Որոնման արդյունքները - Ahmed Bouhouche
- Ցուցադրվում են 1 - 11 արդյունքները 11
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Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients Houyam Tibar, Khalil El Bayad, Ahmed Bouhouche, El Hachmia Ait Ben Haddou, Ali Benomar, Mohamed Yahyaoui, Abdelhamid Benazzouz, W. Regragui
Հրապարակվել է 2018Artigo -
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A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 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
Հրապարակվել է 1999Artigo -
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<i>LRRK2</i> G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease 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
Հրապարակվել է 2017Artigo -
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Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated w... Hamid Azzedine, Alessandra Bolino, T. Taïeb, Nazha Birouk, Marco Di Duca, Ahmed Bouhouche, Soufiène Benamou, A. Mrabet, T. Hammadouche, T. Chkili, Riadh Gouider, Roberto Ravazzolo, Alexis Brice, Jocelyn Laporte, Eric LeGuern
Հրապարակվել է 2003Artigo -
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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia 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
Հրապարակվել է 2016Artigo -
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Characterization of Recessive Parkinson Disease in a Large Multicenter Study Suzanne Lesage, Ariane Lunati, Marion Houot, Sawssan Ben Romdhan, Fabienne Clot, Christelle Tesson, Graziella Mangone, Benjamin Le Toullec, Thomas Courtin, Kathy Larcher, Mustapha Benmahdjoub, Mohamed Arezki, Ahmed Bouhouche, Mathieu Anheim, Emmanuel Roze, François Viallet, François Tison, Emmanuel Broussolle, Murat Emre, Haşmet Hanağası, Başar Bılgıç, Mériem Tazir, Mouna Ben Djebara, Riadh Gouider, Christine Tranchant, Marie Vidailhet, E. Le Guern, Olga Corti, Chokri Mhiri, Ebba Lohmann, Andrew Singleton, Jean‐Christophe Corvol, Alexis Brice
Հրապարակվել է 2020Artigo -
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Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents Sumeet A. Khetarpal, Katrine T. Schjoldager, Christina Christoffersen, Avanthi Raghavan, Andrew C. Edmondson, Heiko Reutter, Ahmed Bouhouche, Réda Ouazzani, Gina M. Peloso, Cecilia Vitali, Wei Zhao, Amritha Varshini Hanasoge Somasundara, John S. Millar, YoSon Park, Gayani Fernando, Valentin Livanov, Seungbum Choi, Eric Noé, Pritesh Patel, Siew Peng Ho, Todd G. Kirchgessner, Hans H. Wandall, Lars Hestbjerg Hansen, Eric Bennett, Sergey Y. Vakhrushev, Danish Saleheen, Sekar Kathiresan, Christopher D. Brown, Rami Abou Jamra, Eric LeGuern, Henrik Clausen, Daniel J. Rader
Հրապարակվել է 2016Artigo -
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Loss of function of GALNT2 lowers high density lipoproteins in humans, nonhuman primates, and rodents Khetarpal, Sumeet A., Schjoldager, Katrine T., Christoffersen, Christina, Raghavan, Avanthi, Edmondson, Andrew C., Reutter, Heiko M., Ahmed, Bouhouche, Ouzzani, R, 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., Jamra, Rami Abou, LeGuern, Eric, Clausen, Henrik, Rader, Daniel J.
Հրապարակվել է 2016Տեքստ -
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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia 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
Հրապարակվել է 2012Artigo -
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Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders 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
Հրապարակվել է 2014Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Gene
Medicine
Disease
Mutation
Phenotype
Hereditary spastic paraplegia
Internal medicine
Parkinson's disease
Candidate gene
Exome sequencing
Missense mutation
Pathology
Pediatrics
Tooth disease
Amyotrophic lateral sclerosis
Bioenergetics
Chromosome
Cohort
Corticospinal tract
Dementia
Depression (economics)
Diffusion MRI
Disease gene identification
Dysautonomia
Dyskinesia
Dystonia
Economics
Endocrinology