Pilar Gómez-Garre - Dissemin

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All papers authored by Pilar Gómez-Garre

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2014 Pilar Gómez-Garre

ORCID

, Silvia Jesús, Fátima Carrillo, Maria Teresa Cáceres-Redondo, Ismael Huertas-Fernández, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Laura Vargas-González, Manuel Carballo, Pablo Mir

ORCID

Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain

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2013 Silvia Jesús, Pilar Gómez-Garre

ORCID

, Fátima Carrillo, María T. Cáceres-Redondo, Ismael Huertas-Fernández, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Laura Vargas-González, Manuel Carballo, Pablo Mir

ORCID

Genetic association of sirtuin genes and Parkinson’s disease

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Ignacio F. Mata, Victoria Alvarez

ORCID

, Renee Ribacoba, Jon Infante, María Sierra, Pilar Gómez-Garre

ORCID

ORCID

, Sarah Waldherr, Dora Yearout, Cyrus P. Zabetian

Novel Lrrk2-p.S1761R Mutation Is Not a Common Cause of Parkinson’s Disease in Spain

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2012 Ra Joundi, Virginia Lopez-Alonso, John-Stuart Brittain, Angel Lago, Miguel Fernandez-Del-Olmo, Pilar Gomez-Garre

ORCID

, Ned Jenkinson

ORCID

ORCID

, Binith Cheeran, Peter Brown

ORCID

The effect of BDNF val66met polymorphism on visuomotor adaptation

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S. Jesús, I. Pérez, M. T. Cáceres-Redondo, F. Carrillo, M. Carballo, P. Gómez-Garre

ORCID

, P. Mir

ORCID

Low serum uric acid concentration in Parkinson's disease in southern Spain

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Pilar Gómez-Garre

ORCID

, Silvia Jesús, Fátima Carrillo, Maria Teresa Cáceres-Redondo, Inmaculada Bernal-Bernal, Manuel Carballo, Lin Gao, Pablo Mir

ORCID

PSMC1Gene in Parkinsons Disease

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Vinko Palada, Sandra Stiern, Nicola Glöckle, Pilar Gómez Garre

ORCID

, Fatima Carrillo, Pablo Mir

ORCID

, Krzysztof Szczaluba, Michele Tinazzi

ORCID

, Domenico Ajena, Marta Romani, Enza Maria Valente, Ulrich Müller, Peter Bauer, Olaf Riess, Thomas Ott and 1 other authors

Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.

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2011 Rosa Guerrero, Santiago Vérnia

ORCID

, Raúl Sanz, Irene Abreu-Rodríguez, Carmen Almaraz, María García-Hoyos, Roberto Michelucci, Carlo Alberto Tassinari, Patrizia Riguzzi, Carlo Nobile, Pascual Sanz

ORCID

, José María Serratosa, Pilar Gómez-Garré

ORCID

A PTG variant contributes to a milder phenotype in Lafora disease

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Alzenira Costa, Lin Gao, Fátima Carrillo, María Teresa Cáceres-Redondo, Manuel Carballo, Juan Díaz-Martín, Pilar Gómez-Garre

ORCID

, Francisco Sobrino, Miguel Lucas, José López-Barneo, Pablo Mir

ORCID

, Elizabeth Pintado

Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease

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2010 M. Fernandez-Del-Olmo, B. Cheeran, P. Gomez-Garre

ORCID

, A. Lago, G. Marquez, G. Koch, J. T. H. Teo, J. C. Rothwell, P. Mir

P20-16 The Rodil Project: Understanding variability in the response to rTMS

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2009 L. Gao, P. Gómez-Garre

ORCID

, F. J. Díaz-Corrales, F. Carrillo, M. Carballo, A. Palomino, J. Díaz-Martín, R. Mejías, P. J. Vime, J. López-Barneo, P. Mir

ORCID

Prevalence and clinical features ofLRRK2mutations in patients with Parkinson’s disease in southern Spain

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2008 Maria Garcia-Hoyos, Isabel Lorda-Sanchez, Pilar Gómez-Garre

ORCID

, Cristina Villaverde, Diego Cantalapiedra, Ana Bustamante, Dan Diego-Alvarez, Elena Vallespin, Jesus Gallego-Merlo, Maria Jose Trujillo, Carmen Ramos, Carmen Ayuso

New Type of Mutations in Three Spanish Families with Choroideremia

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Fernando Daz-Otero, Mar Quesada, Jos Morales-Corraliza, Carlos Martnez-Parra, Pilar Gmez-Garre

ORCID

, Jos M. Serratosa

Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in theCHRNB2gene

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2007 Estrella Gómez-Tortosa, M. Sagrario Barquero, Manuel Barón, M. Jose Sainz, Sagrario Manzano, Maria Payno, Raquel Ros, Carmen Almaraz, Pilar Gómez-Garré

ORCID

, Adriano Jiménez-Escrig

Variability of Age at Onset in Siblings With Familial Alzheimer Disease

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P. Gomez-Garre

ORCID

, P. Gómez Garre, E. Gutiérrez Delicado, C. Gomez-Abad, C. Gómez Abad, J. Morales Corraliza, V. E. Villanueva, S. Rodríguez de Córdoba

ORCID

, J. Larrauri, M. Gutiérrez, J. Berciano, J. M. Serratosa

Hepatic disease as the first manifestation of progressive myoclonus epilepsy of Lafora

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Cristina Gomez-Abad, Zaid Afawi, Amos D. Korczyn, Adel Misk, Stavit A. Shalev, Ronen Spiegel, Tally Lerman-Sagie, Dorit Lev, Katherine L. Kron, Pilar Gómez-Garre

ORCID

, Jose M. Serratosa, Samuel F. Berkovic

Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation

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M. J. Trujillo-Tiebas, P. Gómez-Garré

ORCID

, N. Pérez-González, I. Lorda-Sánchez, J. M. Serratosa, C. Ayuso

Gene symbol: EPM2A.

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M. J. Trujillo-Tiebas, M. Fenollar-Cortés, P. Gómez-Garré

ORCID

, I. Lorda-Sánchez, J. M. Serratosa, C. Ayuso García

Novel human pathological mutations. Gene symbol: EPM2A. Disease: Lafora progressive myoclonus epilepsy.

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2006 Estrella Gomez-Tortosa, Sagrario Barquero, Manuel Baron, Raquel Ros, Sagrario Manzano, Maria J. Sainz, Carmen Almaraz, Pilar Gomez-Garre

ORCID

, Adriano Jimenez-Escrig

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Vicente Villanueva, Juan Alvarez-Linera, Pilar Gomez-Garre

ORCID

, Pilar Gómez-Garre, Jorge Gutiérrez, José M. Serratosa

MRI Volumetry and Proton MR Spectroscopy of the Brain in Lafora Disease

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