Epileptic phenotypes in children with respiratory chain disorders

Sandra Sabbagh, Anne-Sophie Lèbre, Nadia Bahi‐Buisson, +8

Epilepsia

Impact of epilepsy characteristics and behavioral problems on school placement in children

Sandra Sabbagh, C. Soria, Sylvie Escolano, +2

Epilepsy & Behavior

School PlacementChild PsychologyNeuropsychological FunctioningEpilepsy CharacteristicsPediatrics +7

Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase

Nadia Bahi‐Buisson, Sandra Sabbagh, Christine Soufflet, +8

Seizure

Myoclonic Absence EpilepsyPhotoreceptor CellGlutamate DehydrogenaseFunction MutationNeurophysiology +9

Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases

Pratibha Nair, Sandra Sabbagh, Hicham Mansour, +21

Molecular Genetics & Genomic Medicine

Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia

André Mégarbané, Alessandra Pangrazio, Anna Villa, +4

European Journal of Medical Genetics

Thumb HypoplasiaDevelopmental BiologyMendelian DisorderGenetic DisorderSnx10 Gene +7

An unexpected EEG course in Dravet syndrome

Rima Nabbout, Isabelle Desguerre, Sandra Sabbagh, +4

Epilepsy Research

Unexpected Eeg CourseNeuropsychologyNeurophysiologyNeurological DisorderNeuroscience +5

Parental report of cognitive difficulties, quality of life and rehabilitation in children with epilepsy or treated for brain tumour

C. Soria, Delphine Callu, Delphine Viguier, +4

Developmental Neurorehabilitation

<scp>PI4K2A</scp> deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

Hormos Salimi Dafsari, Joshua G. Pemberton, Elizabeth Ferrer, +15

Annals of Clinical and Translational Neurology

Efficacy and tolerability of treatment with lacosamide in children: Postmarketing experience from the Middle East

Ghassan Hmaimess, Sandra Sabbagh, Maya Dirani, +3

Seizure

Infant NutritionPediatricsPharmacotherapyMedicineMiddle East +2

Report on a Patient with a 12q24.31 Microdeletion Inherited from an Insulin-Dependent Diabetes Mellitus Father

Éliane Chouery, Nancy Choucair, Joelle Abou Ghoch, +3

Molecular Syndromology

Developmental AnomalyMendelian DisorderSame DeletionGenetic DisorderGenetics +10