Search Results - "OUAZZANI, Réda"

Sleep quality and mental health in the context of COVID-19 pandemic and lockdown in Morocco by Janati Idrissi, Abdelkrim, Lamkaddem, Abdelaziz, Benouajjit, Abdelilah, Ben El Bouaazzaoui, Manar, El Houari, Farah, Alami, Mohammed, Labyad, Sanae, Chahidi, Abderrahman, Benjelloun, Meryem, Rabhi, Samira, Kissani, Najib, Zarhbouch, Benaissa, Ouazzani, Reda, Kadiri, Fouzia, Alouane, Rachid, Elbiaze, Mohamed, Boujraf, Said, El Fakir, Samira, Souirti, Zouhayr

“…The lockdown of COVID-19 (Coronavirus Disease 2019) is associated with several stressful factors that can negatively affect peoples' sleep quality and mental…”
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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents by Khetarpal, Sumeet A., Schjoldager, Katrine T., Christoffersen, Christina, Raghavan, Avanthi, Edmondson, Andrew C., Reutter, Heiko M., Ahmed, Bouhouche, Ouazzani, Reda, Peloso, Gina M., Vitali, Cecilia, Zhao, Wei, Somasundara, Amritha Varshini Hanasoge, Millar, John S., Park, YoSon, Fernando, Gayani, Livanov, Valentin, Choi, Seungbum, Noé, Eric, Patel, Pritesh, Ho, Siew Peng, Kirchgessner, Todd G., Wandall, Hans H., Hansen, Lars, Bennett, Eric P., Vakhrushev, Sergey Y., Saleheen, Danish, Kathiresan, Sekar, Brown, Christopher D., Abou Jamra, Rami, LeGuern, Eric, Clausen, Henrik, Rader, Daniel J.

“…Human genetics studies have implicated GALNT2, encoding GalNAc-T2, as a regulator of high-density lipoprotein cholesterol (HDL-C) metabolism, but…”
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia by Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Ouled Amar Bencheikh, Bouchra

“…Hereditary spastic paraplegia (HSP) is a genetically and clinically heterogeneous disease characterized by spasticity and weakness of the lower limbs with or…”
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Epilepsy in Morocco: Realities, pitfalls and prospects by Kissani, Najib, Cherkaoui Rhazouani, Oussama, Souirti, Zouhayr, Khramaz, Mounia, Meryem, Chettati, Mebrouk, Yassine, Ouazzani, Reda

“…The World Health Organization (WHO) estimates that about 50 million people of all ages have epilepsy and nearly 85% of whom live in low‐ and middle‐income…”
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Prevalence of epilepsy in Morocco: A population‐based study by Souirti, Zouhayr, Hmidani, Mohammed, Lamkadddem, Abdelaziz, Khabbach, Kawtar, Belakhdar, Salma, Charkani, Doae, Mhandez Tlemcani, Driss, Lahmadi, Nabila, El Akramine, Maroua, Erriouiche, Samira, Berrada, Asmae, Ahniba, Asmae, Omari, Mohammed, El Fakir, Samira, Tachfouti, Nabil, Rafai, Mohammed Abdoh, Chahid, Imane, Meriam, Bentahar, Jilla, Mariam, Ghaname, Aayad, Benmansour, Youssef, Filali Zegzouti, Younes, Kissani, Najib, Lakhdar, Abdelhakim, Belfkih, Rachid, Aggouri, Mohamed, Ouazzani, Reda, Chahidi, Abderrahmane, Janati Idrissi, Abdelkrim

“…ObjectiveIn Morocco, there was a lack of data related to the epidemiology of epilepsy. This data serves as a useful basis for the development of any national…”
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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations by MOULARD, Bruno, GENTON, Pierre, UTERMANN, Barbara, BALDY-MOULINIER, Michel, BELAIDI, Halima, BERTRAN, Francoise, BIRABEN, Arnaud, CHERIF, André Ali, CHKILI, Taieb, CRESPEL, Arielle, DARCEL, Francoise, DULAC, Olivier, GRID, Djamel, GENY, Christian, HUMBERT-CLAUDE, Véronique, KASSIOTIS, Philippe, BURESI, Catherine, MALAFOSSE, Alain, JEANPIERRE, Marc, OUAZZANI, Réda, MRABET, Amel, MORRIS, Mike, LEGUEM, Eric, DRAVET, Charlotte, MAUGUIERE, Francois

“…Unverricht-Lundborg disease (ULD) is a progressive myoclonus epilepsy common in Finland and North Africa, and less common in Western Europe. ULD is mostly…”
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Bilateral brachial plexus injury following acute carbon monoxide poisoning by Rahmani, Mounia, Belaidi, Halima, Benabdeljlil, Maria, Bouchhab, Wafa, El Jazouli, Nadia, El Brini, Asmae, Aidi, Saadia, Ouazzani, Reda M, El Alaoui Faris, Mustapha

“…Carbon monoxide (CO) intoxication is a leading cause of severe neuropsychological impairments. Peripheral nerve injury has rarely been reported. It consists…”
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Cerebral Hemispheric Lateralization Associated with Hippocampal Sclerosis May Affect Interictal Cardiovascular Autonomic Functions in Temporal Lobe Epilepsy by Ghchime, Rokia, Benjelloun, Halima, Kiai, Hajar, Belaidi, Halima, Lahjouji, Fatiha, Ouazzani, Reda

“…It is well established that the temporal lobe epilepsy (TLE) is linked to the autonomic nervous system dysfunctions. Seizures alter the function of different…”
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Amyotrophie monomélique des membres supérieurs en rapport avec une atteinte focale de la corne antérieure de la moelle cervicale by Oumerzouk, Jawad, Birouk, Nazha, Kably, Bouchra, Errguig, Leila, Ouazzani, Réda

“…Les amyotrophies monoméliques (AMM), maladies focales et rares du motoneurone périphérique, représentent un syndrome clinico-électrique et radiologique…”
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Un cas de Flail Leg avec paralysie diaphragmatique by Benmoh, Youssouf, Birouk, Nazha, Ouazzani, Réda

“…La sclérose latérale amyotrophique SLA est une maladie neurodégénérative du motoneurone. Le Flail Leg FL ou forme pseudopolynevritique de P.Marie et Patrikios…”
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Thrombose veineuse rétinienne bilatérale chez une patiente PIDC traité par immunoglobuline intraveineuse by Mnaili, Mohamed Amine, Birouk, Nazha, Ouazzani, Réda

“…Les immunoglobulines intraveineuses (IgIV) sont des concentrées d’immunoglobulines humaines utilisées dans de nombreuses maladies inflammatoires et…”
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Dystrophie musculaire congénitale (DMC) due à une mutation du gène LMNA (L-DMC) : à propos d’une famille marocaine by Belarabi, Laïla, Birouk, Nazha, Quijano-Roy, Susana, Kably, Bouchra, Ouazzani, Réda

“…Les DMC sont un groupe de myopathies hétérogènes, avec une hypotonie précoce et des manifestations orthopédiques et respiratoires. La biologie moléculaire a…”
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Le syndrome de Satoyoshi : à propos d’une observation by Balrhiti, Imane El Alaoui El, Birouk, Nazha, Bnouhanna, Wadii, Benabdeljlil, Maria, Aidi, Sadia, Ouazzani, Réda

“…Le syndrome de Satoyoshi est une entité rare. Il est défini par l’association de spasmes intermittents douloureux d’évolution progressive et d’une alopécie…”
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P14-T Mesio-temporal epilepsy with hippocampal sclerosis: Predictors for long term surgical outcome by Belkadi, Ilhame, Ouazzani, Reda, Lahjouji, Fatiha

“…To Study long-term predictors for surgical outcome of Mesio-temporal epilepsy (MTE) with hippocampal sclerosis (HS) in a Moroccan representative sample and…”
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Atypical onset of amyotrophic lateral sclerosis: Eight cases report by Marzouk, Basma, Birouk, Nazha, Kably, Bouchra, Ergguig, Leila, Ouazzani, Reda

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Motor predominant CIDP with severe respiratory failure by Mouhi, Ikrame, Birouk, Nazha, Kably, Bouchra, Aidi, Sadia, Ouazzani, Reda

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Neuromyotonie : aspects cliniques, éléctro-physiologiques et étiologiques : étude de 6 cas by Benmoh, Youssouf, Birouk, Nazha, Rahmani, Mounia, Kably, Bouchra, Belaidi, Halima, Aïdi, Sadia, Ouazzani, Réda

“…La neuromyotonie est un état d’hyperexcitabilité nerveuse périphérique, rapporté par Denny Brown et décrit par Isaac. Elle comprend une activité musculaire…”
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Carpal tunnel syndrome: Prospective and observational study of 458 cases. Diagnosis accuracy of clinical symptoms and their correlation with ENMG findings by Marzouk, Basma, Mouhi, Ikrame, Kably, Bouchra, Ergguig, Leila, Ouazzani, Reda, Birouk, Nazha

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S186. History of clinicalneurophysiology in Morocco: From an integrated unit in neurology to an independent structure of neurophysiological explorations by Chahidi, Abderrahmane, Souirti, Zouhayr, Chraa, Mohamed, Ouazzani, Reda

“…Neurophysiology is a young discipline in Morocco. The first department of Neurophysiology was created in 2003 in Rabat. It is the fruit of the collaboration of…”
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Advocacy for Epilepsy Surgery in Africa: Moroccan Experience of 132 Cases by El Khamlichi, Abdeslam, El Ouazzani, Reda, Melhaoui, Adyl, Arkha, Yasser, Adeniran Bankole, Nourou Dine, Rifi, Loubna, Lahjouji, Fatiha, Amor, Mourad, Jiddane, Mohamed

“…In Africa, epilepsy is a real burden. Temporal lobe epilepsy is the most common drug-resistant focal epilepsy disorder, and temporal lobectomy is the most…”
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