Resultats de la cerca - Gourfinkel-An, Isabelle

Genetics of inherited human epilepsies per Gourfinkel-An, Isabelle, Baulac, Stéphanie, Brice, Alexis, Leguern, Eric, Baulac, Michel

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Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? per Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Bodeau, Nicolas, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David

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Risk Factors of Acute Behavioral Regression in Psychiatrically Hospitalized Adolescents with Autism per Périsse, Didier, Amiet, Claire, Consoli, Angèle, Thorel, Marie-Vincente, Gourfinkel-An, Isabelle, Bodeau, Nicolas, Guinchat, Vincent, Barthélémy, Catherine, Cohen, David

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A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33 per Baulac, Stéphanie, Gourfinkel-An, Isabelle, Picard, Fabienne, Rosenberg-Bourgin, Myriam, Prud'homme, Jean-François, Baulac, Michel, Brice, Alexis, LeGuern, Eric

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Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism per Couarch, Philippe, Vernia, Santiago, Gourfinkel-An, Isabelle, Lesca, Gaëtan, Gataullina, Svetlana, Fedirko, Estelle, Trouillard, Oriane, Depienne, Christel, Dulac, Olivier, Steschenko, Dominique, Leguern, Eric, Sanz, Pascual, Baulac, Stéphanie

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Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females per Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, LeGuern, Eric

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Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females per Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, LeGuern, Eric

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Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females per Depienne, Christel, Trouillard, Oriane, Bouteiller, Delphine, Gourfinkel-An, Isabelle, Poirier, Karine, Rivier, François, Berquin, Patrick, Nabbout, Rima, Chaigne, Denys, Steschenko, Dominique, Gautier, Agnès, Hoffman-Zacharska, Dorota, Lannuzel, Annie, Lackmy-Port-Lis, Marilyn, Maurey, Hélène, Dusser, Anne, Bru, Marie, Gilbert-Dussardier, Brigitte, Roubertie, Agathe, Kaminska, Anna, Whalen, Sandra, Mignot, Cyril, Baulac, Stéphanie, Lesca, Gaetan, Arzimanoglou, Alexis, LeGuern, Eric

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