Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Abdelilah Oujilal"'
Publikováno v:
Otolaryngology Case Reports, Vol 21, Iss , Pp 100375- (2021)
Objective: To describe a case of inferior vestibular neuritis manifesting with a severe dizziness attack. To review available literature on the clinical features and characteristic presentation of this disease. Methods: Case report with literature re
Externí odkaz:
https://doaj.org/article/e375b642163749c1acdf86ad941896af
Autor:
Azzam Imane, Zahra Sayad, Omar Laassikri, Sophia Nitassi, Razika Bencheikh, Mohammed Anas Benbouzid, Abdelilah Oujilal, Malik Boulaadas, Leila Essakalli Hossyni
Publikováno v:
PAMJ Clinical Medicine, Vol 4, Iss 21 (2020)
Le syndrome de Lemierre « SL » est une maladie rare qui prend son origine très souvent d´une infection oropharyngée se compliquant d´une thrombose septique de la veine jugulaire interne et d´emboles septiques à prédominance pulmonaire dans s
Externí odkaz:
https://doaj.org/article/9e58344ffb45418ca70c9a63429bca44
Publikováno v:
The Pan African Medical Journal, Vol 31, Iss 78 (2018)
Rhinolithiasis is a rare condition often neglected or unknown that tends to disappear in developed countries and corresponds to a solid calcification by gradual deposition of calcareous salts around a central resorbable or non-resorbable foundation o
Externí odkaz:
https://doaj.org/article/d9583ae281ff4e0f93e08d194444b797
Autor:
Jawad Lahma, Zakaria Arkoubi, Reda Hejjouji, Sophia Nitassi, Ali El Ayoubi, Razika Bencheikh, Mohammed Anas Benbouzid, Abdelilah Oujilal, Leila Essakalli
Publikováno v:
The Pan African Medical Journal, Vol 31, Iss 77 (2018)
Kikuchi-Fujimoto's disease KFD is a rare and benign cause of cervical lymphadenopathy. It is an anatomoclinical entity of unknown etiology. The confirmation of the diagnosis is always provided by histological lymph node study. The clinical picture so
Externí odkaz:
https://doaj.org/article/1213b68a8b6643fead5230704f109dfa
Autor:
Mohammed Raoufi, Hicham Sator, Jawad Lahma, Ali El Ayoubi, Sophia Nitassi, Abdelilah Oujilal, Mohammed Anas Benbouzid, Leila Essakalli, Hanane Elouazzani, Ismail Abderrahmane Rhorfi, Ahmed Abid
Publikováno v:
The Pan African Medical Journal, Vol 23, Iss 159 (2016)
Kartagener syndrome is an autosomal recessive genetic ciliary disorder comprising of a classic triad of sinusitis, situs inversus and bronchiectasis. It's the one of primary ciliary dyskinesia disorders with manifestations present from childhood. Mos
Externí odkaz:
https://doaj.org/article/956a8c1676cd4ad3b1c0e8838dddb15b
Autor:
Hafsa El Ouazzani, Imane Azzam, Zainab Benyahya, Rachida Chehrastane, Abdelilah Oujilal, Fouad Zouaidia, Nadia Cherradi
Publikováno v:
Journal of Surgical Case Reports. 2023
Infantile myofibromatosis (IM) is the most common fibrous disorder of infancy and early childhood. Solitary intracranial involvement is rare and often unrecognized. This makes its early diagnosis and adequate management difficult. The majority of les
Autor:
Mohamed Ali GLITI, Niema Benkhraba, Sophia Nitassi, Bencheikh Razika, Benbouzid Mohamed Anas, Abdelilah Oujilal, Leila Essakalli Houssyni
Publikováno v:
EPH - International Journal of Medical and Health Science. 6:19-22
Frontal sinuses that present with abnormally large size are often clinically described as a deformity of the forehead, caused by Pneumosinus dilatans (PD). We report a rare case of Pneumosinus dilatans frontalis which was accidentally discovered by a
Publikováno v:
SAS Journal of Surgery. :22-25
Autor:
Moad El Mekkaoui, Bouchra Dani, Oussama Amraoui, Razika Bencheikh, Anas Benbouzid, Abdelilah Oujilal, Leila Essakalli, Hafsa Elouazzani, Ismail Boujida, Nadia Cherradi
Publikováno v:
Pan African Medical Journal. 43
Autor:
Razika Bencheikh, Sophia Nitassi, Ihssane Allouch, Najoua Belhaj, Abdelilah Oujilal, Chaimae Nekro, Anas Benbouzid, Leila Essakalli
Publikováno v:
Scholars Journal of Applied Medical Sciences. :605-607