-
1
-
-
9444287592
-
Appetite-suppressant drugs and the risk of primary pulmonary hypertension. International Primary Pulmonary Hypertension Study Group
-
Abenhaim L. Moride Y. Brenot F. Rich S. Benichou J. Kurz X. et al. (1996) Appetite-suppressant drugs and the risk of primary pulmonary hypertension. International Primary Pulmonary Hypertension Study Group. N Engl J Med 335: 609–616.
-
(1996)
N Engl J Med
, vol.335
, pp. 609-616
-
-
Abenhaim, L.1
Moride, Y.2
Brenot, F.3
Rich, S.4
Benichou, J.5
Kurz, X.6
-
2
-
-
0022343044
-
Treatment of self-induced photosensitive epilepsy with fenfluramine
-
Aicardi J. Gastaut H. (1985) Treatment of self-induced photosensitive epilepsy with fenfluramine. N Engl J Med 313: 1419.
-
(1985)
N Engl J Med
, vol.313
-
-
Aicardi, J.1
Gastaut, H.2
-
3
-
-
0023811453
-
Syncopal attacks compulsively self-induced by Valsalva's maneuver associated with typical absence seizures. A case report
-
Aicardi J. Gastaut H. Mises J. (1988) Syncopal attacks compulsively self-induced by Valsalva's maneuver associated with typical absence seizures. A case report. Arch Neurol 45: 923–925.
-
(1988)
Arch Neurol
, vol.45
, pp. 923-925
-
-
Aicardi, J.1
Gastaut, H.2
Mises, J.3
-
5
-
-
0032970989
-
A review of central 5-HT receptors and their function
-
Barnes N. Sharp T. (1999) A review of central 5-HT receptors and their function. Neuropharmacology 38: 1083–1152.
-
(1999)
Neuropharmacology
, vol.38
, pp. 1083-1152
-
-
Barnes, N.1
Sharp, T.2
-
6
-
-
84858287762
-
SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome
-
Bender A. Morse R. Scott R. Holmes G. Lenck-Santini P. (2012) SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome. Epilepsy Behav 23: 177–186.
-
(2012)
Epilepsy Behav
, vol.23
, pp. 177-186
-
-
Bender, A.1
Morse, R.2
Scott, R.3
Holmes, G.4
Lenck-Santini, P.5
-
7
-
-
77950857874
-
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009
-
Berg A. Berkovic S. Brodie M. Buchhalter J. Cross J. van Emde Boas W. et al. (2010) Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009. Epilepsia 51: 676–685.
-
(2010)
Epilepsia
, vol.51
, pp. 676-685
-
-
Berg, A.1
Berkovic, S.2
Brodie, M.3
Buchhalter, J.4
Cross, J.5
van Emde Boas, W.6
-
8
-
-
0029737684
-
Add-on therapy of fenfluramine in intractable self-induced epilepsy
-
Boel M. Casaer P. (1996) Add-on therapy of fenfluramine in intractable self-induced epilepsy. Neuropediatrics 27: 171–173.
-
(1996)
Neuropediatrics
, vol.27
, pp. 171-173
-
-
Boel, M.1
Casaer, P.2
-
10
-
-
84900758898
-
Antiepileptic drugs for the treatment of severe myoclonic epilepsy in infancy
-
CD010483.
-
Brigo F. Storti M. (2013) Antiepileptic drugs for the treatment of severe myoclonic epilepsy in infancy. Cochrane Database Syst Rev 11: CD010483.
-
(2013)
Cochrane Database Syst Rev
, vol.11
-
-
Brigo, F.1
Storti, M.2
-
11
-
-
79960909620
-
Comorbidities and predictors of health-related quality of life in Dravet syndrome
-
Brunklaus A. Dorris L. Zuberi S. (2011) Comorbidities and predictors of health-related quality of life in Dravet syndrome. Epilepsia 52: 1476–1482.
-
(2011)
Epilepsia
, vol.52
, pp. 1476-1482
-
-
Brunklaus, A.1
Dorris, L.2
Zuberi, S.3
-
12
-
-
84864704934
-
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
-
Brunklaus A. Ellis R. Reavey E. Forbes G. Zuberi S. (2012) Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome. Brain 135: 2329–2336.
-
(2012)
Brain
, vol.135
, pp. 2329-2336
-
-
Brunklaus, A.1
Ellis, R.2
Reavey, E.3
Forbes, G.4
Zuberi, S.5
-
13
-
-
0036126057
-
Fenfluramine as a potential antiepileptic drug
-
Casaer P. Boel M. (2002) Fenfluramine as a potential antiepileptic drug. Epilepsia 43: 205–206.
-
(2002)
Epilepsia
, vol.43
, pp. 205-206
-
-
Casaer, P.1
Boel, M.2
-
14
-
-
49049116168
-
Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel
-
Cestele S. Scalmani P. Rusconi R. Terragni B. Franceschetti S. Mantegazza M. (2008) Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel. J Neurosci 28: 7273–7283.
-
(2008)
J Neurosci
, vol.28
, pp. 7273-7283
-
-
Cestele, S.1
Scalmani, P.2
Rusconi, R.3
Terragni, B.4
Franceschetti, S.5
Mantegazza, M.6
-
16
-
-
1842850796
-
Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy
-
Ceulemans B. Claes L. Lagae L. (2004) Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy. Pediatr Neurol 30: 236–243.
-
(2004)
Pediatr Neurol
, vol.30
, pp. 236-243
-
-
Ceulemans, B.1
Claes, L.2
Lagae, L.3
-
17
-
-
79953685960
-
The pharmacologic treatment of Dravet syndrome
-
Chiron C. Dulac O. (2011) The pharmacologic treatment of Dravet syndrome. Epilepsia 52(Suppl. 2): 72–75.
-
(2011)
Epilepsia
, vol.52
, pp. 72-75
-
-
Chiron, C.1
Dulac, O.2
-
19
-
-
0023794685
-
Dopamine agonist treatment of self-induced pattern-sensitive epilepsy. A case report
-
Clemens B. (1988) Dopamine agonist treatment of self-induced pattern-sensitive epilepsy. A case report. Epilepsy Res 2: 340–343.
-
(1988)
Epilepsy Res
, vol.2
, pp. 340-343
-
-
Clemens, B.1
-
21
-
-
0036227390
-
Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial
-
Coppola G. Capovilla G. Montagnini A. Romeo A. Spano M. Tortorella G. et al. (2002) Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial. Epilepsy Res 49: 45–48.
-
(2002)
Epilepsy Res
, vol.49
, pp. 45-48
-
-
Coppola, G.1
Capovilla, G.2
Montagnini, A.3
Romeo, A.4
Spano, M.5
Tortorella, G.6
-
22
-
-
84924311057
-
Hippocampal serotonin depletion is related to the presence of generalized tonic–clonic seizures, but not to psychiatric disorders in patients with temporal lobe epilepsy
-
Da Fonseca N. Joaquim H. Talib L. de Vincentiis S. Gattaz W. Valente K. (2015) Hippocampal serotonin depletion is related to the presence of generalized tonic–clonic seizures, but not to psychiatric disorders in patients with temporal lobe epilepsy. Epilepsy Res 111: 18–25.
-
(2015)
Epilepsy Res
, vol.111
, pp. 18-25
-
-
Da Fonseca, N.1
Joaquim, H.2
Talib, L.3
de Vincentiis, S.4
Gattaz, W.5
Valente, K.6
-
23
-
-
0026608645
-
Effects of fluoxetine on convulsions and on brain serotonin as detected by microdialysis in genetically epilepsy-prone rats
-
Dailey J. Yan Q. Mishra P. Burger R. Jobe P. (1992) Effects of fluoxetine on convulsions and on brain serotonin as detected by microdialysis in genetically epilepsy-prone rats. J Pharmacol Exp Ther 260: 533–540.
-
(1992)
J Pharmacol Exp Ther
, vol.260
, pp. 533-540
-
-
Dailey, J.1
Yan, Q.2
Mishra, P.3
Burger, R.4
Jobe, P.5
-
24
-
-
61449230751
-
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH 19 resembles Dravet syndrome but mainly affects females
-
e1000381.
-
Depienne C. Bouteiller D. Keren B. Cheuret E. Poirier K. Trouillard O. et al. (2009) Sporadic infantile epileptic encephalopathy caused by mutations in PCDH 19 resembles Dravet syndrome but mainly affects females. PLoS Genet 5: e1000381.
-
(2009)
PLoS Genet
, vol.5
-
-
Depienne, C.1
Bouteiller, D.2
Keren, B.3
Cheuret, E.4
Poirier, K.5
Trouillard, O.6
-
26
-
-
79953726784
-
The core Dravet syndrome phenotype
-
Dravet C. (2011) The core Dravet syndrome phenotype. Epilepsia 52(Suppl. 2): 3–9.
-
(2011)
Epilepsia
, vol.52
, pp. 3-9
-
-
Dravet, C.1
-
27
-
-
84922662090
-
Efficacy and tolerability of the ketogenic diet in Dravet syndrome - comparison with various standard antiepileptic drug regimen
-
Dressler A. Trimmel-Schwahofer P. Reithofer E. Muhlebner A. Groppel G. Reiter-Fink E. et al. (2015) Efficacy and tolerability of the ketogenic diet in Dravet syndrome - comparison with various standard antiepileptic drug regimen. Epilepsy Res 109: 81–89.
-
(2015)
Epilepsy Res
, vol.109
, pp. 81-89
-
-
Dressler, A.1
Trimmel-Schwahofer, P.2
Reithofer, E.3
Muhlebner, A.4
Groppel, G.5
Reiter-Fink, E.6
-
28
-
-
0038083311
-
The anticonvulsant effect of citalopram as an indirect evidence of serotonergic impairment in human epileptogenesis
-
Favale E. Audenino D. Cocito L. Albano C. (2003) The anticonvulsant effect of citalopram as an indirect evidence of serotonergic impairment in human epileptogenesis. Seizure 12: 316–318.
-
(2003)
Seizure
, vol.12
, pp. 316-318
-
-
Favale, E.1
Audenino, D.2
Cocito, L.3
Albano, C.4
-
30
-
-
70549101203
-
Overview on 5-HT receptors and their role in physiology and pathology of the central nervous system
-
Filip M. Bader M. (2009) Overview on 5-HT receptors and their role in physiology and pathology of the central nervous system. Pharmacol Rep 61: 761–777.
-
(2009)
Pharmacol Rep
, vol.61
, pp. 761-777
-
-
Filip, M.1
Bader, M.2
-
31
-
-
0024161982
-
Mechanisms of effects of D-fenfluramine on brain serotonin metabolism in rats: uptake inhibition versus release
-
Fuller R. Snoddy H. Robertson D. (1988) Mechanisms of effects of D-fenfluramine on brain serotonin metabolism in rats: uptake inhibition versus release. Pharmacol Biochem Behav 30: 715–721.
-
(1988)
Pharmacol Biochem Behav
, vol.30
, pp. 715-721
-
-
Fuller, R.1
Snoddy, H.2
Robertson, D.3
-
32
-
-
0021285639
-
[Efficacy of fenfluramine for the treatment of compulsive behavior disorders in psychotic children]
-
Gastaut H. (1984) [Efficacy of fenfluramine for the treatment of compulsive behavior disorders in psychotic children]. Presse Med 13: 2024–2025.
-
(1984)
Presse Med
, vol.13
, pp. 2024-2025
-
-
Gastaut, H.1
-
33
-
-
0023577711
-
Compulsive respiratory stereotypies in children with autistic features: polygraphic recording and treatment with fenfluramine
-
Gastaut H. Zifkin B. Rufo M. (1987) Compulsive respiratory stereotypies in children with autistic features: polygraphic recording and treatment with fenfluramine. J Autism Develop Disord 17: 391–406.
-
(1987)
J Autism Develop Disord
, vol.17
, pp. 391-406
-
-
Gastaut, H.1
Zifkin, B.2
Rufo, M.3
-
34
-
-
0003627259
-
Antiepileptic effects of fenfluramine: pilot study
-
(abstract).
-
Gastaut H. Zifkin B. (1987) Antiepileptic effects of fenfluramine: pilot study. Ann Neuurol 22: 414–415 (abstract).
-
(1987)
Ann Neuurol
, vol.22
, pp. 414-415
-
-
Gastaut, H.1
Zifkin, B.2
-
35
-
-
0034646342
-
When antiepileptic drugs aggravate epilepsy
-
Genton P. (2000) When antiepileptic drugs aggravate epilepsy. Brain Dev 22: 75–80.
-
(2000)
Brain Dev
, vol.22
, pp. 75-80
-
-
Genton, P.1
-
36
-
-
0033868931
-
Fenfluramine blocks low-Mg2+-induced epileptiform activity in rat entorhinal cortex
-
Gentsch K. Heinemann U. Schmitz B. Behr J. (2000) Fenfluramine blocks low-Mg2+-induced epileptiform activity in rat entorhinal cortex. Epilepsia 41: 925–928.
-
(2000)
Epilepsia
, vol.41
, pp. 925-928
-
-
Gentsch, K.1
Heinemann, U.2
Schmitz, B.3
Behr, J.4
-
39
-
-
84875267737
-
Should antidepressant drugs of the selective serotonin reuptake inhibitor family be tested as antiepileptic drugs?
-
Hamid H. Kanner A. (2013) Should antidepressant drugs of the selective serotonin reuptake inhibitor family be tested as antiepileptic drugs? Epilepsy Behav 26: 261–265.
-
(2013)
Epilepsy Behav
, vol.26
, pp. 261-265
-
-
Hamid, H.1
Kanner, A.2
-
40
-
-
0036155260
-
Truncation of the GABA(A)-receptor Gamma 2 subunit in a family with generalized epilepsy with febrile seizures plus
-
Harkin L. Bowser D. Dibbens L. Singh R. Phillips F. Wallace R. et al. (2002) Truncation of the GABA(A)-receptor Gamma 2 subunit in a family with generalized epilepsy with febrile seizures plus. Am J Hum Genet 70: 530–536.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 530-536
-
-
Harkin, L.1
Bowser, D.2
Dibbens, L.3
Singh, R.4
Phillips, F.5
Wallace, R.6
-
41
-
-
43349103389
-
A screening test for the prediction of Dravet syndrome before one year of age
-
Hattori J. Ouchida M. Ono J. Miyake S. Maniwa S. Mimaki N. et al. (2008) A screening test for the prediction of Dravet syndrome before one year of age. Epilepsia 49: 626–633.
-
(2008)
Epilepsia
, vol.49
, pp. 626-633
-
-
Hattori, J.1
Ouchida, M.2
Ono, J.3
Miyake, S.4
Maniwa, S.5
Mimaki, N.6
-
42
-
-
0025279668
-
Epidemiology of severe myoclonic epilepsy of infancy
-
Hurst D. (1990) Epidemiology of severe myoclonic epilepsy of infancy. Epilepsia 31: 397–400.
-
(1990)
Epilepsia
, vol.31
, pp. 397-400
-
-
Hurst, D.1
-
43
-
-
29544438942
-
The serotonergic and noradrenergic effects of antidepressant drugs are anticonvulsant, not proconvulsant
-
Jobe P. Browning R. (2005) The serotonergic and noradrenergic effects of antidepressant drugs are anticonvulsant, not proconvulsant. Epilepsy Behav 7: 602–619.
-
(2005)
Epilepsy Behav
, vol.7
, pp. 602-619
-
-
Jobe, P.1
Browning, R.2
-
44
-
-
42449091913
-
Topiramate, nutrition and weight change: a prospective study
-
Klein K. Theisen F. Knake S. Oertel W. Hebebrand J. Rosenow F. et al. (2008) Topiramate, nutrition and weight change: a prospective study. J Neurol Neurosurg Psych 79: 590–593.
-
(2008)
J Neurol Neurosurg Psych
, vol.79
, pp. 590-593
-
-
Klein, K.1
Theisen, F.2
Knake, S.3
Oertel, W.4
Hebebrand, J.5
Rosenow, F.6
-
45
-
-
33947575762
-
Topiramate in the treatment of highly refractory patients with Dravet syndrome
-
Kroll-Seger J. Portilla P. Dulac O. Chiron C. (2006) Topiramate in the treatment of highly refractory patients with Dravet syndrome. Neuropediatrics 37: 325–329.
-
(2006)
Neuropediatrics
, vol.37
, pp. 325-329
-
-
Kroll-Seger, J.1
Portilla, P.2
Dulac, O.3
Chiron, C.4
-
46
-
-
84928272450
-
Electroencephalographic features of patients with SCN1A-positive Dravet syndrome
-
Lee H. Chi C. Tsai C. Chen C. Wang C. (2015) Electroencephalographic features of patients with SCN1A-positive Dravet syndrome. Brain Dev 37: 599–611.
-
(2015)
Brain Dev
, vol.37
, pp. 599-611
-
-
Lee, H.1
Chi, C.2
Tsai, C.3
Chen, C.4
Wang, C.5
-
48
-
-
67649985908
-
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis
-
Marini C. Scheffer I. Nabbout R. Mei D. Cox K. Dibbens L. et al. (2009) SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis. Epilepsia 50: 1670–1678.
-
(2009)
Epilepsia
, vol.50
, pp. 1670-1678
-
-
Marini, C.1
Scheffer, I.2
Nabbout, R.3
Mei, D.4
Cox, K.5
Dibbens, L.6
-
50
-
-
84898677304
-
Seizure reduction with fluoxetine in Dravet syndrome
-
Meador K. (2014) Seizure reduction with fluoxetine in Dravet syndrome. Epilepsy Behav Case Rep 2: 54–56.
-
(2014)
Epilepsy Behav Case Rep
, vol.2
, pp. 54-56
-
-
Meador, K.1
-
51
-
-
84929502090
-
The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype
-
Meng H. Xu H.Q. Yu L. Lin G.W. He N. Su T. et al. (2015) The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype. Hum Mutat 36 (6): 573–80.
-
(2015)
Hum Mutat
, vol.36
, Issue.6
, pp. 573-580
-
-
Meng, H.1
Xu, H.Q.2
Yu, L.3
Lin, G.W.4
He, N.5
Su, T.6
-
52
-
-
84893470069
-
Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice
-
Mistry A. Thompson C. Miller A. Vanoye C. George A. Jr Kearney J. (2014) Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice. Neurobiol Dis 65: 1–11.
-
(2014)
Neurobiol Dis
, vol.65
, pp. 1-11
-
-
Mistry, A.1
Thompson, C.2
Miller, A.3
Vanoye, C.4
George, A.5
Kearney, J.6
-
54
-
-
0014011185
-
Treatment of refractory obesity with fenfluramine
-
Munro J. Seaton D. Duncan L. (1966) Treatment of refractory obesity with fenfluramine. Br Med J 2: 624–625.
-
(1966)
Br Med J
, vol.2
, pp. 624-625
-
-
Munro, J.1
Seaton, D.2
Duncan, L.3
-
56
-
-
34249791771
-
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an SCN1A gene mutation
-
Ogiwara I. Miyamoto H. Morita N. Atapour N. Mazaki E. Inoue I. et al. (2007) Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an SCN1A gene mutation. J Neurosci 27: 5903–5914.
-
(2007)
J Neurosci
, vol.27
, pp. 5903-5914
-
-
Ogiwara, I.1
Miyamoto, H.2
Morita, N.3
Atapour, N.4
Mazaki, E.5
Inoue, I.6
-
57
-
-
0029941786
-
The anticonvulsant action of fluoxetine in substantia nigra is dependent upon endogenous serotonin
-
Pasini A. Tortorella A. Gale K. (1996) The anticonvulsant action of fluoxetine in substantia nigra is dependent upon endogenous serotonin. Brain Res 724: 84–88.
-
(1996)
Brain Res
, vol.724
, pp. 84-88
-
-
Pasini, A.1
Tortorella, A.2
Gale, K.3
-
59
-
-
33645528060
-
Stiripentol, a putative antiepileptic drug, enhances the duration of opening of GABA-A receptor channels
-
Quilichini P. Chiron C. Ben-Ari Y. Gozlan H. (2006) Stiripentol, a putative antiepileptic drug, enhances the duration of opening of GABA-A receptor channels. Epilepsia 47: 704–716.
-
(2006)
Epilepsia
, vol.47
, pp. 704-716
-
-
Quilichini, P.1
Chiron, C.2
Ben-Ari, Y.3
Gozlan, H.4
-
60
-
-
84908544395
-
Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome
-
Rubinstein M. Westenbroek R. Yu F. Jones C. Scheuer T. Catterall W. (2015) Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome. Neurobiol Dis 73: 106–117.
-
(2015)
Neurobiol Dis
, vol.73
, pp. 106-117
-
-
Rubinstein, M.1
Westenbroek, R.2
Yu, F.3
Jones, C.4
Scheuer, T.5
Catterall, W.6
-
61
-
-
84865459825
-
Diagnosis and long-term course of Dravet syndrome
-
Scheffer I. (2012) Diagnosis and long-term course of Dravet syndrome. Eur J Paediatr Neurol 16(Suppl. 1): S5–S8.
-
(2012)
Eur J Paediatr Neurol
, vol.16
, pp. S5-S8
-
-
Scheffer, I.1
-
65
-
-
84890151248
-
de novo loss-of-function mutations in CHD 2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
-
Suls A. Jaehn J. Kecskes A. Weber Y. Weckhuysen S. Craiu D. et al. (2013) de novo loss-of-function mutations in CHD 2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. Am J Hum Genet 93: 967–975.
-
(2013)
Am J Hum Genet
, vol.93
, pp. 967-975
-
-
Suls, A.1
Jaehn, J.2
Kecskes, A.3
Weber, Y.4
Weckhuysen, S.5
Craiu, D.6
-
68
-
-
84930194995
-
Seizure precipitants in Dravet syndrome: what events and activities are specifically provocative compared with other epilepsies?
-
Verbeek N. Wassenaar M. van Campen J. Sonsma A. Gunning B. Knoers N. et al. (2015) Seizure precipitants in Dravet syndrome: what events and activities are specifically provocative compared with other epilepsies? Epilepsy Behav 47: 39–44.
-
(2015)
Epilepsy Behav
, vol.47
, pp. 39-44
-
-
Verbeek, N.1
Wassenaar, M.2
van Campen, J.3
Sonsma, A.4
Gunning, B.5
Knoers, N.6
-
69
-
-
0037222315
-
Sodium channels SCN1A, SCN2A and SCN3A in familial autism
-
Weiss L. Escayg A. Kearney J. Trudeau M. Macdonald B. Mori M. et al. (2003) Sodium channels SCN1A, SCN2A and SCN3A in familial autism. Mol Psychiatry 8: 186–194.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 186-194
-
-
Weiss, L.1
Escayg, A.2
Kearney, J.3
Trudeau, M.4
Macdonald, B.5
Mori, M.6
-
70
-
-
33750576365
-
Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings
-
Wolff M. Casse-Perrot C. Dravet C. (2006) Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings. Epilepsia 47(Suppl. 2): 45–48.
-
(2006)
Epilepsia
, vol.47
, pp. 45-48
-
-
Wolff, M.1
Casse-Perrot, C.2
Dravet, C.3
-
72
-
-
0027958856
-
Role of serotonin in the anticonvulsant effect of fluoxetine in genetically epilepsy-prone rats
-
Yan Q. Jobe P. Cheong J. Ko K. Dailey J. (1994) Role of serotonin in the anticonvulsant effect of fluoxetine in genetically epilepsy-prone rats. Naunyn Schmiedebergs Arch Pharmacol 350: 149–152.
-
(1994)
Naunyn Schmiedebergs Arch Pharmacol
, vol.350
, pp. 149-152
-
-
Yan, Q.1
Jobe, P.2
Cheong, J.3
Ko, K.4
Dailey, J.5
-
73
-
-
33748115786
-
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
-
Yu F. Mantegazza M. Westenbroek R. Robbins C. Kalume F. Burton K. et al. (2006) Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy. Nat Neurosci 9: 1142–1149.
-
(2006)
Nat Neurosci
, vol.9
, pp. 1142-1149
-
-
Yu, F.1
Mantegazza, M.2
Westenbroek, R.3
Robbins, C.4
Kalume, F.5
Burton, K.6
-
74
-
-
78651365602
-
Clinical course of young patients with Dravet syndrome after vagal nerve stimulation
-
Zamponi N. Passamonti C. Cappanera S. Petrelli C. (2011) Clinical course of young patients with Dravet syndrome after vagal nerve stimulation. Eur J Paediatr Neurol 15: 8–14.
-
(2011)
Eur J Paediatr Neurol
, vol.15
, pp. 8-14
-
-
Zamponi, N.1
Passamonti, C.2
Cappanera, S.3
Petrelli, C.4
-
75
-
-
84930641989
-
Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine
-
e0125898.
-
Zhang Y. Kecskes A. Copmans D. Langlois M. Crawford A. Ceulemans B. et al. (2015) Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine. PloS ONE 10: e0125898.
-
(2015)
PloS ONE
, vol.10
-
-
Zhang, Y.1
Kecskes, A.2
Copmans, D.3
Langlois, M.4
Crawford, A.5
Ceulemans, B.6
|