Rosa Guerrero-López

Rosa Guerrero-López

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Rosa Guerrero-López

Rosa Guerrero-López

Publications by authors named "Rosa Guerrero-López"

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Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features.

Epilepsy Res 2019 Aug 21;154:39-41. Epub 2019 Apr 21.

Department of Pediatrics, Hospital Universitario Fundación Jiménez Díaz, UAM, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain; Neurology Lab and Epilepsy Unit, Department of Neurology, IIS- Fundación Jiménez Díaz, UAM, Madrid, Spain.

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http://dx.doi.org/10.1016/j.eplepsyres.2019.04.003DOI Listing
August 2019

Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.

Authors:
Patrick May Simon Girard Merle Harrer Dheeraj R Bobbili Julian Schubert Stefan Wolking Felicitas Becker Pamela Lachance-Touchette Caroline Meloche Micheline Gravel Cristina E Niturad Julia Knaus Carolien De Kovel Mohamad Toliat Anne Polvi Michele Iacomino Rosa Guerrero-López Stéphanie Baulac Carla Marini Holger Thiele Janine Altmüller Kamel Jabbari Ann-Kathrin Ruppert Wiktor Jurkowski Dennis Lal Raffaella Rusconi Sandrine Cestèle Benedetta Terragni Ian D Coombs Christopher A Reid Pasquale Striano Hande Caglayan Auli Siren Kate Everett Rikke S Møller Helle Hjalgrim Hiltrud Muhle Ingo Helbig Wolfram S Kunz Yvonne G Weber Sarah Weckhuysen Peter De Jonghe Sanjay M Sisodiya Rima Nabbout Silvana Franceschetti Antonietta Coppola Maria S Vari Dorothée Kasteleijn-Nolst Trenité Betul Baykan Ugur Ozbek Nerses Bebek Karl M Klein Felix Rosenow Dang K Nguyen François Dubeau Lionel Carmant Anne Lortie Richard Desbiens Jean-François Clément Cécile Cieuta-Walti Graeme J Sills Pauls Auce Ben Francis Michael R Johnson Anthony G Marson Bianca Berghuis Josemir W Sander Andreja Avbersek Mark McCormack Gianpiero L Cavalleri Norman Delanty Chantal Depondt Martin Krenn Fritz Zimprich Sarah Peter Marina Nikanorova Robert Kraaij Jeroen van Rooij Rudi Balling M Arfan Ikram André G Uitterlinden Giuliano Avanzini Stephanie Schorge Steven Petrou Massimo Mantegazza Thomas Sander Eric LeGuern Jose M Serratosa Bobby P C Koeleman Aarno Palotie Anna-Elina Lehesjoki Michael Nothnagel Peter Nürnberg Snezana Maljevic Federico Zara Patrick Cossette Roland Krause Holger Lerche

Lancet Neurol 2018 08 17;17(8):699-708. Epub 2018 Jul 17.

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http://dx.doi.org/10.1016/S1474-4422(18)30215-1DOI Listing
August 2018

Behavioral Evolution of Progressive Semantic Aphasia in Comparison with Nonfluent Aphasia.

Dement Geriatr Cogn Disord 2016 2;41(1-2):1-8. Epub 2015 Oct 2.

Department of Neurology, Fundacix00F3;n Jimx00E9;nez Dx00ED;az, Madrid, Spain.

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http://dx.doi.org/10.1159/000439521DOI Listing
September 2016

Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1.

Neuromuscul Disord 2015 Mar 22;25(3):222-4. Epub 2014 Nov 22.

Neurology Lab and Epilepsy Unit, Department of Neurology, IIS- Fundación Jiménez Díaz, UAM, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S09608966140069
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http://dx.doi.org/10.1016/j.nmd.2014.11.007DOI Listing
March 2015

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene.

Epilepsy Res 2014 Oct 7;108(8):1274-8. Epub 2014 Jul 7.

Neurology Lab and Epilepsy Unit, Department of Neurology, IIS - Fundación Jiménez Díaz, UAM, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2014.06.011DOI Listing
October 2014

Hyperexcitability and epileptic seizures in a model of frontotemporal dementia.

Neurobiol Dis 2013 Oct 14;58:200-8. Epub 2013 Jun 14.

Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Madrid, Spain.

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http://dx.doi.org/10.1016/j.nbd.2013.06.005DOI Listing
October 2013