I agree that this site is using cookies. You can find further informations here.
X
Kammoun, Fatma
163  results:
Search for persons X
?
1

Moyamoya Angiopathy: An Underdiagnosed Cause of Ischemic St..:

Bouchaala, Wafa ; Laroussi, Sirine ; Mzid, Yosra...
Pediatric Neurology.  150 (2024)  - p. 3-9 , 2024
Link: https://doi.org/10.1016/..
 
?
2

Development, validity and reliability of the systematic scr..:

Farhat, Faiçal ; Ammar, Achraf ; Kammoun, Mohamed Moncef...
F1000Research.  13 (2024)  - p. 313 , 2024
Link: https://doi.org/10.12688..
 
?
3

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/..
 
?
4

Apport du potentiel évoqué flash dans l'exploration des enc..:

Sellami, Sana ; Triki, Leila ; Chahnez, Triki...
Revue Neurologique.  179 (2023)  - p. S79 , 2023
Link: https://doi.org/10.1016/..
 
?
5

Valeur prédictive des potentiels évoqués auditifs précoces ..:

Sellami, Sana ; Triki, Leila ; Chahnez, Triki...
Revue Neurologique.  179 (2023)  - p. S62-S63 , 2023
Link: https://doi.org/10.1016/..
 
?
6

Mutation in the β‐tubulin gene TUBB4A results in epileptic ..:

Ben Jdila, Marwa ; Kammoun, Fatma ; Abdelmaksoud‐Dammak, Rania..
International Journal of Developmental Neuroscience.  83 (2023)  6 - p. 532-545 , 2023
Link: https://doi.org/10.1002/..
 
?
7

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/..
 
?
8

Relations entre les anomalies de l'EEG et l'évolution neuro..:

Chakroun, Sahar ; Sellami, Sana ; Adouania, Mahdi...
Revue Neurologique.  178 (2022)  - p. S13 , 2022
Link: https://doi.org/10.1016/..
 
?
9

SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and c..:

Ben Ayed, Ikhlas ; Ouarda, Wael ; Frikha, Fakher...
American Journal of Medical Genetics Part A.  185 (2021)  4 - p. 1081-1090 , 2021
Link: https://doi.org/10.1002/..
 
?
10

8q21.11 microdeletion syndrome: Delineation of HEY1 as a ca..:

Ben Ayed, Ikhlas ; Bouzid, Amal ; Kammoun, Fatma...
Molecular Genetics & Genomic Medicine.  9 (2021)  11 - p. , 2021
Link: https://doi.org/10.1002/..
 
?
11

A large consanguineous family with a homozygous Metabotropi..:

Jdila, Marwa Ben ; Mignon-Ravix, Cécile ; Ncir, Sihem Ben...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
?
12

A first description of ataxia with vitamin E deficiency ass..:

Maalej, Marwa ; Kammoun, Fatma ; Kharrat, Marwa...
Acta Neurologica Belgica.  121 (2020)  6 - p. 1733-1740 , 2020
Link: https://doi.org/10.1007/..
 
?
13

First description of an unusual novel double mutation in ME..:

Kharrat, Marwa ; Triki, Chahnez ; Maalej, Marwa...
International Journal of Developmental Neuroscience.  79 (2019)  1 - p. 37-44 , 2019
Link: https://doi.org/10.1016/..
 
?
14

Mitochondrial DNA triplication and punctual mutations in pa..:

Mkaouar-Rebai, Emna ; Felhi, Rahma ; Tabebi, Mouna...
Biochemical and Biophysical Research Communications.  473 (2016)  2 - p. 578-585 , 2016
Link: https://doi.org/10.1016/..
 
?
15

Syndrome des pointes-ondes continues du sommeil et autisme ..:

Kammoun, Ines ; Rekik, Sleh ; Zouari, Hela...
Revue Neurologique.  171 (2015)  - p. A27 , 2015
Link: https://doi.org/10.1016/..
 
1-15