K. Snoussi

Melatonin is useful alternative for sedation in children undergoing auditory brainstem responses testing

M. Essaadi, Amal Hajjij, Ilias Tahiri, 2020, European Journal of Pediatrics.

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

C. Petit, H. Charoute, A. Bakhchane, 2017, Human Genome Variation.

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness

C. Petit, H. Charoute, A. Bakhchane, 2019, Human Heredity.

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

Majida Charif, G. Lenaers, H. Charoute, 2017, International journal of pediatric otorhinolaryngology.

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

H. Charoute, A. Bakhchane, H. Rouba, 2016, European journal of medical genetics.

The Role of Surgery in the Treatment of Cervical Lymph Node Tuberculosis

F. Benariba, M. Essaadi, Ilias Tahiri, 2023, Cureus.