Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Graziella, Mangone"'
Autor:
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Álvarez, Pau Pastor, Alessio Di Fonzo, Kailash P. Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockmann, Huw R. Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean Christophe Corvol, French Parkinson disease Genetics Study Group (PDG)
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-12 (2024)
Abstract Bi-allelic pathogenic variants in PRKN are the most common cause of autosomal recessive Parkinson’s disease (PD). 647 patients with PRKN-PD were included in this international study. The pathogenic variants present were characterised and i
Externí odkaz:
https://doaj.org/article/70e73e8ef588464cb23a2e9bc5b7be18
Autor:
Pauline Dodet, Marion Houot, Smaranda Leu-Semenescu, Jean-Christophe Corvol, Stéphane Lehéricy, Graziella Mangone, Marie Vidailhet, Emmanuel Roze, Isabelle Arnulf
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-11 (2024)
Abstract In Parkinson’s disease (PD), it remains unclear whether sleep disorders including insomnia, REM sleep behavior disorder (RBD), excessive daytime sleepiness (EDS), restless legs syndrome (RLS) and sleep-disordered breathing (SDB), are isola
Externí odkaz:
https://doaj.org/article/3e7d0893364a4647a32532c060491d99
Autor:
Johann Faouzi, Manuela Tan, Fanny Casse, Suzanne Lesage, Christelle Tesson, Alexis Brice, Graziella Mangone, Louise-Laure Mariani, Hirotaka Iwaki, Olivier Colliot, Lasse Pihlstrøm, Jean-Christophe Corvol
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-11 (2024)
Abstract Cognitive decline is common in Parkinson’s disease (PD) and its genetic risk factors are not well known to date, besides variants in the GBA and APOE genes. However, variation in complex traits is caused by numerous variants and is usually
Externí odkaz:
https://doaj.org/article/22c72047f7ba4c65895a99e971717d77
Autor:
Johann Faouzi, Samir Bekadar, Fanny Artaud, Alexis Elbaz, Graziella Mangone, Olivier Colliot, Jean-Christophe Corvol
Publikováno v:
IEEE Open Journal of Engineering in Medicine and Biology, Vol 3, Pp 96-107 (2022)
Goal: Impulse control disorders (ICDs) are frequent non-motor symptoms occurring during the course of Parkinson’s disease (PD). The objective of this study was to estimate the predictability of the future occurrence of these disorders using longitu
Externí odkaz:
https://doaj.org/article/7cf12ec92d2848dab7e7da1815a3706e
Autor:
Marie-Laure Welter, Alexandre Vasseur, Regine Edragas, Hugo Chaumont, Fanny Pineau, Graziella Mangone, Claire Olivier, Isabelle Leber, Sophie Rivaud-Pechoux, Stéphane Lehericy, Cecile Gallea, Lydia Yahia-Cherif, Annie Lannuzel
Publikováno v:
NeuroImage: Clinical, Vol 38, Iss , Pp 103443- (2023)
Introduction: Gait disorders and falls occur early in progressive supranuclear palsy (PSP-RS) and Caribbean atypical parkinsonism (Caribbean AP). However, the link between these signs and brain lesions has never been explored in these patient populat
Externí odkaz:
https://doaj.org/article/4320069c5a264ce7949f28405f5df24a
Autor:
Rahul Gaurav, Romain Valabrègue, Lydia Yahia-Chérif, Graziella Mangone, Sridar Narayanan, Isabelle Arnulf, Marie Vidailhet, Jean-Christophe Corvol, Stéphane Lehéricy
Publikováno v:
NeuroImage: Clinical, Vol 36, Iss , Pp 103250- (2022)
Background: Parkinson’s disease (PD) demonstrates neurodegenerative changes in the substantia nigra pars compacta (SNc) using neuromelanin-sensitive (NM)-MRI. As SNc manual segmentation is prone to substantial inter-individual variability across ra
Externí odkaz:
https://doaj.org/article/8cc340beba6a4e0996942050384bf3f2
Autor:
Laila Khedher, Jean-Marie Bonny, Ana Marques, Elodie Durand, Bruno Pereira, Marie Chupin, Tiphaine Vidal, Carine Chassain, Luc Defebvre, Nicolas Carriere, Valerie Fraix, Elena Moro, Stéphane Thobois, Elise Metereau, Graziella Mangone, Marie Vidailhet, Jean-Christophe Corvol, Stéphane Lehéricy, Nicolas Menjot de Champfleur, Christian Geny, Umberto Spampinato, Wassilios Meissner, Solène Frismand, Emmanuelle Schmitt, Anne Doé de Maindreville, Christophe Portefaix, Philippe Remy, Gilles Fénelon, Jean Luc Houeto, Olivier Colin, Olivier Rascol, Patrice Peran, Franck Durif
Publikováno v:
NeuroImage: Clinical, Vol 36, Iss , Pp 103231- (2022)
Several postmortem studies have shown iron accumulation in the substantia nigra of Parkinson’s disease patients. Iron concentration can be estimated via MRI-R2∗ mapping. To assess the changes in R2∗ occurring in Parkinson’s disease patients c
Externí odkaz:
https://doaj.org/article/964991b807554fe298b3d89933a6a216
Autor:
Matthias Löhle, Graziella Mangone, Wiebke Hermann, Denise Hausbrand, Martin Wolz, Julia Mende, Heinz Reichmann, Andreas Hermann, Jean-Christophe Corvol, Alexander Storch
Publikováno v:
Parkinson's Disease, Vol 2022 (2022)
Identification of individual risk factors for motor complications in Parkinson’s disease (PD) can help to guide personalised medical treatment, particularly since treatment options are still limited. To determine whether common functional gene poly
Externí odkaz:
https://doaj.org/article/6192ce6730d34e4a96b1cdc8102fa2ff
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:
Laetitia Jeancolas, Dijana Petrovska-Delacrétaz, Graziella Mangone, Badr-Eddine Benkelfat, Jean-Christophe Corvol, Marie Vidailhet, Stéphane Lehéricy, Habib Benali
Publikováno v:
Frontiers in Neuroinformatics, Vol 15 (2021)
Many articles have used voice analysis to detect Parkinson's disease (PD), but few have focused on the early stages of the disease and the gender effect. In this article, we have adapted the latest speaker recognition system, called x-vectors, in ord
Externí odkaz:
https://doaj.org/article/2824f6eb36184efa818b863e2d34132c