-
1
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate, A., Chartier-Harlin, M.-C., Mullan, M., Brown, J., Crawford, F., Fidani, L., Giuffra, L., Haynes, A., Irving, N., James, L., Mant, R., Newton, P., Rooke, K., Roques, P., Talbot, C., Pericak-Vance, M., Roses, A., Williamson, R., Rossor, M., Owen, M. and Hardy, J.A., Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease, Nature, 349 (1991) 704-706.
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.-C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.A.21
more..
-
2
-
-
16144367382
-
Presenilin-1 polymorphism and Alzheimer's disease
-
Kehoe, P., Williams, J., Lovestone, S. and Wilcock, G., Owen, M.J. and the UK Alzheimer's Disease Collaborative Group, Presenilin-1 polymorphism and Alzheimer's disease, Lancet, 347 (1996) 1185.
-
(1996)
Lancet
, vol.347
, pp. 1185
-
-
Kehoe, P.1
Williams, J.2
Lovestone, S.3
Wilcock, G.4
Owen, M.J.5
-
3
-
-
0030603564
-
Presenilin-1 polymorphism and Alzheimer's disease
-
Higuchi, S., Muramatsu, T., Matsushita, S., Arai, H. and Sasaki, H., Presenilin-1 polymorphism and Alzheimer's disease, Lancet, 347 (1996) 1186.
-
(1996)
Lancet
, vol.347
, pp. 1186
-
-
Higuchi, S.1
Muramatsu, T.2
Matsushita, S.3
Arai, H.4
Sasaki, H.5
-
4
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad, E., Wasco, W., Poorkaj, P., Romano, D.M., Oshima, J., Pettingell, W.H., Yu, C., Jondro, P.D., Schmidt, S.D., Wang, K., Crowley, A.C., Fu, Y.-H., Guenette, S.Y., Galas, D., Nemens, E., Wijsman, E.M., Bird, T.D., Schellenberg, G.D. and Tanzi, R.E., Candidate gene for the chromosome 1 familial Alzheimer's disease locus, Science, 269 (1995) 973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, W.H.6
Yu, C.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
Crowley, A.C.11
Fu, Y.-H.12
Guenette, S.Y.13
Galas, D.14
Nemens, E.15
Wijsman, E.M.16
Bird, T.D.17
Schellenberg, G.D.18
Tanzi, R.E.19
-
5
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services task force on Alzheimer's disease
-
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D. and Stadlan, E.M., Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services task force on Alzheimer's disease, Neurology, 34 (1984) 939-944.
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
6
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev, E.I., Sherrington, R., Rogaeva, E.A., Levesque, G., Ikeda, M., Liang, Y., Chi, H., Lin, C., Holman, K., Tsuda, T., Mar, L., Sorbi, S., Nacmias, B., Piacentini, S., Amaducci, L., Chumakov, I., Cohen, D., Lannfelt, L., Eraser, P.E., Rommens, J.M. and St George-Hyslop, P.H., Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene, Nature, 376 (1995) 775-778.
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Sorbi, S.12
Nacmias, B.13
Piacentini, S.14
Amaducci, L.15
Chumakov, I.16
Cohen, D.17
Lannfelt, L.18
Eraser, P.E.19
Rommens, J.M.20
St George-Hyslop, P.H.21
more..
-
7
-
-
0028997817
-
Apolipoprotein e genotyping in the differential diagnosis, not prediction, of Alzheimer's disease
-
Roses, A.D., Apolipoprotein E genotyping in the differential diagnosis, not prediction, of Alzheimer's disease, Ann. Neurol., 38 (1995) 6-14.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 6-14
-
-
Roses, A.D.1
-
8
-
-
0030603564
-
Presenilin-1 polymorphism and Alzheimer's disease
-
Scott, W.K., Growdon, J.H., Roses, A.D., Haines, J.H. and Pericak-Vance, M.A., Presenilin-1 polymorphism and Alzheimer's disease, Lancet, 347 (1996) 1186-1187.
-
(1996)
Lancet
, vol.347
, pp. 1186-1187
-
-
Scott, W.K.1
Growdon, J.H.2
Roses, A.D.3
Haines, J.H.4
Pericak-Vance, M.A.5
-
9
-
-
0029004341
-
Cloning of a novel gene bearing missense mutations in early familial Alzheimer's disease
-
Sherrington, R., Rogaev, E.I., Liang, Y., Rogaeva, E.A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Holman, K., Tsuda, T., Mar, L., Foncin, J.-F., Bruni, A.C., Montesi, M.P., Sorbi, S., Rainero, I., Pinessi, L., Nee, L., Chumakov, I., Pollen, D., Brookes, A., Sanseau, P., Polinsky, R.J., Wasco, W., Da Silva, H.A.R., Haines, J.L., Pericak-Vance, M.A., Tanzi, R.E., Roses, A.D., Fraser, P.E., Rommens, J.M. and St George-Hyslop, P.H., Cloning of a novel gene bearing missense mutations in early familial Alzheimer's disease, Nature, 375 (1995) 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Foncin, J.-F.12
Bruni, A.C.13
Montesi, M.P.14
Sorbi, S.15
Rainero, I.16
Pinessi, L.17
Nee, L.18
Chumakov, I.19
Pollen, D.20
Brookes, A.21
Sanseau, P.22
Polinsky, R.J.23
Wasco, W.24
Da Silva, H.A.R.25
Haines, J.L.26
Pericak-Vance, M.A.27
Tanzi, R.E.28
Roses, A.D.29
Fraser, P.E.30
Rommens, J.M.31
St George-Hyslop, P.H.32
more..
-
10
-
-
8944241774
-
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant
-
Sherrington, R., Froelich, S., Sorbi, S., Campion, D., Chi, H., Rogaeva, E.A., Levesque, G., Rogaev, E.I., Lin, C., Liang, Y., Ikeda, M., Mar, L., Brice, A., Agid, Y., Percy, M.E., Clerget-Darpoux, F., Piacentini, S., Marcon, G., Nacmias, B., Amaducci, L., Frebourg, T., Lannfelt, L., Rommens, J.M. and St George-Hyslop, P.H., Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant, Hum. Mol. Genet., 5 (1996) 985-988.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 985-988
-
-
Sherrington, R.1
Froelich, S.2
Sorbi, S.3
Campion, D.4
Chi, H.5
Rogaeva, E.A.6
Levesque, G.7
Rogaev, E.I.8
Lin, C.9
Liang, Y.10
Ikeda, M.11
Mar, L.12
Brice, A.13
Agid, Y.14
Percy, M.E.15
Clerget-Darpoux, F.16
Piacentini, S.17
Marcon, G.18
Nacmias, B.19
Amaducci, L.20
Frebourg, T.21
Lannfelt, L.22
Rommens, J.M.23
St George-Hyslop, P.H.24
more..
-
11
-
-
0027205142
-
APP717 and Alzheimer's disease in Italy
-
Sorbi, S., Nacmias, B., Forleo, P., Piacentini, S., Amaducci, L. and Provinciali, L., APP717 and Alzheimer's disease in Italy, Nature Genet., 4 (1993) 10.
-
(1993)
Nature Genet.
, vol.4
, pp. 10
-
-
Sorbi, S.1
Nacmias, B.2
Forleo, P.3
Piacentini, S.4
Amaducci, L.5
Provinciali, L.6
-
12
-
-
0029001744
-
Epistatic effect of APP717 mutation and apolipoprotein e genotype in familial Alzheimer's disease
-
Sorbi, S., Nacmias, B., Forleo, P., Piacentini, S., Latorraca, S. and Amaducci, L., Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease, Ann. Neurol., 38 (1995) 124-127.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 124-127
-
-
Sorbi, S.1
Nacmias, B.2
Forleo, P.3
Piacentini, S.4
Latorraca, S.5
Amaducci, L.6
-
13
-
-
0029157347
-
Missense mutation of S182 gene in families with early onset Alzheimer's disease
-
Sorbi, S., Nacmias, B., Forleo, P., Piacentini, S., Sherrington, R., Rogaev, E., St George-Hyslop, P.H. and Amaducci, L., Missense mutation of S182 gene in families with early onset Alzheimer's disease, Lancet, 346 (1995) 439-440.
-
(1995)
Lancet
, vol.346
, pp. 439-440
-
-
Sorbi, S.1
Nacmias, B.2
Forleo, P.3
Piacentini, S.4
Sherrington, R.5
Rogaev, E.6
St George-Hyslop, P.H.7
Amaducci, L.8
-
14
-
-
0028137052
-
ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease
-
Sorbi, S., Nacmias, B., Forleo, P., Latorraca, S., Gobbini, I., Bracco, L., Piacentini, S. and Amaducci, L., ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease, Neurosci. Lett., 177 (1994) 100-102.
-
(1994)
Neurosci. Lett.
, vol.177
, pp. 100-102
-
-
Sorbi, S.1
Nacmias, B.2
Forleo, P.3
Latorraca, S.4
Gobbini, I.5
Bracco, L.6
Piacentini, S.7
Amaducci, L.8
-
15
-
-
0030028429
-
Genetic association between intronic polymorphism in presenilin-1 gene and late onset Alzheimer's disease
-
Wragg, M. and Hutton, M., Talbot, C. and the Alzheimer's Disease Collaborative Group, Genetic association between intronic polymorphism in presenilin-1 gene and late onset Alzheimer's disease, Lancet, 347 (1996) 509-512.
-
(1996)
Lancet
, vol.347
, pp. 509-512
-
-
Wragg, M.1
Hutton, M.2
Talbot, C.3
|