Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease

Autor: Evelyn Berger-Sieczkowski, Gian Maria Asioli, Javier Villacieros-Álvarez, Katya Kotschet, Marcus Erdler, Joan Santamaria Cano, Carles Gaig, Teresa Montojo, Alejandro Herrero San Martin, Koldo Berganzo, Morten Blaabjerg, Günter U. Höglinger, Lydia Lopez Manzanares, Giuseppe Plazzi, Josep Dalmau, Thomas Seifert-Held, Maja Patalong-Ogiewa, Barbara Willekens, Federica Provini, Nicola Tambasco, Herburg Liendl, Yaroslau Compta, Jan Lewerenz, Ángela Milán-Tomás, Christian Geis, Alex Iranzo, Inmaculada Puertas, Caroline Giordana, Birgit Högl, Lidia Sabater, Antonio Martin-Bastida, Nora Möhn, Lucio Huebra, Sonia Quintas, Francesc Graus, Pasquale Nigro, Norbert Brüggemann, Markus Hutterer, Maarten J. Titulaer, Maria Elena Erro, Stefan Macher, Florian Schoeberl, N. Téllez, Mateus Mistieri Simabukuro, Franziska S. Thaler, Juan Carlos Garcia-Monco, Jesus Perez Perez, Romana Höftberger, Caspar B Seitz, Anna Heidbreder, Carlos Morata, Yvette S Crijnen, Chen Fei Ng, Tarsis Farias, María José Martí

Publikováno v: Gaig, C, Compta, Y, Heidbreder, A, Marti, M J, Titulaer, M J, Crijnen, Y, Högl, B, Lewerenz, J, Erro, M E, Garcia-Monco, J C, Nigro, P, Tambasco, N, Patalong-Ogiewa, M, Erdler, M, Macher, S, Berger-Sieczkowski, E, Höftberger, R, Geis, C, Hutterer, M, Milán-Tomás, A, Martin-Bastida, A, Manzanares, L L, Quintas, S, Höglinger, G U, Möhn, N, Schoeberl, F, Thaler, F S, Asioli, G M, Provini, F, Plazzi, G, Berganzo, K, Blaabjerg, M, Brüggemann, N, Farias, T, Ng, C F, Giordana, C, Herrero-San Martín, A, Huebra, L, Kotschet, K, Liendl, H, Montojo, T, Morata, C, Perez, J P, Puertas, I, Seifert-Held, T, Seitz, C, Simabukuro, M M, Tellez, N, Villacieros-Álvarez, J, Willekens, B, Sabater, L, Iranzo, A, Cano, J S, Dalmau, J & Graus, F 2021, ' Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease ', Neurology, vol. 97, no. 14, pp. e1367-e1381 . https://doi.org/10.1212/WNL.0000000000012639
NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurology

Background and ObjectivesAnti-IgLON5 disease is a recently described neurologic disease that shares features of autoimmunity and neurodegeneration. Abnormal movements appear to be frequent and important but have not been characterized and are underre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb9bfacd5b844fa5de099b0b5aa5518d
https://portal.findresearcher.sdu.dk/da/publications/bdf1ece5-6028-4911-a2d1-11bd881fcbd6

Altered ioflupane single-photon emission computed tomography in anti-IgLON5 disease: A new case mimicking probable progressive supranuclear palsy and review of the literature

Autor: Carmen González-Ávila, Javier Villacieros-Álvarez, Laura Casado, José Vivancos, Sonia Quintas, Inés Muro García

Publikováno v: European journal of neurologyREFERENCES. 28(4)

Background and purpose Anti-IgLON5 disease is a rare disorder characterized by a heterogeneous myriad of symptoms that may include sleep disorders, bulbar dysfunction, gait problems, movement disorders, cognitive impairment, oculomotor abnormalities,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::708af3175beff42c5ba7386415f9bf0a
https://pubmed.ncbi.nlm.nih.gov/33175431

Teaching Video NeuroImages: Anti-IgLON5 Disease

Autor: Cristina Prieto-Jurczynska, Javier Villacieros-Álvarez, Carles Gaig, Gustavo Torres-Gaona, Ana Díez-Barrio, Carlos M. Ordás

Publikováno v: Neurology. 96:e2901-e2902

A 74-year-old woman presented with a 5-year history of progressive gait instability with recurrent falls, dysphonia, dysphagia, and sleep problems, which included insomnia, breathing difficulties, and complex vocalizations during sleep (talking, sing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b9ae841cfb546bda858bbaec9473d9
https://doi.org/10.1212/wnl.0000000000011381

Fatal familial insomnia: A new case description with early response to immunotherapy

Autor: Javier Villacieros-Álvarez, Erika García Di-Ruggiero, Alejandra Peláez-Hidalgo, Elvira García Cobos, E. Toribio-Díaz, Sonia Quintas

Publikováno v: Journal of Neuroimmunology. 346:577321

Fatal Familial Insomnia (FFI) is a rare prionopathy with autosomal dominant inheritance. Although it owes its name because insomnia is one of the most frequent and core symptoms, its clinical phenotype can be wide and heterogeneous. This usually make

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a160f78e7c2a80cf09a8308c67a3ea5f
https://doi.org/10.1016/j.jneuroim.2020.577321