ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate
Rheims, Sylvain, Herbillon, Vania, Villeneuve, Nathalie, Auvin, Stéphane, Napuri, Silvia, Cances, Claude, Berquin, Patrick, Castelneau, Pierre, Nguyen The Tich, Sylvie, Villega, Frédéric, Isnard, Hervé, Nabbout, Rima, Gaillard, Ségolène, Mercier, Catherine, Kassai, Behrouz, Arzimanoglou, Alexis, Pedespan, Jean‐Michel, Bellescize, Julitta, Keo‐Kosal, Pascale, Panagiotakaki, Eleni, Montavont, Alexandra, Ostrowski‐Coste, Karine, Milh, Mathieu, Chiron, Catherine, Chemaly, Nicole, Bellavoine, Vanina, Barthez, Marie‐Anne
Published in Epilepsia (Copenhagen) (01.07.2016)
Published in Epilepsia (Copenhagen) (01.07.2016)
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Phosphatidylserine enriched with polyunsaturated n‐3 fatty acid supplementation for attention‐deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo‐controlled trial
Rheims, Sylvain, Herbillon, Vania, Gaillard, Ségolène, Mercier, Catherine, Villeuve, Nathalie, Villéga, Frédéric, Cances, Claude, Castelnau, Pierre, Napuri, Silvia, de Saint‐Martin, Anne, Auvin, Stéphane, Nguyen The Tich, Sylvie, Berquin, Patrick, Bellecize, Julitta, Milh, Mathieu, Roy, Pascal, Arzimanoglou, Alexis, Bodennec, Jacques, Bezin, Laurent, Kassai, Behrouz
Published in Epilepsia open (01.04.2024)
Published in Epilepsia open (01.04.2024)
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Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype
Yazbeck, Elise, Maurey, Hélène, Leroy, Carole, Horellou, Philippe, Napuri, Silvia, Lali, Mohammed, Adam, Clovis, Husson, Beatrice, Sevin, Caroline, Deiva, Kumaran
Published in Neuropediatrics (01.08.2021)
Published in Neuropediatrics (01.08.2021)
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Cognitive impairment in children with CACNA1A mutations
Humbertclaude, Veronique, Riant, Florence, Krams, Benjamin, Zimmermann, Valerie, Nagot, Nicolas, Annequin, Daniel, Echenne, Bernard, Tournier‐Lasserve, Elisabeth, Roubertie, Agathe, Bonnemains, Chrystelle, Chabrier, Stéphane, Cheuret, Emmanuel, Doummar, Diane, Dubois, Fanny, Kossorotoff, Manoelle, Leboucq, Nicolas, Leydet, Julie, Lion‐François, Laurence, Meyer, Pierre, Milh, Mathieu, Napuri, Silvia, Nguyen, Marie‐Ange, Nogue, Erika, Panagiotakaki, Eleni, Préclaire, Elodie, Rivier, François, Saint Martin, Anne, Sanchez, Stéphanie, Sarret, Catherine, Spitz, Marie‐Aude, Tardieu, Marc, Tourniaire, Barbara, Walther‐Louvier, Ulrike
Published in Developmental medicine and child neurology (01.03.2020)
Published in Developmental medicine and child neurology (01.03.2020)
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Benign paroxysmal torticollis, benign paroxysmal vertigo, and benign tonic upward gaze are not benign disorders
Humbertclaude, Véronique, Krams, Benjamin, Nogue, Erika, Nagot, Nicolas, Annequin, Daniel, Tourniaire, Barbara, Tournier‐Lasserve, Elisabeth, Riant, Florence, Roubertie, Agathe, Echenne, Bernard, Nguyen, Marie‐Ange, Doummar, Diane, Milh, Mathieu, Napuri, Silvia, Lion‐François, Laurence, Tardieu, Marc, Cheuret, Emmanuel, Spitz, Marie‐Aude, Saint Martin, Anne, Dubois, Fanny, Kossorotoff, Manoelle, Sarret, Catherine, Leboucq, Nicolas, Sanchez, Stéphanie, Préclaire, Elodie, Chabrier, Stéphane, Rivier, François, Panagiotakaki, Eleni, Bonnemains, Chrystelle, Walter‐Louvier, Ulrike
Published in Developmental medicine and child neurology (01.12.2018)
Published in Developmental medicine and child neurology (01.12.2018)
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Epilepsy in young Tsc1+/− mice exhibits age‐dependent expression that mimics that of human tuberous sclerosis complex
Gataullina, Svetlana, Lemaire, Eric, Wendling, Fabrice, Kaminska, Anna, Watrin, Françoise, Riquet, Audrey, Ville, Dorothée, Moutard, Marie‐Laure, Saint Martin, Anne, Napuri, Silvia, Pedespan, Jean‐Michel, Eisermann, Monika, Bahi‐Buisson, Nadia, Nabbout, Rima, Chiron, Catherine, Dulac, Olivier, Huberfeld, Gilles
Published in Epilepsia (Copenhagen) (01.04.2016)
Published in Epilepsia (Copenhagen) (01.04.2016)
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Cognitive impairment in children with CACNA 1A mutations
Humbertclaude, Veronique, Riant, Florence, Krams, Benjamin, Zimmermann, Valerie, Nagot, Nicolas, Annequin, Daniel, Echenne, Bernard, Tournier‐Lasserve, Elisabeth, Roubertie, Agathe
Published in Developmental medicine and child neurology (01.03.2020)
Published in Developmental medicine and child neurology (01.03.2020)
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A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report
Dessein, Anne-Frédérique, Fontaine, Monique, Andresen, Brage S, Gregersen, Niels, Brivet, Michèle, Rabier, Daniel, Napuri-Gouel, Silvia, Dobbelaere, Dries, Mention-Mulliez, Karine, Martin-Ponthieu, Annie, Briand, Gilbert, Millington, David S, Vianey-Saban, Christine, Wanders, Ronald J A, Vamecq, Joseph
Published in Orphanet journal of rare diseases (05.10.2010)
Published in Orphanet journal of rare diseases (05.10.2010)
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Topography of brain damage in metabolic hypoglycaemia is determined by age at which hypoglycaemia occurred
GATAULLINA, SVETLANA, LONLAY, PASCALE DE, DELLATOLAS, GEORGES, VALAYANNAPOULOS, VASSILI, NAPURI, SILVIA, DAMAJ, LÉNA, TOUATI, GUY, ALTUZARRA, CECILA, DULAC, OLIVIER, BODDAERT, NATHALIE
Published in Developmental medicine and child neurology (01.02.2013)
Published in Developmental medicine and child neurology (01.02.2013)
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Factors associated with treatment lag in infantile spasms
NAPURI, SILVIA, LE GALL, EDOUARD, DULAC, OLIVIER, CHAPERON, JACQUES, RIOU, FRANCOISE
Published in Developmental medicine and child neurology (01.12.2010)
Published in Developmental medicine and child neurology (01.12.2010)
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GDP-mannose: GlcNAc2-PP-dolichol mannosyltransferase deficiency (CDG Ik): 5 new patients and 7 novel mutations
Dupré, Thierry, Vuillaumier-Barrot, Sandrine, Chantret, Isabelle, Sadou Yayé, Hassane, Le Bizec, Christiane, Afenjar, Alexandra, Altuzarra, Cecilia, Barnérias, Christine, Burglen, Lydie, de Lonlay, Pascale, Feillet, François, Napuri, Silvia, Seta, Nathalie, Moore, Stuart E. H.
Published in Journal of medical genetics (02.08.2010)
Published in Journal of medical genetics (02.08.2010)
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A novel mutation of the ACADM gene associated with the common c.985AG mutation on the other ACADM allele causes mild MCAD deficiency: a case report
Dessein, Anne-Frédérique, Fontaine, Monique, Andresen, Brage S, Gregersen, Niels, Brivet, Michèle, Rabier, Daniel, Napuri-Gouel, Silvia, Dobbelaere, Dries, Mention-Mulliez, Karine, Ma, Briand, Gilbert, Millington, David S, Vianey-Saban, Christine, Wanders, Ronald JA, Vamecq, Joseph
Published in Orphanet journal of rare diseases (05.10.2010)
Published in Orphanet journal of rare diseases (05.10.2010)
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Journal Article
A novel mutation of the ACADM gene
Dessein, Anne-Frédérique, Fontaine, Monique, Andresen, Brage S, Gregersen, Niels, Brivet, Michèle, Rabier, Daniel, Napuri-Gouel, Silvia, Dobbelaere, Dries, Mention-Mulliez, Karine, Martin-Ponthieu, Annie, Briand, Gilbert, Millington, David S, Vianey-Saban, Christine, Wanders, Ronald JA, Vamecq, Joseph
Published in Orphanet journal of rare diseases (05.10.2010)
Published in Orphanet journal of rare diseases (05.10.2010)
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11 Contexte obstétrical, décision de réanimer en salle de naissance et devenir à deux et quatre ans après une naissance avant 28 semaines d’aménorrhée en ille-et-vilaine
Anne, Busnel, Alain, Beuchée, Gilles, Bretaudeau, Silvia, Napuri, Bernard, Branger
Published in Journal de gynécologie, obstétrique et biologie de la reproduction (01.05.2005)
Published in Journal de gynécologie, obstétrique et biologie de la reproduction (01.05.2005)
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