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

gan Vieira, A.S., Dogini, D.B., Lopes-Cendes, I.
Cyhoeddwyd yn 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.

gan Maciel, P, Lopes-Cendes, I, Kish, S, Sequeiros, J, Rouleau, G A
Cyhoeddwyd 1997

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

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

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

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

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

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

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

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

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

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

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

gan Bruno, D.C.F., Donatti, A., Martin, M., Almeida, V.S., Geraldis, J.C., Oliveira, F.S., Dogini, D.B., Lopes-Cendes, I.
Cyhoeddwyd yn 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.

gan 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.
Cyhoeddwyd 1996

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

gan 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.
Cyhoeddwyd yn Sci Rep (2016)

Patterns of hippocampal abnormalities in malformations of cortical development

gan 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
Cyhoeddwyd 2006

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

gan 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
Cyhoeddwyd 1998

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

gan 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.
Cyhoeddwyd 2001