Search Results - Seni, Marie-Hélène

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  1. 1
    An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

    An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred by 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
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  2. 2
    Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12

    Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12 by 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

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  3. 3
    Repeated Neural Tube Defects and Valproate Monotherapy Suggest a Pharmacogenetic Abnormality

    Repeated Neural Tube Defects and Valproate Monotherapy Suggest a Pharmacogenetic Abnormality by Duncan, Susan, Mercho, Suha, Lopes‐Cendes, Iscia, Seni, Marie‐Helene, Benjamin, Alice, Dubeau, Francois, Andermann, Frederick, Andermann, Eva

    Published in Epilepsia (Copenhagen)
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  4. 4
    Sodium-channel defects in benign familial neonatal-infantile seizures

    Sodium-channel defects in benign familial neonatal-infantile seizures by 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

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