-
1
-
-
0000244405
-
Ueber die Beziehungen der senilen Hirnatrophie zur Aphasia
-
Pick A. Ueber die Beziehungen der senilen Hirnatrophie zur Aphasia. Prag Med Wochenschr 1892;17:165-167
-
(1892)
Prag Med Wochenschr
, vol.17
, pp. 165-167
-
-
Pick, A.1
-
2
-
-
33646906138
-
Uber eigenartige Krankheitsfalle des spateren Alters
-
Alzheimer A. Uber eigenartige Krankheitsfalle des spateren Alters. Z Ges Neurol Psychiatr 1911;4:356-385
-
(1911)
Z Ges Neurol Psychiatr
, vol.4
, pp. 356-385
-
-
Alzheimer, A.1
-
3
-
-
0000952928
-
Anatomische Beitrage zur Lehre von der Pickschen umschriebenen Grosshirnrinden-Atrophie ("Picksche Krankheit")
-
Onari K, Spatz H. Anatomische Beitrage zur Lehre von der Pickschen umschriebenen Grosshirnrinden-Atrophie ("Picksche Krankheit"). Z Ges Neurol Psychiatr 1926;101:470-511
-
(1926)
Z Ges Neurol Psychiatr
, vol.101
, pp. 470-511
-
-
Onari, K.1
Spatz, H.2
-
4
-
-
0020037788
-
Slowly progressive aphasia without generalized dementia
-
Mesulam MM. Slowly progressive aphasia without generalized dementia. Ann Neurol 1982;11:592-598
-
(1982)
Ann Neurol
, vol.11
, pp. 592-598
-
-
Mesulam, M.M.1
-
5
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998;51:1546-1554
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
-
6
-
-
1042299821
-
The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994
-
Knopman DS, Petersen RC, Edland SD, Cha RH, Rocca WA. The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994. Neurology 2004;62:506-508
-
(2004)
Neurology
, vol.62
, pp. 506-508
-
-
Knopman, D.S.1
Petersen, R.C.2
Edland, S.D.3
Cha, R.H.4
Rocca, W.A.5
-
8
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998;51:1546-1554
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
-
9
-
-
0031944218
-
Pick's disease, frontotemporal dementia, and Pick complex: Emerging concepts
-
Kertesz A, Munoz D. Pick's disease, frontotemporal dementia, and Pick complex: emerging concepts. Arch Neurol 1998;55:302-304
-
(1998)
Arch Neurol
, vol.55
, pp. 302-304
-
-
Kertesz, A.1
Munoz, D.2
-
10
-
-
0034764622
-
Clinical and pathological diagnosis of frontotemporal dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease
-
McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ. Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 2001;58:1803-1809
-
(2001)
Arch Neurol
, vol.58
, pp. 1803-1809
-
-
McKhann, G.M.1
Albert, M.S.2
Grossman, M.3
Miller, B.4
Dickson, D.5
Trojanowski, J.Q.6
-
11
-
-
0035375621
-
Clinicoanatomic studies in dysarthria: Review, critique, and directions for research
-
Kent RD, Duffy JR, Slama A, Kent JF, Clift A. Clinicoanatomic studies in dysarthria: review, critique, and directions for research. J Speech Lang Hear Res 2001;44:535-551
-
(2001)
J Speech Lang Hear Res
, vol.44
, pp. 535-551
-
-
Kent, R.D.1
Duffy, J.R.2
Slama, A.3
Kent, J.F.4
Clift, A.5
-
12
-
-
0035071053
-
Primary progressive aphasia
-
Mesulam MM. Primary progressive aphasia. Ann Neurol 2001;49:425-432
-
(2001)
Ann Neurol
, vol.49
, pp. 425-432
-
-
Mesulam, M.M.1
-
13
-
-
25444460934
-
Natural history of primary progressive aphasia
-
Le Rhun E, Richard F, Pasquier F. Natural history of primary progressive aphasia. Neurology 2005;65:887-891
-
(2005)
Neurology
, vol.65
, pp. 887-891
-
-
Le Rhun, E.1
Richard, F.2
Pasquier, F.3
-
14
-
-
0034530634
-
Molecular genetics of chromosome 17 tauopathies
-
Hutton M. Molecular genetics of chromosome 17 tauopathies. Ann NY Acad Sci 2000;920:63-73
-
(2000)
Ann NY Acad Sci
, vol.920
, pp. 63-73
-
-
Hutton, M.1
-
15
-
-
0030977392
-
-
Foster NL, Wilhelmsen K, Sima AA, Jones MZ, D'Amato CJ, Gilman S. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants. Ann Neurol 1997;41:706-715
-
(1997)
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference. Conference Participants. Ann Neurol
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
-
17
-
-
0037595526
-
Cognitive impairment, frontotemporal dementia, and the motor neuron diseases
-
Strong MJ, Lomen-Hoerth C, Caselli RJ, Bigio E, Yang W. Cognitive impairment, frontotemporal dementia, and the motor neuron diseases. Ann Neurol 2003;54(suppl 5):S20-S23
-
(2003)
Ann Neurol
, vol.54
, Issue.SUPPL. 5
-
-
Strong, M.J.1
Lomen-Hoerth, C.2
Caselli, R.J.3
Bigio, E.4
Yang, W.5
-
18
-
-
0033546981
-
Pathologic heterogeneity in clinically diagnosed corticobasal degeneration
-
Boeve BF, Maraganore DM, Parisi JE, et al. Pathologic heterogeneity in clinically diagnosed corticobasal degeneration. Neurology 1999;53:795-800
-
(1999)
Neurology
, vol.53
, pp. 795-800
-
-
Boeve, B.F.1
Maraganore, D.M.2
Parisi, J.E.3
-
19
-
-
33645729013
-
Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP
-
Josephs KA, Petersen RC, Knopman DS, et al. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP. Neurology 2006;66:41-48
-
(2006)
Neurology
, vol.66
, pp. 41-48
-
-
Josephs, K.A.1
Petersen, R.C.2
Knopman, D.S.3
-
20
-
-
0038270733
-
Laboratory investigations and treatment in frontotemporal dementia
-
Pasquier F, Fukui T, Sarazin M, et al. Laboratory investigations and treatment in frontotemporal dementia. Ann Neurol 2003;54(suppl 5):S32-S35
-
(2003)
Ann Neurol
, vol.54
, Issue.SUPPL. 5
-
-
Pasquier, F.1
Fukui, T.2
Sarazin, M.3
-
21
-
-
33645828452
-
Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration
-
Whitwell JL, Jack CR Jr, Senjem ML, Josephs KA. Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration. Neurology 2006;66:102-104
-
(2006)
Neurology
, vol.66
, pp. 102-104
-
-
Whitwell, J.L.1
Jack Jr, C.R.2
Senjem, M.L.3
Josephs, K.A.4
-
22
-
-
22844452585
-
Different patterns of magnetic resonance imaging atrophy for frontotemporal lobar degeneration syndromes
-
Short RA, Broderick DF, Patton A, Arvanitakis Z, Graff-Radford NR. Different patterns of magnetic resonance imaging atrophy for frontotemporal lobar degeneration syndromes. Arch Neurol 2005;62:1106-1110
-
(2005)
Arch Neurol
, vol.62
, pp. 1106-1110
-
-
Short, R.A.1
Broderick, D.F.2
Patton, A.3
Arvanitakis, Z.4
Graff-Radford, N.R.5
-
23
-
-
0016211732
-
Pick's disease: Histological and clinical correlations
-
Constantinidis J, Richard J, Tissot R. Pick's disease: histological and clinical correlations. Eur Neurol 1974;11:208-217
-
(1974)
Eur Neurol
, vol.11
, pp. 208-217
-
-
Constantinidis, J.1
Richard, J.2
Tissot, R.3
-
25
-
-
0038270736
-
The neuropathology and biochemistry of frontotemporal dementia
-
Munoz DG, Dickson DW, Bergeron C, Mackenzie I, Delacourte A, Zhukareva V. The neuropathology and biochemistry of frontotemporal dementia. Ann Neurol 2003;54(suppl 5):S24-S28
-
(2003)
Ann Neurol
, vol.54
, Issue.SUPPL. 5
-
-
Munoz, D.G.1
Dickson, D.W.2
Bergeron, C.3
Mackenzie, I.4
Delacourte, A.5
Zhukareva, V.6
-
26
-
-
0025341975
-
Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
-
Knopman DS, Mastri AR, Frey WH II, Sung JH, Rustan T. Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia. Neurology 1990;40:251-256
-
(1990)
Neurology
, vol.40
, pp. 251-256
-
-
Knopman, D.S.1
Mastri, A.R.2
Frey II, W.H.3
Sung, J.H.4
Rustan, T.5
-
27
-
-
12244259054
-
Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cM interval
-
Rademakers R, Cruts M, Dermaut B, et al. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. Mol Psychiatry 2002;7:1064-1074
-
(2002)
Mol Psychiatry
, vol.7
, pp. 1064-1074
-
-
Rademakers, R.1
Cruts, M.2
Dermaut, B.3
-
28
-
-
23044471011
-
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
-
Skibinski G, Parkinson NJ, Brown JM, et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet 2005;37:806-808
-
(2005)
Nat Genet
, vol.37
, pp. 806-808
-
-
Skibinski, G.1
Parkinson, N.J.2
Brown, J.M.3
-
29
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
Hosler BA, Siddique T, Sapp PC, et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA 2000;284:1664-1669
-
(2000)
JAMA
, vol.284
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
-
30
-
-
18244381306
-
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
-
Kovach MJ, Waggoner B, Leal SM, et al. Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Mol Genet Metab 2001;74:458-475
-
(2001)
Mol Genet Metab
, vol.74
, pp. 458-475
-
-
Kovach, M.J.1
Waggoner, B.2
Leal, S.M.3
-
31
-
-
27744488802
-
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy
-
Rademakers R, Melquist S, Cruts M, et al. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy. Hum Mol Genet 2005;14:3281-3292
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3281-3292
-
-
Rademakers, R.1
Melquist, S.2
Cruts, M.3
-
32
-
-
24644502474
-
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration
-
Pittman AM, Myers AJ, Abou-Sleiman P, et al. Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration. J Med Genet 2005;42:837-846
-
(2005)
J Med Genet
, vol.42
, pp. 837-846
-
-
Pittman, A.M.1
Myers, A.J.2
Abou-Sleiman, P.3
-
33
-
-
33846913146
-
Presenilin mutations: Variations in the behavioral phenotype with an emphasis on the frontotemporal dementia phenotype
-
Cummings J, Hardy J, Poncet M, Christen Y, eds, Berlin: Springer-Verlag;
-
Graff-Radford N. Presenilin mutations: variations in the behavioral phenotype with an emphasis on the frontotemporal dementia phenotype. In: Cummings J, Hardy J, Poncet M, Christen Y, eds. Genotype-Proteotype-Phenotype Relationships on Neurodegenerative Diseases. Berlin: Springer-Verlag; 2005:93-101
-
(2005)
Genotype-Proteotype-Phenotype Relationships on Neurodegenerative Diseases
, pp. 93-101
-
-
Graff-Radford, N.1
-
34
-
-
0034788203
-
Analysis of tauopathies with transgenic mice
-
Hutton M, Lewis J, Dickson D, Yen SH, McGowan E. Analysis of tauopathies with transgenic mice. Trends Mol Med 2001;7:467-470
-
(2001)
Trends Mol Med
, vol.7
, pp. 467-470
-
-
Hutton, M.1
Lewis, J.2
Dickson, D.3
Yen, S.H.4
McGowan, E.5
|