-
1
-
-
0001855752
-
Pathological findings in epilepsy
-
Engel Jr. J. (Ed), Raven Press, New York
-
Babb T.L., and Brown W.J. Pathological findings in epilepsy. In: Engel Jr. J. (Ed). Surgical Treatment of the Epilepsies (1987), Raven Press, New York 511-540
-
(1987)
Surgical Treatment of the Epilepsies
, pp. 511-540
-
-
Babb, T.L.1
Brown, W.J.2
-
2
-
-
18144416596
-
The presence of valine at residue 129 in human prion protein accelerates amyloid formation
-
Baskakov I., Disterer P., Breydo L., Shaw M., Gill A., James W., and Tahiri-Alaoui A. The presence of valine at residue 129 in human prion protein accelerates amyloid formation. FEBS Lett. 44 (2005) 6776-6787
-
(2005)
FEBS Lett.
, vol.44
, pp. 6776-6787
-
-
Baskakov, I.1
Disterer, P.2
Breydo, L.3
Shaw, M.4
Gill, A.5
James, W.6
Tahiri-Alaoui, A.7
-
3
-
-
0035833934
-
Genetic association studies: genes in search of diseases
-
Bird T.D., Jarvik G.P., and Wood N.W. Genetic association studies: genes in search of diseases. Neurology 57 7 (2001) 1153-1154
-
(2001)
Neurology
, vol.57
, Issue.7
, pp. 1153-1154
-
-
Bird, T.D.1
Jarvik, G.P.2
Wood, N.W.3
-
4
-
-
0034872877
-
Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene
-
Bratosiewicz J., Liberski P.P., Kulczycki J., and Kordek R. Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene. Acta Neurobiol. Exp. (Warsz) 61 3 (2001) 151-156
-
(2001)
Acta Neurobiol. Exp. (Warsz)
, vol.61
, Issue.3
, pp. 151-156
-
-
Bratosiewicz, J.1
Liberski, P.P.2
Kulczycki, J.3
Kordek, R.4
-
5
-
-
5644302491
-
High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC
-
Castro R.M., Landemberger M.C., Walz R., Carlotti Jr. C.G., Huang N., Cunha D.R., Moura R., Caballero O.L., Sakamoto A.C., Nitrini R., Brentani R.R., and Martins V.R. High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC. J. Neurosci. Methods 139 2 (2004) 263-269
-
(2004)
J. Neurosci. Methods
, vol.139
, Issue.2
, pp. 263-269
-
-
Castro, R.M.1
Landemberger, M.C.2
Walz, R.3
Carlotti Jr., C.G.4
Huang, N.5
Cunha, D.R.6
Moura, R.7
Caballero, O.L.8
Sakamoto, A.C.9
Nitrini, R.10
Brentani, R.R.11
Martins, V.R.12
-
6
-
-
0025859996
-
Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease
-
Collinge J., Palmer M.S., and Dryden A.J. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 337 8755 (1991) 1441-1442
-
(1991)
Lancet
, vol.337
, Issue.8755
, pp. 1441-1442
-
-
Collinge, J.1
Palmer, M.S.2
Dryden, A.J.3
-
7
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J., Whittington M.A., Sidle K.C., Smith C.J., Palmer M.S., Clarke A.R., and Jefferys J.G. Prion protein is necessary for normal synaptic function. Nature 370 6487 (1994) 295-297
-
(1994)
Nature
, vol.370
, Issue.6487
, pp. 295-297
-
-
Collinge, J.1
Whittington, M.A.2
Sidle, K.C.3
Smith, C.J.4
Palmer, M.S.5
Clarke, A.R.6
Jefferys, J.G.7
-
8
-
-
0041843758
-
Early cognitive decline is associated with prion protein codon 129 polymorphism
-
Croes E.A., Dermaut B., Houwing-Duistermaat J.J., Van den Broeck M., Crust M., Breteler M.M.B., Hofman A., van Broeckhoven C., and van Duijin C.M. Early cognitive decline is associated with prion protein codon 129 polymorphism. Ann Neurol. 54 2 (2003) 275-276
-
(2003)
Ann Neurol.
, vol.54
, Issue.2
, pp. 275-276
-
-
Croes, E.A.1
Dermaut, B.2
Houwing-Duistermaat, J.J.3
Van den Broeck, M.4
Crust, M.5
Breteler, M.M.B.6
Hofman, A.7
van Broeckhoven, C.8
van Duijin, C.M.9
-
9
-
-
0037465373
-
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy
-
Gambardella A., Manna I., Labate A., Chifari R., La Russa A., Serra P., Cittadella R., Bonavita S., Andreoli V., LePiane E., Sasanelli F., Di Costanzo A., Zappia M., Tedeschi G., Aguglia U., and Quattrone A. GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. Neurology 60 4 (2003) 560-563
-
(2003)
Neurology
, vol.60
, Issue.4
, pp. 560-563
-
-
Gambardella, A.1
Manna, I.2
Labate, A.3
Chifari, R.4
La Russa, A.5
Serra, P.6
Cittadella, R.7
Bonavita, S.8
Andreoli, V.9
LePiane, E.10
Sasanelli, F.11
Di Costanzo, A.12
Zappia, M.13
Tedeschi, G.14
Aguglia, U.15
Quattrone, A.16
-
10
-
-
19944433841
-
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy
-
Gambardella A., Aguglia U., Chifari R., Labate A., Manna I., Serra P., Romeo N., Sibilia G., Le Piane E., Russa A.L., Ventura P., Cittadella R., Sasanelli F., Colosimo E., Leggio U., Zappia M., and Quattrone A. ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. Epilepsia 46 1 (2005) 110-117
-
(2005)
Epilepsia
, vol.46
, Issue.1
, pp. 110-117
-
-
Gambardella, A.1
Aguglia, U.2
Chifari, R.3
Labate, A.4
Manna, I.5
Serra, P.6
Romeo, N.7
Sibilia, G.8
Le Piane, E.9
Russa, A.L.10
Ventura, P.11
Cittadella, R.12
Sasanelli, F.13
Colosimo, E.14
Leggio, U.15
Zappia, M.16
Quattrone, A.17
-
11
-
-
0016784773
-
Relative frequency of different types of epilepsy: a study employing the classification of the International League Against Epilepsy
-
Gastaut H., Gastaut J.L., Goncalves e Silva G.E., and Fernandez Sanchez G.R. Relative frequency of different types of epilepsy: a study employing the classification of the International League Against Epilepsy. Epilepsia 16 (1975) 457-461
-
(1975)
Epilepsia
, vol.16
, pp. 457-461
-
-
Gastaut, H.1
Gastaut, J.L.2
Goncalves e Silva, G.E.3
Fernandez Sanchez, G.R.4
-
12
-
-
0033570367
-
Evidence of presynaptic location and function of the prion protein
-
Herms J., Tings T., Gall S., Madlung A., Giese A., Siebert H., Schurmann P., Windl O., Brose N., and Kretzschmar H. Evidence of presynaptic location and function of the prion protein. J. Neurosci. 19 20 (1999) 8866-8875
-
(1999)
J. Neurosci.
, vol.19
, Issue.20
, pp. 8866-8875
-
-
Herms, J.1
Tings, T.2
Gall, S.3
Madlung, A.4
Giese, A.5
Siebert, H.6
Schurmann, P.7
Windl, O.8
Brose, N.9
Kretzschmar, H.10
-
13
-
-
33645001630
-
MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy
-
Labate A., Ventura P., Gambardella A., Le Piane E., Colosimo E., Leggio U., Ambrosio R., Condino F., Messina D., Lanza P., Aguglia U., and Quattrone A. MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy. Neurology 66 4 (2006) 562-566
-
(2006)
Neurology
, vol.66
, Issue.4
, pp. 562-566
-
-
Labate, A.1
Ventura, P.2
Gambardella, A.3
Le Piane, E.4
Colosimo, E.5
Leggio, U.6
Ambrosio, R.7
Condino, F.8
Messina, D.9
Lanza, P.10
Aguglia, U.11
Quattrone, A.12
-
14
-
-
0036470471
-
Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration
-
Mallucci G.R., Ratte S., Asante E.A., Linehan J., Gowland I., Jefferys J.G., and Collinge J. Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration. EMBO J. 21 3 (2002) 202-210
-
(2002)
EMBO J.
, vol.21
, Issue.3
, pp. 202-210
-
-
Mallucci, G.R.1
Ratte, S.2
Asante, E.A.3
Linehan, J.4
Gowland, I.5
Jefferys, J.G.6
Collinge, J.7
-
15
-
-
0037070220
-
Cellular prion protein: on the road for functions
-
Martins V.R., Linden R., Prado M.A., Walz R., Sakamoto A.C., Izquierdo I., and Brentani R.R. Cellular prion protein: on the road for functions. FEBS Lett. 512 1-3 (2002) 25-28
-
(2002)
FEBS Lett.
, vol.512
, Issue.1-3
, pp. 25-28
-
-
Martins, V.R.1
Linden, R.2
Prado, M.A.3
Walz, R.4
Sakamoto, A.C.5
Izquierdo, I.6
Brentani, R.R.7
-
16
-
-
0002511516
-
Hippocampal sclerosis in epilepsy
-
Lüders H. (Ed), Raven Press, New York
-
Meencke H.J., and Veith G. Hippocampal sclerosis in epilepsy. In: Lüders H. (Ed). Epilepsy Surgery (1991), Raven Press, New York 705-715
-
(1991)
Epilepsy Surgery
, pp. 705-715
-
-
Meencke, H.J.1
Veith, G.2
-
17
-
-
0024536973
-
Genetics of the partial epilepsies: a review
-
Ottman R. Genetics of the partial epilepsies: a review. Epilepsia 30 (1989) 107-111
-
(1989)
Epilepsia
, vol.30
, pp. 107-111
-
-
Ottman, R.1
-
18
-
-
0025332889
-
A codon 129 polymorphism in the PRIP gene
-
Owen F., Poulter M., Collinge J., and Crow T.J. A codon 129 polymorphism in the PRIP gene. Nucleic Acids Res. 18 10 (1990) 3103
-
(1990)
Nucleic Acids Res.
, vol.18
, Issue.10
, pp. 3103
-
-
Owen, F.1
Poulter, M.2
Collinge, J.3
Crow, T.J.4
-
19
-
-
0025910229
-
Molecular biology of prion diseases
-
Prusiner S.B. Molecular biology of prion diseases. Science 252 5012 (1991) 1515-1522
-
(1991)
Science
, vol.252
, Issue.5012
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
20
-
-
0030773705
-
A prion-linked psychiatric disorder
-
Samaia H.B., Mari J.J., Vallada H.P., Moura R.P., Simpson A.J., and Brentani R.R. A prion-linked psychiatric disorder. Nature 390 6657 (1997) 241
-
(1997)
Nature
, vol.390
, Issue.6657
, pp. 241
-
-
Samaia, H.B.1
Mari, J.J.2
Vallada, H.P.3
Moura, R.P.4
Simpson, A.J.5
Brentani, R.R.6
-
21
-
-
10744222194
-
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant
-
Walz R., Castro R.M., Velasco T.R., Alexandre Jr. V., Lopes M.H., Leite J.P., Santos A.C., Assirati Jr. J.A., Wichert-Ana L., Terra-Bustamante V.C., Bianchin M.M., Maciag P.C., Ribeiro K.B., Guarnieri R., Araujo D., Cabalero O., Moura R., Salim A.C., Kindlmann K., Landemberger M.C., Marques Jr. W., Fernandes R.M., Serafini L.N., Machado H.R., Carlotti Jr. C.G., Brentani R.R., Sakamoto A.C., and Martins V.R. Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant. Neurology 61 9 (2003) 1204-1210
-
(2003)
Neurology
, vol.61
, Issue.9
, pp. 1204-1210
-
-
Walz, R.1
Castro, R.M.2
Velasco, T.R.3
Alexandre Jr., V.4
Lopes, M.H.5
Leite, J.P.6
Santos, A.C.7
Assirati Jr., J.A.8
Wichert-Ana, L.9
Terra-Bustamante, V.C.10
Bianchin, M.M.11
Maciag, P.C.12
Ribeiro, K.B.13
Guarnieri, R.14
Araujo, D.15
Cabalero, O.16
Moura, R.17
Salim, A.C.18
Kindlmann, K.19
Landemberger, M.C.20
Marques Jr., W.21
Fernandes, R.M.22
Serafini, L.N.23
Machado, H.R.24
Carlotti Jr., C.G.25
Brentani, R.R.26
Sakamoto, A.C.27
Martins, V.R.28
more..
-
22
-
-
3543054070
-
Cortical malformations are associated with a rare polymorphism of cellular prion protein
-
Walz R., Castro R.M., Landemberger M.C., Velasco T.R., Terra-Bustamante V.C., Bastos A.C., Bianchin M., Wichert-Ana L., Araujo D., Alexandre Jr. V., Santos A.C., Machado H.R., Carlotti Jr. C.G., Brentani R.R., Martins V.R., and Sakamoto A.C. Cortical malformations are associated with a rare polymorphism of cellular prion protein. Neurology 63 3 (2004) 557-560
-
(2004)
Neurology
, vol.63
, Issue.3
, pp. 557-560
-
-
Walz, R.1
Castro, R.M.2
Landemberger, M.C.3
Velasco, T.R.4
Terra-Bustamante, V.C.5
Bastos, A.C.6
Bianchin, M.7
Wichert-Ana, L.8
Araujo, D.9
Alexandre Jr., V.10
Santos, A.C.11
Machado, H.R.12
Carlotti Jr., C.G.13
Brentani, R.R.14
Martins, V.R.15
Sakamoto, A.C.16
-
23
-
-
0032806450
-
Increased sensitivity to seizures in mice lacking cellular prion protein
-
Walz R., Amaral O.B., Rockenbach I.C., Roesler R., Izquierdo I., Cavalheiro E.A., Martins V.R., and Brentani R.R. Increased sensitivity to seizures in mice lacking cellular prion protein. Epilepsia 40 12 (1999) 1679-1682
-
(1999)
Epilepsia
, vol.40
, Issue.12
, pp. 1679-1682
-
-
Walz, R.1
Amaral, O.B.2
Rockenbach, I.C.3
Roesler, R.4
Izquierdo, I.5
Cavalheiro, E.A.6
Martins, V.R.7
Brentani, R.R.8
-
24
-
-
0036625255
-
Cellular prion protein: implications in seizures and epilepsy
-
Walz R., Castro R.M., Velasco T.R., Carlotti Jr. C.G., Sakamoto A.C., Brentani R.R., and Martins V.R. Cellular prion protein: implications in seizures and epilepsy. Cell. Mol. Neurobiol. 22 3 (2002) 249-257
-
(2002)
Cell. Mol. Neurobiol.
, vol.22
, Issue.3
, pp. 249-257
-
-
Walz, R.1
Castro, R.M.2
Velasco, T.R.3
Carlotti Jr., C.G.4
Sakamoto, A.C.5
Brentani, R.R.6
Martins, V.R.7
|