Role of non-coding RNAs in non-aging-related neurological disorders

por Vieira, A.S., Dogini, D.B., Lopes-Cendes, I.
Publicado en Braz J Med Biol Res (2018)

Mosaicism of the CAG repeat in CNS tissue in relation to age at death in spinocerebellar ataxia type 1 and Machado-Joseph disease patients.

por Maciel, P, Lopes-Cendes, I, Kish, S, Sequeiros, J, Rouleau, G A
Publicado 1997

Abnormalities of hippocampal signal intensity in patients with familial mesial temporal lobe epilepsy

por Coan A.C., Kobayashi E., Lopes-Cendes I., Li L.M., Cendes F.
Publicado 2004-01-01

A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2

por Lopes-Cendes, I., Scheffer, I. E., Berkovic, S. F., Rousseau, M., Andermann, E., Rouleau, G. A.
Publicado 2000

Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease

por Lopes-Ramos, C.M., Pereira, T.C., Dogini, D.B., Gilioli, R., Lopes-Cendes, I.
Publicado en Braz J Med Biol Res (2016)

Thalamic metabolic abnormalities in patients with Huntington's disease measured by magnetic resonance spectroscopy

por Casseb, R.F., D'Abreu, A., Ruocco, H.H., Lopes-Cendes, I., Cendes, F., Castellano, G.
Publicado 2013

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

por Lopes-Cendes, I., Andermann, E., Attig, E., Cendes, F., Bosch, S., Wagner, M., Gerstenbrand, F., Andermann, F., Rouleau, G. A.
Publicado 1994

Circulating nucleic acids in the plasma and serum as potential biomarkers in neurological disorders

por Bruno, D.C.F., Donatti, A., Martin, M., Almeida, V.S., Geraldis, J.C., Oliveira, F.S., Dogini, D.B., Lopes-Cendes, I.
Publicado en Braz J Med Biol Res (2020)

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

por Casaubon, L. K., Melanson, M., Lopes-Cendes, I., Marineau, C., Andermann, E., Andermann, F., Weissenbach, J., Prévost, C., Bouchard, J. P., Mathieu, J., Rouleau, G. A.
Publicado 1996

RNA sequencing reveals region-specific molecular mechanisms associated with epileptogenesis in a model of classical hippocampal sclerosis

por Vieira, A. S., de Matos, A. H., do Canto, A. M., Rocha, C. S., Carvalho, B. S., Pascoal, V. D. B., Norwood, B., Bauer, S., Rosenow, F., Gilioli, R., Cendes, F., Lopes-Cendes, I.
Publicado en Sci Rep (2016)

Patterns of hippocampal abnormalities in malformations of cortical development

por Montenegro, M A, Kinay, D, Cendes, F, Bernasconi, A, Bernasconi, N, Coan, A C, Li, L M, Guerreiro, M M, Guerreiro, C A M, Lopes‐Cendes, I, Andermann, E, Dubeau, F, Andermann, F
Publicado 2006

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24.

por Phillips, H A, Scheffer, I E, Crossland, K M, Bhatia, K P, Fish, D R, Marsden, C D, Howell, S J, Stephenson, J B, Tolmie, J, Plazzi, G, Eeg-Olofsson, O, Singh, R, Lopes-Cendes, I, Andermann, E, Andermann, F, Berkovic, S F, Mulley, J C
Publicado 1998

Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study

por Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., Silveira, I., Maciel, P., Coutinho, P., Lima, M., Zhou, Y.-X., Soong, B.-W., Watanabe, M., Giunti, P., Stevanin, G., Riess, O., Sasaki, H., Hsieh, M., Nicholson, G. A., Brunt, E., Higgins, J. J., Lauritzen, M., Tranebjaerg, L., Volpini, V., Wood, N., Ranum, L., Tsuji, S., Brice, A., Sequeiros, J., Rouleau, G. A.
Publicado 2001