תוצאות חיפוש - Gourfinkel-An, Isabelle

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

קבל טקסט מלא קבל טקסט מלא

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

קבל טקסט מלא קבל טקסט מלא קבל טקסט מלא

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

קבל טקסט מלא קבל טקסט מלא

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

קבל טקסט מלא קבל טקסט מלא

Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism מאת 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

קבל טקסט מלא קבל טקסט מלא קבל טקסט מלא

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females מאת 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

קבל טקסט מלא קבל טקסט מלא קבל טקסט מלא

Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females מאת 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

קבל טקסט מלא קבל טקסט מלא

Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females מאת 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

קבל טקסט מלא קבל טקסט מלא קבל טקסט מלא