Rahma Felhi

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Topics

Oxidative Stress

Mitochondrial Dna

Top Venues

Metabolic brain disease

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

This page only lists publications with an associated author ORCID identifier.

Publications

Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease 39 (4) (2024)
Marwa Maalej, Lamia Sfaihi, Olfa-Alila Fersi, Boudour Khabou, Marwa Ammar, Rahma Felhi, Marwa Kharrat, Jihen Chouchen, Thouraya Kammoun, Abdelaziz Tlili, Faiza Fakhfakh
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity. Metabolic brain disease (2024)
Rahma Felhi, Lamia Sfaihi, Majida Charif, Fakher Frikha, Nissaf Aoiadni, Thouraya Kammoun, Guy Lenaers, Faiza Fakhfakh
Vitamin B1 deficiency leads to high oxidative stress and mtDNA depletion caused by SLC19A3 mutation in consanguineous family with Leigh syndrome. Metabolic brain disease (2023)
Rahma Felhi, Kamel Monastiri, Hayet Ben Hamida, Marwa Ammar, Fatma Zohra Chioukh, Brahim Tabarki, Jihene Chouchen, Faiza Fakhfakh, Abdelaziz Tlili, Emna Mkaouar-Rebai
First description of the MEGDEHL syndrome in the Tunisian population via whole-exome sequencing: Novel nonsense mutation in SERAC1 gene. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 82 (8) (2022)