1
Müller-Myshok, B.2
Wszolek, Z.K.3
Dürr, A.4
Vaughan, J.R.5
Bonifati, V.6
Meco, G.7
Bereznai, B.8
Oehlmann, R.9
Agid, Y.10
Brice, A.11
Wood, N.12
-
5
-
-
0025344485
-
A large kindred with autosomal dominant Parkinson's disease
-
Golbe LI, Di Iorio G, Bonavita V, Miller DC, Duvoisin RC (1990): A large kindred with autosomal dominant Parkinson's disease. Ann Neurol 27:276-282.
-
(1990)
Ann Neurol
, vol.27
, pp. 276-282
-
-
Golbe, L.I.1
Di Iorio, G.2
Bonavita, V.3
Miller, D.C.4
Duvoisin, R.C.5
-
7
-
-
0021344005
-
Easy calculations of LOD scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM (1984):Easy calculations of LOD scores and genetic risks on small computers. Am J Hum Genet 36:460-465.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
9
-
-
0022646961
-
Construction of human genetic linkage maps: Likelihood calculations for multilocus analysis
-
Lathrop GM, Lalouel JM, White RL (1986): Construction of human genetic linkage maps: Likelihood calculations for multilocus analysis. Genet Epidemiol 3:39-52.
-
(1986)
Genet Epidemiol
, vol.3
, pp. 39-52
-
-
Lathrop, G.M.1
Lalouel, J.M.2
White, R.L.3
-
10
-
-
0027948959
-
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex
-
Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AAF, Keohane D, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC (1994): Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology 44:1878-1884.
-
(1994)
Neurology
, vol.44
, pp. 1878-1884
-
-
Lynch, T.1
Sano, M.2
Marder, K.S.3
Bell, K.L.4
Foster, N.L.5
Defendini, R.F.6
Sima, A.A.F.7
Keohane, D.8
Nygaard, T.G.9
Fahn, S.10
Mayeux, R.11
Rowland, L.P.12
Wilhelmsen, K.C.13
-
11
-
-
0026786260
-
Prevalence of Parkinson's disease and other types of parkinsonism: A door to door survey in 3 Sicilian municipalities
-
Morgante L, Rocca WA, Di Rosa AE, De Domineco P, Grigoletto F, Meneghini F, Reggio A, Savettieri G, Castiglione MG, Patti F, Di Perri R (1992): Prevalence of Parkinson's disease and other types of parkinsonism: A door to door survey in 3 Sicilian municipalities. Neurology 42: 1901-1907.
-
(1992)
Neurology
, vol.42
, pp. 1901-1907
-
-
Morgante, L.1
Rocca, W.A.2
Di Rosa, A.E.3
De Domineco, P.4
Grigoletto, F.5
Meneghini, F.6
Reggio, A.7
Savettieri, G.8
Castiglione, M.G.9
Patti, F.10
Di Perri, R.11
-
12
-
-
0001724075
-
A familial Parkinson-dementia syndrome
-
Muenter MD, Howard FM, Okazaki H, Forno LS, Kish SJ, Hornykiewicz O (1986): A familial Parkinson-dementia syndrome. Neurology 36 (suppl):115.
-
(1986)
Neurology
, vol.36
, Issue.SUPPL.
, pp. 115
-
-
Muenter, M.D.1
Howard, F.M.2
Okazaki, H.3
Forno, L.S.4
Kish, S.J.5
Hornykiewicz, O.6
-
13
-
-
84878766698
-
Hereditary form of Parkinsonism-Dementia
-
in press
-
Muenter MD, Forno LS, Hornykiewicz O, Kish SJ, Maraganore DM, Caselli RJ, Okazaki H, Howard FM, Snow BJ, Calne DB (1997): Hereditary form of Parkinsonism-Dementia. Ann. Neurol. (in press).
-
(1997)
Ann. Neurol.
-
-
Muenter, M.D.1
Forno, L.S.2
Hornykiewicz, O.3
Kish, S.J.4
Maraganore, D.M.5
Caselli, R.J.6
Okazaki, H.7
Howard, F.M.8
Snow, B.J.9
Calne, D.B.10
-
14
-
-
0024602536
-
Estimating the power of a proposed linkage study for a complex genetic trait
-
Ploughman LM, Boehnke M (1989): Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet 44:543-551.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 543-551
-
-
Ploughman, L.M.1
Boehnke, M.2
-
15
-
-
10544234193
-
A locus for Parkinson's disease on chromosome 4
-
Polymeropoulos MH, Higgins JJ, Golbe LI, Johnson WG, Ide SE, Di Iorio G, Sange G, Stenrros E, Pho LT, Schaffer AA, Lazzarini AM, Nuss-baum RL, Duvoisin RC (1996): A locus for Parkinson's disease on chromosome 4. Science 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
Di Iorio, G.6
Sange, G.7
Stenrros, E.8
Pho, L.T.9
Schaffer, A.A.10
Lazzarini, A.M.11
Nuss-baum, R.L.12
Duvoisin, R.C.13
-
16
-
-
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, Papapetropoulos T, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL (1997): Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 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
Athanassiadou13
Papapetropoulos, T.14
Lazzarini, A.M.15
Duvoisin, R.C.16
Di Iorio, G.17
Golbe, L.I.18
Nussbaum, R.L.19
-
17
-
-
0030822568
-
Genetic complexity and Parkinson's disease
-
Scott WK, Stajich JM, Yamaoka LH, Speer MC, Vance JM, Roses AD, Pericak-Vance RIA and the Deane Laboratory Parkinson Disease Research Group (1997): Genetic complexity and Parkinson's disease. Science 277:387-388.
-
(1997)
Science
, vol.277
, pp. 387-388
-
-
Scott, W.K.1
Stajich, J.M.2
Yamaoka, L.H.3
Speer, M.C.4
Vance, J.M.5
Roses, A.D.6
Pericak-Vance, R.I.A.7
-
18
-
-
0000355052
-
Report of familial cases of parkinsonism
-
Spellman GG (1962): Report of familial cases of parkinsonism. JAMA 179: 160-162.
-
(1962)
JAMA
, vol.179
, pp. 160-162
-
-
Spellman, G.G.1
-
19
-
-
0028127866
-
Autosomal dominant Lewy body parkinsonism in a four generation family
-
Waters CH, Miller CA (1994): Autosomal dominant Lewy body parkinsonism in a four generation family. Ann Neurol 35:59-64.
-
(1994)
Ann Neurol
, vol.35
, pp. 59-64
-
-
Waters, C.H.1
Miller, C.A.2
|