-
2
-
-
78651024089
-
The problem of anticipation in pedigrees of dystonia myotonica
-
Penrose LS. The problem of anticipation in pedigrees of dystonia myotonica. Ann Eugen 1948;14:125-132.
-
(1948)
Ann Eugen
, vol.14
, pp. 125-132
-
-
Penrose, L.S.1
-
4
-
-
0013475839
-
A large kindred with Parkinson's disease: Onset age, segregation ratios, and anticipation
-
Golbe LI, Di Iorio G, Lazzarini AM, Bonavita V, Duvoisin RC. A large kindred with Parkinson's disease: onset age, segregation ratios, and anticipation [abstract]. Mov Disord 1993;8: 406.
-
(1993)
Mov Disord
, vol.8
, pp. 406
-
-
Golbe, L.I.1
Di Iorio, G.2
Lazzarini, A.M.3
Bonavita, V.4
Duvoisin, R.C.5
-
5
-
-
0027970947
-
Anticipation of onset age in familial Parkinson's disease
-
Bonifati V, Vanacore N, Meco G. Anticipation of onset age in familial Parkinson's disease. Neurology 1994;44:1978-1979.
-
(1994)
Neurology
, vol.44
, pp. 1978-1979
-
-
Bonifati, V.1
Vanacore, N.2
Meco, G.3
-
6
-
-
10544237412
-
A Greek-American family with autosomal dominant levodopa-responsive parkinsonism
-
Markopoulou K, Wszolek ZK, Pfeiffer RF. A Greek-American family with autosomal dominant levodopa-responsive parkinsonism [abstract]. Ann Neurol 1994;36:280.
-
(1994)
Ann Neurol
, vol.36
, pp. 280
-
-
Markopoulou, K.1
Wszolek, Z.K.2
Pfeiffer, R.F.3
-
7
-
-
0028869758
-
Genetic anticipation in Parkinson's disease
-
Payami H, Bernard S, Larsen K, Kaye J, Nutt J. Genetic anticipation in Parkinson's disease. Neurology 1995;45:135-138.
-
(1995)
Neurology
, vol.45
, pp. 135-138
-
-
Payami, H.1
Bernard, S.2
Larsen, K.3
Kaye, J.4
Nutt, J.5
-
8
-
-
10544240155
-
Familial aggregation, segregation analysis and transmission patterns in Parkinson's disease
-
Lazzarini AM, Myers RH, Zimmerman TR Jr, et al. Familial aggregation, segregation analysis and transmission patterns in Parkinson's disease [abstract]. New Trends Clin Neuropharmacol 1994;8:119.
-
(1994)
New Trends Clin Neuropharmacol
, vol.8
, pp. 119
-
-
Lazzarini, A.M.1
Myers, R.H.2
Zimmerman Jr., T.R.3
-
9
-
-
8544261234
-
Clinical and genetic study of familial Parkinson's disease
-
Mazzetti P, Bonnet AM, Vidailhet M, et al. Clinical and genetic study of familial Parkinson's disease [abstract]. Neurology 1993;43(suppl 2):A238.
-
(1993)
Neurology
, vol.43
, Issue.2 SUPPL.
-
-
Mazzetti, P.1
Bonnet, A.M.2
Vidailhet, M.3
-
10
-
-
7144229702
-
Familial Parkinson's disease: Clinical and genetic considerations on 13 Italian kindreds
-
Bonifati V, Fabrizio E, Buttarelli FR, Di Legge S, Vanacore N, Meco G. Familial Parkinson's disease: Clinical and genetic considerations on 13 Italian kindreds [abstract]. Mov Disord 1994;9(suppl 1):30.
-
(1994)
Mov Disord
, vol.9
, Issue.1 SUPPL.
, pp. 30
-
-
Bonifati, V.1
Fabrizio, E.2
Buttarelli, F.R.3
Di Legge, S.4
Vanacore, N.5
Meco, G.6
-
11
-
-
0025834561
-
A clinical and genetic study of familial Parkinson's disease
-
Maraganore DM, Harding AE, Marsden CD. A clinical and genetic study of familial Parkinson's disease. Mov Disord 1991;6:205-211.
-
(1991)
Mov Disord
, vol.6
, pp. 205-211
-
-
Maraganore, D.M.1
Harding, A.E.2
Marsden, C.D.3
-
12
-
-
0018736142
-
Bias in analytic research
-
Sackett DL. Bias in analytic research. J Chron Dis 1979;32: 51-63.
-
(1979)
J Chron Dis
, vol.32
, pp. 51-63
-
-
Sackett, D.L.1
-
14
-
-
0027742974
-
Phenotypic variability in autosomal dominant cerebellar ataxia type 1 is unrelated to genetic heterogeneity
-
Durr A, Chneiweiss H, Khati C, et al. Phenotypic variability in autosomal dominant cerebellar ataxia type 1 is unrelated to genetic heterogeneity. Brain 1993;116:1497-1508.
-
(1993)
Brain
, vol.116
, pp. 1497-1508
-
-
Durr, A.1
Chneiweiss, H.2
Khati, C.3
-
15
-
-
0026786260
-
Prevalence of Parkinson's disease and other types of parkinsonism: A door-to-door survey in three Sicilian municipalities
-
Morgante L, Rocca WA, Di Rosa AE, et al. Prevalence of Parkinson's disease and other types of parkinsonism: a door-to-door survey in three Sicilian municipalities. Neurology 1992;42:1901-1907.
-
(1992)
Neurology
, vol.42
, pp. 1901-1907
-
-
Morgante, L.1
Rocca, W.A.2
Di Rosa, A.E.3
-
16
-
-
0027504703
-
Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology
-
Golbe LI, Lazzarini AM, Schwarz KO, Mark MH, Dickson DW, Duvoisin RC. Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology. Neurology 1993;43:2222-2227.
-
(1993)
Neurology
, vol.43
, pp. 2222-2227
-
-
Golbe, L.I.1
Lazzarini, A.M.2
Schwarz, K.O.3
Mark, M.H.4
Dickson, D.W.5
Duvoisin, R.C.6
-
17
-
-
0029090839
-
A Greek-American kindred with autosomal dominant parkinsonism and anticipation
-
Markopoulou K, Wzolek ZK, Pfeiffer RF. A Greek-American kindred with autosomal dominant parkinsonism and anticipation. Neurology 1995;38:373-378.
-
(1995)
Neurology
, vol.38
, pp. 373-378
-
-
Markopoulou, K.1
Wzolek, Z.K.2
Pfeiffer, R.F.3
-
19
-
-
0028127866
-
Autosomal dominant Lewy body parkinsonism in a four-generation family
-
Waters CH, Miller CA. Autosomal dominant Lewy body parkinsonism in a four-generation family. Ann Neurol 1994;35: 59-64.
-
(1994)
Ann Neurol
, vol.35
, pp. 59-64
-
-
Waters, C.H.1
Miller, C.A.2
-
20
-
-
0029049738
-
Western Nebraska family (family D) with autosomal dominant parkinsonism
-
Wszolek ZK, Pfeiffer B, Fulgham JR, et al. Western Nebraska family (family D) with autosomal dominant parkinsonism. Neurology 1995;45:502-505.
-
(1995)
Neurology
, vol.45
, pp. 502-505
-
-
Wszolek, Z.K.1
Pfeiffer, B.2
Fulgham, J.R.3
-
21
-
-
0028787434
-
No evidence for association of familial Parkinson's disease with CAG repeat expansion
-
Carrero-Valenzuela R, Lindblad K, Payami H, et al. No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology 1995;45:1760-1763.
-
(1995)
Neurology
, vol.45
, pp. 1760-1763
-
-
Carrero-Valenzuela, R.1
Lindblad, K.2
Payami, H.3
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