Intra-Parotid Recurrent Nasopharyngeal Carcinoma Following Intensity-Modulated Radiation Therapy: A Case Report

Autor: Abderrahim Bourial, Othmane Nourallah Laraqui, Chirwa Abdillahi Mahamoud, Hiba Elhani, Reyzane Elmjabber, Loubna Taali, Said Anajar, Mustapha Essaadi, Khalid Snoussi, Zineb Dahbi, Amal Hajjij

Publikováno v: Clinical Medicine Insights: Case Reports, Vol 17 (2024)

Introduction: Intra-parotid metastasis refers to the spread of cancerous cells from a primary tumor to the lymph nodes within the parotid gland. To our best knowledge, we report the first described case in the literature of a patient who received IMR

Externí odkaz: https://doaj.org/article/4fbb0c0f085c48ad8736ae11a133e45e

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

Autor: Amina Bakhchane, Khalid Snoussi, Crystel Bonnet, Christine Petit, Amale Bousfiha, Hicham Charoute, Zied Riahi, Abdelhamid Barakat, Lamiae Elkhattabi

Publikováno v: Human Heredity. 84:109-116

Mutations in the mesenchymal epithelial transition factor (MET) gene are frequently associated with multiple human cancers but can also lead to human non-syndromic autosomal recessive deafness (DFNB97). In the present study, we identified a novel hom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::03645daef43209a3b7a3b537a8baf3c3
https://doi.org/10.1159/000503450

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

Autor: Said Anajar, Amal Hajjij, Khalid Snoussi, Ilias Tahiri, Mustapha Essaadi

Publikováno v: European journal of pediatrics. 179(9)

Auditory brainstem responses testing (ABRs) is frequently required to assess auditory function in children. It is done usually in outpatient fashion and requires deep sleep to avoid artefacts. Sedation method used for the test should allow a deep sle

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5806ad48d81c5951573a1f60c00b72
https://pubmed.ncbi.nlm.nih.gov/32179981

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

Autor: Zied Riahi, Crystel Bonnet, Christine Petit, Abdelhamid Barakat, Amale Bousfiha, Khalid Snoussi, Amina Bakhchane, Hicham Charoute, Hassan Rouba

Publikováno v: Human Genome Variation
Human Genome Variation, Nature Publishing Group, 2017, 4 (1), pp.17009. ⟨10.1038/hgv.2017.9⟩
Human Genome Variation, 2017, 4 (1), pp.17009. ⟨10.1038/hgv.2017.9⟩

International audience; Mutations in the PEX1 gene are usually associated with recessive inherited diseases including Zellweger spectrum disorders. In this work, we identified a new pathogenic missense homozygous PEX1 mutation (p.Leu1026Pro, c.3077T>

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bcae21bbb3e0c3a043ea3004eb39418
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219646

A novel

Autor: Amale, Bousfiha, Amina, Bakhchane, Hicham, Charoute, Zied, Riahi, Khalid, Snoussi, Hassan, Rouba, Crystel, Bonnet, Christine, Petit, Abdelhamid, Barakat

Publikováno v: Human Genome Variation

Mutations in the PEX1 gene are usually associated with recessive inherited diseases including Zellweger spectrum disorders. In this work, we identified a new pathogenic missense homozygous PEX1 mutation (p.Leu1026Pro, c.3077T>C) in two Moroccan syndr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7e9205871f4c373387686e4d8e8726be
https://pubmed.ncbi.nlm.nih.gov/28446956