Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
Billingsley, Kimberley J, Barbosa, Ines A, Bandrés-Ciga, Sara, Quinn, John P, Bubb, Vivien J, Deshpande, Charu, Botia, Juan A, Reynolds, Regina H, Zhang, David, Simpson, Michael A, Blauwendraat, Cornelis, Gan-Or, Ziv, Gibbs, J Raphael, Nalls, Mike A, Singleton, Andrew, Ryten, Mina, Koks, Sulev
Published in NPJ Parkinson's Disease (22.05.2019)
Published in NPJ Parkinson's Disease (22.05.2019)
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Integrating genetic and clinical data to predict impulse control disorders in Parkinson's disease
Jesús, S., Periñán, M. T., Cortés, C., Buiza‐Rueda, D., Macías‐García, D., Adarmes, A., Muñoz‐Delgado, L., Labrador‐Espinosa, M. Á., Tejera‐Parrado, C., Gómez‐Garre, M. P., Mir, P.
Published in European journal of neurology (01.02.2021)
Published in European journal of neurology (01.02.2021)
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Low serum uric acid concentration in Parkinson's disease in southern Spain
Jesús, S., Pérez, I., Cáceres-Redondo, M. T., Carrillo, F., Carballo, M., Gómez-Garre, P., Mir, P.
Published in European journal of neurology (01.01.2013)
Published in European journal of neurology (01.01.2013)
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Lafora disease due to EPM2B mutations: a clinical and genetic study
Gómez-Abad, C, Gómez-Garre, P, Gutiérrez-Delicado, E, Saygi, S, Michelucci, R, Tassinari, C A, Rodríguez de Córdoba, S, Serratosa, J M
Published in Neurology (22.03.2005)
Published in Neurology (22.03.2005)
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Prevalence and clinical features of LRRK2 mutations in patients with Parkinson’s disease in southern Spain
Gao, L., Gómez‐Garre, P., Díaz‐Corrales, F. J., Carrillo, F., Carballo, M., Palomino, A., Díaz‐Martín, J., Mejías, R., Vime, P. J., López‐Barneo, J., Mir, P.
Published in European journal of neurology (01.08.2009)
Published in European journal of neurology (01.08.2009)
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Hepatic disease as the first manifestation of progressive myoclonus epilepsy of Lafora
Gómez-Garre, P, Gutiérrez-Delicado, E, Gómez-Abad, C, Morales-Corraliza, J, Villanueva, V E, Rodríguez de Córdoba, S, Larrauri, J, Gutiérrez, M, Berciano, J, Serratosa, J M
Published in Neurology (24.04.2007)
Published in Neurology (24.04.2007)
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Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation
Gómez-Garre, P, Seijo, M, Gutiérrez-Delicado, E, Castro del Río, M, de la Torre, C, Gómez-Abad, C, Morales-Corraliza, J, Puig, M, Serratosa, J M
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Gene symbol: EPM2A
Trujillo-Tiebas, Maria J, Gómez-Garré, P, Fenolla-Cortés, M, Lorda-Sánchez, I, Serratosa, J M, Ayuso, C
Published in Human genetics (01.04.2007)
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Published in Human genetics (01.04.2007)
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A Novel Protein Tyrosine Phosphatase Gene Is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (EPM2)
Serratosa, José M., Gómez-Garre, Pilar, Gallardo, Ma Esther, Anta, Berta, de Bernabé, Daniel Beltrán-Valero, Lindhout, Dick, Augustijn, Paul B., Tassinari, Carlo A., Michelucci, Roberto, Malafosse, Alain, Topcu, Meral, Grid, Djamel, Dravet, Charlotte, Berkovic, Samuel F., de Córdoba, Santiago Rodríguez
Published in Human molecular genetics (01.02.1999)
Published in Human molecular genetics (01.02.1999)
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P20-16 The Rodil Project: Understanding variability in the response to rTMS
Fernandez-del-Olmo, M, Cheeran, B, Gomez-Garre, P, Lago, A, Marquez, G, Koch, G, Teo, J.T.H, Rothwell, J.C, Mir, P
Published in Clinical neurophysiology (2010)
Published in Clinical neurophysiology (2010)
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Genetic analysis of CHCHD2 in a southern Spanish population
Tejera-Parrado, C, Jesús, S, Huertas-Fernández, I, Bernal-Bernal, I, Bonilla-Toribio, M, Córdoba-Tevar, I, Abreu-Rodríguez, I, Carrillo, F, Bernal-Escudero, M, Vargas-González, L, Carballo, M, Gómez-Garre, P, Mir, P
Published in Neurobiology of aging (01.02.2017)
Published in Neurobiology of aging (01.02.2017)
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Gene symbol: EPM2A
Trujillo-Tiebas, Maria J, Gómez-Garré, P, Pérez-González, N, Lorda-Sánchez, I, Serratosa, J M, Ayuso, C
Published in Human genetics (01.04.2007)
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Published in Human genetics (01.04.2007)
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Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions
Gómez-Garre, P, Sanz, Y, Rodríguez De Córdoba, S R, Serratosa, J M
Published in European journal of human genetics : EJHG (01.12.2000)
Published in European journal of human genetics : EJHG (01.12.2000)
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Enfermedad de Lafora. Confirmación diagnóstica por genética molecular de un nuevo caso
Martínez Bermejo, Antonio, López Martín, Valentín, Serratosa Fernández, José María, Gutiérrez Molina, Manuel, Gómez Garre, P., Arcas Martínez, Joaquín, Tendero Gormaz, Adrián, Roche Herrero, Mª Carmen, Pérez Mies, B.
Published in Revista de neurologiá (2002)
Published in Revista de neurologiá (2002)
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Non-motor symptom burden in patients with Parkinson's disease with impulse control disorders and compulsive behaviours: results from the COPPADIS cohort
Jesús, S, Labrador-Espinosa, M A, Adarmes, A D, Méndel-Del Barrio, C, Martínez-Castrillo, J C, Alonso-Cánovas, A, Sánchez Alonso, P, Novo-Ponte, S, Alonso-Losada, M G, López Ariztegui, N, Segundo Rodríguez, J C, Morales, M I, Gastón, I, Lacruz Bescos, F, Clavero Ibarra, P, Kulisevsky, J, Pagonabarraga, J, Pascual-Sedano, B, Martínez-Martín, P, Santos-García, D, Mir, P
Published in Scientific reports (09.10.2020)
Published in Scientific reports (09.10.2020)
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Effects of Motor Symptom Laterality on Clinical Manifestations and Quality of Life in Parkinson’s Disease
Cubo, Esther, Martínez-Martín, Pablo, González-Bernal, Jerónimo, Casas, Elena, Arnaiz, Sandra, Miranda, Javier, Gámez, Pedro, Santos-García, Diego
Published in Journal of Parkinson's disease (01.01.2020)
Published in Journal of Parkinson's disease (01.01.2020)
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Lafora disease. A new case of confirmation of diagnosis on molecular genetic studies
Martínez-Bermejo, A, López-Martín, V, Serratosa, J M, Gutiérrez-Molina, M, Gómez-Garre, P, Arcas, J, Tendero, A, Roche, C, Pérez-Mies, B
Published in Revista de neurologiá (16.01.2002)
Published in Revista de neurologiá (16.01.2002)
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COPPADIS‐2015 (COhort of Patients with PArkinson's DIsease in Spain, 2015): an ongoing global Parkinson's disease project about disease progression with more than 1000 subjects included. Results from the baseline evaluation
Santos García, D., Jesús, S., Aguilar, M., García Caldentey, J., Caballol, N., Legarda, I., Hernández Vara, J., López Manzanares, L., González Aramburu, I., Ávila Rivera, M. A., López Díaz, L., Puente, V., García Moreno, J. M., Borrué, C., Solano Vila, B., Álvarez Sauco, M., Vela, L., Escalante, S., Cubo, E., Sánchez Alonso, P., Alonso Losada, M. G., Gastón, I., Kulisevsky, J., Menéndez González, M., Seijo, M., Rúiz Martínez, J., Valero, C., Kurtis, M., Fábregues‐Boixar, O., Prieto Jurczynska, C., Martinez‐Martin, P., Mir, P., Adarmes Astrid, D., Alonso Cánovas, A., Alonso Frech, F., Aneiros Díaz, A., Arnáiz, S., Ascunce Vidondo, A., Bernardo Lambrich, N., Bejr‐Kasem, H., Blázquez Estrada, M., Botí, M., Cabello González, C., Carrillo, F., Casas, E., Clavero, P., Cortina Fernández, A., Cots Foraster, A., Crespo Cuevas, A., de Deus Fonticoba, T., Díez‐Fairen, M., Estelrich Peyret, E., Fernández Guillán, N., Gámez, P., Gallego, M., García Campos, C., Gómez Garre, M. P., González Aloy, J., González García, B., González Palmás, M. J., González Toledo, G. R., Golpe Díaz, A., Grau Solá, M., Infante, J., Lacruz, F., Lage Castro, M., López Seoane, B., Macías, Y., Mata, M., Martí Andres, G., Martí, M. J., McAfee, D., Meitín, M. T., Méndez del Barrio, C., Moreno Diéguez, A., Nogueira, V., Novo Amado, A., Pagonabarraga, J., Pascual‐Sedano, B., Pastor, P., Pérez Fuertes, A., Prats, M. A., Pueyo Morlans, M., Redondo Rafales, N., Rodríguez Méndez, L., Rodríguez Pérez, A. B., Ruíz De Arcos, M., Sánchez‐Carpintero, M., Sánchez Díez, G., Sánchez Rodríguez, A., Santacruz, P., Segundo Rodríguez, J. C., Serarols, A., Sierra Peña, M., Suárez Castro, E., Tartari, J. P., Vázquez Gómez, R., Villanueva, C., Vives, B., Villar, M. D.
Published in European journal of neurology (01.11.2019)
Published in European journal of neurology (01.11.2019)
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