Ikhlass Hadj Salem

New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures

Nourhène Fendri-Kriaa, F. Kammoun, Ikhlass Hadj Salem et al. · European Journal of Neurology · 2010 · 26 citations

Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus

Nourhène Fendri-Kriaa, F. Kammoun, Ahmed Rebaï et al. · European Journal of Neurology · 2009 · 18 citations

Impact of single-nucleotide polymorphisms at the TP53-binding and responsive promoter region of BCL2 gene in modulating the phenotypic variability of LGMD2C patients

Ikhlass Hadj Salem, Fatma Kamoun, Nacim Louhichi et al. · Molecular Biology Reports · 2012 · 13 citations

Bcl2 Gene, Lgmd2c Patients, Genetics +6

Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient

Fakhri Kallabi, Ikhlass Hadj Salem, Amel Ben Chehida et al. · Neuroscience Research · 2015 · 12 citations

Genetic Disorder, Genetics, Partial Intron Retention +5

Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease

Nadege Kammoun Jellouli, Ikhlass Hadj Salem, Emna Ellouz et al. · Gene · 2012 · 12 citations

Autoimmune Disease, Founder Mutation C.-167a, Disease Mechanism +11