-
1
-
-
0034957202
-
A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology
-
J.EngelJr. A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology. Epilepsia2001; 42: 796–803.
-
(2001)
Epilepsia
, vol.42
, pp. 796-803
-
-
Engel, J.1
-
3
-
-
0033054216
-
Effect of precollicular transection on audiogenic seizures in genetically epilepsy-prone rats
-
R.A.BrowningC.WangD.K.Nelson. Effect of precollicular transection on audiogenic seizures in genetically epilepsy-prone rats. Exp Neurol1999; 155: 295–301.
-
(1999)
Exp Neurol
, vol.155
, pp. 295-301
-
-
Browning, R.A.1
Wang, C.2
Nelson, D.K.3
-
4
-
-
0013913719
-
Subcortical mechanisms of audiogenic seizures
-
R.P.Kesner. Subcortical mechanisms of audiogenic seizures. Exp Neurol1966; 15: 192–205.
-
(1966)
Exp Neurol
, vol.15
, pp. 192-205
-
-
Kesner, R.P.1
-
5
-
-
0036020142
-
A critical review on the participation of inferior colliculus in acoustic-motor and acoustic-limbic networks involved in the expression of acute and kindled audiogenic seizures
-
N.Garcia-Cairasco. A critical review on the participation of inferior colliculus in acoustic-motor and acoustic-limbic networks involved in the expression of acute and kindled audiogenic seizures. Hear Res2002; 168: 208–222.
-
(2002)
Hear Res
, vol.168
, pp. 208-222
-
-
Garcia-Cairasco, N.1
-
7
-
-
0023879183
-
Audiogenic seizures in Wistar rats before and after repeated auditory stimuli: clinical, pharmacological, and electroencephalographic studies
-
M.KiesmannC.MarescauxM.Vergnes. Audiogenic seizures in Wistar rats before and after repeated auditory stimuli: clinical, pharmacological, and electroencephalographic studies. J Neural Transm1988; 72: 235–244.
-
(1988)
J Neural Transm
, vol.72
, pp. 235-244
-
-
Kiesmann, M.1
Marescaux, C.2
Vergnes, M.3
-
8
-
-
0032563178
-
Evidence for a unique profile of levetiracetam in rodent models of seizures and epilepsy
-
H.KlitgaardA.MatagneK.Gobert. Evidence for a unique profile of levetiracetam in rodent models of seizures and epilepsy. Eur J Pharmacol1998; 353: 191–206.
-
(1998)
Eur J Pharmacol
, vol.353
, pp. 191-206
-
-
Klitgaard, H.1
Matagne, A.2
Gobert, K.3
-
9
-
-
26944485922
-
Long-lasting antiepileptic effects of levetiracetam against epileptic seizures in the spontaneously epileptic rat (SER): differentiation of levetiracetam from conventional antiepileptic drugs
-
C.Ji-qunK.IshiharaT.Nagayama. Long-lasting antiepileptic effects of levetiracetam against epileptic seizures in the spontaneously epileptic rat (SER): differentiation of levetiracetam from conventional antiepileptic drugs. Epilepsia2005; 46: 1362–1370.
-
(2005)
Epilepsia
, vol.46
, pp. 1362-1370
-
-
Ji-qun, C.1
Ishihara, K.2
Nagayama, T.3
-
10
-
-
0028825031
-
The novel antiepileptic drug levetiracetam (ucb L059) appears to act via a specific binding site in CNS membranes
-
M.NoyerM.GillardA.Matagne. The novel antiepileptic drug levetiracetam (ucb L059) appears to act via a specific binding site in CNS membranes. Eur J Pharmacol1995; 286: 137–146.
-
(1995)
Eur J Pharmacol
, vol.286
, pp. 137-146
-
-
Noyer, M.1
Gillard, M.2
Matagne, A.3
-
11
-
-
1642355074
-
Localization and photoaffinity labelling of the levetiracetam binding site in rat brain and certain cell lines
-
B.FuksM.GillardP.Michel. Localization and photoaffinity labelling of the levetiracetam binding site in rat brain and certain cell lines. Eur J Pharmacol2003; 478: 11–19.
-
(2003)
Eur J Pharmacol
, vol.478
, pp. 11-19
-
-
Fuks, B.1
Gillard, M.2
Michel, P.3
-
12
-
-
0035852626
-
Suppression of post-hypoxic and post encephalitic myoclonus with levetiracetam
-
200;
-
G.L.KraussA.BerginR.E.Kramer. Suppression of post-hypoxic and post encephalitic myoclonus with levetiracetam. Neurology 200; 56: 411–412.
-
Neurology
, vol.56
, pp. 411-412
-
-
Krauss, G.L.1
Bergin, A.2
Kramer, R.E.3
-
13
-
-
39749166363
-
Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures
-
S.NoachtarE.AndermannP.Meyvisch. Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures. Neurology2008; 70: 607–616.
-
(2008)
Neurology
, vol.70
, pp. 607-616
-
-
Noachtar, S.1
Andermann, E.2
Meyvisch, P.3
-
14
-
-
67349156067
-
Levetiracetam as add-on therapy for idiopathic generalized epilepsy syndromes with onset during adolescence: analysis of two randomized, double-blind, placebo-controlled studies
-
W.E.RosenfeldS.BenbadisP.Edrich. Levetiracetam as add-on therapy for idiopathic generalized epilepsy syndromes with onset during adolescence: analysis of two randomized, double-blind, placebo-controlled studies. Epilepsy Res2009; 85: 72–80.
-
(2009)
Epilepsy Res
, vol.85
, pp. 72-80
-
-
Rosenfeld, W.E.1
Benbadis, S.2
Edrich, P.3
-
15
-
-
0020168752
-
Sound and its significance for laboratory animals
-
M.R.Gamble. Sound and its significance for laboratory animals. Biol Rev Camb Philos Soc1982; 57: 395–421.
-
(1982)
Biol Rev Camb Philos Soc
, vol.57
, pp. 395-421
-
-
Gamble, M.R.1
-
17
-
-
84880297409
-
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human
-
N.CharizopoulouA.LelliM.Schraders. Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. Nat Commun2011; 2: 201.
-
(2011)
Nat Commun
, vol.2
, pp. 201
-
-
Charizopoulou, N.1
Lelli, A.2
Schraders, M.3
-
18
-
-
84880364986
-
LGI proteins in the nervous system
-
L.KegelE.AuninD.Meijer. LGI proteins in the nervous system. ASN Neuro2013; 5: 167–181.
-
(2013)
ASN Neuro
, vol.5
, pp. 167-181
-
-
Kegel, L.1
Aunin, E.2
Meijer, D.3
-
19
-
-
84865063217
-
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR cases DFNB98 profound deafness
-
S.DelmaghaniA.AghaieN.Michalski. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR cases DFNB98 profound deafness. Hum Mol Genet2012; 21: 3835–3844.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 3835-3844
-
-
Delmaghani, S.1
Aghaie, A.2
Michalski, N.3
-
20
-
-
84856057629
-
LGI2 truncation causes a remitting focal epilepsy in dogs
-
E.H.SeppäläT.S.JokinenFukata. LGI2 truncation causes a remitting focal epilepsy in dogs. PLoS Genet2011; 7: e1002194.
-
(2011)
PLoS Genet
, vol.7
, pp. e1002194
-
-
Seppälä, E.H.1
Jokinen, T.S.2
Fukata3
-
21
-
-
0035974897
-
A novel gene causing a mendelian audiogenic mouse epilepsy
-
S.L.SkradskiA.M.ClarkH.Jiang. A novel gene causing a mendelian audiogenic mouse epilepsy. Neuron2001; 31: 537–544.
-
(2001)
Neuron
, vol.31
, pp. 537-544
-
-
Skradski, S.L.1
Clark, A.M.2
Jiang, H.3
-
22
-
-
13244261194
-
Vlgr1 knockout mice show audiogenic seizure susceptibility
-
H.YagiY.TakamuraT.Yoneda. Vlgr1 knockout mice show audiogenic seizure susceptibility. J Neurochem2005; 92: 191–202.
-
(2005)
J Neurochem
, vol.92
, pp. 191-202
-
-
Yagi, H.1
Takamura, Y.2
Yoneda, T.3
-
23
-
-
2942633028
-
Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice
-
D.R.McMillanP.C.White. Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice. Mol Cell Neurosci2004; 26: 322–329.
-
(2004)
Mol Cell Neurosci
, vol.26
, pp. 322-329
-
-
McMillan, D.R.1
White, P.C.2
-
24
-
-
16244371351
-
The Mass1 frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC
-
K.R.JohnsonQ.Y.ZhengM.D.Weston. The Mass1 frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC. Genomics2005; 85: 582–590.
-
(2005)
Genomics
, vol.85
, pp. 582-590
-
-
Johnson, K.R.1
Zheng, Q.Y.2
Weston, M.D.3
-
25
-
-
15044357259
-
Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects
-
A.ShahwanM.FarrellN.Delanty. Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects. Lancet Neurol2005; 4: 239–248.
-
(2005)
Lancet Neurol
, vol.4
, pp. 239-248
-
-
Shahwan, A.1
Farrell, M.2
Delanty, N.3
-
27
-
-
77954660164
-
A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund
-
D.N.SandersF.H.FariasG.S.Johnson. A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund. Mol Genet Metab2010; 100: 349–356.
-
(2010)
Mol Genet Metab
, vol.100
, pp. 349-356
-
-
Sanders, D.N.1
Farias, F.H.2
Johnson, G.S.3
-
28
-
-
33748966447
-
A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis
-
T.AwanoM.L.KatzD.P.O’Brien. A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis. Mol Genet Metab2006; 89: 254–260.
-
(2006)
Mol Genet Metab
, vol.89
, pp. 254-260
-
-
Awano, T.1
Katz, M.L.2
O’Brien, D.P.3
-
29
-
-
23244466313
-
A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs
-
S.A.MelvilleC.L.WilsonC.S.Chiang. A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs. Genomics2005; 86: 287–294.
-
(2005)
Genomics
, vol.86
, pp. 287-294
-
-
Melville, S.A.1
Wilson, C.L.2
Chiang, C.S.3
-
30
-
-
79952231932
-
A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis
-
M.L.KatzF.H.FariasD.N.Sanders. A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis. J Biomed Biotechnol2011; 2011: 198042.
-
(2011)
J Biomed Biotechnol
, vol.2011
, pp. 198042
-
-
Katz, M.L.1
Farias, F.H.2
Sanders, D.N.3
-
31
-
-
11144341883
-
A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis
-
M.L.KatzS.KhanT.Awano. A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis. Biochem Biophys Res Commun2005; 327: 541–547.
-
(2005)
Biochem Biophys Res Commun
, vol.327
, pp. 541-547
-
-
Katz, M.L.1
Khan, S.2
Awano, T.3
-
32
-
-
33645130942
-
A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis
-
T.AwanoM.L.KatzD.P.O’Brien. A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis. Mol Genet Metab2006; 87: 341–348.
-
(2006)
Mol Genet Metab
, vol.87
, pp. 341-348
-
-
Awano, T.1
Katz, M.L.2
O’Brien, D.P.3
-
33
-
-
79954629520
-
A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers
-
F.H.FariasR.ZengG.S.Johnson. A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiol Dis2011; 42: 468–474.
-
(2011)
Neurobiol Dis
, vol.42
, pp. 468-474
-
-
Farias, F.H.1
Zeng, R.2
Johnson, G.S.3
-
34
-
-
77957069126
-
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis
-
M.AbitbolJ.L.ThibaudN.J.Olby. A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis. Proc Natl Acad Sci U S A2010; 107: 14775–14780.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 14775-14780
-
-
Abitbol, M.1
Thibaud, J.L.2
Olby, N.J.3
-
35
-
-
85013844538
-
Familial myoclonic epilepsy with skeletal muscle polyglucosan bodies in the miniature wirehaired dachshund
-
S.N.FitzmauriceH.C.PowellG.D.Shelton. Familial myoclonic epilepsy with skeletal muscle polyglucosan bodies in the miniature wirehaired dachshund. J Vet Intern Med1999; 13: 239.
-
(1999)
J Vet Intern Med
, vol.13
, pp. 239
-
-
Fitzmaurice, S.N.1
Powell, H.C.2
Shelton, G.D.3
-
37
-
-
70350187890
-
Treatment of Lafora disease (inherited myoclonic epilepsy) in dogs
-
C.RusbridgeS.N.FitzmauriceH.Lohi. Treatment of Lafora disease (inherited myoclonic epilepsy) in dogs. J Vet Intern Med2005; 19: 289.
-
(2005)
J Vet Intern Med
, vol.19
, pp. 289
-
-
Rusbridge, C.1
Fitzmaurice, S.N.2
Lohi, H.3
-
38
-
-
0026178844
-
Lafora’s disease (progressive myoclonus epilepsy) in the Basset Hound – early diagnosis by muscle biopsy
-
E.KaiserK.KrauserD.Schwartz-Porsche. Lafora’s disease (progressive myoclonus epilepsy) in the Basset Hound – early diagnosis by muscle biopsy. Tierärztl Prax1991; 19: 290–295.
-
(1991)
Tierärztl Prax
, vol.19
, pp. 290-295
-
-
Kaiser, E.1
Krauser, K.2
Schwartz-Porsche, D.3
-
39
-
-
0014747914
-
Lafora’s disease in the dog. A comparative study
-
J.M.HollandW.C.DavisD.J.Prieur. Lafora’s disease in the dog. A comparative study. Am J Pathol1970; 58: 509–530.
-
(1970)
Am J Pathol
, vol.58
, pp. 509-530
-
-
Holland, J.M.1
Davis, W.C.2
Prieur, D.J.3
-
40
-
-
0002119724
-
Lafora’s disease in an epileptic Basset hound
-
Z.JianM.R.AlleyJ.Cayzer. Lafora’s disease in an epileptic Basset hound. N Z Vet J1990; 38: 75–79.
-
(1990)
N Z Vet J
, vol.38
, pp. 75-79
-
-
Jian, Z.1
Alley, M.R.2
Cayzer, J.3
-
41
-
-
0344502958
-
Familial Lafora’s disease in the beagle dog
-
T.L.Tomchick. Familial Lafora’s disease in the beagle dog. Fed Proc1973; 32: 821.
-
(1973)
Fed Proc
, vol.32
, pp. 821
-
-
Tomchick, T.L.1
-
42
-
-
0017156720
-
Inherited progressive epilepsy of the dog with comparisons to Lafora’s disease of man
-
G.A.HegrebergG.A.Padgett. Inherited progressive epilepsy of the dog with comparisons to Lafora’s disease of man. Fed Proc1976; 35: 1202–1205.
-
(1976)
Fed Proc
, vol.35
, pp. 1202-1205
-
-
Hegreberg, G.A.1
Padgett, G.A.2
-
44
-
-
85026681893
-
-
American Association of Veterinary Laboratory Diagnosticians, 21st Annual Proceedings, Madison, WI
-
D.L.Whitenack. Neuronal glycoproteinosis (Lafora’s disease) in the dog. American Association of Veterinary Laboratory Diagnosticians, 21st Annual Proceedings; 1978, Madison, WI. 1978, pp 493–496.
-
(1978)
Neuronal glycoproteinosis (Lafora’s disease) in the dog
, pp. 493-496
-
-
Whitenack, D.L.1
-
45
-
-
0017142768
-
Canine neuronal glycoproteinosis – Lafora’s disease in the dog
-
P.K.CusickA.M.CameronA.J.Parker. Canine neuronal glycoproteinosis – Lafora’s disease in the dog. J Am Anim Hosp Assoc1976; 12: 518–521.
-
(1976)
J Am Anim Hosp Assoc
, vol.12
, pp. 518-521
-
-
Cusick, P.K.1
Cameron, A.M.2
Parker, A.J.3
-
46
-
-
0036515932
-
Polyglucosan storage disease in a dog resembling Lafora’s disease
-
T.SchoemanJ.WilliamsE.van Wilpe. Polyglucosan storage disease in a dog resembling Lafora’s disease. J Vet Intern Med2002; 16: 201–207.
-
(2002)
J Vet Intern Med
, vol.16
, pp. 201-207
-
-
Schoeman, T.1
Williams, J.2
van Wilpe, E.3
-
48
-
-
70350163400
-
Lafora disease as a cause of visually exacerbated myoclonic attacks in a dog
-
A.A.WebbC.McMillanC.L.Cullen. Lafora disease as a cause of visually exacerbated myoclonic attacks in a dog. Can Vet J2009; 50: 963–967.
-
(2009)
Can Vet J
, vol.50
, pp. 963-967
-
-
Webb, A.A.1
McMillan, C.2
Cullen, C.L.3
-
49
-
-
17344362307
-
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
-
B.A.MinassianJ.R.LeeJ.A.Herbrick. Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nat Genet1998; 20: 171–174.
-
(1998)
Nat Genet
, vol.20
, pp. 171-174
-
-
Minassian, B.A.1
Lee, J.R.2
Herbrick, J.A.3
-
50
-
-
0042831105
-
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22
-
E.M.ChanD.E.BulmanA.D.Paterson. Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22. J Med Genet2003; 40: 671–675.
-
(2003)
J Med Genet
, vol.40
, pp. 671-675
-
-
Chan, E.M.1
Bulman, D.E.2
Paterson, A.D.3
-
51
-
-
15244352202
-
Lafora disease due to EPM2B mutations: a clinical and genetic study
-
C.Gómez-AbadP.Gómez-GarreE.Gutiérrez-Delicado. Lafora disease due to EPM2B mutations: a clinical and genetic study. Neurology2005; 64: 982–986.
-
(2005)
Neurology
, vol.64
, pp. 982-986
-
-
Gómez-Abad, C.1
Gómez-Garre, P.2
Gutiérrez-Delicado, E.3
-
52
-
-
0016161147
-
Neuronal ceroid-lipofuscin storage in Siamese cats
-
P.D.GreenP.B.Little. Neuronal ceroid-lipofuscin storage in Siamese cats. Can J Comp Med1974; 38: 207–212.
-
(1974)
Can J Comp Med
, vol.38
, pp. 207-212
-
-
Green, P.D.1
Little, P.B.2
-
54
-
-
67650457932
-
Neuronal ceroid-lipofuscinosis in a Japanese domestic shorthair cat
-
M.KuwamuraM.NakagawaM.Nabe. Neuronal ceroid-lipofuscinosis in a Japanese domestic shorthair cat. J Vet Med Sci2009; 71: 665–667.
-
(2009)
J Vet Med Sci
, vol.71
, pp. 665-667
-
-
Kuwamura, M.1
Nakagawa, M.2
Nabe, M.3
-
55
-
-
84872417574
-
Mutational analysis of the feline CLN3 gene and an ultrastructural evaluation of lysosomal storage materials in a cat with neuronal ceroid lipofuscinosis: an investigation into the molecular basis of the disease
-
Y.FurusawaK.MizukamiA.Yabuki. Mutational analysis of the feline CLN3 gene and an ultrastructural evaluation of lysosomal storage materials in a cat with neuronal ceroid lipofuscinosis: an investigation into the molecular basis of the disease. Vet J2012; 194: 425–428.
-
(2012)
Vet J
, vol.194
, pp. 425-428
-
-
Furusawa, Y.1
Mizukami, K.2
Yabuki, A.3
-
56
-
-
84907464254
-
Characterization of neuronal ceroid-lipofuscinosis in 3 cats
-
M.D.ChalkleyA.G.ArmienD.H.Gilliam. Characterization of neuronal ceroid-lipofuscinosis in 3 cats. Vet Pathol2014; 51: 796–804.
-
(2014)
Vet Pathol
, vol.51
, pp. 796-804
-
-
Chalkley, M.D.1
Armien, A.G.2
Gilliam, D.H.3
|