-
1
-
-
78651171840
-
Symptomatic occult hydrocephalus with 'normal' cerebrospinal fluid pressure. A treatable syndrome
-
Adams R.D., Fisher C.M., Hakim S., Ojemann R.G., Sweet W.H. Symptomatic occult hydrocephalus with 'normal' cerebrospinal fluid pressure. A treatable syndrome. N. Engl. J. Med. 273:1965;117-126.
-
(1965)
N. Engl. J. Med.
, vol.273
, pp. 117-126
-
-
Adams, R.D.1
Fisher, C.M.2
Hakim, S.3
Ojemann, R.G.4
Sweet, W.H.5
-
2
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder E.H., Saunders A.M., Strittmatter W.J., Schmechel D.E., Gaskel P.C., Small G.W., Roses A.D., Haines J.L., Pericak-Vance M.A. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 261:1993;921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskel, P.C.5
Small, G.W.6
Roses, A.D.7
Haines, J.L.8
Pericak-Vance, M.A.9
-
4
-
-
84965186510
-
Communicating hydrocephalus from subarachnoid bleeding
-
Foltz E.L., Ward A.A. Communicating hydrocephalus from subarachnoid bleeding. J. Neurosurg. 13:1956;546-548.
-
(1956)
J. Neurosurg.
, vol.13
, pp. 546-548
-
-
Foltz, E.L.1
Ward, A.A.2
-
5
-
-
0014635442
-
Pre and post-operative evaluation of cerebral blood flow in low-pressure hydrocephalus
-
Greitz T.V.B., Grepe A.O.L., Kalmar M.S.F. Pre and post-operative evaluation of cerebral blood flow in low-pressure hydrocephalus. J. Neurosurg. 31:1969;644-651.
-
(1969)
J. Neurosurg.
, vol.31
, pp. 644-651
-
-
Greitz, T.V.B.1
Grepe, A.O.L.2
Kalmar, M.S.F.3
-
6
-
-
0013785967
-
The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics
-
Hakim S., Adams R.D. The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics. J. Neurol. Sci. 2:1965;307-327.
-
(1965)
J. Neurol. Sci.
, vol.2
, pp. 307-327
-
-
Hakim, S.1
Adams, R.D.2
-
7
-
-
0030066605
-
Apolipoprotein E polymorphism in patients with different neurodegenerative disorders
-
Helisalmi S., Linnaranta K., Lehtovirta M., Mannermaa A., Heinonen O., Ryynanen M., Riekkinen P., Soininen H. Apolipoprotein E polymorphism in patients with different neurodegenerative disorders. Neurosci. Lett. 205:1996;61-64.
-
(1996)
Neurosci. Lett.
, vol.205
, pp. 61-64
-
-
Helisalmi, S.1
Linnaranta, K.2
Lehtovirta, M.3
Mannermaa, A.4
Heinonen, O.5
Ryynanen, M.6
Riekkinen, P.7
Soininen, H.8
-
8
-
-
0023633020
-
MR findings in normal-pressure hydrocephalus: Significance and comparison with other forms of dementia
-
Jack C.R., Mokri B., Laws E.R., Houser O.W., Baker H.L., Petersen R.C. MR findings in normal-pressure hydrocephalus: significance and comparison with other forms of dementia. J. Comput. Assist. Tomogr. 11:1987;923-931.
-
(1987)
J. Comput. Assist. Tomogr.
, vol.11
, pp. 923-931
-
-
Jack, C.R.1
Mokri, B.2
Laws, E.R.3
Houser, O.W.4
Baker, H.L.5
Petersen, R.C.6
-
10
-
-
0029662327
-
1-antichymotrypsin polymorphism in Alzheimer's disease
-
1-antichymotrypsin polymorphism in Alzheimer's disease. Ann. Neurol. 40:1996;678-680.
-
(1996)
Ann. Neurol.
, vol.40
, pp. 678-680
-
-
Nacmias, B.1
Tedde, A.2
Latorraca, S.3
Piacentini, S.4
Bracco, L.5
Amaducci, L.6
Guarnieri, M.G.7
Petruzzi, C.8
Ortenzi, L.9
Sorbi, S.10
-
11
-
-
0028346903
-
Apolipoprotein E4 and Alzheimer's disease pathology in Lewy body disease and other β-amyloid-forming diseases
-
Pickering-Brown S.M., Mann D.M.A., Bourke J.P., Roberts D.A., Balderson D., Burns A., Byrne J., Owen F. Apolipoprotein E4 and Alzheimer's disease pathology in Lewy body disease and other β-amyloid-forming diseases. Lancet. 343:1994;1155.
-
(1994)
Lancet
, vol.343
, pp. 1155
-
-
Pickering-Brown, S.M.1
Mann, D.M.A.2
Bourke, J.P.3
Roberts, D.A.4
Balderson, D.5
Burns, A.6
Byrne, J.7
Owen, F.8
-
12
-
-
0027337858
-
Apolipoprotein E ε4 allele distribution in late-onset Alzheimer's disease and in other amyloid-forming diseases
-
Saunders A.M., Schmader K., Breitner J.C.S., Benson M.D., Brown W.T., Goldfarb L., Goldgaber D., Manwaring M.G., Szymanski M.H., McCown N., Schmechel D.E., Strittmatter W.J., Pericak-Vance M.A., Roses A.D. Apolipoprotein E ε4 allele distribution in late-onset Alzheimer's disease and in other amyloid-forming diseases. Lancet. 342:1993;710-711.
-
(1993)
Lancet
, vol.342
, pp. 710-711
-
-
Saunders, A.M.1
Schmader, K.2
Breitner, J.C.S.3
Benson, M.D.4
Brown, W.T.5
Goldfarb, L.6
Goldgaber, D.7
Manwaring, M.G.8
Szymanski, M.H.9
McCown, N.10
Schmechel, D.E.11
Strittmatter, W.J.12
Pericak-Vance, M.A.13
Roses, A.D.14
-
13
-
-
0029036661
-
Apolipoprotein E genotype in diverse neurodegenerative disorders
-
Schneider J.A., Gearing M., Robbins R.S., de l'Aune W., Mirra S.S. Apolipoprotein E genotype in diverse neurodegenerative disorders. Ann. Neurol. 38:1995;131-135.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 131-135
-
-
Schneider, J.A.1
Gearing, M.2
Robbins, R.S.3
De L'Aune, W.4
Mirra, S.S.5
-
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
-
-
0031046087
-
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease
-
Sorbi S., Nacmias B., Tedde A., Forleo P., Piacentini S., Latorraca S., Amaducci L. Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. Neurosci. Lett. 222:1997;132-134.
-
(1997)
Neurosci. Lett.
, vol.222
, pp. 132-134
-
-
Sorbi, S.1
Nacmias, B.2
Tedde, A.3
Forleo, P.4
Piacentini, S.5
Latorraca, S.6
Amaducci, L.7
-
16
-
-
0029867041
-
Polymorphism in AACT gene may lower age of onset of Alzheimer's disease
-
Talbot C., Houlden H., Craddock N., Crook R., Huttonn M., Lendon C., Prihar G., Morris J.C., Hardy J., Goate A. Polymorphism in AACT gene may lower age of onset of Alzheimer's disease. NeuroReport. 7:1996;534-536.
-
(1996)
NeuroReport
, vol.7
, pp. 534-536
-
-
Talbot, C.1
Houlden, H.2
Craddock, N.3
Crook, R.4
Huttonn, M.5
Lendon, C.6
Prihar, G.7
Morris, J.C.8
Hardy, J.9
Goate, A.10
-
17
-
-
0030028429
-
Genetic association between intronic polymorphism in Presenilin-1 gene and late onset Alzheimer's disease
-
Wragg M., Hutton M., Talbot C., 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
Alzheimer'S Disease Collaborative Group4
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