Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study

Autor: Zuzanna Michalak, Marek Parowicz, Georgina Hollingsworth, Claudio Zucca, Ingrid E. Scheffer, Juan P. Kaski, Sergiu Groppa, Michael P. Carboni, Vesna Brankovic, Jacek Pilch, Ann M.E. Bye, Leticia Pias-Peleteiro, Roser Pons, Michela Stagnaro, Jan Novy, Ana Potic, Bassil Kherallah, Daniel S. Sinden, Carmen Fons, Charlotte E. Miller, Sanjay M. Sisodiya, A. Arzimanoglou, Maria Mazurkiewicz-Bełdzińska, Melissa McLean, Francesca Ragona, Rosaria Vavassori, Geoffrey S. Pitt, Raquel Samões, Eleni Panagiotakaki, Michael Ashworth, Elisa De Grandis, J. Helen Cross, Monique M. Ryan, Sarah Weckhuysen, Lyndsey Prange, Arsen S. Hunanyan, Jaume Campistol, Alessandra Gagliardi, Mohamad A. Mikati, Tiziana Granata, Inês Carrilho, Andrew M. Davis, Maria Thom, Livia Pisciotta, Allison Brashear, Aikaterini Vezyroglou, Reyes Álvarez-García-Rovés, Christopher Semsarian, Quasar S. Padiath, Andrew Tinker, Simona Balestrini, Nardo Nardocci, Karolina Dzieżyc, Edvige Veneselli

Publikováno v: Neurology
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu

ObjectiveTo define the risks and consequences of cardiac abnormalities in ATP1A3-related syndromes.MethodsPatients meeting clinical diagnostic criteria for rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood (AHC), and cerebe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47205323ba751dcf5cc2a1c8324afb32
http://hdl.handle.net/11567/1024573