Search Results - Ali Benomar

Ali Benomar

Ali Benomar (born 9 May 1988) is a Dutch footballer who plays as a midfielder for amateur side Nieuwerkerk. Provided by Wikipedia
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  1. 1
    Cost of Treatment of Cerebral Aneurysm Embolization: Study of Associated Factors

    Cost of Treatment of Cerebral Aneurysm Embolization: Study of Associated Factors by Cheikh, Amine, Rachid, Razine, Jehanne, Aasfara, Adil, Ababou, Ali, Benomar, Cherrah, Yahya, Amine, El Hassani, Abdeljalil, El Quessar

    Published 2016
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  2. 2
    Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients

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

    Published 2018
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  3. 3
    A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

    A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 by Ahmed Bouhouche, Ali Benomar, Nazha Birouk, Angélique Mularoni, Farid Meggouh, Jean‐Pol Tassin, D. Grid, Antoon Vandenberghe, Mohamed Yahyaoui, T. Chkili, Alexis Brice, Eric LeGuern

    Published 1999
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  4. 4
    <i>LRRK2</i> G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease

    <i>LRRK2</i> G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease by Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, Khalil El Bayad, Rachid Razıne, S. Tazrout, A. Skalli, Naïma Bouslam, Loubna Elouardi, Ali Benomar, Mohammed Yahyaoui, W. Regragui

    Published 2017
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  5. 5
    Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients

    Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients by Isabelle Le Ber, Naïma Bouslam, Sophie Rivaud-Péchoux, João Tiago Guimarães, Ali Benomar, Céline Chamayou, Cyril Goizet, Maria-Ceù Moreira, Sandra Klur, Mohamed Yahyaoui, Y. Agid, Michel Kœnig, Giovanni Stévanin, Alexis Brice, Alexandra Dürr

    Published 2004
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  6. 6
    An expanded CAG repeat sequence in spinocerebellar ataxia type 7.

    An expanded CAG repeat sequence in spinocerebellar ataxia type 7. by K Lindblad, M L Savontaus, Giovanni Stévanin, Monica Holmberg, Kathleen B. Digre, Cecilia Zander, Hans Ehrsson, Gilles David, Ali Benomar, Eeva Nikoskelainen, Yvon Trottier, Gösta Holmgren, L J Ptácek, Anu Anttinen, Alexis Brice, Martin Schalling

    Published 1996
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  7. 7
    Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

    Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome by Sylvain Hanein, Elodie Martin, Amir Boukhris, P. Byrne, Cyril Goizet, Abdelmadjid Hamri, Ali Benomar, Alexander Lossos, Paola S. Denora, José Carlos Fernández Fernández, Nizar Elleuch, Sylvie Forlani, Alexandra Dürr, Imed Feki, Michael Hutchinson, Filippo M. Santorelli, Chokri Mhiri, Alexis Brice, Giovanni Stévanin

    Published 2008
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  8. 8
    Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families

    Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families by Géraldine Cancel‐Tassin, Alexandra Dürr, Olivier Didierjean, G. Imbert, Katrin Bürk, Agnès Lézin, Samir Belal, Ali Benomar, M. Abada-Bendib, Christophe Vial, J. Guimarães, Hervé Chneiweiss, Giovanni Stévanin, Gaël Yvert, N. Abbas, Frédéric Saudou, Anne Sophie Lebre, M. Yahyaoui, Fayçal Hentati, J C Vernant, Thomas Klockgether, Jean‐Louis Mandel, Y. Agid, Alexis Brice

    Published 1997
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  9. 9
    Intergenerational instability of the CAG repeat of the gene for Machado- Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat

    Intergenerational instability of the CAG repeat of the gene for Machado- Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular... by S. Igarashi, Yoshihisa Takiyama, Géraldine Cancel‐Tassin, Ekaterina Rogaeva, Hidenao Sasaki, Akemi Wakisaka, Yongxing Zhou, Hiroki Takano, K. Endo, Kazuhiro Sanpei, Mutsuo Oyake, Hajime Tanaka, Giovanni Stévanin, N. Abbas, Alexandra Dürr, Е. И. Рогаев, Robin Sherrington, T. Tsuda, Masaki Ikeda, E Cassa, Mayumi Nishizawa, Ali Benomar, Jean‐Philippe Julien, Jean Weissenbach, Gao‐Xue Wang, Y. Agid, Peter St George–Hyslop, Alexis Brice, Shoji Tsuji

    Published 1996
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  10. 10
    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia by Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B. Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B. Laurent, Daniel Rochefort, Dan Spiegelman, Alexandre Dionne‐Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed Yahyaoui, Réda Ouazzani, Grace Yoon, Nicolas Dupré, Oksana Suchowersky, François V. Bolduc, J. Alex Parker, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau, Bouchra Ouled Amar Bencheikh

    Published 2016
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  11. 11
    Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

    Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia by Christelle Tesson, Magdalena Nawara, Mustafa A. Salih, Rodrigue Rossignol, Maha S. Zaki, Mohammed Al Balwi, Rebecca Schüle, Cyril Mignot, Émilie Obre, Ahmed Bouhouche, Filippo M. Santorelli, Christelle Durand, Andrés Caballero-Oteyza, Khalid H. El-Hachimi, Abdulmajeed Al Drees, Naïma Bouslam, Foudil Lamari, Salah A. Elmalik, Mohammad M. Kabiraj, Mohammed Zain Seidahmed, Typhaine Esteves, Marion Gaussen, Marie-Lorraine Monin, Gàbor Gyapay, Doris Lechner, Michael Gonzalez, Christel Depienne, Fanny Mochel, Julie Lavie, Lüdger Schöls, Didier Lacombe, Mohamed Yahyaoui, Ibrahim Al Abdulkareem, Stephan Züchner, Atsushi Yamashita, Ali Benomar, Cyril Goizet, Alexandra Dürr, Joseph G. Gleeson, Frédéric Darios, Alexis Brice, Giovanni Stévanin

    Published 2012
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  12. 12
    Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

    Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders by Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Matan Hofree, Jennifer L. Silhavy, Andrew Heiberg, Mostafa Abdellateef, Başak Rosti, Eric Scott, Lobna Mansour, Amira Masri, Hülya Kayserili, Jumana Y. Al‐Aama, Ghada M. H. Abdel‐Salam, Ariana Karminejad, Majdi Kara, Bülent Kara, Babak Bozorgmehri, Tawfeg Ben‐Omran, Faezeh Mojahedi, Iman G. Mahmoud, Naïma Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Laure Raymond, Sylvie Forlani, Massimo Mascaro, Laila Selim, Nabil Shehata, Nasir Al‐Allawi, Parayil Sankaran Bindu, Matloob Azam, Murat Günel, Ahmet Okay Çağlayan, Kaya Bilgüvar, Aslıhan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily Spencer, Rasim Özgür Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Dürr, Alexis Brice, Giovanni Stévanin, Stacy Gabriel, Trey Ideker, Joseph G. Gleeson

    Published 2014
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  13. 13
    Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

    Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment by Thomas Roux, Mathieu Barbier, Mélanie Papin, Claire-Sophie Davoine, Sabrina Sayah, Giulia Coarelli, Perrine Charles, Cécilia Marelli, Livia Parodi, Christine Tranchant, Cyril Goizet, Stephan Klebe, Ebba Lohmann, Lionel Van Maldergem, Christine Van Broeckhoven, Marie Coutelier, Christelle Tesson, Giovanni Stévanin, Charles Duyckaerts, Alexis Brice, Alexandra Dürr, Alexandra Durr, Giovanni Stévanin, Alexis Brice, Frédéric Darios, Sylvie Forlani, Pitié-Salpêtrière Site, Guillaume Banneau, Cécile Cazeneuve, Perrine Charles, Charles Duyckaerts, Bertrand Fontaine, Jean‐Philippe Azulay, Odile Boesfplug-Tanguy, Cyril Goizet, Didier Hannequin, Jamïlé Hazan, Andrea Burgo, Christophe Verny, M. Kœnig, Pierre Labauge, Cécilia Marelli, Karine N’guyen, Diana Rodriguez, Soraya Belarbi, Abdelmadjid Hamri, Mériem Tazir, Sylvia Boesch, Massimo Pandolfo, Jardim Laura, Velina Guergueltcheva, Ivalo Tournev, Olga Lucia Pedraza Linarès, Jørgen E. Nielsen, Kirsten Svenstrup, Maha S. Zaki, Peter Bauer, Lüdger Schöls, Rebecca Schüle, Alexander Lossos, Maria-Teresa Bassi, Manuela Basso, Enrico Bertini, Alfredo Brusco, Carlo Casali, Giorgio Casari, Chiara Criscuolo, Alessandro Filla, Laura Orsi, Filippo M. Santorelli, Enza Maria Valente, Marinela Vavla, Giovanni Vazza, André Mégarbané, Ali Benomar, Berry Kremer, Willeke M. C. van Roon‐Mom, Richard Roxburgh, Anne Kjersti Erichsen, Chantal Tallaksen, Isabel Alonso, Paula Coutinho, José Léal Loureiro, Jorge Sequeiros, Mustapha Salih, Vladimir Kostić, Idoia Rouco Axpe, Liena E. O. Elsayed, Martin Paucar, Samir Roumani, Soong Bing-Wen, Evan Reid, Suran Nethisinghe, Thomas T. Warner, Nicholas Wood

    Published 2020
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  14. 14
    Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

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

    Published 2020
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