Severe Myoclonic Epilepsy of Infancy: Extended Spectrum of GEFS+?
Singh, R., Andermann, E., Whitehouse, W. P. A., Harvey, A. S., Keene, D. L., Seni, M‐H., Crossland, K. M., Andermann, F., Berkovic, S. F., Scheffer, I. E.
Published in Epilepsia (Copenhagen) (01.07.2001)
Published in Epilepsia (Copenhagen) (01.07.2001)
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Congenital malformations due to antiepileptic drugs
Kaneko, S, Battino, D, Andermann, E, Wada, K, Kan, R, Takeda, A, Nakane, Y, Ogawa, Y, Avanzini, G, Fumarola, C, Granata, T, Molteni, F, Pardi, G, Minotti, L, Canger, R, Dansky, L, Oguni, M, Lopes-Cendas, I, Sherwin, A, Andermann, F, Seni, M.-H, Okada, M, Teranishi, T
Published in Epilepsy research (01.02.1999)
Published in Epilepsy research (01.02.1999)
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Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion
Montermini, L, Richter, A, Morgan, K, Justice, C M, Julien, D, Castellotti, B, Mercier, J, Poirier, J, Capozzoli, F, Bouchard, J P, Lemieux, B, Mathieu, J, Vanasse, M, Seni, M H, Graham, G, Andermann, F, Andermann, E, Melançon, S B, Keats, B J, Di Donato, S, Pandolfo, M
Published in Annals of neurology (01.05.1997)
Published in Annals of neurology (01.05.1997)
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Intrauterine growth in the offspring of epileptic women: a prospective multicenter study
Battino, D, Kaneko, S, Andermann, E, Avanzini, G, Canevini, M.P, Canger, R, Croci, D, Fumarola, C, Guidolin, L, Mamoli, D, Molteni, F, Pardi, G, Vignoli, A, Fukushima, Y, Kan, R, Takeda, A, Nakane, Y, Ogawa, Y, Dansky, L, Oguni, M, Lopez-Ciendas, I, Sherwin, A, Andermann, F, Seni, M.-H, Otani, K, Teranishi, T, Goto, M
Published in Epilepsy research (01.08.1999)
Published in Epilepsy research (01.08.1999)
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Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12
Xiong, Lan, Labuda, Malgorzata, Li, Dong-Sheng, Hudson, Thomas J., Desbiens, Richard, Patry, Georges, Verret, Simon, Langevin, Pierre, Mercho, Suha, Seni, Marie-Hélène, Scheffer, Ingrid, Dubeau, François, Berkovic, Samuel F., Andermann, Frederick, Andermann, Eva, Pandolfo, Massimo
Published in American journal of human genetics (01.12.1999)
Published in American journal of human genetics (01.12.1999)
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Journal Article
Genetic predisposition to phenytoin-induced birth defects
Strickler, S M, Dansky, L V, Miller, M A, Seni, M H, Andermann, E, Spielberg, S P
Published in The Lancet (British edition) (05.10.1985)
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Published in The Lancet (British edition) (05.10.1985)
Journal Article
Repeated Neural Tube Defects and Valproate Monotherapy Suggest a Pharmacogenetic Abnormality
Duncan, Susan, Mercho, Suha, Lopes‐Cendes, Iscia, Seni, Marie‐Helene, Benjamin, Alice, Dubeau, Francois, Andermann, Frederick, Andermann, Eva
Published in Epilepsia (Copenhagen) (01.06.2001)
Published in Epilepsia (Copenhagen) (01.06.2001)
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Journal Article
Evidence for abnormal regulation of insulin receptors in Friedreich's ataxia
Fantus, I G, Seni, M H, Andermann, E
Published in The journal of clinical endocrinology and metabolism (01.01.1993)
Published in The journal of clinical endocrinology and metabolism (01.01.1993)
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Journal Article
Sodium-channel defects in benign familial neonatal-infantile seizures
Heron, Sarah E, Crossland, Kathryn M, Andermann, Eva, Phillips, Hilary A, Hall, Allison J, Bleasel, Andrew, Shevell, Michael, Mercho, Suha, Seni, Marie-Helene, Guiot, Marie-Christine, Mulley, John C, Berkovic, Samuel F, Scheffer, Ingrid E
Published in The Lancet (British edition) (14.09.2002)
Published in The Lancet (British edition) (14.09.2002)
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Journal Article
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred
Gros-Louis, François, Meijer, Inge A., Hand, Collette K., Dubé, Marie-Pierre, MacGregor, Daune L., Seni, Marie-Hélène, Devon, Rebecca S., Hayden, Michael R., Andermann, Frederick, Andermann, Eva, Rouleau, Guy A.
Published in Annals of neurology (01.01.2003)
Published in Annals of neurology (01.01.2003)
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Journal Article
Genetic predisposition to phenytoin-induced birth defects
Strickler, S M, Dansky, LV, Miller, MA, Seni, M-H, Andermann, E, Spielberg, S P
Published in The Lancet (North American edition) (01.01.1985)
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Published in The Lancet (North American edition) (01.01.1985)
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