Julitta de Bellescize: search on Z-Library

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1

Troubles du sommeil, TDAH et absences typiques de lâenfant et de lâadolescentÂ : une Ã©tude observationnelle

Thieux, Marine, Duca, Maddalena, Putois, Benjamin, Herbillon, Vania, Toulouse, Joseph, Panagiotakaki, Eleni, Ilski-Lecoanet, Faustine, De Bellescize, Julitta, Arzimanoglou, Alexis, Franco, Patricia

Journal:

Year:

2020

File:

PDF, 228 KB

2020

2

Impacts cognitifs des anomalies paroxystiques intercritiques chez l’enfant épileptique : aspects EEG et neuropsychologiques, présentation d’un test cognitif synchronisé à l’EEG

Herbillon, Vania, Perrone, Marcela, de Bellescize, Julitta

Journal:

Neurophysiologie Clinique/Clinical Neurophysiology

Year:

2016

Language:

french

File:

PDF, 59 KB

french, 2016

3

Ring 14 chromosome presenting as early-onset isolated partial epilepsy

DOROTHÉE VILLE, JULITTA DE BELLESCIZE, MARIE ANGE NGUYEN, HERVÉ TESTARD, AGNÈS GAUTIER, JULIE PERRIER, MARIANNE TILL, VINCENT DES PORTES

Journal:

Developmental Medicine & Child Neurology

Year:

2009

Language:

english

File:

PDF, 330 KB

english, 2009

4

Myoclonic epilepsy in infancy: one or two diseases?

Stéphane Auvin,Julitta de Bellescize,Charlotte Dravet

Journal:

Epileptic Disorders

Year:

2013

Language:

english

File:

PDF, 65 KB

english, 2013

5

Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation

Zimmern, Vincent, Riant, Florence, Roze, Emmanuel, Ranza, Emmanuelle, Lehmann-Horn, Frank, Bellescize, Julitta de, Ville, Dorothée, Lesca, Gaetan, Korff, Christian M.

Journal:

Neuropediatrics

Year:

2019

Language:

english

File:

PDF, 155 KB

english, 2019

6

Neural correlates of verbal working memory in children with epilepsy with centro-temporal spikes

Ciumas, Carolina, Montavont, Alexandra, Ilski, Faustine, Laurent, Agathe, Saignavongs, Mani, Lachaux, Jean-Philippe, de Bellescize, Julitta, Panagiotakaki, Eleni, Ostrowsky-Coste, Karine, Herbillon, V

Journal:

NeuroImage: Clinical

Year:

2020

File:

PDF, 4.49 MB

2020

7

Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes

Rudolf, Gabrielle, de Bellescize, Julitta, de Saint Martin, Anne, Arzimanoglou, Alexis, Valenti Hirsch, Maria Paola, Labalme, Audrey, Boulay, Clotilde, Simonet, Thomas, Boland, Anne, Deleuze, Jean Fra

Journal:

European Journal of Paediatric Neurology

Year:

2020

File:

PDF, 714 KB

2020

8

Effets de la méthylphenydate sur les EEG des enfants épileptiques

Dadah, Samy Mohamed Lemine, De Bellescize, Julitta, Ostrowski-Coste, Karine, Kosal, Pascale Keo, Herbillon, Vania, Panagiotakaki, Elenie, Ilski, Faustine, Rheims, Sylvain, Arzimanoglou, Alexis

Journal:

Neurophysiologie Clinique/Clinical Neurophysiology

Year:

2016

Language:

french

File:

PDF, 47 KB

french, 2016

9

Myoclonic epilepsy in infancy : one or two diseases ?

Auvin, Stéphane, Bellescize, Julitta De, Dravet, Charlotte

Year:

2013

Language:

english

File:

PDF, 65 KB

english, 2013

10

Electrical status epilepticus in sleep, a constitutive feature of Christianson Syndrome?

Mathieu, Marie-Laure, de Bellescize, Julitta, Till, Marianne, Flurin, Vincent, Labalme, Audrey, Chatron, Nicolas, Sanlaville, Damien, Chemaly, Nicole, Portes, Vincent des, Ostrowsky, Karine, Arzimanog

Journal:

European Journal of Paediatric Neurology

Year:

2018

Language:

english

File:

PDF, 8.24 MB

english, 2018

11

Behavioral and fMRI responses to fearful faces are altered in benign childhood epilepsy with centrotemporal spikes (BCECTS)

Ciumas, Carolina, Laurent, Agathe, Saignavongs, Mani, Ilski, Faustine, de Bellescize, Julitta, Panagiotakaki, Eleni, Ostrowsky-Coste, Karine, Arzimanoglou, Alexis, Herbillon, Vania, Ibarrola, Danielle

Journal:

Year:

2017

Language:

english

File:

PDF, 1.03 MB

english, 2017

12

Functional connectivity of insular efferences

Almashaikhi, Talal, Rheims, Sylvain, Jung, Julien, Ostrowsky-Coste, Karine, Montavont, Alexandra, De Bellescize, Julitta, Arzimanoglou, Alexis, Keo Kosal, Pascale, Guénot, Marc, Bertrand, Olivier, Ryv

Journal:

Human Brain Mapping

Year:

2014

Language:

english

File:

PDF, 705 KB

english, 2014

13

GRIN2A -related disorders: genotype and functional consequence predict phenotype

Strehlow, Vincent, Heyne, Henrike O, Vlaskamp, Danique R M, Marwick, Katie F M, Rudolf, Gabrielle, de Bellescize, Julitta, Biskup, Saskia, Brilstra, Eva H, Brouwer, Oebele F, Callenbach, Petra M C, He

Journal:

Year:

2018

Language:

english

File:

PDF, 1.20 MB

english, 2018

14

Molecular characterization of a cohort of 73 patients with infantile spasms syndrome

Boutry-Kryza, Nadia, Labalme, Audrey, Ville, Dorothee, de Bellescize, Julitta, Touraine, Renaud, Prieur, Fabienne, Dimassi, Sarra, Poulat, Anne-Lise, Till, Marianne, Rossi, Massimiliano, Bourel-Ponche

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 849 KB

english, 2015

15

Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy

Rudolf, Gabrielle, Lesca, Gaetan, Mehrjouy, Mana M, Labalme, Audrey, Salmi, Manal, Bache, Iben, Bruneau, Nadine, Pendziwiat, Manuela, Fluss, Joel, de Bellescize, Julitta, Scholly, Julia, Møller, Rikke

Journal:

European Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.77 MB

english, 2016

16

Intrainsular functional connectivity in human

Almashaikhi, Talal, Rheims, Sylvain, Ostrowsky-Coste, Karine, Montavont, Alexandra, Jung, Julien, De Bellescize, Julitta, Arzimanoglou, Alexis, Keo Kosal, Pascal, Guénot, Marc, Bertrand, Olivier, Ryvl

Journal:

Human Brain Mapping

Year:

2014

Language:

english

File:

PDF, 363 KB

english, 2014

17

Correlation between sleep disorders and ADHD in children with absence epilepsy: An observational study

Duca, Maddalena, Cottone, Carlo, Maltoni, Lucia, Migliori, Matteo, Parmeggiani, Antonia, Franzoni, Emilio, Nollace, Leslie, Herbillon, Vania, Ilski-Lecoanet, Faustine, De Bellescize, Julitta, Panagiot

Journal:

European Journal of Paediatric Neurology

Year:

2017

Language:

english

File:

PDF, 171 KB

english, 2017

18

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, Pierre Genton, Jacques Motte, Anne de Saint Martin, Maria-Paola Valenti, Clotilde Boulay, Julitta De Bellescize, Pa

Journal:

Year:

2012

Language:

english

File:

PDF, 141 KB

english, 2012

19

A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes

Julitta de Bellescize, Nadia Boutry, Elodie Chabrol, Nathalie André-Obadia, Alexis Arzimanoglou, Eric Leguern, Stéphanie Baulac, Alain Calender, Philippe Ryvlin, Gaetan Lesca

Journal:

Epilepsy Research

Year:

2009

Language:

english

File:

PDF, 537 KB

english, 2009

20

Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability

Poulat, Anne-Lise, Ville, Dorothée, de Bellescize, Julitta, André-Obadia, Nathalie, Cacciagli, Pierre, Milh, Mathieu, Villard, Laurent, Lesca, Gaetan

Journal:

Epilepsy Research

Year:

2015

Language:

english

File:

PDF, 1.21 MB

english, 2015

21

Epileptic encephalopathy caused by BRAT1 mutations: Description of a novel patient

Putoux, Audrey, Chatron, Nicolas, Eyraud-Rousselle, Anne-Sophie, Labalme, Audrey, Streichenberger, Nathalie, Meyronet, David, De-Regnauld-De-Bellescize, Julitta, Sanlaville, Damien, Edery, Patrick, Le

Journal:

European Journal of Paediatric Neurology

Year:

2017

Language:

english

File:

PDF, 55 KB

english, 2017

22

Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers

Weckhuysen, Sarah, Holmgren, Philip, Hendrickx, Rik, Jansen, Anna C., Hasaerts, Daniele, Dielman, Charlotte, de Bellescize, Julitta, Boutry-Kryza, Nadia, Lesca, Gaetan, Spiczak, Sarah Von, Helbig, Ing

Journal:

Year:

2013

Language:

english

File:

PDF, 212 KB

english, 2013

23

West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1

Alfaiz, Ali Abdullah, Müller, Verena, Boutry-Kryza, Nadia, Ville, Dorothée, Guex, Nicolas, de Bellescize, Julitta, Rivier, Clotilde, Labalme, Audrey, des Portes, Vincent, Edery, Patrick, Till, Mariann

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.44 MB

english, 2015

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