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Felhi, Rahma
18
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Search for persons
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Online (18)
Mediatypes
Articles (Online) (15)
OpenAccess-fulltext (3)
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1
Molecular and in silico investigation of a novel ECHS1 gene..:
Maalej, Marwa
;
Sfaihi, Lamia
;
Fersi, Olfa-Alila
...
Metabolic Brain Disease. 39 (2024) 4 - p. 611-623 , 2024
Link:
https://doi.org/10.1007/..
?
2
Vitamin B1 deficiency leads to high oxidative stress and mt..:
Felhi, Rahma
;
Sfaihi, Lamia
;
Charif, Majida
...
Metabolic Brain Disease. 38 (2023) 7 - p. 2489-2497 , 2023
Link:
https://doi.org/10.1007/..
?
3
A novel thymidine phosphorylase mutation in a family with M..:
Ammar, Marwa
;
Safi, Wajdi
;
Tlili, Abdelaziz
...
International Journal of Developmental Neuroscience. 82 (2022) 7 - p. 626-638 , 2022
Link:
https://doi.org/10.1002/..
?
4
First description of the MEGDEHL syndrome in the Tunisian p..:
Felhi, Rahma
;
Monastiri, Kamel
;
Ben Hamida, Hayet
...
International Journal of Developmental Neuroscience. 82 (2022) 8 - p. 735-746 , 2022
Link:
https://doi.org/10.1002/..
?
5
Severe Wolfram Syndrome Caused by aNovel Frameshift Mutatio..:
Tabebi, Mouna
;
Felhi, Rahma
;
Mrabet, Houcem Elomma
...
Open Journal of Genetics. 11 (2021) 4 - p. 77-92 , 2021
Link:
https://doi.org/10.4236/..
?
6
Mitochondrial disease patients with novel ND4 12058A > C an..:
Mkaouar-Rebai, Emna
;
Ammar, Marwa
;
Sfaihi, Lamia
...
Molecular Biology Reports. , 2021
Link:
https://doi.org/10.1007/..
?
7
Mutations in aARS genes revealed by targeted next-generatio..:
Felhi, Rahma
;
Charif, Majida
;
Sfaihi, Lamia
...
Molecular Biology Reports. 47 (2020) 5 - p. 3779-3787 , 2020
Link:
https://doi.org/10.1007/..
?
8
The first concurrent detection of mitochondrial DNA m.3243A..:
Tabebi, Mouna
;
Safi, Wajdi
;
Felhi, Rahma
...
Molecular Genetics & Genomic Medicine. 8 (2020) 7 - p. , 2020
Link:
https://doi.org/10.1002/..
?
9
Next generation sequencing in family with MNGIE syndrome as..:
Felhi, Rahma
;
Sfaihi, Lamia
;
Charif, Majida
...
Clinica Chimica Acta. 488 (2019) - p. 104-110 , 2019
Link:
https://doi.org/10.1016/..
?
10
Clinical, Molecular, and Computational Analysis in two case..:
Maalej, Marwa
;
Tej, Amel
;
Bouguila, Jihène
...
Biochemical and Biophysical Research Communications. 495 (2018) 2 - p. 1730-1737 , 2018
Link:
https://doi.org/10.1016/..
?
11
Cytochrome C oxydase deficiency: SURF1 gene investigation i..:
Maalej, Marwa
;
Kammoun, Thouraya
;
Alila-Fersi, Olfa
...
Biochemical and Biophysical Research Communications. 497 (2018) 4 - p. 1043-1048 , 2018
Link:
https://doi.org/10.1016/..
?
12
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/..
?
13
Mutational screening in patients with profound sensorineura..:
Ammar, Marwa
;
Tabebi, Mouna
;
Sfaihi, Lamia
...
Biochemical and Biophysical Research Communications. 474 (2016) 4 - p. 702-708 , 2016
Link:
https://doi.org/10.1016/..
?
14
Mutational analysis in patients with neuromuscular disorder..:
Felhi, Rahma
;
Mkaouar-Rebai, Emna
;
Sfaihi-Ben Mansour, Lamia
...
Biochemical and Biophysical Research Communications. 473 (2016) 1 - p. 61-66 , 2016
Link:
https://doi.org/10.1016/..
?
15
Severe Wolfram Syndrome Caused by a Novel Frameshift Mutati..:
Tabebi, Mouna
;
Felhi, Rahma
;
Mrabet, Houcem Elomma
...
Open Journal of Genetics, 2162-4453, 2021, 11:04, s. 77-92. , 2021
Link:
http://urn.kb.se/resolve..
1-15