A large consanguineous family with a homozygous Metabotropic Glutamate Receptor 7 (mGlu7) variant and developmental epileptic encephalopathy: Effect on protein structure and ligand affinity
Jdila, Marwa Ben, Mignon-Ravix, Cécile, Ncir, Sihem Ben, Kammoun, Fatma, Fakhfakh, Faiza, Villard, Laurent, Triki, Chahnez
Published in Orphanet journal of rare diseases (17.07.2021)
Published in Orphanet journal of rare diseases (17.07.2021)
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Journal Article
Unusual double mutation in MECP2 and CDKL5 genes in Rett-like syndrome: Correlation with phenotype and genes expression
Jdila, Marwa Ben, Triki, Chahnez Charfi, Ghorbel, Rania, Bouchalla, Wafa, Ncir, Sihem Ben, Kamoun, Fatma, Fakhfakh, Faiza
Published in Clinica chimica acta (01.09.2020)
Published in Clinica chimica acta (01.09.2020)
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Journal Article
Knowledge and attitudes toward epilepsy among people in Sfax region, Tunisia
Charfi Triki, Chahnez, Mguidich, Thouraya, Bouchaala, Wafa, Ben Ncir, Sihem, Chaari, Hayet, Fourati, Emna, Ketata, Sourour, Kallel, Raida, Kamoun, Fatma
Published in Epilepsy & behavior (01.09.2021)
Published in Epilepsy & behavior (01.09.2021)
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Journal Article
Les hypersomnies de l’enfant : particularités cliniques et thérapeutiques
Fourati, Emna, Ben Ncir, Sihem, Bouchala, Wafa, Kamoun, Fatma, Chahanez, Triki
Published in Revue neurologique (01.04.2022)
Published in Revue neurologique (01.04.2022)
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Journal Article