-
1
-
-
0030483182
-
Genetic factors in Alzheimer's disease: A review of recent advances
-
Levy-Lahad E, Bird TD. Genetic factors in Alzheimer's disease: a review of recent advances. Ann Neurol 1996;40:829-840.
-
(1996)
Ann Neurol
, vol.40
, pp. 829-840
-
-
Levy-Lahad, E.1
Bird, T.D.2
-
2
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen KC, Lynch T, Pavolu E, 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, T.2
Pavolu, E.3
-
3
-
-
0024324177
-
Familial dementia with PrP-positive amyloid plaques: A variant of Gerstmann-Straussler syndrome
-
Nochlin D, Sumi SM, Bird TD, et al. Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Straussler syndrome. Neurology 1989;39:910-918.
-
(1989)
Neurology
, vol.39
, pp. 910-918
-
-
Nochlin, D.1
Sumi, S.M.2
Bird, T.D.3
-
4
-
-
0026567475
-
Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala
-
Sumi SM, Bird TD, Nochlin D, Raskind MA. Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala. Neurology 1992;42:120-127.
-
(1992)
Neurology
, vol.42
, pp. 120-127
-
-
Sumi, S.M.1
Bird, T.D.2
Nochlin, D.3
Raskind, M.A.4
-
5
-
-
0342801885
-
Familial aphasic dementia with degeneration of the cerebral cortex, striatum, and substantia nigra
-
Sumi SM, Gambetti P, Bird TD. Familial aphasic dementia with degeneration of the cerebral cortex, striatum, and substantia nigra. Ann Neurol 1991;30:254.
-
(1991)
Ann Neurol
, vol.30
, pp. 254
-
-
Sumi, S.M.1
Gambetti, P.2
Bird, T.D.3
-
6
-
-
0021132642
-
Hereditary dysphasic dementia and the Pick-Alzheimer spectrum
-
Morris JC, Cole M, Banker BQ, Wright D. Hereditary dysphasic dementia and the Pick-Alzheimer spectrum. Ann Neurol 1984;16:455-466.
-
(1984)
Ann Neurol
, vol.16
, pp. 455-466
-
-
Morris, J.C.1
Cole, M.2
Banker, B.Q.3
Wright, D.4
-
7
-
-
0027430805
-
Chromosome-14 and late-onset familial Alzheimer disease (FAD)
-
Schellenberg GD, Payami H, Wijsman EM, et al. Chromosome-14 and late-onset familial Alzheimer disease (FAD). Am J Hum Genet 1993;53:619-628.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 619-628
-
-
Schellenberg, G.D.1
Payami, H.2
Wijsman, E.M.3
-
8
-
-
0029150716
-
A familial Alzheimer's disease locus on chromosome 1
-
Levy-Lahad E, Wijsman EM, Nemens E, et al. A familial Alzheimer's disease locus on chromosome 1. Science 1995;269: 970-973.
-
(1995)
Science
, vol.269
, pp. 970-973
-
-
Levy-Lahad, E.1
Wijsman, E.M.2
Nemens, E.3
-
9
-
-
0016302483
-
Estimation of the recombination fraction in human pedigrees: Efficient computation of likelihood for human linkage studies
-
Ott J. Estimation of the recombination fraction in human pedigrees: efficient computation of likelihood for human linkage studies. Am J Hum Genet 1974;26:588-597.
-
(1974)
Am J Hum Genet
, vol.26
, pp. 588-597
-
-
Ott, J.1
-
10
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer disease locus
-
Levy-Lahad E, Wasco W, Poorkaj P, et al. Candidate gene for the chromosome 1 familial Alzheimer disease locus. Science 1995;269:973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
-
11
-
-
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
-
12
-
-
0029944376
-
The neuropathology of chromosome 17-linked dementia
-
Sima AAF, Defendini R, Keohane C, et al. The neuropathology of chromosome 17-linked dementia. Ann Neurol 1996;39:734-743.
-
(1996)
Ann Neurol
, vol.39
, pp. 734-743
-
-
Sima, A.A.F.1
Defendini, R.2
Keohane, C.3
-
13
-
-
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, Holters EC, et al. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21. Hum Mol Genet 1996;5:151-154.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 151-154
-
-
Wijker, M.1
Wszolek, Z.K.2
Holters, E.C.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
-
-
0029064004
-
Familial progressive subcortical gliosis: Presence of prions and linkage to chromosome 17
-
Petersen RB, Tabaton M, Chen SG, et al. Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17. Neurology 1995;45:1062-1067.
-
(1995)
Neurology
, vol.45
, pp. 1062-1067
-
-
Petersen, R.B.1
Tabaton, M.2
Chen, S.G.3
-
16
-
-
0342801882
-
Hereditary fronto-temporal dementia with linkage to chromosome 17
-
in press
-
Heutink P, Van Swieten J, Stevens M, et al. Hereditary fronto-temporal dementia with linkage to chromosome 17. Ann Neurol 1997 (in press).
-
(1997)
Ann Neurol
-
-
Heutink, P.1
Van Swieten, J.2
Stevens, M.3
-
18
-
-
0019858957
-
Familial dementia of adult onset with pathological findings of a "non-specific" nature
-
Kim RC, Collins GH, Parisi JE, et al. Familial dementia of adult onset with pathological findings of a "non-specific" nature. Brain 1981;104:61-78.
-
(1981)
Brain
, vol.104
, pp. 61-78
-
-
Kim, R.C.1
Collins, G.H.2
Parisi, J.E.3
-
19
-
-
0029119112
-
Familial non-specific dementia maps to chromosome 3
-
Brown J, Ashworth A, Gydesen S, et al. Familial non-specific dementia maps to chromosome 3. Hum Mol Genet 1995;4: 1625-1628.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1625-1628
-
-
Brown, J.1
Ashworth, A.2
Gydesen, S.3
-
20
-
-
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: 42-48.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 42-48
-
-
Spillantini, M.G.1
Crowther, R.A.2
Goedert, M.3
-
21
-
-
19244362853
-
Linkage of frontotemporal dementia to chromosome 17: Clinical and neuropathological characterization of phenotype
-
Yamaoka LH, Welsh-Bohmer KA, Hulette CM, et al. Linkage of frontotemporal dementia to chromosome 17: Clinical and neuropathological characterization of phenotype. Am J Hum Genet 1996;59:1306-1312.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1306-1312
-
-
Yamaoka, L.H.1
Welsh-Bohmer, K.A.2
Hulette, C.M.3
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