Global high-order numerical schemes for the time evolution of the general relativistic radiation magneto-hydrodynamics equations von Izquierdo, M R, Pareschi, L, Miñano, B, Massó, J, Palenzuela, C

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Simflowny 3: An upgraded platform for scientific modeling and simulation von Palenzuela, C., Miñano, B., Arbona, A., Bona-Casas, C., Bona, C., Massó, J.

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Simflowny 2: An upgraded platform for scientific modelling and simulation von Arbona, A., Miñano, B., Rigo, A., Bona, C., Palenzuela, C., Artigues, A., Bona-Casas, C., Massó, J.

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LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene von Sáenz, A., Leturcq, F., Cobo, A. M., Poza, J. J., Ferrer, X., Otaegui, D., Camaño, P., Urtasun, M., Vílchez, J., Gutiérrez-Rivas, E., Emparanza, J., Merlini, L., Paisán, C., Goicoechea, M., Blázquez, L., Eymard, B., Lochmuller, H., Walter, M., Bonnemann, C., Figarella-Branger, D., Kaplan, J. C., Urtizberea, J. A., Martí-Massó, J. F., de Munain, A. López

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Association between COMMD1 gene polymorphism rs11125908 and rheumatoid arthritis in the Cuban population von Carpio Alvarez, M, Cintado Benitez, A, Diaz Argudin, T, Nodarse Cuni, H, Dominguez Horta, M D C, Fernández Massó, J R

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Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area von Andrés, N, Poza, J J, Martí Massó, J F

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Simflowny: A general-purpose platform for the management of physical models and simulation problems von Arbona, A., Artigues, A., Bona-Casas, C., Massó, J., Miñano, B., Rigo, A., Trias, M., Bona, C.

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Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1 von Sistiaga, A., Urreta, I., Jodar, M., Cobo, A. M., Emparanza, J., Otaegui, D., Poza, J. J., Merino, J. J., Imaz, H., Martí-Massó, J. F., López de Munain, A.

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LRRK2 G2019S and R1441G mutations associated with Parkinson’s disease are common in the Basque Country, but relative prevalence is determined by ethnicity von Gorostidi, A., Ruiz-Martínez, J., Lopez de Munain, A., Alzualde, A., Martí Massó, J. F.

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Bioactive versus bare platinum coils in the treatment of intracranial aneurysms: the MAPS (Matrix and Platinum Science) trial von McDougall, C G, Johnston, S Claiborne, Gholkar, A, Barnwell, S L, Vazquez Suarez, J C, Massó Romero, J, Chaloupka, J C, Bonafe, A, Wakhloo, A K, Tampieri, D, Dowd, C F, Fox, A J, Imm, S J, Carroll, K, Turk, A S

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New formalism for numerical relativity von Bona, C, Massó, J, Seidel, E, Stela, J

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Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q von Poza, J. J., Sáenz, A., Martínez-Gil, A., Cheron, N., Cobo, A. M., Urtasun, M., Martí-Massó, J. F., Grid, D., Beckmann, J. S., Prud'Homme, J. F., López De Munain, A.

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Mitochondrial polymporphisms in Parkinson's Disease von Otaegui, D., Paisán, C., Sáenz, A., Martí, I., Ribate, M., Martí-Massó, J.F., Pérez-Tur, J., López de Munain, A.

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Prevalence of Parkinson's disease and other types of parkinsonism: A door-to-door survey in Bidasoa, Spain von BERGARECHE, A, DE LA PUENTE, E, LOPEZ DE MUNAIN, A, SARASQUETA, C, DE ARCE, A, POZA, J. J, MARTI-MASSO, J. F

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Phenotypic variability in familial prion diseases due to the D178N mutation von Zarranz, J J, Digon, A, Atarés, B, Rodríguez-Martínez, A B, Arce, A, Carrera, N, Fernández-Manchola, I, Fernández-Martínez, M, Fernández-Maiztegui, C, Forcadas, I, Galdos, L, Gómez-Esteban, J C, Ibáñez, A, Lezcano, E, López de Munain, A, Martí-Massó, J F, Mendibe, M M, Urtasun, M, Uterga, J M, Saracibar, N, Velasco, F, de Pancorbo, M M

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Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect von Sistiaga, A., Camaño, P., Otaegui, D., Ibáñez, B., Ruiz‐Martinez, J., Martí‐Massó, J. F., López de Munain, A.

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P-025 Freezing of the semen sample by the patient at home is clinically effective von Pujal, B, Montalvo, V, Massó, J, Garcia-Faura, Á, Garcia, F, Marqués, B, López-Teijón, M

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Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease von Brockmann, K., Schulte, C., Schneiderhan‐Marra, N., Apel, A., Pont‐Sunyer, C., Vilas, D., Ruiz‐Martinez, J., Langkamp, M., Corvol, J.‐C., Cormier, F., Knorpp, T., Joos, T. O., Bernard, A., Gasser, T., Marras, C., Schüle, B., Aasly, J. O., Foroud, T., Marti‐Masso, J. F., Brice, A., Tolosa, E., Berg, D., Maetzler, W.

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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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Frontotemporoparietal dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation von MORENO, F, INDAKOETXEA, B, LOPEZ DE MUNAIN, A, BARANDIARAN, M, ALZUALDE, A, GABILONDO, A, ESTANGA, A, RUIZ, J, RUIBAL, M, BERGARECHE, A, MARTI-MASSO, J. F

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