Epilepsy Pioneers in Tunisia and Current Educational Programs in Tunisia

Chahnez Charfi Triki; Najoua Ben Khaled Miladi

doi:10.1055/s-0039-1685192

Journal of Pediatric Epilepsy, Table of Contents

Journal of Pediatric Epilepsy 2019; 08(01): 019-020
DOI: 10.1055/s-0039-1685192

Historical Vignette

Georg Thieme Verlag KG Stuttgart · New York

Epilepsy Pioneers in Tunisia and Current Educational Programs in Tunisia

Authors

Chahnez Charfi Triki

¹Department of Child Neurology, Hedi Chaker University Hospital, Sfax, Tunisia
Najoua Ben Khaled Miladi

²Department of Child Neurology, Maghreb Medical Tunis, Tunisia

Abstract

Full Text

References

References
1 Triki CC, Miladi NBK. L'association tunisienne de lutte contre l'épilepsie: parcours historique, objectifs et moyens. Epilepsies 2006; 18 (01) 51-53
2 Mrabet Khiari H, Khemiri E, Parain D, Hattab N, Proust F, Mrabet A. Epilepsy surgery program in Tunisia: an example of a Tunisian French collaboration. Seizure 2010; 19 (02) 74-78
3 Mrabet H, Mrabet A, Zouari B, Ghachem R. Health-related quality of life of people with epilepsy compared with a general reference population: a Tunisian study. Epilepsia 2004; 45 (07) 838-843
4 Attia-Romdhane N, Mrabet A, Ben Hamida M. Prevalence of epilepsy in Kelibia, Tunisia. Epilepsia 1993; 34 (06) 1028-1032
5 Fendri-Kriaa N, Boujilbene S, Kammoun F. , et al. A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome. Biochem Biophys Res Commun 2011; 408 (04) 654-657
6 Fendri-Kriaa N, Kammoun F, Salem IH. , et al. New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures. Eur J Neurol 2011; 18 (05) 695-702
7 Fendri-Kriaa N, Louhichi N, Mkaouar-Rebai E. , et al. The first genome-wide scan in a tunisian family with generalized epilepsy with febrile seizure plus (GEFS+). J Child Neurol 2010; 25 (11) 1362-1368
8 Jdila MB, Issa AB, Khabou B. , et al. Novel mutations in the CDKL5 gene in complex genotypes associated with West syndrome with variable phenotype: First description of somatic mosaic state. Clin Chim Acta 2017; 473: 51-59
9 Jdila MB, Triki C, Rhouma BB. , et al. A novel C-terminal truncated mutation in hCDKL5 protein causing a severe West syndrome: Comparison with previous truncated mutations and genotype/phenotype correlation. Int J Dev Neurosci 2019; 72: 22-30