Publications by authors named "Khalid Snoussi"

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Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Zied Riahi, Sophie Boucher, Samia Abdi, Fabienne Wong Jun Tai, Amrit Singh-Estivalet, Khalid Snoussi

Proc Natl Acad Sci U S A· December 2025

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CSF gushers in cochlear implantation: surgical planning and management.
Amal Hajjij, Hiba El Hani, Abderrahim Bourial, Khadija El Bouhmadi, Sara Benchikh, Khalid Snoussi

BMC Surg· November 2025

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Ambulatory pediatric cochlear implantation: safety, efficacy, and feasibility - first multicentric Moroccan study on 681 children.
Amal Hajjij, Khadija Elbouhmadi, Oussama El Gamali, Anas Benjilali, Sara Benchikh, Khalid Snoussi

BMC Pediatr· October 2025

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Spontaneous Retropharyngeal and Cervical Hematoma: A Case Report.
Hatim Bensouda Korachi, Safa Darouich, Said Anajar, Khalid Snoussi, Mustapha Essaadi

Clin Med Insights Case Rep· April 2025

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Intra-Parotid Recurrent Nasopharyngeal Carcinoma Following Intensity-Modulated Radiation Therapy: A Case Report.
Abderrahim Bourial, Othmane Nourallah Laraqui, Chirwa Abdillahi Mahamoud, Hiba Elhani, Reyzane Elmjabber, Khalid Snoussi

Clin Med Insights Case Rep· November 2024

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A case report of labyrinthine infarction: a 'central' cause of vertigo with 'peripheral' presentation.
Khadija El Bouhmadi, Safa Darouich, Myriam Youbi, Said Anajar, Mustapha Essaadi, Khalid Snoussi

Ann Med Surg (Lond)· November 2024

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Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
Imane AitRaise, Ghita Amalou, Salaheddine Redouane, Hicham Charoute, Khalid Snoussi

Mol Biol Rep· December 2023

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The Role of Surgery in the Treatment of Cervical Lymph Node Tuberculosis.
Ilias Tahiri, Rim Yacoubi, Othman Elhouari, Said Anajar, Taali Loubna, Khalid Snoussi

Cureus· May 2023

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Melatonin is useful alternative for sedation in children undergoing auditory brainstem responses testing.
Amal Hajjij, Ilias Tahiri, Said Anajar, Mustapha Essaadi, Khalid Snoussi

Eur J Pediatr· September 2020

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Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.
Amale Bousfiha, Zied Riahi, Lamiae Elkhattabi, Amina Bakhchane, Hicham Charoute, Khalid Snoussi

Hum Hered· May 2020

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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.
Sara Salime, Majida Charif, Amale Bousfiha, Soukaina Elrharchi, Amina Bakhchane, Khalid Snoussi

Int J Pediatr Otorhinolaryngol· October 2017

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A novel mutation in a Moroccan family with Zellweger spectrum disorders.
Amale Bousfiha, Amina Bakhchane, Hicham Charoute, Zied Riahi, Khalid Snoussi

Hum Genome Var· April 2017

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Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.
Amina Bakhchane, Amale Bousfiha, Hicham Charoute, Sara Salime, Mustapha Detsouli, Khalid Snoussi

Eur J Med Genet· June 2016

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