Publications by authors named "Jacques Motte"

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WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.
Mara Cavallin, Maria A Rujano, Nathalie Bednarek, Daniel Medina-Cano, Antoinette Bernabe Gelot, Jacques Motte

Brain· October 2017

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Efficacy of a ketogenic diet in resistant myoclono-astatic epilepsy: A French multicenter retrospective study.
Elodie Stenger, Mickael Schaeffer, Claude Cances, Jacques Motte, Stéphane Auvin

Epilepsy Res· March 2017

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Word Detection in Sung and Spoken Sentences in Children With Typical Language Development or With Specific Language Impairment.
Clément Planchou, Sylvain Clément, Renée Béland, Nia Cason, Jacques Motte

Adv Cogn Psychol· January 2016

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Singing abilities in children with Specific Language Impairment (SLI).
Sylvain Clément, Clément Planchou, Renée Béland, Jacques Motte, Séverine Samson

Front Psychol· April 2015

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Social cognition in ADHD: irony understanding and recursive theory of mind.
Stéphanie Caillies, Vincine Bertot, Jacques Motte, Christine Raynaud, Michel Abely

Res Dev Disabil· November 2014

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A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.
Sarra Dimassi, Audrey Labalme, Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Jacques Motte

Epilepsia· February 2014

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GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
Gaetan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Jacques Motte

Nat Genet· September 2013

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Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth.
Lionel Van Maldergem, Qingming Hou, Vera M Kalscheuer, Marlène Rio, Martine Doco-Fenzy, Jacques Motte

Hum Mol Genet· August 2013

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The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients.
Camille Leroy, Emilie Landais, Sylvain Briault, Albert David, Olivier Tassy, Jacques Motte

Eur J Hum Genet· June 2013

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Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion.
Ksenija Vucurovic, Emilie Landais, Cécile Delahaigue, Julien Eutrope, Anouck Schneider, Jacques Motte

Eur J Med Genet· November 2012

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.
Robin Cloarec, Nadine Bruneau, Gabrielle Rudolf, Annick Massacrier, Manal Salmi, Jacques Motte

Neurology· November 2012

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Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Domitille Gras, Laurence Jonard, Emmanuel Roze, Sandra Chantot-Bastaraud, Jeanette Koht, Jacques Motte

J Neurol Neurosurg Psychiatry· October 2012

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Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.
Gaetan Lesca, Gabrielle Rudolf, Audrey Labalme, Edouard Hirsch, Alexis Arzimanoglou, Jacques Motte

Epilepsia· September 2012

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Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability.
Claire Beneteau, Emilie Landais, Martine Doco-Fenzy, Cyrille Gavazzi, Christophe Philippe, Jacques Motte

J Med Genet· September 2011

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Idiopathic hypersomnia: a report of three adolescent-onset cases in a two-generation family.
Sona Janácková, Jacques Motte, Serge Bakchine, Emilia Sforza

J Child Neurol· April 2011

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Four family cases of acute renal failure. Diagnosis: Orellanus syndrome.
Déborah Talmud, Alain Wynckel, Francis Grossenbacher, Sélim Saad, Jacques Motte

Pediatr Nephrol· March 2011

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Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome.
Jacques Rochette, Patrice Roll, Ying-Hui Fu, Anne Gaëlle Lemoing, Barbara Royer, Jacques Motte

Epileptic Disord· September 2010

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Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders.
Constance Flamand-Rouvière, Emilie Guettard, Caroline Moreau, Nadia Bahi-Buisson, Vassili Valayannopoulos, Jacques Motte

Mov Disord· August 2010

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Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome.
Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlène Rio, Valérie Malan, Jacques Motte

Hum Mutat· April 2009

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Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation.
Martine Doco-Fenzy, Emilie Landais, Joris Andrieux, Anouck Schneider, Brigitte Delemer, Jacques Motte

Eur J Med Genet· March 2009

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Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients.
Cyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, Constance Flamand-Rouvière, Nathalie Boddaert, Jacques Motte

Mov Disord· December 2008

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Human Bocavirus quantitative DNA detection in French children hospitalized for acute bronchiolitis.
Jérôme Jacques, Hélène Moret, Fanny Renois, Nicolas Lévêque, Jacques Motte

J Clin Virol· October 2008

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The three stages of epilepsy in patients with CDKL5 mutations.
Nadia Bahi-Buisson, Anna Kaminska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar, Jacques Motte

Epilepsia· June 2008

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Clinical and virological features of an aseptic meningitis outbreak in North-Eastern France, 2005.
Delphine Brunel, Nicolas Lévêque, Jérôme Jacques, Fanny Renois, Jacques Motte

J Clin Virol· June 2008

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Epidemiological, molecular, and clinical features of enterovirus respiratory infections in French children between 1999 and 2005.
Jérôme Jacques, Hélène Moret, Delphine Minette, Nicolas Lévêque, Nicolas Jovenin, Jacques Motte

J Clin Microbiol· January 2008

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