Cervical myelopathy as a form of presentation of Whipple disease
Pérez Álvarez, Á.I., Morís de la Tassa, G.
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Published in Neurología (Barcelona, English ed. ) (01.10.2020)
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Expert tutoring system for teaching mechanical engineering
Tucho, R., Sierra, J.M., Fernández, J.E., Vijande, R., Morı́s, G.
Published in Expert systems with applications (01.05.2003)
Published in Expert systems with applications (01.05.2003)
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The Distinctive Headache of the Occipital Condyle Syndrome: A Report of Four Cases
Morís, G., Roig, C., Misiego, M., Alvarez, A., Berciano, J., Pascual, J.
Published in Headache (01.04.1998)
Published in Headache (01.04.1998)
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VP.92 Autonomic symptoms are frequent in myotonic dystrophy type 1
Alonso, S., Alvarez, N., Amaral, N., Morís, G.
Published in Neuromuscular disorders : NMD (01.10.2022)
Published in Neuromuscular disorders : NMD (01.10.2022)
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SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V
Sánchez-Ferrero, E, Coto, E, Beetz, C, Gámez, J, Corao, AI, Díaz, M, Esteban, J, del Castillo, E, Moris, G, Infante, J, Menéndez, M, Pascual-Pascual, SI, López de Munaín, A, Garcia-Barcina, MJ, Alvarez, V
Published in Clinical genetics (01.03.2013)
Published in Clinical genetics (01.03.2013)
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Outbreaks of monophasic Salmonella enterica serovar 4,[5],12:i:- in Luxembourg, 2006
Mossong, J, Marques, P, Ragimbeau, C, Huberty-Krau, P, Losch, S, Meyer, G, Moris, G, Strottner, C, Rabsch, W, Schneider, F
Published in Euro surveillance : bulletin européen sur les maladies transmissibles (01.06.2007)
Published in Euro surveillance : bulletin européen sur les maladies transmissibles (01.06.2007)
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Association between an α2 Macroglobulin DNA Polymorphism and Late-Onset Alzheimer's Disease
Alvarez, Victoria, Alvarez, Ruth, Lahoz, C.H., Martı́nez, C., Peña, J., Guisasola, L.M., Salas-Puig, J., Morı́s, G., Urı́a, D., Menes, B.B., Ribacoba, R., Vidal, J.A., Sánchez, J.M., Coto, Eliecer
Published in Biochemical and biophysical research communications (14.10.1999)
Published in Biochemical and biophysical research communications (14.10.1999)
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Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease
Gutiérrez Gutiérrez, G., Díaz-Manera, J., Almendrote, M., Azriel, S., Eulalio Bárcena, J., Cabezudo García, P., Camacho Salas, A., Casanova Rodríguez, C., Cobo, A.M., Díaz Guardiola, P., Fernández-Torrón, R., Gallano Petit, M.P., García Pavía, P., Gómez Gallego, M., Gutiérrez Martínez, A.J., Jericó, I., Kapetanovic García, S., López de Munaín Arregui, A., Martorell, L., Morís de la Tassa, G., Moreno Zabaleta, R., Muñoz-Blanco, J.L., Olivar Roldán, J., Pascual Pascual, S.I., Peinado Peinado, R., Pérez, H., Poza Aldea, J.J., Rabasa, M., Ramos, A., Rosado Bartolomé, A., Rubio Pérez, M.Á., Urtizberea, J.A., Zapata-Wainberg, G., Gutiérrez-Rivas, E.
Published in Neurología (Barcelona, English ed. ) (01.04.2020)
Published in Neurología (Barcelona, English ed. ) (01.04.2020)
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International Validation of the Erasmus Guillain–Barré Syndrome Respiratory Insufficiency Score
Doets, Alex Y., Walgaard, Christa, Yamagishi, Yuko, Dimachkie, Mazen M., Waheed, Waqar, Kolb, Noah, Gorson, Kenneth C., Islam, Zhahirul, Mohammad, Quazi Deen, Harbo, Thomas, Chavada, Govindsinh, Davidson, Amy, Willison, Hugh J., Bateman, Kathleen, Miller, James A.L., Berg, Bianca, Verboon, Christine, Benedetti, Luana, Monges, Soledad, Pereon, Yann, Bürmann, Jan, Kuitwaard, Krista, Kleyweg, Ruud P., Marchesoni, Cintia, Sedano Tous, María J., Schenone, Angelo, Pardo, Julio, Vermeij, Frederique H., Gutiérrez‐Gutiérrez, Gerardo, Barroso, Fabio A., Dardiotis, Efthimios, Wirtz, Paul W., Gilhuis, H. Jacobus, Hadden, Robert D.M., Sheikh, Kazim A., Feasby, Thomas E., Kramers, J.C.H.M. (Hans), Roberts, Rhys C., Silvestri, Nicholas J., Fazio, Raffaella, Dijk, Gert W., Verschuuren, Jan G.G.M., Hughes, R.A.C., Hartung, H.P., Koning, L.C., Woerkom, M., Ajroud‐Driss, S., Bella, I.R., Bhavaraju‐Sanka, R., Brand, P., Brannagan, T.H., Briani, Chiara, Chao, C.C., Chen, S., Claeys, K.G., Conti, M.E., Cosgrove, J.S., Dalakas, M.C., Derejko, M.A., Coeur, C. Dornonville, Echaniz‐Laguna, A., Fokke, C., Fulgenzi, E.A., Goyal, N.A., Grimbergen, Y.A.M., Grisanti, S., Gutmann, L., Holbech, J.V., Htut, M., Jellema, K., Pascual, I. Jericó, Jimeno‐Montero, M.C., Kaida, K., Kimpinski, K., Kokubun, N., Kwan, J.Y., Lassen, L. Landschoff, Pan, E. Lee, Lunn, M.P.T., Magot, A., Martín‐Aguilar, L., McDermott, C.J., Tassa, G. Morís, Nascimbene, C., Nedkova, V., Nowak, R.J., Balaguer, P. Orizaola, Prada, V., Pulley, M.T., Sachs, G.M., Samukawa, M., Sommer, C.L., Stino, A.M., Tan, C‐Y., Twydell, P.T., Damme, P., Ree, T., Koningsveld, R., Zhou, L., Zivkovic, S.
Published in Annals of neurology (01.04.2022)
Published in Annals of neurology (01.04.2022)
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IMAGING
Dominguez-Gonzalez, C., Fernandez-Torron, R., Moore, U., Velez, B., Perez, J. Alonso, Gonzalez-Mera, L., Olivé, M., García, J. García, Morís, G., Hernández, J. León, Muelas, N., de Fuenmayor Fernández de la H, C., Martín, M., Díaz-Manera, J., Paradas, C.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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IMAGING: EP.333 Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis
Dominguez-Gonzalez, C., Fernandez-Torron, R., Moore, U., Velez, B., Perez, J. Alonso, Gonzalez-Mera, L., Olivé, M., García, J. García, Morís, G., Hernández, J. León, Muelas, N., de Fuenmayor Fernández de la H, C., Martín, M., Díaz-Manera, J., Paradas, C.
Published in Neuromuscular disorders : NMD (01.10.2021)
Published in Neuromuscular disorders : NMD (01.10.2021)
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LRRK2 mutations are a common cause of Parkinson's disease in Spain
Mata, I. F., Ross, O. A., Kachergus, J., Huerta, C., Ribacoba, R., Moris, G., Blazquez, M., Guisasola, L. M., Salvador, C., Martinez, C., Farrer, M., Alvarez, V.
Published in European journal of neurology (01.04.2006)
Published in European journal of neurology (01.04.2006)
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Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease
Alvarez, Ruth, Alvarez, Victoria, Lahoz, Carlos H, Martínez, Carmen, Peña, Joaquín, Sánchez, José M, Guisasola, Luis M, Salas-Puig, Javier, Morís, Germán, Vidal, José A, Ribacoba, René, Menes, Bernardino B, Uría, Dionisio, Coto, Eliecer
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1999)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.1999)
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Conference Proceeding
Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert
Gutiérrez Gutiérrez, G., Díaz-Manera, J., Almendrote, M., Azriel, S., Eulalio Bárcena, J., Cabezudo García, P., Camacho Salas, A., Casanova Rodríguez, C., Cobo, A.M., Díaz Guardiola, P., Fernández-Torrón, R., Gallano Petit, M.P., García Pavía, P., Gómez Gallego, M., Gutiérrez Martínez, A.J., Jericó, I., Kapetanovic García, S., López de Munaín Arregui, A., Martorell, L., Morís de la Tassa, G., Moreno Zabaleta, R., Muñoz-Blanco, J.L., Olivar Roldán, J., Pascual Pascual, S.I., Peinado Peinado, R., Pérez, H., Poza Aldea, J.J., Rabasa, M., Ramos, A., Rosado Bartolomé, A., Rubio Pérez, M.Á., Urtizberea, J.A., Zapata-Wainberg, G., Gutiérrez-Rivas, E.
Published in Neurología (Barcelona, Spain) (01.04.2020)
Published in Neurología (Barcelona, Spain) (01.04.2020)
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Two cases of neurosarcoidosis with atypical manifestations
Gómez, H., Martínez, J., Colunga, D., Morís, G., Carbajo, C., Cárcaba, V.
Published in European journal of internal medicine (01.10.2013)
Published in European journal of internal medicine (01.10.2013)
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