Afif Ben Mahmoud

发表

Antagonist effects of Bacillus spp. strains against Fusarium graminearum for protection of durum wheat (Triticum turgidum L. subsp. durum).

Hannatu K. Ali, S. Tounsi, S. Sellami, 2016, Microbiological research.

Identification of a novel m.9588G > A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men

F. Fakhfakh, A. Sellami, E. Mkaouar-Rebai, 2014, Journal of Assisted Reproduction and Genetics.

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.

N. Charfi, M. Abid, F. Fakhfakh, 2015, Biochemical and biophysical research communications.

A novel MT-CO2 m.8249G > A pathogenic variation and the MT-TW m.5521G > A mutation in patients with mitochondrial myopathy

F. Fakhfakh, M. Hachicha, I. Chamkha, 2014, Mitochondrial DNA.

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men

F. Fakhfakh, A. Sellami, E. Mkaouar-Rebai, 2013, Molecular Biology Reports.

First functional analysis of a novel splicing mutation in the B3GALTL gene by an ex vivo approach in Tunisian patients with typical Peters plus syndrome.

F. Fakhfakh, N. Belguith, R. B. Mansour, 2013, Gene.

A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG–Binding Protein 2 Confers Phenotypic Variability in 3 Cases of Tunisian Rett Patients

F. Fakhfakh, C. Triki, N. Fendri-Kriaa, 2015, Journal of child neurology.

Do GSTM1 and GSTT1 polymorphisms influence the risk of developing mitochondrial diseases in a Tunisian population?

F. Fakhfakh, Ghada Ben Salah, I. Chamkha, 2018, Environmental Science and Pollution Research.

A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome.

Ahmed Rebai, F. Kammoun, F. Fakhfakh, 2011, Biochemical and biophysical research communications.

Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.

N. Charfi, M. Abid, A. Tlili, 2017, Journal of diabetes and its complications.

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men

F. Fakhfakh, A. Sellami, E. Mkaouar-Rebai, 2013, Molecular reproduction and development.