-
1
-
-
37349022446
-
Genetics of Parkinson disease
-
Pankratz N, Foroud T. Genetics of Parkinson disease. Genet Med 2007;9:801-811.
-
(2007)
Genet Med
, vol.9
, pp. 801-811
-
-
Pankratz, N.1
Foroud, T.2
-
2
-
-
7244261867
-
Distribution, type, and origin of Parkin mutations: Review and case studies
-
Hedrich K, Eskelson C, Wilmot B, et al. Distribution, type, and origin of Parkin mutations: review and case studies. Mov Disord 2004;19:1146-1157.
-
(2004)
Mov Disord
, vol.19
, pp. 1146-1157
-
-
Hedrich, K.1
Eskelson, C.2
Wilmot, B.3
-
3
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, et al. 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
-
4
-
-
0032564235
-
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group
-
Lucking CB, Abbas N, Durr A, et al. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group. Lancet 1998;352:1355-1356.
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
Abbas, N.2
Durr, A.3
-
5
-
-
0345490853
-
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
-
Abbas N, Lucking CB, Ricard S, et al. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. Hum Mol Genet 1999;8:567-574.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 567-574
-
-
Abbas, N.1
Lucking, C.B.2
Ricard, S.3
-
6
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
Lucking CB, Durr A, Bonifati V, et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. N Engl J Med 2000;342:1560-1567.
-
(2000)
N Engl J Med
, vol.342
, pp. 1560-1567
-
-
Lucking, C.B.1
Durr, A.2
Bonifati, V.3
-
7
-
-
0037161261
-
Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations
-
Hedrich K, Marder K, Harris J, et al. Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations. Neurology 2002;58:1239-1246.
-
(2002)
Neurology
, vol.58
, pp. 1239-1246
-
-
Hedrich, K.1
Marder, K.2
Harris, J.3
-
8
-
-
0036229267
-
Role of parkin mutations in 111 community-based patients with earlyonset parkinsonism
-
Kann M, Jacobs H, Mohrmann K, et al. Role of parkin mutations in 111 community-based patients with earlyonset parkinsonism. Ann Neurol 2002;51:621-625.
-
(2002)
Ann Neurol
, vol.51
, pp. 621-625
-
-
Kann, M.1
Jacobs, H.2
Mohrmann, K.3
-
9
-
-
18444419131
-
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families
-
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;39:489-492.
-
(2002)
J Med Genet
, vol.39
, pp. 489-492
-
-
Nichols, W.C.1
Pankratz, N.2
Uniacke, S.K.3
-
10
-
-
18444398035
-
Complex relationship between Parkin mutations and Parkinson disease
-
West A, Periquet M, Lincoln S, et al. Complex relationship between Parkin mutations and Parkinson disease. Am J Med Genet 2002;114:584-591.
-
(2002)
Am J Med Genet
, vol.114
, pp. 584-591
-
-
West, A.1
Periquet, M.2
Lincoln, S.3
-
11
-
-
12244262766
-
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
-
Foroud T, Uniacke SK, Liu L, et al. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. Neurology 2003;60:796-801.
-
(2003)
Neurology
, vol.60
, pp. 796-801
-
-
Foroud, T.1
Uniacke, S.K.2
Liu, L.3
-
12
-
-
0034848395
-
Lewy bodies and parkinsonism in families with parkin mutations
-
Farrer M, Chan P, Chen R, et al. Lewy bodies and parkinsonism in families with parkin mutations. Ann Neurol 2001;50:293-300.
-
(2001)
Ann Neurol
, vol.50
, pp. 293-300
-
-
Farrer, M.1
Chan, P.2
Chen, R.3
-
13
-
-
0033933192
-
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
-
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;48:65-71.
-
(2000)
Ann Neurol
, vol.48
, pp. 65-71
-
-
Klein, C.1
Pramstaller, P.P.2
Kis, B.3
-
14
-
-
33745091901
-
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: The GenePD study
-
Sun M, Latourelle JC, Wooten GF, et al. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. Arch Neurol 2006;63:826-832.
-
(2006)
Arch Neurol
, vol.63
, pp. 826-832
-
-
Sun, M.1
Latourelle, J.C.2
Wooten, G.F.3
-
15
-
-
0000224448
-
UPDRS Development Committee. Unified Parkinson's disease rating scale
-
Fahn S, Marsden CD, Goldstein M, eds, New York: Macmillan Healthcare Information;
-
Fahn S, Elton RL; UPDRS Development Committee. Unified Parkinson's disease rating scale. In: Fahn S, Marsden CD, Goldstein M, eds. Recent Developments in Parkinson's Disease. New York: Macmillan Healthcare Information; 1987:153-163.
-
(1987)
Recent Developments in Parkinson's Disease
, pp. 153-163
-
-
Fahn, S.1
Elton, R.L.2
-
16
-
-
0001265104
-
Projection technique for evaluating surgery in Parkinson's disease
-
Gillingham F, Donaldson I, eds, Edinburgh: E&S Livingstone;
-
Schwab R, England A. Projection technique for evaluating surgery in Parkinson's disease. In: Gillingham F, Donaldson I, eds. Third Symposium on Parkinson's Disease. Edinburgh: E&S Livingstone; 1969:152-157.
-
(1969)
Third Symposium on Parkinson's Disease
, pp. 152-157
-
-
Schwab, R.1
England, A.2
-
17
-
-
0014082977
-
Parkinsonism: Onset, progression and mortality
-
Hoehn MM, Yahr MD. Parkinsonism: onset, progression and mortality. Neurology 1967;17:427-442.
-
(1967)
Neurology
, vol.17
, pp. 427-442
-
-
Hoehn, M.M.1
Yahr, M.D.2
-
18
-
-
0016823810
-
Mini-Mental State: A practical method for grading the cognitive state of patients for the clinician
-
Folstein MF, Folstein SE, McHugh PR. "Mini-Mental State": a practical method for grading the cognitive state of patients for the clinician J Psychiatr Res 1975;12:189-198.
-
(1975)
J Psychiatr Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
19
-
-
0020286558
-
Development and validation of a geriatric depression screening scale: A preliminary report
-
Yesavage JA, Brink TL, Rose TL, et al. Development and validation of a geriatric depression screening scale: a preliminary report. J Psychiatr Res 1982;17:37-49.
-
(1982)
J Psychiatr Res
, vol.17
, pp. 37-49
-
-
Yesavage, J.A.1
Brink, T.L.2
Rose, T.L.3
-
20
-
-
0014313861
-
The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects
-
Blessed G, Tomlinson BE, Roth M. The association between quantitative measures of dementia and of senile change in the cerebral grey matter of elderly subjects. Br J Psychiatry 1968;114:797-811.
-
(1968)
Br J Psychiatry
, vol.114
, pp. 797-811
-
-
Blessed, G.1
Tomlinson, B.E.2
Roth, M.3
-
21
-
-
18444364221
-
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations
-
Pankratz N, Nichols WC, Uniacke SK, et al. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. Am J Hum Genet 2002;71:124-135.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 124-135
-
-
Pankratz, N.1
Nichols, W.C.2
Uniacke, S.K.3
-
22
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 2005;365:410-412.
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
-
23
-
-
33846463019
-
Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease
-
Pankratz N, Pauciulo MW, Elsaesser VE, et al. Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease. Mov Disord 2006;21:2257-2260.
-
(2006)
Mov Disord
, vol.21
, pp. 2257-2260
-
-
Pankratz, N.1
Pauciulo, M.W.2
Elsaesser, V.E.3
-
24
-
-
35848937961
-
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
-
Nichols WC, Elsaesser VE, Pankratz N, et al. LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. Neurology 2007;69:1737-1744.
-
(2007)
Neurology
, vol.69
, pp. 1737-1744
-
-
Nichols, W.C.1
Elsaesser, V.E.2
Pankratz, N.3
-
25
-
-
58149100151
-
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
-
Pankratz N, Wilk JB, Latourelle JC, et al. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet 2009;124:593-605.
-
(2009)
Hum Genet
, vol.124
, pp. 593-605
-
-
Pankratz, N.1
Wilk, J.B.2
Latourelle, J.C.3
-
26
-
-
33749519563
-
Mutations in DJ-1 are rare in familial Parkinson disease
-
Pankratz N, Pauciulo MW, Elsaesser VE, et al. Mutations in DJ-1 are rare in familial Parkinson disease. Neurosci Lett 2006;408:209-213.
-
(2006)
Neurosci Lett
, vol.408
, pp. 209-213
-
-
Pankratz, N.1
Pauciulo, M.W.2
Elsaesser, V.E.3
-
27
-
-
33846833930
-
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients
-
Kay DM, Moran D, Moses L, et al. Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients. Ann Neurol 2007;61:47-54.
-
(2007)
Ann Neurol
, vol.61
, pp. 47-54
-
-
Kay, D.M.1
Moran, D.2
Moses, L.3
-
28
-
-
0032937416
-
Polymorphism in the parkin gene in sporadic Parkinson's disease
-
Wang M, Hattori N, Matsumine H, et al. 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
Matsumine, H.3
-
29
-
-
61449133324
-
Clinical correlates of depressive symptoms in familial Parkinson's disease
-
Pankratz N, Marder KS, Halter CA, et al. Clinical correlates of depressive symptoms in familial Parkinson's disease. Mov Disord 2008;23:2216-2223.
-
(2008)
Mov Disord
, vol.23
, pp. 2216-2223
-
-
Pankratz, N.1
Marder, K.S.2
Halter, C.A.3
-
30
-
-
68249128792
-
Features associated with parkin mutation status in probands in the Core-PD Study
-
Marder KS, Clark L, Mejia-Santana H, et al. Features associated with parkin mutation status in probands in the Core-PD Study. Ann Neurol 2007;62(suppl):S38.
-
(2007)
Ann Neurol
, vol.62
, Issue.SUPPL.
-
-
Marder, K.S.1
Clark, L.2
Mejia-Santana, H.3
|