J. Motte

A. Nehlig, J. Motte, Brigitte Voutsinos-Porche, 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

Developmental delay and epilepsy

J. Motte, N. Bednarek, 2006 .

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

Y. Agid, A. Bonnet, M. Vidailhet, 2000, Brain : a journal of neurology.

Effects of pentylenetetrazol-induced status epilepticus on c-Fos and HSP72 immunoreactivity in the immature rat brain.

C. Marescaux, A. Nehlig, J. Motte, 1997, Brain research. Molecular brain research.

Hereditary sensory neuropathy with spastic paraplegia.

P. Sabouraud, J. Motte, N. Bednarek, 2004, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

Anne de Saint Martin, N. Burnashev, T. Tsintsadze, 2013, Nature Genetics.

Midbrain disconnection: an aetiology of severe central neonatal hypotonia.

P. Sabouraud, J. Motte, N. Bednarek, 2005, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Association of respiratory picornaviruses with acute bronchiolitis in French infants.

B. Lina, J. Motte, L. Andréoletti, 2006, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Human Bocavirus quantitative DNA detection in French children hospitalized for acute bronchiolitis

J. Motte, N. Lévêque, L. Andréoletti, 2008, Journal of Clinical Virology.

Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS).

Yves Chaix, S. Peudenier, J. Motte, 2006, Epileptic disorders : international epilepsy journal with videotape.

The BREV neuropsychological test: Part II. Results of validation in children with epilepsy

L. Vallée, J. Motte, C. Billard, 2002, Developmental medicine and child neurology.

Cognitive function in adolescents and young adults in complete remission from benign childhood epilepsy with centro-temporal spikes.

C. Hommet, J. Motte, C. Billard, 2001, Epileptic disorders : international epilepsy journal with videotape.

A young adult with sarcosinemia. No benefit from long duration treatment with memantine.

S. Bakchine, J. Motte, P. Gillery, 2012, JIMD reports.

Clinical and virological features of an aseptic meningitis outbreak in North-Eastern France, 2005.

J. Motte, N. Lévêque, L. Andréoletti, 2008, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Short communication Clinical and virological features of an aseptic meningitis outbreak in

J. Motte, F. Renois, D. Brunel, 2008 .

Pentylenetetrazol seizures induce cell suffering but not death in the immature rat brain.

A. Nehlig, C. Charriaut-Marlangue, J. Motte, 1999, Brain research. Developmental brain research.

Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome

Ying-Hui Fu, P. Berquin, A. Hunter, 2010, Epileptic disorders : international epilepsy journal with videotape.

Topiramate: efficacy and tolerability in children according to epilepsy syndromes

L. Vallée, M. Bourgeois, O. Dulac, 2003, Epilepsy Research.

Semiology of typical and atypical Rolandic epilepsy: a video-EEG analysis.

C. Marescaux, A. Arzimanoglou, M. Metz-Lutz, 2002, Epileptic disorders : international epilepsy journal with videotape.

Sinus pericranii: advantages of MR imaging

J. Motte, J. Bigot, P. Dhellemmes, 2000, Pediatric Radiology.

Spatial and temporal evolution of neuronal activation, stress and injury in lithium–pilocarpine seizures in adult rats

Astrid Nehlig, Tallie Z. Baram, A. Nehlig, 1998, Brain Research.

Benign Myoclonic Epilepsy in Infants: Electroclinical Features and Long‐term Follow‐up of 34 Patients

L. Vallée, S. Auvin, J. Motte, 2006, Epilepsia.

Lamotrigine for generalized seizures associated with the Lennox-Gastaut syndrome. Lamictal Lennox-Gastaut Study Group.

J. Motte, E. Trevathan, P. Manasco, 1997, The New England journal of medicine.

Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients

M. Vidailhet, N. Boddaert, D. Devos, 2008, Movement disorders : official journal of the Movement Disorder Society.

[Cutaneous granulomatous lesions disclosing ataxia-telangiectasia].

J. Motte, M. Munzer, E. Grosshans, 1999, Annales de dermatologie et de venereologie.

[Epidemiological and clinical study of Mycoplasma pneumoniae respiratory infections in children hospitalized in a pediatric ward between 1999 and 2005 at the Reims University Hospital].

D. Laplanche, J. Motte, L. Andréoletti, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Epilepsy and other neurological disorders Developmental delay and epilepsy

J. Motte, N. Bednarek, 2006 .

Fatal Echovirus 18 Leukoencephalitis in a Child

J. Motte, L. Andréoletti, J. Jacques, 2007, Journal of Clinical Microbiology.

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).

B. Echenne, L. Meiners, O. Dulac, 1998, Human molecular genetics.

Lennox-Gastaut syndrome ( LGS ) Author : Professor

J. Motte, J. Campos-castelló, 2004 .

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells

N. Boddaert, A. Verloes, P. Nitschké, 2017, Brain : a journal of neurology.

Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.

A. Monaco, M. Lathrop, A. Lemainque, 2001, American journal of human genetics.

A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2

P. Ryvlin, A. Arzimanoglou, E. Hirsch, 2014, Epilepsia.

Efficacy of a ketogenic diet in resistant myoclono-astatic epilepsy: A French multicenter retrospective study

S. Auvin, M. Schaeffer, R. Nabbout, 2017, Epilepsy Research.

C-fos expression after single and kindled audiogenic seizures in Wistar rats

L. Danober, M. Vergnes, C. Marescaux, 1994, Neuroscience Letters.

Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism

Edouard Hirsch, Damien Sanlaville, Alexis Arzimanoglou, 2012, Epilepsia.

Mutational, functional, and expression studies of the TCF4 gene in Pitt‐Hopkins syndrome

A. Munnich, C. Picard, N. Boddaert, 2009, Human mutation.

CASE REPORTS Fatal Echovirus 18 Leukoencephalitis in a Child

J. Motte, L. Andréoletti, D. Brunel, 2007 .

New Reverse Transcription-PCR Assay for Rapid and Sensitive Detection of Enterovirus Genomes in Cerebrospinal Fluid Specimens of Patients with Aseptic Meningitis

J. Motte, L. Andréoletti, V. Brodard, 2003, Journal of Clinical Microbiology.

Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation.

J. Andrieux, J. Motte, V. Sulmont, 2008, European journal of medical genetics.

Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion.

J. Motte, M. Doco‐Fenzy, A. Schneider, 2012, European journal of medical genetics.

Familial rectal pain: a familial autonomic disorder as a cause of paroxysmal attacks in the newborn baby.

P. Sabouraud, P. Plouin, J. Motte, 2005, Epileptic disorders : international epilepsy journal with videotape.

Evidence of Late‐Onset Infantile Spasms

O. Dulac, P. Plouin, J. Motte, 1998, Epilepsia.

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

M. Vidailhet, A. Durr, M. Polak, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Encephalopathy with calcifications of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new cases.

B. Echenne, O. Dulac, P. Lebon, 1989, Neuropediatrics.

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.

D. Smadja, P. Billuart, O. Dulac, 1997, Journal of medical genetics.

X-linked malformations of neuronal migration

D. Ledbetter, C. Walsh, M. Ross, 1996, Neurology.

Detection of Human Metapneumovirus RNA Sequences in Nasopharyngeal Aspirates of Young French Children with Acute Bronchiolitis by Real-Time Reverse Transcriptase PCR and Phylogenetic Analysis

B. Lina, J. Motte, L. Andréoletti, 2005, Journal of Clinical Microbiology.

Perinatal/Neonatal Case Presentation: Neonatal Acute Renal Failure Secondary to Maternal Exposure to Telmisartan, Angiotensin II Receptor Antagonist

J. Motte, C. Pietrement, B. Roussel, 2003, Journal of Perinatology.

Regional cerebral glucose metabolism in children with deterioration of one or more cognitive functions and continuous spike-and-wave discharges during sleep.

P. Maquet, C. Marescaux, G. Franck, 1995, Brain : a journal of neurology.

[Benign infantile convulsions. French collaborative study].

P. Berquin, O. Dulac, J. Motte, 1999, Archives de pédiatrie.

Ambiguity Detection in Adolescents with Asperger Syndrome: Is Central Coherence or Theory of Mind Impaired?.

F. Gierski, S. Caillies, J. Motte, 2011 .

A prospective open-labeled trial with levetiracetam in pediatric epilepsy syndromes: Continuous spikes and waves during sleep is definitely a target

O. Dulac, C. Chiron, J. Motte, 2011, Seizure.

Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability

C. Bénéteau, C. Philippe, P. Jonveaux, 2011, Journal of Medical Genetics.

[Bilateral frontal polymicrogyria and Ehlers-Danlos syndrome].

P. Sabouraud, J. Motte, N. Bednarek, 2005, Archives de pédiatrie.

Social cognition in ADHD: irony understanding and recursive theory of mind.

S. Caillies, J. Motte, M. Abély, 2014, Research in developmental disabilities.

Inference Processing in Adolescents with Asperger Syndrome: Relationship with Theory of Mind Abilities.

F. Gierski, S. Caillies, J. Motte, 2009 .

Sonographic diagnosis of lissencephaly

J. Motte, M. Cymbalista, P. Morville, 2006, Pediatric Radiology.

[Neuroimaging in pediatric epilepsy].

J. Motte, C. Hoeffel, N. Bednarek, 2012, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Neurofibromatosis type one and West syndrome: a relatively benign association.

O. Dulac, J. Motte, Z. Sfaello, 1992, Epilepsia.

Early infantile epileptic encephalopathy Author : Doctor

R. Nabbout, J. Motte, 2004 .

Chronic Infantile Neurological, Cutaneous, and Articular Syndrome with Severe Early Articular Manifestations

C. Leys, A. Prieur, J. Motte, 2005, Pediatric dermatology.

Landau–Kleffner syndrome: sleep EEG characteristics at onset

C. Marescaux, M. Metz-Lutz, E. Hirsch, 2000, Clinical Neurophysiology.

Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders

M. Vidailhet, D. Grabli, C. Moreau, 2010, Movement disorders : official journal of the Movement Disorder Society.

[Benign intracranial hypertension (17 cases) and cerebral venous thromboses (49 cases). Comparative study].

J. Motte, M. Bernard, A. Vieillart, 1985, Neuro-chirurgie.

PENCEA, V, KD BÍNGAMAN, LJ FREEDMAN, and MB LUSKIN, 200 1. Neurogenesis in the subventricular zone and rostral migra-tory stream of the neonatal and adult primate forebrain. Exp. Neural. 172: 1-16

O. Reiner, E. Andermann, J. Motte, 2004 .

Flunarizine in Alternating Hemiplegia in Childhood. An International Study in 12 Children

J. Aicardi, J. Motte, H. Szliwowski, 1987, Neuropediatrics.

Laryngospasm and sudden unexpected death syndrome.

J. Motte, B. Menanteau, M. Cymbalista, 1986, Annales de radiologie.

[Ifosfamide induced encephalopathy: 15 observations].

A. Paci, J. Grill, P. Sabouraud, 2006, Archives de pédiatrie.

Mapping of neuronal networks underlying generalized seizures induced by increasing doses of pentylenetetrazol in the immature and adult rat: a c‐Fos immunohistochemical study

C. Marescaux, A. Nehlig, J. Motte, 1998, The European journal of neuroscience.

Idiopathic Hypersomnia: A Report of Three Adolescent-Onset Cases in a Two-Generation Family

E. Sforza, S. Bakchine, J. Motte, 2011, Journal of child neurology.

Lamotrigine for generalized seizures associated with the Lennox-Gastaut syndrome.

J. Motte, E. Trevathan, P. Manasco, 1997, The New England journal of medicine.

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

P. Genton, Ying-Hui Fu, A. Hunter, 2012, Neurology.