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Alila-Fersi, Olfa
21  results:
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1

Mitochondrial genes modulate the phenotypic expression of c..:

Alila-Fersi, Olfa ; Tej, Amel ; Maalej, Marwa...
Gene.  914 (2024)  - p. 148388 , 2024
Link: https://doi.org/10.1016/..
 
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2

A Novel Mutation in the MAP7D3 Gene in Two Siblings with Se..:

Kharrat, Marwa ; Issa, Abir Ben ; Tlili, Abdelaziz...
Journal of Molecular Neuroscience.  73 (2023)  9-10 - p. 853-864 , 2023
Link: https://doi.org/10.1007/..
 
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3

A novel homozygous PIGO mutation associated with severe inf..:

Aguech, Ameni ; Sfaihi, Lamia ; Alila-Fersi, Olfa...
Metabolic Brain Disease.  , 2023
Link: https://doi.org/10.1007/..
 
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4

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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5

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/..
 
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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/..
 
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7

Mutations in GAA Gene in Tunisian Families with Infantile O..:

Alila-Fersi, Olfa ; Aloulou, Hajer ; Werteni, Ines...
Journal of Molecular Neuroscience.  70 (2020)  7 - p. 1100-1109 , 2020
Link: https://doi.org/10.1007/..
 
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8

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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9

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/..
 
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10

Whole mitochondrial genome screening of a family with mater..:

Tabebi, Mouna ; Charfi, Nadia ; Kallabi, Fakhri...
Journal of Diabetes and its Complications.  31 (2017)  1 - p. 253-259 , 2017
Link: https://doi.org/10.1016/..
 
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11

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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12

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/..
 
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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/..
 
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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/..
 
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15

A novel MT-CO1 m.6498C>A variation associated with the m.74..:

Mkaouar-Rebai, Emna ; Chamkha, Imen ; Kammoun, Thouraya...
Biochemical and Biophysical Research Communications.  430 (2013)  2 - p. 585-591 , 2013
Link: https://doi.org/10.1016/..
 
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