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Felhi, Rahma
18  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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 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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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

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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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..
 
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