Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Constance Flamand-Rouvière"'
Autor:
Emmanuel Roze, Jean-Michel Mayer, Marie Vidailhet, Constance Flamand-Rouvière, Michel Gonce, Anne Le Floch, Emmanuel Broussolle, David Grabli
Publikováno v:
Movement Disorders. 25:394-397
Focal task-specific dystonia (FTSD) occurs exclusively during a specific activity that usually involves a highly skilled movement. Classical FTSD dystonias include writer's cramp and musician's dystonia. Few cases of sport-related dystonia have been
Autor:
Nathalie Boddaert, Constance Flamand-Rouvière, Brigitte Chabrol, Vassili Valayannopoulos, Jacques Motte, Emmanuel Roze, Karine Mention, Kiyoka Kinugawa, Emmanuelle Apartis, François Feillet, Dries Dobbelaere, Marie Vidailhet, Guy Touati, Nadia Bahi-Buisson, Cyril Gitiaux, Diana Rodriguez, Agathe Roubertie, David Devos
Publikováno v:
Movement Disorders. 23:2392-2397
Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to glutaryl CoA dehydrogenase deficiency. Comprehensive descriptions of GA1-associated movement disorders are rare. In order to refine the description of the motor p
Autor:
Damien Galanaud, Eric Bardinet, Bernard Pidoux, Pierre Pollak, Soledad Navarro, Emmanuel Roze, Marie Vidailhet, Marie-Laure Welter, Philippe Cornu, Constance Flamand-Rouvière, Magaly Aya-Kombo, José Fidel Baizabal-Carvallo, Luigi Romito, David Grabli
Publikováno v:
Parkinsonism & Related Disorders, Vol. 19, No 5 (2013) pp. 566-8
Parkinsonism & Related Disorders
Parkinsonism & Related Disorders, 2013, 19 (5), pp.566-8. ⟨10.1016/j.parkreldis.2013.01.010⟩
Parkinsonism and Related Disorders
Parkinsonism and Related Disorders, Elsevier, 2013, 19 (5), pp.566-8. ⟨10.1016/j.parkreldis.2013.01.010⟩
Parkinsonism & Related Disorders
Parkinsonism & Related Disorders, 2013, 19 (5), pp.566-8. ⟨10.1016/j.parkreldis.2013.01.010⟩
Parkinsonism and Related Disorders
Parkinsonism and Related Disorders, Elsevier, 2013, 19 (5), pp.566-8. ⟨10.1016/j.parkreldis.2013.01.010⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a71ec2e4608ccaf4d651038adafba3d
https://archive-ouverte.unige.ch/unige:33602
https://archive-ouverte.unige.ch/unige:33602
Autor:
Irène Ceballos-Picot, Caroline Moreau, Constance Flamand-Rouvière, Diana Rodriguez, Nadia Bahi-Buisson, Agathe Roubertie, Lisa Maintigneux, Emilie Guettard, David R. Adams, Vassili Valayannopoulos, Emmanuel Roze, Marie Vidailhet, David Grabli, Isabelle Kemlin, Jacques Motte
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(11)
Speech disturbances are frequent and potentially disabling in patients with dystonia or chorea due to neurometabolic disorders (DCND), but their precise characteristics are poorly documented. We prospectively studied 29 consecutive patients with DCND
Autor:
Anne, Le Floch, Marie, Vidailhet, Constance, Flamand-Rouvière, David, Grabli, Jean-Michel, Mayer, Michel, Gonce, Emmanuel, Broussolle, Emmanuel, Roze
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(3)
Focal task-specific dystonia (FTSD) occurs exclusively during a specific activity that usually involves a highly skilled movement. Classical FTSD dystonias include writer's cramp and musician's dystonia. Few cases of sport-related dystonia have been
Autor:
Cyril, Gitiaux, Emmanuel, Roze, Kiyoka, Kinugawa, Constance, Flamand-Rouvière, Nathalie, Boddaert, Emmanuelle, Apartis, Vassili, Valayannopoulos, Guy, Touati, Jacques, Motte, David, Devos, Karine, Mention, Dries, Dobbelaere, Diana, Rodriguez, Agathe, Roubertie, Brigitte, Chabrol, François, Feillet, Marie, Vidailhet, Nadia, Bahi-Buisson
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 23(16)
Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to glutaryl CoA dehydrogenase deficiency. Comprehensive descriptions of GA1-associated movement disorders are rare. In order to refine the description of the motor p
Autor:
Emmanuel Roze, Fanny Pineau, Claire Ewenczyk, Mathieu Anheim, Constance Flamand-Rouvière, Emmanuelle Apartis, Sandrine Vuillaumier-Barrot, Florence Riant, Elisabeth Maillart
Publikováno v:
Journal of Neurology. 258:316-317
Heterozygous mutations in the SLC2A1 gene, which encodes glucose transport protein type 1 (GLUT1), are responsible for GLUT1 deficiency, leading to cerebral energy failure associated with low cerebrospinal fluid (CSF) glucose concentrations [3, 6]. M