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Triki, Chahnez Charfi
108
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Search for persons
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Format
Online (108)
Mediatypes
Articles (Online) (97)
Bookchapter (Online) (1)
OpenAccess-fulltext (10)
Languages
french (26)
english (74)
Sorted by: Relevance
Sorted by: Year
?
1
Treatment of seizures in the neonate: Guidelines and consen..:
Pressler, Ronit M.
;
Abend, Nicholas S.
;
Auvin, Stéphan
...
Epilepsia. 64 (2023) 10 - p. 2550-2570 , 2023
Link:
https://doi.org/10.1111/..
?
2
Case report: Functional analysis of the p.Arg507Trp variant..:
Ben Ayed, Ikhlas
;
Jallouli, Olfa
;
Murakami, Yoshiko
...
Frontiers in Neurology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Timing of referral to evaluate for epilepsy surgery: Expert..:
Jehi, Lara
;
Jette, Nathalie
;
Kwon, Churl‐Su
...
Epilepsia. 63 (2022) 10 - p. 2491-2506 , 2022
Link:
https://doi.org/10.1111/..
?
4
Combined in Silico Prediction Methods, Molecular Dynamic Si..:
Kharrat, Marwa
;
Triki, Chahnez Charfi
;
Alila-Fersi, Olfa
...
Journal of Molecular Neuroscience. 72 (2022) 8 - p. 1695-1705 , 2022
Link:
https://doi.org/10.1007/..
?
5
Global survey on disruption and mitigation of neurological ..:
Triki, Chahnez Charfi
;
Leonardi, Matilde
;
Mallouli, Salma Zouari
...
Journal of Neurology. 269 (2021) 1 - p. 26-38 , 2021
Link:
https://doi.org/10.1007/..
?
6
Unusual double mutation in MECP2 and CDKL5 genes in Rett-li..:
Jdila, Marwa Ben
;
Triki, Chahnez Charfi
;
Ghorbel, Rania
...
Clinica Chimica Acta. 508 (2020) - p. 287-294 , 2020
Link:
https://doi.org/10.1016/..
?
7
Position Statement:Emerging genetic therapies for rare diso..:
Samia, Pauline
;
Kirton, Adam
;
Dale, Russell
...
Journal of the International Child Neurology Association. , 2019
Link:
https://doi.org/10.17724..
?
8
First report of Tunisian patients with CDKL5‐related enceph..:
Charfi Triki, Chahnez
;
Zouari Mallouli, Salma
;
Ben Jdila, Marwa
...
Epilepsia Open. 9 (2024) 3 - p. 906-917 , 2024
Link:
https://doi.org/10.1002/..
?
9
Customized targeted massively parallel sequencing enables t..:
Ben Said, Mariem
;
Jallouli, Olfa
;
Ben Aissa, Abir
...
Epilepsia Open. , 2024
Link:
https://doi.org/10.1002/..
?
10
Case report: Compound heterozygous variants detected by nex..:
Ammous-Boukhris, Nihel
;
Abdelmaksoud-Dammak, Rania
;
Ben Ayed-Guerfali, Dorra
...
Frontiers in Neurology. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
11
Characterization of a missense variant in COG5 in a Tunisia..:
Khabou, Boudour
;
Sahari, Umar Bin Mohamad
;
ben Issa, Abir
...
Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
12
Complex genotypes in family with metachromatic leukodystrop..:
Ben Issa, Abir
;
Kamoun, Fatma
;
Bouchaala, Wafa
..
International Journal of Developmental Neuroscience. 84 (2023) 1 - p. 35-46 , 2023
Link:
https://doi.org/10.1002/..
?
13
A new case with the recurrent PURA p.(Phe233del) pathogenic..:
Ben Issa, Abir
;
Ben Ayed, Ikhlas
;
Jallouli, Olfa
...
International Journal of Developmental Neuroscience. 83 (2023) 4 - p. 383-395 , 2023
Link:
https://doi.org/10.1002/..
?
14
Knowledge and attitudes toward epilepsy among people in Sfa..:
Charfi Triki, Chahnez
;
Mguidich, Thouraya
;
Bouchaala, Wafa
...
Epilepsy & Behavior. 122 (2021) - p. 108151 , 2021
Link:
https://doi.org/10.1016/..
?
15
Acute Demyelinating Syndromes: A report of child neurology ..:
Zouari Mallouli, Salma
;
Ben Nsir, Sihem
;
Bouchaala, Wafa
..
Multiple Sclerosis and Related Disorders. 56 (2021) - p. 103291 , 2021
Link:
https://doi.org/10.1016/..
1-15