-
1
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
Conrad C, Andreadis A, Trojanowsky JQ, et al. Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann Neurol 1997;41:277-281
-
(1997)
Ann Neurol
, vol.41
, pp. 277-281
-
-
Conrad, C.1
Andreadis, A.2
Trojanowsky, J.Q.3
-
2
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M, Litvan I, Houlden H, et al. Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum Mol Genet 1999;8:711-715
-
(1999)
Hum Mol Genet
, vol.8
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
-
3
-
-
0031869343
-
Significant changes in the σ A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection
-
Oliva R, Tolosa E, Ezquerra M, et al. Significant changes in the σ A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection. Arch Neurol 1998;55: 1122-1124
-
(1998)
Arch Neurol
, vol.55
, pp. 1122-1124
-
-
Oliva, R.1
Tolosa, E.2
Ezquerra, M.3
-
4
-
-
0018372161
-
Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia
-
Wisniewski K, Jervis GA, Moretz RC, Wisniewski HM. Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia. Ann Neurol 1979;5:288-294
-
(1979)
Ann Neurol
, vol.5
, pp. 288-294
-
-
Wisniewski, K.1
Jervis, G.A.2
Moretz, R.C.3
Wisniewski, H.M.4
-
5
-
-
0027178388
-
Dementia in Parkinson's disease: Biochemical evidence for cortical involvement using the immunodetection of abnormal tau proteins
-
Vermersch P, Delacourte A, Javoy-Agid F, et al. Dementia in Parkinson's disease: biochemical evidence for cortical involvement using the immunodetection of abnormal tau proteins. Ann Neurol 1993;33:445-450
-
(1993)
Ann Neurol
, vol.33
, pp. 445-450
-
-
Vermersch, P.1
Delacourte, A.2
Javoy-Agid, F.3
-
6
-
-
0031719117
-
Alzheimer's disease and Parkinson's disease: Distinct entities or extremes of a spectrum of neurodegeneration?
-
Perl DP, Olanow CW, Calne D. Alzheimer's disease and Parkinson's disease: distinct entities or extremes of a spectrum of neurodegeneration? Ann Neurol 1998;44(Suppl 1):S19-S31
-
(1998)
Ann Neurol
, vol.44
, Issue.SUPPL. 1
-
-
Perl, D.P.1
Olanow, C.W.2
Calne, D.3
-
7
-
-
0024343410
-
Parkinsonism and neurofibrillary tangle pathology in pigmented nuclei
-
Rajput AH, Uitti RJ, Stidhakar S, Rozdilsky B. Parkinsonism and neurofibrillary tangle pathology in pigmented nuclei. Ann Neurol 1989;25:602-606
-
(1989)
Ann Neurol
, vol.25
, pp. 602-606
-
-
Rajput, A.H.1
Uitti, R.J.2
Stidhakar, S.3
Rozdilsky, B.4
-
8
-
-
0023898945
-
The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
-
Gibb WRG, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988;51:745-752
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, pp. 745-752
-
-
Gibb, W.R.G.1
Lees, A.J.2
-
9
-
-
0030056696
-
Risk of Parkinson's disease among first-degree relatives: A community-based study
-
Marder K, Tang MX, Mejia H, et al. Risk of Parkinson's disease among first-degree relatives: a community-based study. Neurology 1996;47:155-160
-
(1996)
Neurology
, vol.47
, pp. 155-160
-
-
Marder, K.1
Tang, M.X.2
Mejia, H.3
-
10
-
-
0033554882
-
α1-antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease
-
Muñoz E, Obach V, Oliva R, et al. α1-Antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease. Neurology 1999;52:297-301
-
(1999)
Neurology
, vol.52
, pp. 297-301
-
-
Muñoz, E.1
Obach, V.2
Oliva, R.3
-
12
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group
-
McKhann G, Drackman D, Folstein M, et al. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group. Neurology 1984;34:939-944
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drackman, D.2
Folstein, M.3
-
13
-
-
0026629509
-
What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study
-
Hughes AJ, Ben-Shlomo Y, Daniel SE, Lees AJ. What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. Neurology 1992;42:1142-1146
-
(1992)
Neurology
, vol.42
, pp. 1142-1146
-
-
Hughes, A.J.1
Ben-Shlomo, Y.2
Daniel, S.E.3
Lees, A.J.4
-
14
-
-
0001384856
-
Tau intronic polymorphism in Parkinson's disease and progressive supranuclear palsy
-
Abstract
-
Lazzarini AM, Golhe LI, Dennis NJ, et al. Tau intronic polymorphism in Parkinson's disease and progressive supranuclear palsy. Neurology 1997;48:A427 (Abstract)
-
(1997)
Neurology
, vol.48
-
-
Lazzarini, A.M.1
Golhe, L.I.2
Dennis, N.J.3
-
15
-
-
0032892668
-
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases
-
Morris HK, Janssen JC, Bandmann O, et al. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. J Neurol Neurosurg Psychiatry 1999;66:665-667
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.66
, pp. 665-667
-
-
Morris, H.K.1
Janssen, J.C.2
Bandmann, O.3
-
16
-
-
0024551353
-
The presence of tau distinguishes Lewy bodies of diffuse Lewy body disease from those of idiopathic Parkinson's disease
-
Galloway PG, Bergeron C, Perry G. The presence of tau distinguishes Lewy bodies of diffuse Lewy body disease from those of idiopathic Parkinson's disease. Neurosci Lett 1989;100:6-10
-
(1989)
Neurosci Lett
, vol.100
, pp. 6-10
-
-
Galloway, P.G.1
Bergeron, C.2
Perry, G.3
-
17
-
-
0032543684
-
Association of a missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P. et al. Association of a missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998;393:702-705
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
-
18
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird T, Wijsman E, et al. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 1998;43:815-825
-
(1998)
Ann Neurol
, vol.43
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.2
Wijsman, E.3
-
19
-
-
0031045491
-
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families
-
Heutink P, Stevens M, Rizzu P, et al. Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families. Ann Neurol 1997;41:150-159
-
(1997)
Ann Neurol
, vol.41
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
-
20
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen KC, Lynch E, Pavlou M, et al. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 1994;55:1159-1165
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1159-1165
-
-
Wilhelmsen, K.C.1
Lynch, E.2
Pavlou, M.3
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