Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mustapha Benmahdjoub"'
Autor:
Suzanne Lesage, Graziella Mangone, Christelle Tesson, Hélène Bertrand, Mustapha Benmahdjoub, Selma Kesraoui, Mohamed Arezki, Andrew Singleton, Jean-Christophe Corvol, Alexis Brice
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Autosomal recessive early-onset parkinsonism is clinically and genetically heterogeneous. Mutations of three genes, PRKN, PINK1, and DJ-1 cause pure phenotypes usually characterized by levodopa-responsive Parkinson's disease. By contrast, mutations o
Externí odkaz:
https://doaj.org/article/3192991556b54f2d86a73c02e4800b12
Autor:
Thomas Courtin, Ahmed Bouhouche, Mouna Ben Djebara, Riadh Gouider, Olga Corti, Mathieu Anheim, Eric Le Guern, Kathy Larcher, Mustapha Benmahdjoub, Meriem Tazir, Christine Tranchant, Ariane Lunati, Hasmet Hanagasi, Chokri Mhiri, Christelle Tesson, Başar Bilgiç, Marie Vidailhet, Fabienne Clot, François Tison, Mohammed Arezki, Graziella Mangone, Sawssan Ben Romdhan, Marion Houot, Ebba Lohmann, Andrew B. Singleton, Emmanuel Roze, Suzanne Lesage, Benjamin Le Toullec, Emmanuel Broussolle, Jean-Christophe Corvol, Alexis Brice, François Viallet, Murat Emre
Publikováno v:
Annals of Neurology
Annals of Neurology, Wiley, 2020, 88 (4), pp.843-850. ⟨10.1002/ana.25787⟩
Ann Neurol
Annals of Neurology, Wiley, 2020, 88 (4), pp.843-850. ⟨10.1002/ana.25787⟩
Ann Neurol
Studies of the phenotype and population distribution of rare genetic forms of parkinsonism are required, now that gene-targeting approaches for Parkinson's disease have reached the clinical trial stage. We evaluated the frequencies of PRKN, PINK1, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db2a6b777b8501b234a62242808cfe7
https://doi.org/10.1002/ana.25787
https://doi.org/10.1002/ana.25787
Autor:
Jean-Christophe Corvol, Andrew B. Singleton, Selma Kesraoui, Graziella Mangone, Hélène Bertrand, Mustapha Benmahdjoub, Alexis Brice, Mohamed Arezki, Suzanne Lesage, Christelle Tesson
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Frontiers, 2021, 12, pp.648457. ⟨10.3389/fneur.2021.648457⟩
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology, 2021, 12, pp.648457. ⟨10.3389/fneur.2021.648457⟩
Frontiers in Neurology, Frontiers, 2021, 12, pp.648457. ⟨10.3389/fneur.2021.648457⟩
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology, 2021, 12, pp.648457. ⟨10.3389/fneur.2021.648457⟩
Autosomal recessive early-onset parkinsonism is clinically and genetically heterogeneous. Mutations of three genes, PRKN, PINK1, and DJ-1 cause pure phenotypes usually characterized by levodopa-responsive Parkinson's disease. By contrast, mutations o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc8611dac08283e0d116b1682a91a4f
http://europepmc.org/articles/PMC8027075
http://europepmc.org/articles/PMC8027075
Publikováno v:
Revue Neurologique. 178:S14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f43ad1441370a5a92e38fa630adb643
https://doi.org/10.1016/j.neurol.2022.02.150
https://doi.org/10.1016/j.neurol.2022.02.150
Autor:
François Tison, Ariane Lunati, Olga Corti, Kathy Larcher, Suzanne Lesage, Thomas Courtin, Andrew Singleton, Meriem Tazir, François Viallet, Ebba Lohmann, Chokri Mhiri, Fabienne Clot, Emmanuel Broussolle, Mohammed Arezki, Jean Christophe Corvol, Mustapha Benmahdjoub, A Brice, Mathieu Anheim, Eric Le Guern, Emmanuel Roze, Ahmed Bouhouche, Graziella Mangone, Benjamin Le Toullec, Marie Vidailhet, Christelle Tesson, Christine Tranchant, Marion Houot, Murat Emre, Sawssan Benromdhan
Publikováno v:
SSRN Electronic Journal.
Background: Genetic mutations causing autosomal recessive Parkinson's disease account for a significant proportion of patients with early-onset disease. However, no large multicentre studies of known recessive Parkinson's disease-linked genes have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c600f7b97219e4d6ac2db0d30daf177c
https://doi.org/10.2139/ssrn.3409309
https://doi.org/10.2139/ssrn.3409309
Autor:
Mustapha Benmahdjoub, Mohamed Arezki
Publikováno v:
Revue Neurologique. 171:A6
Introduction La maladie de parkinson est rarement observee chez la femme en âge de procreer. Nous rapportons deux observations de patientes atteintes de maladie de parkinson ayant eu chacune plusieurs grossesses durant la maladie. Observation La pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10a08516d5f6fc446ad7625074924c05
https://doi.org/10.1016/j.neurol.2015.01.008
https://doi.org/10.1016/j.neurol.2015.01.008