-
1
-
-
0027948959
-
Clinical characteristics of a family with chromosome 17 linked disinhibition-dementia-parkinsonism-amyotrophy complex
-
Lynch T, Sano M, Marder KS, et al. Clinical characteristics of a family with chromosome 17 linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology 1994;44:1878-1884.
-
(1994)
Neurology
, vol.44
, pp. 1878-1884
-
-
Lynch, T.1
Sano, M.2
Marder, K.S.3
-
2
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, et al. Association of 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
-
3
-
-
0034081234
-
Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
-
Spillantini MG, Van Sweiten JC, Goedert M. Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Neurogenetics 2000;2:193-205.
-
(2000)
Neurogenetics
, vol.2
, pp. 193-205
-
-
Spillantini, M.G.1
Van Sweiten, J.C.2
Goedert, M.3
-
4
-
-
0003374626
-
Tau protein pathology in neurodegenerative diseases
-
Spillantini MG, Goedert M. Tau protein pathology in neurodegenerative diseases. Trends Neurosci 1998;21:428-433.
-
(1998)
Trends Neurosci.
, vol.21
, pp. 428-433
-
-
Spillantini, M.G.1
Goedert, M.2
-
5
-
-
0032897924
-
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
-
Bird TD, Nochlin D. Poorkaj P, et al. A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L). Brain 1999;122:741-756.
-
(1999)
Brain
, vol.122
, pp. 741-756
-
-
Bird, T.D.1
Nochlin, D.2
Poorkaj, P.3
-
7
-
-
0033059975
-
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
-
Bugiani O, Murrell JR, Giaccone G, et al. Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. J Neuropathol Exp Neurol 1999;58:667-677.
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 667-677
-
-
Bugiani, O.1
Murrell, J.R.2
Giaccone, G.3
-
8
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau-isoforms of hereditary FTDP-17
-
Hong M, Zhukareva V, Vogelsberg-Ragaglia V, et al. Mutation-specific functional impairments in distinct tau-isoforms of hereditary FTDP-17. Science 1998;282:1917-4.
-
(1998)
Science
, vol.282
, pp. 1917-1924
-
-
Hong, M.1
Zhukareva, V.2
Vogelsberg-Ragaglia, V.3
-
9
-
-
0036205905
-
Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene
-
Pickering-Brown SM, Richardson AM, Snowden JS, et al. Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain 2002;125:732-751.
-
(2002)
Brain
, vol.125
, pp. 732-751
-
-
Pickering-Brown, S.M.1
Richardson, A.M.2
Snowden, J.S.3
-
10
-
-
0034756333
-
The genetic and pathological classification of familial frontotemporal dementia
-
Morris HR, Khan MN, Janssen JC, et al. The genetic and pathological classification of familial frontotemporal dementia. Arch Neurol 2001;58:1813-1816.
-
(2001)
Arch. Neurol.
, vol.58
, pp. 1813-1816
-
-
Morris, H.R.1
Khan, M.N.2
Janssen, J.C.3
-
11
-
-
0032724611
-
FTDP-17: An early phenotype with parkinsonism and epileptic seizures caused by a novel mutation
-
Sperfeld AD, Collatz MB, Baier H, et al. FTDP-17: an early phenotype with parkinsonism and epileptic seizures caused by a novel mutation. Ann Neurol 1999;46:708-715.
-
(1999)
Ann. Neurol.
, vol.46
, pp. 708-715
-
-
Sperfeld, A.D.1
Collatz, M.B.2
Baier, H.3
-
12
-
-
0034711149
-
A Japanese patient with frontotemporal dementia and parkinsonism by a Tau P301S mutation
-
Yasuda M, Yokoyama K, Nakayasu T, et al. A Japanese patient with frontotemporal dementia and parkinsonism by a Tau P301S mutation. Neurology 2000;55:1224-1227.
-
(2000)
Neurology
, vol.55
, pp. 1224-1227
-
-
Yasuda, M.1
Yokoyama, K.2
Nakayasu, T.3
-
13
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, 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.D.2
Wijsman, E.3
-
14
-
-
0026775551
-
Rapidly progressive autosomal dominant parkinsonism and dementia with pallidoponto nigral degeneration
-
Wszolek ZK, Pfeiffer RF, Bhatt MH, et al. Rapidly progressive autosomal dominant parkinsonism and dementia with pallidoponto nigral degeneration. Ann Neurol 1992;32:312-320.
-
(1992)
Ann. Neurol.
, vol.32
, pp. 312-320
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Bhatt, M.H.3
-
15
-
-
0001124925
-
Magnetic resonance imaging studies in rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto nigral degeneration
-
Cordes M, Wszolek ZK, Calne DB, Rodnitzky RL, Pfeiffer RF. Magnetic resonance imaging studies in rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto nigral degeneration. Neurodegeneration 1992;1:217-224.
-
(1992)
Neurodegeneration
, vol.1
, pp. 217-224
-
-
Cordes, M.1
Wszolek, Z.K.2
Calne, D.B.3
Rodnitzky, R.L.4
Pfeiffer, R.F.5
-
16
-
-
9044220964
-
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral-degeneration to chromosome 17q21
-
Wijker M, Wszolek ZK, Wolters E, et al. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral-degeneration to chromosome 17q21. Hum Mol Gen 1996;1:151-154.
-
(1996)
Hum. Mol. Gen.
, vol.1
, pp. 151-154
-
-
Wijker, M.1
Wszolek, Z.K.2
Wolters, E.3
-
17
-
-
0035116282
-
Positron emission tomography in pallido-ponto nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene)
-
Pal PK, Wszolek DK, Kishore A, et al. Positron emission tomography in pallido-ponto nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene). Parkinsonism Relat Disord 2001; 7:81-88.
-
(2001)
Parkinsonism Relat. Disord.
, vol.7
, pp. 81-88
-
-
Pal, P.K.1
Wszolek, D.K.2
Kishore, A.3
-
18
-
-
0032976201
-
From genotype to phenotype: A clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
-
Nasreddine ZS, Loginov M, Clark LN, et al. From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation. Ann Neurol 1999;45:704-715.
-
(1999)
Ann. Neurol.
, vol.45
, pp. 704-715
-
-
Nasreddine, Z.S.1
Loginov, M.2
Clark, L.N.3
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