Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Ali, Benomar"'
Autor:
Amine Cheikh, Mohamed Rida Ajaja, Hicham Rhazali, Mustapha Bouatia, Ali Benomar, Anas Slaoui, Yahia Cherrah, Redouane Abouqal, Amine El Hassani, Younes Cheikhaoui
Publikováno v:
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Postoperative bleeding in cardiovascular surgery is a frequent and complicated situation for the surgical team, and may also be responsible for significant hospital expenditures. Fibrin glue are indicated in surgery to improve hem
Externí odkaz:
https://doaj.org/article/333b6c06d8fa48e08aa3140d39673d2f
Autor:
Jehanne Aasfara, Wafa Regragui, Loubna El Ouardi, El Hachmia Ait Ben Haddou, Ali Benomar, Mohammed Yahyaoui
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 2 (2019)
Ischemic stroke can result from multiple etiologies. It can also be a complication of tuberculous meningoencephalitis and determine its outcome. stroke secondary to tuberculous meningoencephalitis, occurs in 30% cases in the basal ganglia region, unu
Externí odkaz:
https://doaj.org/article/f0ca4ddf0cbb4b73b2562d1c166e4d03
Autor:
Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouche
Publikováno v:
Journal of Molecular Neuroscience.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c31751d34e20c00c1c58bf1d1f7f0669
https://doi.org/10.1007/s12031-023-02128-9
https://doi.org/10.1007/s12031-023-02128-9
Autor:
Ghita Cherkaoui, Amine Cheikh, Rachid Razine, Wadii Bnouhanna, Wafae Regragui, Ali Benomar, Yahia Cherrah
Publikováno v:
Revue d'Épidémiologie et de Santé Publique. 70:75-81
Epilepsy is one of the most common chronic neurological diseases. In Morocco, it is the second most common reason for consulting a neurologist. Its prevalence was estimated in Casablanca in 1998 at 1.1%. This study was carried out with the aim of eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9cfe3599ca476bc972578b8781db748
https://doi.org/10.1016/j.respe.2022.01.127
https://doi.org/10.1016/j.respe.2022.01.127
Autor:
Mounia Rahmani, Maria Benabdeljlil, Fouad Bellakhdar, Mustapha El Alaoui Faris, Mohamed Jiddane, Khalil El Bayad, Fatima Boutbib, Rachid Razine, Rachid Gana, Moulay R. El Hassani, Nizar El Fatemi, Meryem Fikri, Siham Sanhaji, Hennou Tassine, Imane El Alaoui Balrhiti, Souad El Hadri, Najwa Ech-Cherif Kettani, Najia El Abbadi, Mourad Amor, Abdelmjid Moussaoui, Afifa Semlali, Saadia Aidi, El Hachmia Ait Benhaddou, Ali Benomar, Ahmed Bouhouche, Mohamed Yahyaoui, Abdeslam El Khamlichi, Abdessamad El Ouahabi, Rachid El Maaqili, Houyam Tibar, Yasser Arkha, Adyl Melhaoui, Abdelhamid Benazzouz, Wafa Regragui
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Introduction: Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is known as a therapy of choice of advanced Parkinson's disease. The present study aimed to assess the beneficial and side effects of STN DBS in Moroccan Parkinsonian patient
Externí odkaz:
https://doaj.org/article/01c2d0a03d95451fb4dc0bf8d3def84d
Autor:
Houyam Tibar, Khalil El Bayad, Ahmed Bouhouche, El Hachmia Ait Ben Haddou, Ali Benomar, Mohamed Yahyaoui, Abdelhamid Benazzouz, Wafa Regragui
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
BackgroundNon-motor symptoms (NMSs) are a real burden in Parkinson’s disease (PD). They may appear in early pre-symptomatic stage as well as throughout the disease course. However, their relationship with the deterioration of the patient’s qualit
Externí odkaz:
https://doaj.org/article/6488c5b485d844ffa878045ccb8c3c57
Autor:
Ahmed Bouhouche, Houyam Tibar, Yamna Kriouale, Mohammed Jiddane, Imane Smaili, Naima Bouslam, Ali Benomar, Mohamed Yahyaoui, Elmostafa El Fahime
Publikováno v:
Case Reports in Genetics, Vol 2018 (2018)
GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder due to mutations in the lysosomal acid 3-galactosidase gene, GLB1. It is usually classified into three forms, infantile, juvenile, or adult, based on age at onset and severity of
Externí odkaz:
https://doaj.org/article/fd3c6829c46240aaa791c579a95b452c
Publikováno v:
In Multiple Sclerosis and Related Disorders March 2023 71
Autor:
Ahmed Bouhouche, Christelle Tesson, Wafaa Regragui, Mounia Rahmani, Valérie Drouet, Houyam Tibar, Zouhayr Souirti, Rafiqua Ben El Haj, Naima Bouslam, Mohamed Yahyaoui, Alexis Brice, Ali Benomar, Suzanne Lesage
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
During the last two decades, 15 different genes have been reported to be responsible for the monogenic form of Parkinson’s disease (PD), representing a worldwide frequency of 5–10%. Among them, 10 genes have been associated with autosomal recessi
Externí odkaz:
https://doaj.org/article/7d19805c66a144fbaea0ae953be271c0
Autor:
Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, Khalil El Bayad, Rachid Razine, Sanaa Tazrout, Asmae Skalli, Naima Bouslam, Loubna Elouardi, Ali Benomar, Mohammed Yahyaoui, Wafa Regragui
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Background. The LRRK2 G2019S mutation is the most common genetic determinant of Parkinson’s disease (PD) identified to date. This mutation, reported in both familial and sporadic PD, occurs at elevated frequencies in Maghreb population. In the pres
Externí odkaz:
https://doaj.org/article/8adb26575b174d94aee5d9a5851268ea