-
1
-
-
0042970162
-
Dementia associated with Parkinson's disease
-
Emre M. Dementia associated with Parkinson's disease. Lancet Neurol 2 (2003) 229-237
-
(2003)
Lancet Neurol
, vol.2
, pp. 229-237
-
-
Emre, M.1
-
2
-
-
42449147949
-
A modern hypothesis: the distinct pathologies of dementia associated with Parkinson's disease versus Alzheimer's disease
-
Farlow M.R., and Cummings J. A modern hypothesis: the distinct pathologies of dementia associated with Parkinson's disease versus Alzheimer's disease. Dement Geriatr Cogn Disord 25 (2008) 301-308
-
(2008)
Dement Geriatr Cogn Disord
, vol.25
, pp. 301-308
-
-
Farlow, M.R.1
Cummings, J.2
-
3
-
-
0024317904
-
Prevalence of Alzheimer's disease in a community population of older persons higher than previously reported
-
Evans D.A., Funkenstein H.H., Albert M.S., Scherr P.R., Cook N.R., Herbert L.E., et al. Prevalence of Alzheimer's disease in a community population of older persons higher than previously reported. JAMA 262 (1989) 2551-2556
-
(1989)
JAMA
, vol.262
, pp. 2551-2556
-
-
Evans, D.A.1
Funkenstein, H.H.2
Albert, M.S.3
Scherr, P.R.4
Cook, N.R.5
Herbert, L.E.6
-
4
-
-
0037335814
-
Prevalence and characteristics of dementia in Parkinson's disease: an 8-year prospective study
-
Aarsland D., Andersen K., Larsen J.P., Lolk A., and Kragh-Sorensen P. Prevalence and characteristics of dementia in Parkinson's disease: an 8-year prospective study. Arch Neurol 60 (2003) 387-837
-
(2003)
Arch Neurol
, vol.60
, pp. 387-837
-
-
Aarsland, D.1
Andersen, K.2
Larsen, J.P.3
Lolk, A.4
Kragh-Sorensen, P.5
-
5
-
-
0347123264
-
Onset and progression of disease in familial and sporadic Parkinson's disease
-
Inzelberg R., Schecthman E., Paleacu D., Zach L., Bonwitt R., Carasso R.L., et al. Onset and progression of disease in familial and sporadic Parkinson's disease. Am J Med Genet 124 (2004) 255-258
-
(2004)
Am J Med Genet
, vol.124
, pp. 255-258
-
-
Inzelberg, R.1
Schecthman, E.2
Paleacu, D.3
Zach, L.4
Bonwitt, R.5
Carasso, R.L.6
-
6
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., Lavedan C., Leroy E., et al. 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
-
7
-
-
0030882856
-
Alpha-synuclein in Lewy bodies
-
Spillantini M.G., Schmidt M.L., Lee V.M.-Y., Trojanowski J.Q., Jakes R., and Goedert M. Alpha-synuclein in Lewy bodies. Nature 388 (1997) 839-840
-
(1997)
Nature
, vol.388
, pp. 839-840
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.-Y.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
8
-
-
4644295844
-
Parkinson's disease and dementia with Lewy bodies: a difference in dose?
-
Singleton A., and Gwinn-Hardy K. Parkinson's disease and dementia with Lewy bodies: a difference in dose?. Lancet 364 (2004) 1105-1106
-
(2004)
Lancet
, vol.364
, pp. 1105-1106
-
-
Singleton, A.1
Gwinn-Hardy, K.2
-
9
-
-
0034602442
-
Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions
-
Giasson B.I., Duda J.E., Murray I.V.J., Chen Q., Souza J.M., Hurtig H.I., et al. Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions. Science 290 (2000) 985-989
-
(2000)
Science
, vol.290
, pp. 985-989
-
-
Giasson, B.I.1
Duda, J.E.2
Murray, I.V.J.3
Chen, Q.4
Souza, J.M.5
Hurtig, H.I.6
-
10
-
-
33749570292
-
Phosphorylation of ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body disease
-
Anderson J.P., Walker D.E., Goldstein J.M., de Laat R., Banducci K., Caccavello R.J., et al. Phosphorylation of ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body disease. J Biol Chem 281 (2006) 29739-29752
-
(2006)
J Biol Chem
, vol.281
, pp. 29739-29752
-
-
Anderson, J.P.1
Walker, D.E.2
Goldstein, J.M.3
de Laat, R.4
Banducci, K.5
Caccavello, R.J.6
-
11
-
-
0036142959
-
Parkinson disease neuropathology: later-developing dementia and loss of the levodopa response
-
Apaydin H., Ahlskog J.E., Parisi J.E., Boeve B.F., and Dickson D.W. Parkinson disease neuropathology: later-developing dementia and loss of the levodopa response. Arch Neurol 59 (2002) 102-112
-
(2002)
Arch Neurol
, vol.59
, pp. 102-112
-
-
Apaydin, H.1
Ahlskog, J.E.2
Parisi, J.E.3
Boeve, B.F.4
Dickson, D.W.5
-
12
-
-
0034705015
-
Alpha-synuclein cortical Lewy bodies correlate with dementia in Parkinson's disease
-
Hurtig H.I., Trojanowski J.Q., Galvin J., Ewbank D., Schmidt M.L., Lee V.M., et al. Alpha-synuclein cortical Lewy bodies correlate with dementia in Parkinson's disease. Neurology 54 (2000) 1916-1921
-
(2000)
Neurology
, vol.54
, pp. 1916-1921
-
-
Hurtig, H.I.1
Trojanowski, J.Q.2
Galvin, J.3
Ewbank, D.4
Schmidt, M.L.5
Lee, V.M.6
-
13
-
-
32044453611
-
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease
-
Nishioka K., Hayashi S., Farrer M.J., Singleton A.B., Yoshino H., Imai H., et al. Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease. Ann Neurol 59 (2006) 298-309
-
(2006)
Ann Neurol
, vol.59
, pp. 298-309
-
-
Nishioka, K.1
Hayashi, S.2
Farrer, M.J.3
Singleton, A.B.4
Yoshino, H.5
Imai, H.6
-
14
-
-
37849012348
-
Alpha-synuclein gene duplication is present in sporadic Parkinson disease
-
Ahn T.-B., Kim S.Y., Kim J.Y., Park S.-S., Lee D.S., Min H.J., et al. Alpha-synuclein gene duplication is present in sporadic Parkinson disease. Neurology 70 (2008) 43-49
-
(2008)
Neurology
, vol.70
, pp. 43-49
-
-
Ahn, T.-B.1
Kim, S.Y.2
Kim, J.Y.3
Park, S.-S.4
Lee, D.S.5
Min, H.J.6
-
15
-
-
34147109175
-
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication
-
Fuchs J., Nilsson C., Kachergus J., Munz M., Larsson E.-M., Schule B., et al. Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication. Neurology 68 (2007) 916-922
-
(2007)
Neurology
, vol.68
, pp. 916-922
-
-
Fuchs, J.1
Nilsson, C.2
Kachergus, J.3
Munz, M.4
Larsson, E.-M.5
Schule, B.6
-
16
-
-
38649119157
-
Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseases
-
Beyer K., Domingo-Sabat M., Lao J.I., Carrato C., Ferrer I., and Ariza A. Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseases. Neurogenetics 9 (2008) 15-23
-
(2008)
Neurogenetics
, vol.9
, pp. 15-23
-
-
Beyer, K.1
Domingo-Sabat, M.2
Lao, J.I.3
Carrato, C.4
Ferrer, I.5
Ariza, A.6
-
17
-
-
0034069848
-
Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p
-
Gwinn-Hardy K., Mehta N.D., Farrer M., Maraganore D., Muenter M., Yen S.-H., et al. Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p. Acta Neuropath 99 (2000) 663-672
-
(2000)
Acta Neuropath
, vol.99
, pp. 663-672
-
-
Gwinn-Hardy, K.1
Mehta, N.D.2
Farrer, M.3
Maraganore, D.4
Muenter, M.5
Yen, S.-H.6
-
18
-
-
10744227740
-
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications
-
Farrer M., Kachergus J., Forno L., Lincoln S., Wang D.-S., Hulihan M., et al. Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications. Ann Neurol 55 (2004) 174-179
-
(2004)
Ann Neurol
, vol.55
, pp. 174-179
-
-
Farrer, M.1
Kachergus, J.2
Forno, L.3
Lincoln, S.4
Wang, D.-S.5
Hulihan, M.6
-
19
-
-
0000355051
-
Report of familial cases of parkinsonism: evidence of a dominant trait in a patient's family
-
Spellman G.G. Report of familial cases of parkinsonism: evidence of a dominant trait in a patient's family. JAMA 179 (1962) 372-374
-
(1962)
JAMA
, vol.179
, pp. 372-374
-
-
Spellman, G.G.1
-
20
-
-
38149131788
-
Clinicopathological study of a SNCA duplication patient with Parkinson disease and dementia
-
Obi T., Nishioka K., Ross O.A., Terada T., Yamazaki K., Sugiura A., et al. Clinicopathological study of a SNCA duplication patient with Parkinson disease and dementia. Neurology 70 (2008) 238-241
-
(2008)
Neurology
, vol.70
, pp. 238-241
-
-
Obi, T.1
Nishioka, K.2
Ross, O.A.3
Terada, T.4
Yamazaki, K.5
Sugiura, A.6
-
21
-
-
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 392 (1998) 605-608
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
-
22
-
-
0342368772
-
-
Lucking CB, Durr A, Bonifati V, XXXet al. Association between early-onset Parkinson's disease and mutations in the parkin gene. New Eng J Med 2000;342: 1560-7.
-
Lucking CB, Durr A, Bonifati V, XXXet al. Association between early-onset Parkinson's disease and mutations in the parkin gene. New Eng J Med 2000;342: 1560-7.
-
-
-
-
23
-
-
0032716207
-
Autosomal recessive juvenile parkinsonism in a Jewish Yemenite kindred: Mutation of Parkin gene
-
Nisipeanu P., Inzelberg R., Blumen S.C., Carasso R.L., Hattori N., Matsumine H., et al. Autosomal recessive juvenile parkinsonism in a Jewish Yemenite kindred: Mutation of Parkin gene. Neurology 53 (1999) 1602-1604
-
(1999)
Neurology
, vol.53
, pp. 1602-1604
-
-
Nisipeanu, P.1
Inzelberg, R.2
Blumen, S.C.3
Carasso, R.L.4
Hattori, N.5
Matsumine, H.6
-
24
-
-
0035849493
-
Parkin gene causing benign autosomal recessive juvenile parkinsonism
-
Nisipeanu P., Inzelberg R., Abo Mouch S., Carasso R.L., Blumen S.C., Zhang J., et al. Parkin gene causing benign autosomal recessive juvenile parkinsonism. Neurology 56 (2001) 1573-1575
-
(2001)
Neurology
, vol.56
, pp. 1573-1575
-
-
Nisipeanu, P.1
Inzelberg, R.2
Abo Mouch, S.3
Carasso, R.L.4
Blumen, S.C.5
Zhang, J.6
-
25
-
-
0037461313
-
Camptocormia, axial dystonia and parkinsonism: phenotypic heterogeneity of a parkin mutation
-
Inzelberg R., Hattori N., Nisipeanu P., Abo Mouch S., Blumen S.C., Carasso R.L., et al. Camptocormia, axial dystonia and parkinsonism: phenotypic heterogeneity of a parkin mutation. Neurology 60 (2003) 1393-1394
-
(2003)
Neurology
, vol.60
, pp. 1393-1394
-
-
Inzelberg, R.1
Hattori, N.2
Nisipeanu, P.3
Abo Mouch, S.4
Blumen, S.C.5
Carasso, R.L.6
-
26
-
-
0033814671
-
An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene
-
Hayashi S., Wakabayashi K., Ishikawa A., Nagai H., Saito M., Maruyama M., et al. An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene. Mov Disord 15 (2000) 884-888
-
(2000)
Mov Disord
, vol.15
, pp. 884-888
-
-
Hayashi, S.1
Wakabayashi, K.2
Ishikawa, A.3
Nagai, H.4
Saito, M.5
Maruyama, M.6
-
27
-
-
0035957112
-
Clinical and pathologic abnormalities in a family with parkinsonism and parkin disease
-
Van de Warrenburg B.P.C., Lammens M., Lucking C.B., Denefle P., Wesseling P., Booij J., et al. Clinical and pathologic abnormalities in a family with parkinsonism and parkin disease. Neurology 56 (2001) 553-557
-
(2001)
Neurology
, vol.56
, pp. 553-557
-
-
Van de Warrenburg, B.P.C.1
Lammens, M.2
Lucking, C.B.3
Denefle, P.4
Wesseling, P.5
Booij, J.6
-
28
-
-
34247185238
-
Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations
-
Ephraty L., Porat O., Israeli D., Cohen O.S., Tunkel O., Yael S., et al. Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations. Mov Disord 22 (2007) 566-569
-
(2007)
Mov Disord
, vol.22
, pp. 566-569
-
-
Ephraty, L.1
Porat, O.2
Israeli, D.3
Cohen, O.S.4
Tunkel, O.5
Yael, S.6
-
29
-
-
34247231543
-
Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations
-
Steinlechner S., Stahlberg J., Völkel B., Djarmati A., Hagenah J., Hiller A., et al. Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations. J Neurol Neurosurg Psychiatry 78 (2007) 532-535
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 532-535
-
-
Steinlechner, S.1
Stahlberg, J.2
Völkel, B.3
Djarmati, A.4
Hagenah, J.5
Hiller, A.6
-
30
-
-
33746923419
-
Recessive Parkinson's disease
-
Kubo S., Hattori N., and Mizuno Y. Recessive Parkinson's disease. Mov Disord 21 (2006) 885-893
-
(2006)
Mov Disord
, vol.21
, pp. 885-893
-
-
Kubo, S.1
Hattori, N.2
Mizuno, Y.3
-
31
-
-
0038662544
-
Parkin disease: a phenotypic study of a large case series
-
Khan N.L., Graham E., Critchley P., Schrag A.E., Wood N.W., Lees A.J., et al. Parkin disease: a phenotypic study of a large case series. Brain 126 (2003) 1279-1292
-
(2003)
Brain
, vol.126
, pp. 1279-1292
-
-
Khan, N.L.1
Graham, E.2
Critchley, P.3
Schrag, A.E.4
Wood, N.W.5
Lees, A.J.6
-
32
-
-
0034972560
-
A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees
-
Lindholm E., Ekholm B., Shaw S., Jalonen P., Johansson G., Pettersson U., et al. A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees. Am J Hum Genet 69 (2001) 96-105
-
(2001)
Am J Hum Genet
, vol.69
, pp. 96-105
-
-
Lindholm, E.1
Ekholm, B.2
Shaw, S.3
Jalonen, P.4
Johansson, G.5
Pettersson, U.6
-
33
-
-
20444399801
-
M, Bellacchio E, Elia AE, Dallapiccola B. The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease
-
Albanese A., and Valente E.M. M, Bellacchio E, Elia AE, Dallapiccola B. The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease. Neurology 64 (2005) 1958-1960
-
(2005)
Neurology
, vol.64
, pp. 1958-1960
-
-
Albanese, A.1
Valente, E.M.2
-
34
-
-
20444377223
-
Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism
-
Li Y., Tomiyama H., Sato K., Hatano Y., Yoshino H., Atsumi M., et al. Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism. Neurology 64 (2005) 1955-1957
-
(2005)
Neurology
, vol.64
, pp. 1955-1957
-
-
Li, Y.1
Tomiyama, H.2
Sato, K.3
Hatano, Y.4
Yoshino, H.5
Atsumi, M.6
-
35
-
-
52649172321
-
Familial Parkinsonism with digenic parkin and PINK1 mutations
-
Funayama M., Li Y., Tsoi T.H., Lam C.W., Ohi T., Yazawa S., et al. Familial Parkinsonism with digenic parkin and PINK1 mutations. Mov Disord 23 (2008) 1461-1465
-
(2008)
Mov Disord
, vol.23
, pp. 1461-1465
-
-
Funayama, M.1
Li, Y.2
Tsoi, T.H.3
Lam, C.W.4
Ohi, T.5
Yazawa, S.6
-
36
-
-
33645130652
-
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
-
Tomiyama H., Li Y., Funayama M., Hasegawa K., Yoshino H., Kubo S.I., 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
Hasegawa, K.4
Yoshino, H.5
Kubo, S.I.6
-
37
-
-
32044466285
-
LRRK2 and Lewy body disease
-
Ross O.A., Toft M., Whittle A.J., Johnson J.L., Papapetropoulos S., Mash D.C., et al. LRRK2 and Lewy body disease. Ann Neurol 59 (2006) 388-393
-
(2006)
Ann Neurol
, vol.59
, pp. 388-393
-
-
Ross, O.A.1
Toft, M.2
Whittle, A.J.3
Johnson, J.L.4
Papapetropoulos, S.5
Mash, D.C.6
-
38
-
-
33750331692
-
LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP
-
Spanaki C., Latsoudis H., and Plaitakis A. LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP. Neurology 67 (2006) 1518-1519
-
(2006)
Neurology
, vol.67
, pp. 1518-1519
-
-
Spanaki, C.1
Latsoudis, H.2
Plaitakis, A.3
-
39
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder E.H., Saunders A.M., Strittmatter W.J., Schmechel D.E., Gaskell P.C., Small G.W., et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261 (1993) 92-93
-
(1993)
Science
, vol.261
, pp. 92-93
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
-
40
-
-
33847007700
-
Apolipoprotein E gene polymorphism, total plasma cholesterol level, and Parkinson disease dementia
-
Jasinska-Myga B., Opala G., Goetz C.G., Tustanowski J., Ochudlo S., Gorzkowska A., et al. Apolipoprotein E gene polymorphism, total plasma cholesterol level, and Parkinson disease dementia. Arch Neurol 64 (2007) 261-265
-
(2007)
Arch Neurol
, vol.64
, pp. 261-265
-
-
Jasinska-Myga, B.1
Opala, G.2
Goetz, C.G.3
Tustanowski, J.4
Ochudlo, S.5
Gorzkowska, A.6
-
42
-
-
74149090734
-
-
Paleacu D, Inzelberg R, Chapman J, Orlov Y, Asherov A, Korczyn AD. Apolipoprotein E ε4 allele does not influence the development of dementia in Parkinsonian patients. In: Fisher IH, Yashida M, editors, Advances in Behavioral Biology, New York, Plenum Press,1998;47:817-821
-
Paleacu D, Inzelberg R, Chapman J, Orlov Y, Asherov A, Korczyn AD. Apolipoprotein E ε4 allele does not influence the development of dementia in Parkinsonian patients. In: Fisher IH, Yashida M, editors, Advances in Behavioral Biology, New York, Plenum Press,1998;47:817-821
-
-
-
-
43
-
-
0032466990
-
Apolipoprotein E4 in Parkinson's disease and dementia: new data and meta-analysis of published studies
-
Inzelberg R., Chapman J., Treves T.A., Asherov A., Kipervasser S., Hilkewicz O., et al. Apolipoprotein E4 in Parkinson's disease and dementia: new data and meta-analysis of published studies. Alz Disease Assoc Disord 12 (1998) 45-48
-
(1998)
Alz Disease Assoc Disord
, vol.12
, pp. 45-48
-
-
Inzelberg, R.1
Chapman, J.2
Treves, T.A.3
Asherov, A.4
Kipervasser, S.5
Hilkewicz, O.6
-
44
-
-
26444534522
-
Apolipoprotein E4 and catechol-O-methyltransferase alleles in autopsy-proven Parkinson's disease: relationship to dementia and hallucinations
-
Camicioli R., Rajput A., Rajput M., Reece C., Payami H., and Hao C. Apolipoprotein E4 and catechol-O-methyltransferase alleles in autopsy-proven Parkinson's disease: relationship to dementia and hallucinations. Mov Disord. 20 (2005) 989-994
-
(2005)
Mov Disord.
, vol.20
, pp. 989-994
-
-
Camicioli, R.1
Rajput, A.2
Rajput, M.3
Reece, C.4
Payami, H.5
Hao, C.6
|