Incidence of varicella zoster virus infections of the central nervous system in the elderly: a large tertiary hospital-based series (2007–2014) von Arruti, M., Piñeiro, LD, Salicio, Y., Cilla, G., Goenaga, MA, López de Munain, A.

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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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Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3 von Kramerova, I, Kudryashova, E, Ermolova, N, Saenz, A, Jaka, O, López de Munain, A, Spencer, M 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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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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Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene von Alzualde, A., Moreno, F., Martínez-Lage, P., Ferrer, I., Gorostidi, A., Otaegui, D., Blázquez, L., Atares, B., Cardoso, S., Martínez de Pancorbo, M., Juste, R., Rodríguez-Martínez, A.B., Indakoetxea, B., de Munain, A. López

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Neurocognitive disorder detection based on feature vectors extracted from VBM analysis of structural MRI von Savio, A, García-Sebastián, M.T, Chyzyk, D, Hernandez, C, Graña, M, Sistiaga, A, López de Munain, A, Villanúa, J

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Brain fog of post-COVID-19 condition and Chronic Fatigue Syndrome, same medical disorder? von Azcue, N, Gómez-Esteban, J C, Acera, M, Tijero, B, Fernandez, T, Ayo-Mentxakatorre, N, Pérez-Concha, T, Murueta-Goyena, A, Lafuente, J V, Prada, Á, López de Munain, A, Ruiz-Irastorza, G, Ribacoba, L, Gabilondo, I, Del Pino, R

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Phenotypic correlations in a large single‐center cohort of patients with BSCL2 nerve disorders: a clinical, neurophysiological and muscle magnetic resonance imaging study von Fernández‐Eulate, G., Fernández‐Torrón, R., Guisasola, A., Gaspar, M. T. I., Diaz‐Manera, J., Maneiro, M., Zulaica, M., Olasagasti, V., Formica, A. F., Espinal, J. B., Ruiz, M., Schlüter, A., Pujol, A., Poza, J. J., López de Munain, A.

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CD24 V/V is an allele associated with the risk of developing multiple sclerosis in the Spanish population von Otaegui, D, Sáenz, A, Camaño, P, Blázquez, L, Goicoechea, M, Ruíz-Martínez, J, Olaskoaga, J, Emparanza, J A, de Munain, A López

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Blood miRNA expression pattern is a possible risk marker for natalizumab-associated progressive multifocal leukoencephalopathy in multiple sclerosis patients von Muñoz-Culla, M, Irizar, H, Castillo-Triviño, T, Sáenz-Cuesta, M, Sepúlveda, L, Lopetegi, I, de Munain, A López, Olascoaga, J, Baranzini, SE, Otaegui, D

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Understanding the olfactory role in post-COVID cognitive and neuropsychiatric manifestations von Azcue, N, Del Pino, Rocio, Saenz de Argandoña, Olatz, Ortiz de Echevarría, Amaia, Acera, Marian, Fernández-Valle, T, Ayo-Mentxakatorre, N, Lafuente, Jose Vicente, Ruiz-Lopez, Marta, López de Munain, A, Gabilondo, Inigo, Gómez-Esteban, J C, Tijero-Merino, B

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Dysautonomia and small fiber neuropathy in post-COVID condition and Chronic Fatigue Syndrome von Azcue, N, Del Pino, R, Acera, M, Fernández-Valle, T, Ayo-Mentxakatorre, N, Pérez-Concha, T, Murueta-Goyena, A, Lafuente, J V, Prada, A, López de Munain, A, Ruiz Irastorza, G, Martín-Iglesias, D, Ribacoba, L, Gabilondo, I, Gómez-Esteban, J C, Tijero-Merino, B

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Cerebrotendinous xanthomatosis: Neuropathological findings von Pilo de la Fuente, B., Ruiz, I., Lopez de Munain, A., Jimenez-Escrig, A.

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Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis von Blázquez, L., Azpitarte, M., Sáenz, A., Goicoechea, M., Otaegui, D., Ferrer, X., Illa, I., Gutierrez-Rivas, E., Vilchez, J. J., López de Munain, A.

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Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpression of CELF2 but not by MBNL1 silencing von Dhaenens, C.M., Tran, H., Frandemiche, M.-L., Carpentier, C., Schraen-Maschke, S., Sistiaga, A., Goicoechea, M., Eddarkaoui, S., Van Brussels, E., Obriot, H., Labudeck, A., Gevaert, M.H., Fernandez-Gomez, F., Charlet-Berguerand, N., Deramecourt, V., Maurage, C.A., Buée, L., de Munain, A. Lopez, Sablonnière, B., Caillet-Boudin, M.L., Sergeant, N.

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Patient-specific iPSC-derived cellular models of LGMDR1 von Mateos-Aierdi, A.J., Dehesa-Etxebeste, M., Goicoechea, M., Aiastui, A., Richaud-Patin, Y., Jiménez-Delgado, S., Raya, A., Naldaiz-Gastesi, N., López de Munain, A.

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Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect von Claramunt, R, Pedrola, L, Sevilla, T, López de Munain, A, Berciano, J, Cuesta, A, Sánchez-Navarro, B, Millán, J M, Saifi, G M, Lupski, J R, Vílchez, J J, Espinós, C, Palau, F

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Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy? von Krahn, M, Goicoechea, M, Hanisch, F, Groen, E, Bartoli, M, Pécheux, C, Garcia-Bragado, F, Leturcq, F, Jeannet, P-Y, Lobrinus, JA, Jacquemont, S, Strober, J, Urtizberea, JA, Saenz, A, Bushby, K, Lévy, N, Lopez de Munain, A

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Calpainopathy—A Survey of Mutations and Polymorphisms von Richard, I., Roudaut, C., Saenz, A., Pogue, R., Grimbergen, J.E.M.A., Anderson, L.V.B., Beley, C., Cobo, A-M, de Diego, C., Eymard, B., Gallano, P., Ginjaar, H.B., Lasa, A., Pollitt, C., Topaloglu, H., Urtizberea, J.A., de Visser, M., van der Kooi, A., Bushby, K., Bakker, E., Lopez de Munain, A., Fardeau, M., Beckmann, J.S.

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