Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Emmanuelle, Apartis"'
Autor:
Clément Tarrano, Cécile Galléa, Cécile Delorme, Eavan M. McGovern, Cyril Atkinson-Clement, Vanessa Brochard, Stéphane Thobois, Christine Tranchant, David Grabli, Bertrand Degos, Jean Christophe Corvol, Jean-Michel Pedespan, Pierre Krystkowiak, Jean-Luc Houeto, Adrian Degardin, Luc Defebvre, Benoit Beranger, Davide Martino, Emmanuelle Apartis, Marie Vidailhet, Emmanuel Roze, Yulia Worbe
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Psychiatric symptoms are common in neurodevelopmental movement disorders, including some types of dystonia. However, research has mainly focused on motor manifestations and underlying circuits. Myoclonus-dystonia is a rare and homogeneous ne
Externí odkaz:
https://doaj.org/article/c1866a1963714179a033c4666633d649
Publikováno v:
Brain Stimulation, Vol 16, Iss 2, Pp 647-649 (2023)
Externí odkaz:
https://doaj.org/article/3ebb26519c674282b80b7695a58bfb9d
Autor:
Vincent Van Iseghem, Eavan McGovern, Emmanuelle Apartis, Boris Keren, Marie Vidailhet, Emmanuel Roze, Bertrand Degos
Publikováno v:
Tremor and Other Hyperkinetic Movements, Vol 10, Iss 0, Pp 1-4 (2020)
Externí odkaz:
https://doaj.org/article/0e0e39f94c9641459d8e8f4ca0964443
Autor:
Enrica Marchionni, Aurélie Méneret, Boris Keren, Judith Melki, Christian Denier, Alexandra Durr, Emmanuelle Apartis, Odile Boespflug-Tanguy, Fanny Mochel
Publikováno v:
Tremor and Other Hyperkinetic Movements, Vol 9, Iss 0, Pp 1-4 (2019)
Background: KIF1C (Kinesin Family Member 1C) variants have been associated with hereditary spastic paraplegia and spastic ataxia. Case report: We report fraternal twins presenting with cerebellar ataxia and dystonic tremor. Their brain MRI showed a h
Externí odkaz:
https://doaj.org/article/a5ae91c4916e48d8b9c2cb4b79ca94dc
Autor:
Pedro Manzke, Talyta Grippe, Georgia L. Tavares, Lucas C. Leal, Emmanuel Roze, Emmanuelle Apartis, Ronaldo M. Dias, André G. Ferreira
Publikováno v:
Tremor and Other Hyperkinetic Movements, Pp 1-3 (2018)
Background: The clinical spectrum of anti-glutamic acid decarboxylase (GAD) antibody-associated neurologic syndromes is expanding, with focal, generalized, and atypical forms. Case Report: We describe a 59-year-old female showing continuous right
Externí odkaz:
https://doaj.org/article/a4b366ebfbba42d6a1807c68a811a3e5
Autor:
Lucie Maugest, Eavan M. McGovern, Katia Mazalovic, Mohamed Doulazmi, Emmanuelle Apartis, Mathieu Anheim, Frédéric Bourdain, Eve Benchetrit, Virginie Czernecki, Emmanuel Broussolle, Cecilia Bonnet, Bruno Falissard, Marjan Jahanshahi, Marie Vidailhet, Emmanuel Roze
Publikováno v:
Frontiers in Neurology, Vol 8 (2018)
BackgroundPrimary orthostatic tremor (POT) is a movement disorder characterized by unsteadiness upon standing still due to a tremor affecting the legs. It is a gradually progressive condition with limited treatment options. Impairments in health-rela
Externí odkaz:
https://doaj.org/article/d441c31092094c30b2f1e81817ff8174
Autor:
Laurent Bailly, Marie Mongin, Cecile Delorme, Emmanuelle Apartis, Samir Saheb, Karine Viala, Emmanuel Roze
Publikováno v:
Tremor and Other Hyperkinetic Movements, Pp 1-2 (2018)
Background: Tremor is an underrecognized feature in certain neuropathy subtypes. Phenomenology shown: We show a patient with a disabling neuropathic tremor and mild cerebellar syndrome associated with chronic inflammatory demyelinating polyneuropa
Externí odkaz:
https://doaj.org/article/2d92ff2ddbd144e0a09233f803fa4934
Publikováno v:
Revue Neurologique. 178:398-399
Autor:
Marion Simonetta-Moreau, Emmanuel Roze, Jean-Charles Lamy, Sophien Mehdi, Pasquale Varriale, Emmanuelle Apartis, Anne Blancher-Meinadier, Sabine Meunier, Solène Frismand, Zuzana Kosutzka, Marie Vidailhet, Bertrand Degos
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 36(8)
Background Primary orthostatic tremor (POT) is a rare disorder, characterized by 13 to 18 Hz tremor in the legs when standing and is often refractory to medical treatment. Epidural spinal cord stimulation has been proposed as an alternative treatment
Autor:
Diane Doummar, Marie-Laure Moutard, Christine Ioos, Anna Loussouarn, Fanny Mochel, Christel Depienne, Delphine Héron, Julia Metreau, Nathalie Dorison, Boris Keren, Solveig Heide, Claudia Ravelli, Emmanuelle Apartis, Yara Beaugendre, Perrine Charles, Thierry Bienvenu, Cyril Mignot
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 34
The phenotypic spectrum of STXBP1-related encephalopathy ranges from infantile epileptic encephalopathy to intellectual disability with nonsyndromic or absent epilepsy. Although being frequently reported, the tremor associated with STXBP1 has not bee