Mohammed Ridal

Ocular motor impairment in early-stage multiple sclerosis: a video-oculography assessment

N. Ouattassi, S. Bouchal, Salma El Alaoui El Ghoul, 2023, The Egyptian Journal of Otolaryngology.

Hemangioma of the maxillary sinus: A benign and rare cause of epistaxis

B. Alami, M. Maaroufi, Y. Lamrani, 2022, Radiology case reports.

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

H. Rouba, A. Barakat, Redouane Boulouiz, 2007, International journal of pediatric otorhinolaryngology.

[Etiologic profile of severe and profound sensorineural hearing loss in children in the region of north-central Morocco].

Redouane Boulouiz, N. Benmansour, Z. Zaki, 2014, The Pan African medical journal.

A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2

L. Bouguenouch, K. Ouldim, M. Abbassi, 2023, American journal of medical genetics. Part A.