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Mkaouar-Rebai, Emna
50
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Online (50)
Mediatypes
Articles (Online) (49)
OpenAccess-fulltext (1)
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1
Identification of a novel homozygous mutation in NAXE gene ..:
Maalej, Marwa
;
Sfaihi, Lamia
;
Ammar, Marwa
...
neurogenetics. 23 (2022) 4 - p. 257-270 , 2022
Link:
https://doi.org/10.1007/..
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2
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/..
?
3
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/..
?
4
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/..
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5
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/..
?
6
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/..
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7
First description of a novel mitochondrial mutation in the ..:
Alila-Fersi, Olfa
;
Tabebi, Mouna
;
Maalej, Marwa
...
Biochemical and Biophysical Research Communications. 497 (2018) 4 - p. 1049-1054 , 2018
Link:
https://doi.org/10.1016/..
?
8
Co segregation of the m.1555A>G mutation in the MT-RNR1 gen..:
Alila-Fersi, Olfa
;
Chamkha, Imen
;
Majdoub, Imen
...
Biochemical and Biophysical Research Communications. 484 (2017) 1 - p. 71-78 , 2017
Link:
https://doi.org/10.1016/..
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9
Do GSTM1 and GSTT1 polymorphisms influence the risk of deve..:
Ghorbel, Raouia
;
Ben Salah, Ghada
;
Ghorbel, Rania
...
Environmental Science and Pollution Research. 25 (2017) 6 - p. 5779-5787 , 2017
Link:
https://doi.org/10.1007/..
?
10
In silico investigation of the impact of synonymous variant..:
Khabou, Boudour
;
Siala-Sahnoun, Olfa
;
Gargouri, Lamia
...
Computational Biology and Chemistry. 65 (2016) - p. 103-109 , 2016
Link:
https://doi.org/10.1016/..
?
11
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/..
?
12
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/..
?
13
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/..
?
14
Evaluation of the effect of c.2946+1G>T mutation on splicin..:
Ben Mahmoud, Afif
;
Ben Mansour, Riadh
;
Driss, Fatma
...
Computational Biology and Chemistry. 54 (2015) - p. 44-48 , 2015
Link:
https://doi.org/10.1016/..
?
15
A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mu..:
Tabebi, Mouna
;
Mkaouar-Rebai, Emna
;
Mnif, Mouna
...
Biochemical and Biophysical Research Communications. 459 (2015) 3 - p. 353-360 , 2015
Link:
https://doi.org/10.1016/..
1-15