-
1
-
-
16444380313
-
LRRK2 mutations and Parkinsonism
-
M. Albrecht, LRRK2 mutations and Parkinsonism, Lancet 365 (2005), 1230.
-
(2005)
Lancet
, vol.365
, pp. 1230
-
-
Albrecht, M.1
-
2
-
-
0030858820
-
The clock drawing test for dementia of the alzheimer's type: A comparison of three scoring methods in a memory disorders clinic
-
H. Brodaty and C.M. Moore, The Clock Drawing Test for dementia of the Alzheimer's type: A comparison of three scoring methods in a memory disorders clinic, Int J Geriatr Psychiatry 12 (1997), 619-627.
-
(1997)
Int J Geriatr Psychiatry
, vol.12
, pp. 619-627
-
-
Brodaty, H.1
Moore, C.M.2
-
3
-
-
0016823810
-
"mini-mental state". A practical method for grading the cognitive state of patients for the clinician
-
M.F. Folstein, S.E. Folstein and P.R. McHugh, "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician, J Psychiatr Res 12 (1975), 189-198.
-
(1975)
J Psychiatr Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
4
-
-
24644468116
-
LRRK2: Both a cause and a risk factor for parkinson disease?
-
T. Foroud, LRRK2: both a cause and a risk factor for Parkinson disease? Neurology 65 (2005), 664-665.
-
(2005)
Neurology
, vol.65
, pp. 664-665
-
-
Foroud, T.1
-
5
-
-
34147125812
-
Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in parkinson disease
-
S. Goldwurm, M. Zini, L. Mariani et al., Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease, Neurology 68 (2007), 1141-1143.
-
(2007)
Neurology
, vol.68
, pp. 1141-1143
-
-
Goldwurm, S.1
Zini, M.2
Mariani, L.3
-
6
-
-
33746267531
-
Kinase activity is required for the toxic effects of mutant LRRK2/dardarin
-
E. Greggio, S. Jain, A. Kingsbury et al., Kinase activity is required for the toxic effects of mutant LRRK2/dardarin, Neurobiol Dis 23 (2006), 329-341.
-
(2006)
Neurobiol Dis
, vol.23
, pp. 329-341
-
-
Greggio, E.1
Jain, S.2
Kingsbury, A.3
-
7
-
-
24644474856
-
The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases
-
D. Hernandez, C. Paisan-Ruiz, A. Crawley et al., The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases, Neurosci Lett 389 (2005), 137-139.
-
(2005)
Neurosci Lett
, vol.389
, pp. 137-139
-
-
Hernandez, D.1
Paisan-Ruiz, C.2
Crawley, A.3
-
8
-
-
20044394901
-
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2
-
D.G. Hernandez, C. Paiśan-Rúyz, A. McInerney-Leo et al., Clinical and positron emission tomography of Parkinson's disease caused by LRRK2, Ann Neurol 57 (2005), 453-456.
-
(2005)
Ann Neurol
, vol.57
, pp. 453-456
-
-
Hernandez, D.G.1
Paiśan-Rúyz, C.2
McInerney-Leo, A.3
-
9
-
-
59649089328
-
The Parkinson diasease protein leucine-rich repeat kinase 2 transduces death signals via fas-associated protein with death domain and caspase-8 in a cellular model of neurodegeneration
-
C.C. Ho, H.J. Rideout, E. Ribe et al., The Parkinson diasease protein leucine-rich repeat kinase 2 transduces death signals via Fas-associated protein with death domain and caspase-8 in a cellular model of neurodegeneration, J Neurosci 29 (2009), 1011-1016.
-
(2009)
J Neurosci
, vol.29
, pp. 1011-1016
-
-
Ho, C.C.1
Rideout, H.J.2
Ribe, E.3
-
10
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across european populations
-
J. Kachergus, I.F. Mata, M. Hulihan et al., Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations, Am J Hum Genet 76 (2005), 672-680.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
-
11
-
-
33745766262
-
LRRK2 G2019S and I2020T mutations are not common in alzheimer's disease and vascular dementia
-
E. Lee, S. Hui, G. Ho et al., LRRK2 G2019S and I2020T mutations are not common in Alzheimer's disease and vascular dementia, Am J Med Genet B Neuropsychiatr Genet 141 (2006), 549-550.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141
, pp. 549-550
-
-
Lee, E.1
Hui, S.2
Ho, G.3
-
12
-
-
33646151866
-
LRRK2 in Parkinson's disease: Protein domains and functional insights
-
I.F. Mata, W.J. Wedemeyer, M.J. Farrer et al., LRRK2 in Parkinson's disease: protein domains and functional insights, Trends Neurosci 29 (2006), 286-293.
-
(2006)
Trends Neurosci
, vol.29
, pp. 286-293
-
-
Mata, I.F.1
Wedemeyer, W.J.2
Farrer, M.J.3
-
13
-
-
33749463769
-
LRRK2 expression in normal and pathologic human brain and in human cell lines
-
J. Miklossy, T. Arai, J.P. Guo et al., LRRK2 expression in normal and pathologic human brain and in human cell lines, J Neuropathol Exp Neurol 65 (2006), 953-963.
-
(2006)
J Neuropathol Exp Neurol
, vol.65
, pp. 953-963
-
-
Miklossy, J.1
Arai, T.2
Guo, J.P.3
-
14
-
-
4444353636
-
Regulation of protein kinases; Controlling activity through activation segment conformation
-
B. Nolen, S. Taylor and G. Ghosh, Regulation of protein kinases; controlling activity through activation segment conformation, Mol Cell 15 (2004), 661-675.
-
(2004)
Mol Cell
, vol.15
, pp. 661-675
-
-
Nolen, B.1
Taylor, S.2
Ghosh, G.3
-
15
-
-
0030770726
-
Complete genomic screen in late-onset familial alzheimer disease. Evidence for a new locus on chromosome 12
-
M.A. Pericak-Vance, M.P. Bass, L.H. Yamaoka et al., Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12, JAMA 278 (1997), 1237-1241.
-
(1997)
JAMA
, vol.278
, pp. 1237-1241
-
-
Pericak-Vance, M.A.1
Bass, M.P.2
Yamaoka, L.H.3
-
16
-
-
39149100952
-
A study of LRRK2 mutations and parkinson's disease in Brazil
-
M.M. Pimentel, K.C. Moura, C.B. Abdalla et al., A study of LRRK2 mutations and Parkinson's disease in Brazil, Neurosci Lett 433 (2008), 17-21.
-
(2008)
Neurosci Lett
, vol.433
, pp. 17-21
-
-
Pimentel, M.M.1
Moura, K.C.2
Abdalla, C.B.3
-
17
-
-
33750406222
-
Absence/rarity of commonly reported LRRK2 mutations in Indian parkinson's disease patients
-
S. Punia, M. Behari, S.T. Govindappa et al., Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients, Neurosci Lett 409 (2006), 83-88.
-
(2006)
Neurosci Lett
, vol.409
, pp. 83-88
-
-
Punia, S.1
Behari, M.2
Govindappa, S.T.3
-
18
-
-
37549039817
-
No Association between the LRRK2 G2019S mutation and alzheimer's disease in Italy
-
A. Tedde, S. Bagnoli, E. Cellini et al., No Association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy, Cell Mol Neurobiol 27 (2007), 877-881.
-
(2007)
Cell Mol Neurobiol
, vol.27
, pp. 877-881
-
-
Tedde, A.1
Bagnoli, S.2
Cellini, E.3
-
19
-
-
25144468286
-
LRRK2 mutations are not common in alzheimer's disease
-
M. Toft, S.B. Sando, S. Melquist et al, LRRK2 mutations are not common in Alzheimer's disease, Mech Ageing Dev 126 (2005), 1201-1205.
-
(2005)
Mech Ageing Dev
, vol.126
, pp. 1201-1205
-
-
Toft, M.1
Sando, S.B.2
Melquist, S.3
-
20
-
-
33645130652
-
Clinicogenetic study of mutations in LRRK2 exon 41 in parkinson's disease patients from 18 countries
-
H. Tomiyama, Y. Li, M. Funayama et al., Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries, Mov Disord 21 (2006), 1102-1108.
-
(2006)
Mov Disord
, vol.21
, pp. 1102-1108
-
-
Tomiyama, H.1
Li, Y.2
Funayama, M.3
-
21
-
-
28044460070
-
Parkinson's diseaseassociated mutations in leucine-rich repeat kinase 2 augment kinase activity
-
A.B. West, D.J. Moore, S. Biskup et al., Parkinson's diseaseassociated mutations in leucine-rich repeat kinase 2 augment kinase activity, Proc Natl Acad Sci USA 102 (2005), 16842-16847.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 16842-16847
-
-
West, A.B.1
Moore, D.J.2
Biskup, S.3
-
22
-
-
30344459394
-
Analysis of the LRRK2 G2019S mutation in alzheimer disease
-
C.P. Zabetian, C.J. Lauricella, D.W. Tsuang et al., Analysis of the LRRK2 G2019S mutation in Alzheimer Disease, Arch Neurol 63 (2006), 156-157.
-
(2006)
Arch Neurol
, vol.63
, pp. 156-157
-
-
Zabetian, C.P.1
Lauricella, C.J.2
Tsuang, D.W.3
-
23
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
A. Zimprich, S. Biskup, P. Leitner et al., Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology, Neuron 44 (2004), 601-607.
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
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