Tau/α‐synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study von Delgado‐Alvarado, Manuel, Gago, Belén, Gorostidi, Ana, Jiménez‐Urbieta, Haritz, Dacosta‐Aguayo, Rosalía, Navalpotro‐Gómez, Irene, Ruiz‐Martínez, Javier, Bergareche, Alberto, Martí‐Massó, José F., Martínez‐Lage, Pablo, Izagirre, Andrea, Rodríguez‐Oroz, María C.

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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy von Morante-Redolat, José M., Gorostidi-Pagola, Ana, Piquer-Sirerol, Salomé, Sáenz, Amets, Poza, Juan J., Galán, Juan, Gesk, Stefan, Sarafidou, Theologia, Mautner, Victor-F., Binelli, Simona, Staub, Eike, Hinzmann, Bernd, French, Lisa, Prud'homme, Jean-F., Passarelli, Daniela, Scannapieco, Paolo, Tassinari, Carlo A., Avanzini, Giuliano, Martí-Massó, José F., Kluwe, Lan, Deloukas, Panagiotis, Moschonas, Nicholas K., Michelucci, Roberto, Siebert, Reiner, Nobile, Carlo, Pérez-Tur, Jordi, López de Munain, Adolfo

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Cinnarizine-induced parkinsonism: Ten years later von Martí-Massó, José F., Poza, Juan J.

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Αlpha-synuclein levels in blood plasma from LRRK2 mutation carriers von Gorostidi, Ana, Bergareche, Alberto, Ruiz-Martínez, Javier, Martí-Massó, José F, Cruz, María, Varghese, Shiji, Qureshi, Mohamed M, Alzahmi, Fatimah, Al-Hayani, Abdulmonem, López de Munáin, Adolfo, El-Agnaf, Omar M A

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The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics von Moreno, Fermin, Indakoetxea, Begoña, Barandiaran, Myriam, Caballero, María Cristina, Gorostidi, Ana, Calafell, Francesc, Gabilondo, Alazne, Tainta, Mikel, Zulaica, Miren, Martí Massó, José F, López de Munain, Adolfo, Sánchez-Juan, Pascual, Lee, Suzee E

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Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2 von Ruiz-Martínez, Javier, de la Riva, Patricia, Rodríguez-Oroz, Maria C., Mondragón Rezola, Elisabet, Bergareche, Alberto, Gorostidi, Ana, Gago, Belen, Estanga, Ainara, Larrañaga, Nerea, Sarasqueta, Cristina, López de Munain, Adolfo, Martí Massó, José F.

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Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia von Paisán-Ruiz, Coro, Ruiz-Martinez, Javier, Ruibal, Marta, Mok, Kin Y., Indakoetxea, Begona, Gorostidi, Ana, Massó, José F. Martí

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Rombencefalitis y endocarditis por Listeria monocytogenes : una asociación no descrita von Tainta Cuezva, Mikel, de la Riva Juez, Patricia, González, Félix, Martí Massó, José Félix, Goenaga, Miguel Ángel

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Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease von Kalia, Lorraine V, Lang, Anthony E, Hazrati, Lili-Naz, Fujioka, Shinsuke, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A, Van Deerlin, Vivianna M, Trojanowski, John Q, Hurtig, Howard I, Alcalay, Roy N, Marder, Karen S, Clark, Lorraine N, Gaig, Carles, Tolosa, Eduardo, Ruiz-Martínez, Javier, Marti-Masso, Jose F, Ferrer, Isidre, López de Munain, Adolfo, Goldman, Samuel M, Schüle, Birgitt, Langston, J. William, Aasly, Jan O, Giordana, Maria T, Bonifati, Vincenzo, Puschmann, Andreas, Canesi, Margherita, Pezzoli, Gianni, Maues De Paula, Andre, Hasegawa, Kazuko, Duyckaerts, Charles, Brice, Alexis, Stoessl, A. Jon, Marras, Connie

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Selection of Entropy Based Features for Automatic Analysis of Essential Tremor von López-de-Ipiña, Karmele, Solé-Casals, Jordi, Faundez-Zanuy, Marcos, Calvo, Pilar, Sesa, Enric, Martinez de Lizarduy, Unai, De La Riva, Patricia, Marti-Masso, Jose, Beitia, Blanca, Bergareche, Alberto

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Prion Protein Codon 129 Polymorphism Modifies Age at Onset of Frontotemporal Dementia With the C.709-1 G>A Progranulin Mutation von MORENO, Fermin, ALZUALDE, Ainhoa, CAMBLOR, Pablo Martinez, BARANDIARAN, Myriam, VAN DEERLIN, Vivianna M, GABILONDO, Alazne, MARTI MASSO, José F, LOPEZ DE MUNAIN, Adolfo, INDAKOETXEA, Begoña

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Rhomboencephalitis and endocarditis caused by Listeria monocytogenes: an unreported association von Tainta, M, de la Riva, P, Gonzalez, F, Marti-Masso, J F, Goenaga, M A

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Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease von Kalia, Lorraine V, Lang, Anthony E, Hazrati, Lili-Naz, Fujioka, Shinsuke, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A, Van Deerlin, Vivianna M, Trojanowski, John Q, Hurtig, Howard I, Alcalay, Roy N, Marder, Karen S, Clark, Lorraine N, Gaig Ventura, Carles, Tolosa, Eduardo, Ruiz-Martínez, Javier, Marti-Masso, Jose F, Ferrer, Isidro (Ferrer Abizanda), López de Munain, Adolfo, Goldman, Samuel M, Schüle, Birgitt, Langston, J. William, Aasly, Jan O, Giordana, Maria T, Bonifati, Vincenzo, Puschmann, Andreas, Canesi, Margherita, Pezzoli, Gianni, Maues De Paula, Andre, Hasegawa, Kazuko, Duyckaerts, Charles, Brice, Alexis, Stoessl, A. Jon, Marras, Connie

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Olfactory Deficits and Cardiac 123I-MIBG in Parkinson's Disease Related to the LRRK2 R1441 G and G2019S Mutations von RUIZ-MARTINEZ, Javier, GOROSTIDI, Ana, GOYENECHEA, Estibaliz, ALZUALDE, Ainhoa, POZA, Juan Jose, RODRIGUEZ, Francisco, BERGARECHE, Alberto, MORENO, Fermín, LOPEZ DE MUNAIN, Adolfo, MARTI MASSO, Jose F

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Mutations in the LGl1/epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy von MORANTE-REDOLAT, José M, GOROSTIDI-PAGOLA, Ana, STAUB, Eike, HINZMANN, Bernd, FRENCH, Lisa, PRUD'HOMME, Jean-F, PASSARELLI, Daniela, SCANNAPIECO, Paolo, TASSINARI, Carlo A, AVANZINI, Giuliano, MARTI-MASSO, José F, KLUWE, Lan, PIQUER-SIREROL, Salomé, DELOUKAS, Panagiotis, MOSCHONAS, Nicholas K, MICHELUCCI, Roberto, SIEBERT, Reiner, NOBILE, Carlo, PEREZ-TUR, Jordi, LOPEZ DE MUNAIN, Adolfo, SAENZ, Amets, POZA, Juan J, GALAN, Juan, GESK, Stefan, SARAFIDOU, Theologia, MAUTNER, Victor-F, BINELLI, Simona

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Reply von Martì-Massò, Josè F., Poza, Juan J.

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Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease von Paisán-Ruı́z, Coro, Jain, Shushant, Evans, E.Whitney, Gilks, William P., Simón, Javier, van der Brug, Marcel, de Munain, Adolfo López, Aparicio, Silvia, Gil, Angel Martı́nez, Khan, Naheed, Johnson, Janel, Martinez, Javier Ruiz, Nicholl, David, Carrera, Itxaso Marti, Peňa, Amets Saénz, de Silva, Rohan, Lees, Andrew, Martı́-Massó, José Félix, Pérez-Tur, Jordi, Wood, Nick W., Singleton, Andrew B.

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Cinnarizine-induced parkinsonism: Ten years later von Negrotti, A., Calzetti, S.

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Sobre la descripción inicial del síndrome de pseudomigraña con pleocitosis de líquido cefalorraquídeo von Martí Massó, José Félix

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Selection of Entropy Based Features for Automatic Analysis of Essential Tremor von Lopez-de-Ipiña, Karmele, Solé-Casals, Jordi, Faundez-Zanuy, Marcos, Calvo, Pilar, Sesa Nogueras, Enric, Martinez de Lizardui, Unai, De La Riva, Patricia, Marti-Masso, Jose F, Beitia, Blanca, Bergareche, Alberto

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