-
1
-
-
0023194309
-
Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis
-
Gustafson L. Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis. Arch Gerontol Geriatr 1987;6:209-23.
-
(1987)
Arch Gerontol Geriatr
, vol.6
, pp. 209-223
-
-
Gustafson, L.1
-
3
-
-
0026091772
-
Frontal lobe degeneration: Clinical, neuropsychological, and SPECT characteristics
-
Miller DL, Cummings JL, Villanueva-Meyer J, Boone K, Mehringer CM, Lesser IM, et al. Frontal lobe degeneration: Clinical, neuropsychological, and SPECT characteristics. Neurology 1991;41:1374-82.
-
(1991)
Neurology
, vol.41
, pp. 1374-1382
-
-
Miller, D.L.1
Cummings, J.L.2
Villanueva-Meyer, J.3
Boone, K.4
Mehringer, C.M.5
Lesser, I.M.6
-
4
-
-
0028223015
-
Clinical and neuropathological criteria for frontotemporal dementia
-
The Lund and Manchester Groups. Clinical and neuropathological criteria for frontotemporal dementia. J Neurol Neurosurg Psychiatry 1994;57:416-8.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 416-418
-
-
-
5
-
-
0042996783
-
Chromosome 17-linked dementias
-
Markesbery WR, editor. New York: Oxford University Press
-
Wilhelmsen KC, Clark LN. Chromosome 17-linked dementias. In: Markesbery WR, editor. Neuropathology of dementing disorders. New York: Oxford University Press, 1998.
-
(1998)
Neuropathology of Dementing Disorders
-
-
Wilhelmsen, K.C.1
Clark, L.N.2
-
6
-
-
0014097167
-
Progressive subcortical gliosis, a rare form of presenile dementia
-
Neumann MA, Cohn R. Progressive subcortical gliosis, a rare form of presenile dementia. Brain 1967;90:405-18.
-
(1967)
Brain
, vol.90
, pp. 405-418
-
-
Neumann, M.A.1
Cohn, R.2
-
7
-
-
0025156914
-
Dementia of frontal lobe type
-
Neary D. Dementia of frontal lobe type. J Am Geriatr Soc 1990;38: 71-2.
-
(1990)
J Am Geriatr Soc
, vol.38
, pp. 71-72
-
-
Neary, D.1
-
8
-
-
0025341975
-
Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
-
Knopman DS, Mastri AR, Frey WH, Sung JH, Rustan T. Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia. Neurology 1990;40:251-6.
-
(1990)
Neurology
, vol.40
, pp. 251-256
-
-
Knopman, D.S.1
Mastri, A.R.2
Frey, W.H.3
Sung, J.H.4
Rustan, T.5
-
9
-
-
0039267660
-
Identification of a kindred with autosomal dominant thaIamic dementia
-
Wilhelmsen KC, Defendini R, Dooneief G, Bell K, Marder K, Sano M, et al. Identification of a kindred with autosomal dominant thaIamic dementia. Neurology 1991;41(1 Suppl):176.
-
(1991)
Neurology
, vol.41
, Issue.1 SUPPL.
, pp. 176
-
-
Wilhelmsen, K.C.1
Defendini, R.2
Dooneief, G.3
Bell, K.4
Marder, K.5
Sano, M.6
-
10
-
-
0028324209
-
Familial dementia with Pick cells: A case report of probable Pick's disease
-
Gaughran F, Keohane C, Buckley M. Familial dementia with Pick cells: A case report of probable Pick's disease. Ir J Psychol Med 1994; 11:34-8.
-
(1994)
Ir J Psychol Med
, vol.11
, pp. 34-38
-
-
Gaughran, F.1
Keohane, C.2
Buckley, M.3
-
11
-
-
4244190337
-
The clinical and pathologic presentation of Moynihan's disease: Familial dementia-parkinsonism-amyotrophy complex
-
Lynch T, Bell K, Sano M, Marder K, Nygaard TG, Keohane C, et al. The clinical and pathologic presentation of Moynihan's disease: Familial dementia-parkinsonism-amyotrophy complex. Neurology 1994;44(2 Suppl):A260-1.
-
(1994)
Neurology
, vol.44
, Issue.2 SUPPL.
-
-
Lynch, T.1
Bell, K.2
Sano, M.3
Marder, K.4
Nygaard, T.G.5
Keohane, C.6
-
12
-
-
0345221208
-
Hereditary dysphasic dementia (HDD) and disinhibition-dementiaparkinsonism-amyotrophy complex (DDPAC) are linked to the wld locus on chromosome 17q21-22
-
Lynch T, Lendon C, Busfield F, Morris JC, Craddock N, Fahn S, et al. Hereditary dysphasic dementia (HDD) and disinhibition-dementiaparkinsonism-amyotrophy complex (DDPAC) are linked to the wld locus on chromosome 17q21-22. Mov Disord 1996;11(1 Supplement):86.
-
(1996)
Mov Disord
, vol.11
, Issue.1 SUPPL.
, pp. 86
-
-
Lynch, T.1
Lendon, C.2
Busfield, F.3
Morris, J.C.4
Craddock, N.5
Fahn, S.6
-
13
-
-
0028000011
-
A new eponym: Wilhelmsen-Lynch disease
-
Fahn S, Mayeux R, Rowland LP. A new eponym: Wilhelmsen-Lynch disease [letter]. Neurology 1994;44:1980.
-
(1994)
Neurology
, vol.44
, pp. 1980
-
-
Fahn, S.1
Mayeux, R.2
Rowland, L.P.3
-
14
-
-
0344358520
-
Neuronal and glial inclusions in familial progressive limbic lobe sclerosis
-
Abstract
-
Sima AAF, D'Amato C, Foster NL, Lynch T, Defendini R, Wilhelmsen KC. Neuronal and glial inclusions in familial progressive limbic lobe sclerosis. J Neuropathol Exp Neurol 1995;54:459. Abstract.
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 459
-
-
Sima, A.A.F.1
D'Amato, C.2
Foster, N.L.3
Lynch, T.4
Defendini, R.5
Wilhelmsen, K.C.6
-
15
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 1994;55:1159-65.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1159-1165
-
-
Wilhelmsen, K.C.1
Lynch, T.2
Pavlou, E.3
Higgins, M.4
Nygaard, T.G.5
-
16
-
-
0027948959
-
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex
-
Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, et al. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology 1994;44:1878-84.
-
(1994)
Neurology
, vol.44
, pp. 1878-1884
-
-
Lynch, T.1
Sano, M.2
Marder, K.S.3
Bell, K.L.4
Foster, N.L.5
Defendini, R.F.6
-
17
-
-
0019925346
-
Hereditary Pick's disease: Second re-examination of the large family and discussion of other hereditary cases, with particular reference to electroencephalography, a computerized tomography
-
Groen JJ, Endtz LJ. Hereditary Pick's disease: Second re-examination of the large family and discussion of other hereditary cases, with particular reference to electroencephalography, a computerized tomography. Brain 1982;105:443-59.
-
(1982)
Brain
, vol.105
, pp. 443-459
-
-
Groen, J.J.1
Endtz, L.J.2
-
19
-
-
0027272449
-
Clinical picture of frontal lobe degeneration of non-Alzheimer type
-
Gustafson L. Clinical picture of frontal lobe degeneration of non-Alzheimer type. Dementia 1993;4:143-8.
-
(1993)
Dementia
, vol.4
, pp. 143-148
-
-
Gustafson, L.1
-
20
-
-
0031799683
-
Hereditary dysphasic disinhibition dementia: A frontotemporal dementia linked to 17q21-22
-
Lendon CL, Lynch T, Norton J, McKeel DW Jr, Busfield F, Craddock N, et al. Hereditary dysphasic disinhibition dementia: A frontotemporal dementia linked to 17q21-22. Neurology 1998;50: 1546-55.
-
(1998)
Neurology
, vol.50
, pp. 1546-1555
-
-
Lendon, C.L.1
Lynch, T.2
Norton, J.3
McKeel Jr., D.W.4
Busfield, F.5
Craddock, N.6
-
21
-
-
0028040918
-
Familial progressive subcortical gliosis
-
Lanska DJ, Currier RD, Cohen M, Gambetti P, Smith EE, Bebin J, et al. Familial progressive subcortical gliosis. Neurology 1994;44: 1633-43.
-
(1994)
Neurology
, vol.44
, pp. 1633-1643
-
-
Lanska, D.J.1
Currier, R.D.2
Cohen, M.3
Gambetti, P.4
Smith, E.E.5
Bebin, J.6
-
22
-
-
0026775551
-
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration
-
Wszolek ZK, Pfeiffer RF, Bhatt MH, Schelper RL, Cordes M, Snow BJ, et al. Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration. Ann Neurol 1992; 32:312-20.
-
(1992)
Ann Neurol
, vol.32
, pp. 312-320
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Bhatt, M.H.3
Schelper, R.L.4
Cordes, M.5
Snow, B.J.6
-
23
-
-
0030812529
-
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17
-
Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, et al. Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. Am J Hum Genet 1997;61: 1131-8.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1131-1138
-
-
Murrell, J.R.1
Koller, D.2
Foroud, T.3
Goedert, M.4
Spillantini, M.G.5
Edenberg, H.J.6
-
24
-
-
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, Bakker E, Kros JM, Tibben A, et al. Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families. Ann Neurol 1997;41:150-9.
-
(1997)
Ann Neurol
, vol.41
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
Bakker, E.4
Kros, J.M.5
Tibben, A.6
-
25
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
Foster NL, Wilhelmsen K, Sima AAF, Jones MZ, D'Amato C, Gilman S, et al. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference. Ann Neurol 1997;41:706-15.
-
(1997)
Ann Neurol
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.F.3
Jones, M.Z.4
D'Amato, C.5
Gilman, S.6
-
27
-
-
0027422739
-
Examination of the presynaptic dopaminergic system using positron emission tomography in a family with autosomal dominant parkinsonism and dementia due to pallido-ponto-nigral degeneration (PPNO)
-
Berl
-
Cordes M, Wszolek ZK, Pfeiffer RF, Calne DB. Examination of the presynaptic dopaminergic system using positron emission tomography in a family with autosomal dominant parkinsonism and dementia due to pallido-ponto-nigral degeneration (PPNO). Radiol Diagn (Berl) 1993;34:141-5.
-
(1993)
Radiol Diagn
, vol.34
, pp. 141-145
-
-
Cordes, M.1
Wszolek, Z.K.2
Pfeiffer, R.F.3
Calne, D.B.4
-
28
-
-
0030445619
-
A family intervention to delay nursing home placement of patients with Alzheimer's disease: A randomized controlled trial
-
Mittelman MS, Ferris SH, Shulman E, Steinberg G, Levin B. A family intervention to delay nursing home placement of patients with Alzheimer's disease: A randomized controlled trial. JAMA 1996;276: 1725-31.
-
(1996)
JAMA
, vol.276
, pp. 1725-1731
-
-
Mittelman, M.S.1
Ferris, S.H.2
Shulman, E.3
Steinberg, G.4
Levin, B.5
-
29
-
-
0029944376
-
The neuropathology of chromosome 17-linked dementia
-
Sima AA, Defendini R, Keohane C, D'Amato C, Foster NL, Parchi P, et al. The neuropathology of chromosome 17-linked dementia. Ann Neurol 1996;39:734-43.
-
(1996)
Ann Neurol
, vol.39
, pp. 734-743
-
-
Sima, A.A.1
Defendini, R.2
Keohane, C.3
D'Amato, C.4
Foster, N.L.5
Parchi, P.6
-
30
-
-
0031949084
-
Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies
-
Spillantini MG, Bird TD, Ghetti B. Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies. Brain Pathol 1998;8:387-402.
-
(1998)
Brain Pathol
, vol.8
, pp. 387-402
-
-
Spillantini, M.G.1
Bird, T.D.2
Ghetti, B.3
-
31
-
-
0342327018
-
The genetics of Pick complex and adult onset dementia
-
Kertesz A, Munoz DG, editors. New York: Wiley-Liss
-
Clark LN, Wilhelmsen KC. The genetics of Pick complex and adult onset dementia. In: Kertesz A, Munoz DG, editors. Pick's disease and pick complex. New York: Wiley-Liss, 1998.
-
(1998)
Pick's Disease and Pick Complex
-
-
Clark, L.N.1
Wilhelmsen, K.C.2
-
32
-
-
0030000867
-
Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
-
Spillantini MG, Crowther RA, Goedert M. Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles. Acta Neuropathol 1996;92:42-8.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 42-48
-
-
Spillantini, M.G.1
Crowther, R.A.2
Goedert, M.3
-
33
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998;393:702-5.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
-
34
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
U S A
-
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci U S A 1998;95:7737-41.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
35
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, et al. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 1998;43:815-25.
-
(1998)
Ann Neurol
, vol.43
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
-
36
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease
-
Goedert M, Spillantini MG, Jakes R, Rutherford D, Crowther RA. Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron 1989;3:519-26.
-
(1989)
Neuron
, vol.3
, pp. 519-526
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Rutherford, D.4
Crowther, R.A.5
-
37
-
-
0032573083
-
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
U S A
-
Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, et al. Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Proc Natl Acad Sci U S A 1998; 95:13103-7.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 13103-13107
-
-
Clark, L.N.1
Poorkaj, P.2
Wszolek, Z.3
Geschwind, D.H.4
Nasreddine, Z.S.5
Miller, B.6
-
38
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
-
Hong M, Zhukareva V, Vogelsberg-Ragaglia V, Wszolek Z, Reed L, Miller BI, et al. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science 1998;282:1914-7.
-
(1998)
Science
, vol.282
, pp. 1914-1917
-
-
Hong, M.1
Zhukareva, V.2
Vogelsberg-Ragaglia, V.3
Wszolek, Z.4
Reed, L.5
Miller, B.I.6
-
39
-
-
0025863618
-
Neuropathological staging of Alzheimer-related changes
-
Berl
-
Braak H, Braak E. Neuropathological staging of Alzheimer-related changes. Acta Neuropathol (Berl) 1991;82:239-59.
-
(1991)
Acta Neuropathol
, vol.82
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
-
40
-
-
0030681215
-
Consensus recommendations for the postmortem diagnosis of Alzheimer's disease
-
The National Institute on Aging and Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer's Disease. Consensus recommendations for the postmortem diagnosis of Alzheimer's disease. Neurobiol Aging 1997;18:S1-2.
-
(1997)
Neurobiol Aging
, vol.18
-
-
-
41
-
-
0021673238
-
Cortical abnormalities in Alzheimer's disease
-
Foster NL, Chase TN, Mansi L, Brooks R, Fedio P, Patronas N, et al. Cortical abnormalities in Alzheimer's disease. Ann Neurol 1984; 16:649-54.
-
(1984)
Ann Neurol
, vol.16
, pp. 649-654
-
-
Foster, N.L.1
Chase, T.N.2
Mansi, L.3
Brooks, R.4
Fedio, P.5
Patronas, N.6
-
42
-
-
0030771894
-
Huntingtin localization in brains of normal and Huntington's disease patients
-
Sapp E, Schwarz C, Chase K, Bhide PG, Young AB, Penney J, et al. Huntingtin localization in brains of normal and Huntington's disease patients. Ann Neurol 1997;42:604-12.
-
(1997)
Ann Neurol
, vol.42
, pp. 604-612
-
-
Sapp, E.1
Schwarz, C.2
Chase, K.3
Bhide, P.G.4
Young, A.B.5
Penney, J.6
-
43
-
-
0030040304
-
Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions
-
Gilman S, Sima AA, Junck L, Kluin KJ, Koeppe RA, Lohman ME, et al. Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions. Ann Neurol 1996;39:241-55.
-
(1996)
Ann Neurol
, vol.39
, pp. 241-255
-
-
Gilman, S.1
Sima, A.A.2
Junck, L.3
Kluin, K.J.4
Koeppe, R.A.5
Lohman, M.E.6
-
44
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
Conrad C, Andreadis A, Trojanowski JQ, Dickson DW, Kang D, Chen X, et al. Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann Neurol 1997;41:277-81.
-
(1997)
Ann Neurol
, vol.41
, pp. 277-281
-
-
Conrad, C.1
Andreadis, A.2
Trojanowski, J.Q.3
Dickson, D.W.4
Kang, D.5
Chen, X.6
|