Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Zouhair, Najib"'
Autor:
Zouhair, Najib1 (AUTHOR) najib_zouhair@hotmail.fr, Mkhatri, Amine1 (AUTHOR), Chaouki, Anass1 (AUTHOR), Oukessou, Youssef1 (AUTHOR), Rouadi, Sami1 (AUTHOR), Abada, Redallah Laarabi1 (AUTHOR), Roubal, Mohamed1 (AUTHOR), Mahtar, Mohamed1 (AUTHOR)
Publikováno v:
Indian Journal of Otolaryngology & Head & Neck Surgery. 2022 Suppl, Vol. 74, p3643-3648. 6p.
Autor:
Zouhair, Najib1 Najib_zouhair@hotmail.com, Mallouk, Sanaa1, Oukessou, Youssef1, Rouadi, Sami1, Abada, Redallah Larbi1, Roubal, Mohamed1, Mahtar, Mohamed1
Publikováno v:
Pan African Medical Journal. Sep-Dec2020, Vol. 37, p1-11. 11p.
Autor:
Anass Chaouki, Mohammed Roubal, Omar Berrada, Sami Rouadi, Reda Allah Abada, Zouhair Najib, Mohammed Mahtar, Youssef Oukessou
Publikováno v:
Annals of Medicine and Surgery
Introduction Malignant melanomas (MM) of the parotid gland are rather rare and when discovered in the parotid gland without an identifiable primary site, they are considered even rarer. Presentation of case We report a case of a 27 years-old woman wh
Autor:
Meryem Lahjaouj, Mohamed Roubal, Sami Rouadi, Mohamed Mahtar, Youssef Oukessou, Zouhair Najib, Omar Berrada, Reda Allah Abada
Publikováno v:
Annals of Medicine and Surgery
Introduction The cervical lymphoepithelial or branchial cleft cyst are benign dysembryologic cystic tumors developing in the anterolateral region of the neck. They are relatively uncommon anomalies. The aims of this study are to analyze the anatomocl
Autor:
Zouhair Najib, Mohamed Roubal, Mohamed Mahtar, Redalah Elarabi Abada, Sami Rouadi, Youssef Oukessou
Publikováno v:
Carcinogenesis and Mutagenesis Case Reports. :1-2
Introduction: Mucoepidermoid carcinoma (MEC) is a rare malignant tumor that develops from the salivary glands. Its treatment includes surgery associated or not with radiotherapy depending on the histological grade. We report the case of a 38-year-old
Autor:
Zouhair Najib, Sami Rouad, Reda Abada, Omar Iziki, Sana Mallouk, Mohamed Roubal, Youssef Oukessou, Mohamed Mahtar
Publikováno v:
International Journal of Otorhinolaryngology. 6:23
BACKGROUND: Pendred syndrome (PS) is an autosomal recessive disorder, caused by biallelic mutations in the SLC26A4 gene which codes for the pendrin protein. It is characterized by sensorineural hearing loss associated with dyshormonogenic goiter. Whi
Autor:
Merzouqi, Boutaina, El Bouhmadi, Khadija, Zouhair, Najib, Oukessou, Youssef, Rouadi, Sami, Abada, Redallah Larbi, Roubal, Mohamed, Mahtar, Mohamed
Publikováno v:
In Annals of Medicine and Surgery April 2021 64
Autor:
Zouhair, Najib, Chaouki, Anass, Ballage, Amine, Abada, Redalah Elarabi, Rouadi, Sami, Roubal, Mohamed, Mahtar, Mohamed
Publikováno v:
International Journal of Surgery Case Reports; 2019, Vol. 59, p136-139, 4p