Search Results - "BENOMAR, Ali"

Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients by Tibar, Houyam, El Bayad, Khalil, Bouhouche, Ahmed, Ait Ben Haddou, El Hachmia, Benomar, Ali, Yahyaoui, Mohamed, Benazzouz, Abdelhamid, Regragui, Wafa

“…Non-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…”
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Headache and Status Epilepticus Reveal Paget's Disease of the Bone by Ouhabi, Dahab, Tibar, Houyam, Benomar, Ali, Jiddane, Mohamed, Regragui, Wafa

“…Paget's disease of the bone (PDB) is a benign osteodystrophy of the elderly characterized by excessive remodeling of bone tissue, mainly in the pelvis, femur,…”
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Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment by Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra

“…Purpose Pathogenic variants in STUB1 were initially described in autosomal recessive spinocerebellar ataxia type 16 and dominant cerebellar ataxia with…”
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Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease by Smaili, Imane, Tesson, Christelle, Regragui, Wafa, Bertrand, Hélène, Rahmani, Mounia, Bouslam, Naima, Benomar, Ali, Brice, Alexis, Lesage, Suzanne, Bouhouche, Ahmed

“…In the past two decades, genetic studies of familial forms of Parkinson’s disease (PD) have shown evidence that PD has a significant genetic component. Indeed,…”
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Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome by Hanein, Sylvain, Martin, Elodie, Boukhris, Amir, Byrne, Paula, Goizet, Cyril, Hamri, Abdelmadjid, Benomar, Ali, Lossos, Alexander, Denora, Paola, Fernandez, José, Elleuch, Nizar, Forlani, Sylvie, Durr, Alexandra, Feki, Imed, Hutchinson, Michael, Santorelli, Filippo M., Mhiri, Chokri, Brice, Alexis, Stevanin, Giovanni

“…Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders. Both “uncomplicated” and “complicated” forms have been…”
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Evidence for prehistoric origins of the G2019S mutation in the North African Berber population by Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed

“…The most common cause of the monogenic form of Parkinson's disease known so far is the G2019S mutation of the leucine-rich repeat kinase 2 (LRRK2) gene. Its…”
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LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease by Benomar, Ali, Yahyaoui, Mohamed, Regragui, Wafaa, Bouslam, Naima, Skalli, Asmae, Tazrout, Sanaa, Razine, Rachid, El Bayad, Khalil, Ben El Haj, Rafiqua, Tibar, Houyam, Bouhouche, Ahmed, Elouardi, Loubna

“…Background. The LRRK2 G2019S mutation is the most common genetic determinant of Parkinson’s disease (PD) identified to date. This mutation, reported in both…”
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Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment by Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Durr, Alexandra, Stevanin, Giovanni, Brice, Alexis, Darios, Frédéric, Forlani, Sylvie, Site, Pitié-Salpêtrière, Banneau, Guillaume, Cazeneuve, Cécile, Charles, Perrine, Duyckaerts, Charles, Fontaine, Bertrand, Azulay, Jean-Philippe, Boesfplug-Tanguy, Odile, Goizet, Cyril, Hannequin, Didier, Hazan, Jamilé, Burgo, Andrea, Verny, Christophe, Koenig, Michel, Labauge, Pierre, Marelli, Cecilia, N’guyen, Karine, Rodriguez, Diana, Belarbi, Soraya, Hamri, Abdelmadjid, Tazir, Meriem, Boesch, Sylvia, Pandolfo, Massimo, Laura, Jardim, Guergueltcheva, Velina, Tournev, Ivalo, Pedraza Linarès, Olga Lucia, Nielsen, Jørgen E., Svenstrup, Kirsten, Zaki, Maha, Bauer, Peter, Schöls, Lüdger, Schüle, Rebecca, Lossos, Alexander, Bassi, Maria-Teresa, Basso, Manuela, Bertini, Enrico, Brusco, Alfredo, Casali, Carlo, Casari, Giorgio, Criscuolo, Chiara, Filla, Alessandro, Orsi, Laura, Santorelli, Filippo M., Valente, Enza Maria, Vavla, Marinela, Vazza, Giovanni, Megarbane, André, Benomar, Ali, Kremer, Berry, Van Roon-Mom, Willeke, Roxburgh, Richard, Erichsen, Anne Kjersti, Tallaksen, Chantal, Alonso, Isabel, Coutinho, Paula, Loureiro, José Léal, Sequeiros, Jorge, Salih, Mustapha, Kostic, Vladimir S, Rouco Axpe, Idoia, Elsayed, Liena, Paucar, Martin Arce, Roumani, Samir, Bing-Wen, Soong, Reid, Evan, Suran, Nethisinghe, Warner, Thomas, Wood, Nicholas

“…A Correction to this paper has been published: https://doi.org/10.1038/s41436-020-01064-y…”
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A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis by Aasfara, Jehanne, Regragui, Wafa, Ouardi, Loubna El, Haddou, El Hachmia Ait Ben, Benomar, Ali, Yahyaoui, Mohammed

“…Ischemic stroke can result from multiple etiologies. It can also be a complication of tuberculous meningoencephalitis and determine its outcome. stroke…”
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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel by Bouhouche, Ahmed, Tesson, Christelle, Regragui, Wafaa, Rahmani, Mounia, Drouet, Valérie, Tibar, Houyam, Souirti, Zouhayr, Ben El Haj, Rafiqua, Bouslam, Naima, Yahyaoui, Mohamed, Brice, Alexis, Benomar, Ali, Lesage, Suzanne

“…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…”
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Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study by Cheikh, Amine, Ajaja, Mohamed Rida, Rhazali, Hicham, Bouatia, Mustapha, Benomar, Ali, Slaoui, Anas, Cherrah, Yahia, Abouqal, Redouane, El Hassani, Amine, Cheikhaoui, Younes

“…Postoperative bleeding in cardiovascular surgery is a frequent and complicated situation for the surgical team, and may also be responsible for significant…”
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Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat by Rahmani, Mounia, Benabdeljlil, Maria, Bellakhdar, Fouad, Faris, Mustapha El Alaoui, Jiddane, Mohamed, Bayad, Khalil El, Boutbib, Fatima, Razine, Rachid, Gana, Rachid, Hassani, Moulay R El, Fatemi, Nizar El, Fikri, Meryem, Sanhaji, Siham, Tassine, Hennou, Balrhiti, Imane El Alaoui, Hadri, Souad El, Kettani, Najwa Ech-Cherif, Abbadi, Najia El, Amor, Mourad, Moussaoui, Abdelmjid, Semlali, Afifa, Aidi, Saadia, Benhaddou, El Hachmia Ait, Benomar, Ali, Bouhouche, Ahmed, Yahyaoui, Mohamed, Khamlichi, Abdeslam El, Ouahabi, Abdessamad El, Maaqili, Rachid El, Tibar, Houyam, Arkha, Yasser, Melhaoui, Adyl, Benazzouz, Abdelhamid, Regragui, Wafa

“…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…”
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Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion by Mandel, Jean-Louis, David, Gilles, Abbas, Nacer, Dürr, Alexandra, Brice, Alexis, Saudou, Frédéric, Stevanin, Giovanni, Yvert, Gaël, Weber, Chantal, Gemmill, Robert, Drabkin, Harry, Cancel, Géraldine, Agid, Yves, Giunti, Paola, Ruberg, Merle, Imbert, Georges, Benomar, Ali, Antoniou, Eric, Wood, Nick

“…The gene for spinocerebellar ataxia 7 (SCA7) has been mapped to chromosome 3p12-13. By positional cloning, we have identified a new gene of unknown function…”
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Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing by El Fahime, Elmostafa, Yahyaoui, Mohamed, Bouslam, Naima, Smaili, Imane, Jiddane, Mohammed, Kriouale, Yamna, Tibar, Houyam, Bouhouche, Ahmed, Benomar, Ali

“…GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder due to mutations in the lysosomal acid 3-galactosidase gene, GLB1. It is usually…”
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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) by Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni

“…Pure hereditary spastic paraplegias are characterized by isolated and progressive spasticity in the lower limbs. We mapped the spastic paraplegia 28 (SPG28)…”
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Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features by Dürr, A, Stevanin, G, Cancel, G, Duyckaerts, C, Abbas, N, Didierjean, O, Chneiweiss, H, Benomar, A, Lyon-Caen, O, Julien, J, Serdaru, M, Penet, C, Agid, Y, Brice, A

“…Patients with spinocerebellar ataxia 3 (SCA3) and Machado-Joseph disease (MJD) carry an expanded CAG repeat in the MJD1 gene. One hundred twenty families of…”
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An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3 by Bouhouche, Ahmed, Benomar, Ali, Errguig, Leila, Lachhab, Lamiae, Bouslam, Naima, Aasfara, Jehanne, Sefiani, Sanaa, Chabraoui, Layachi, El Fahime, Elmostafa, El Quessar, Abdeljalil, Jiddane, Mohamed, Yahyaoui, Mohamed

“…Single-gene disorders related to ischemic stroke seem to be an important cause of stroke in young patients without known risk factors. To identify new genes…”
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Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families by ELLEUCH, Nizar, BOUSLAM, Naima, BACQ, Delphine, TAZIR, Meriem, ZELENIKA, Diana, ARGOV, Zohar, DURR, Alexandra, YAHYAOUI, Mohamed, BENOMAR, Ali, BRICE, Alexis, STEVANIN, Giovanni, HANEIN, Sylvain, LOSSES, Alexander, HAMRI, Abdelmadjid, KLEBE, Stephan, MEINER, Vardiella, BIROUK, Nezha, LERER, Israela, GRID, Djamel

“…Hereditary spastic paraplegia (HSP) type 15 is an autosomal recessive (AR) form of complicated HSP mainly characterized by slowly progressive spastic…”
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Efficacy and Safety in Patients with Multiple Sclerosis Treated with Ocrelizumab by Moufakkir, Rim, Tibar, Houyam, Nassiri, Hajar, Regragui, Wafa, Benomar, Ali

“…Ocrelizumab (Ocrevus®) is a humanized monoclonal antibody directed against CD20 protein. It has marketing authorization for the treatment of adult patients…”
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The Use of Rituximab in the Treatment of Multiple Sclerosis in Morrocco by Siham, Asri, Houyam, Tibar, Amal, Souidi, Ali, Benomar, Wafaa, Regragui

“…Multiple sclerosis (MS) is a chronic and disabling neurological condition. It is the first non-traumatic cause of acquired motor disability in young people…”
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