E. de Mattos

E-mail:
e.de.mattos umcg.nl

Research

  1. 2019
  2. 2018
  3. Sena, L. S., Castilhos, R. M., Mattos, E. P., Furtado, G. V., Pedroso, J. L., Barsottini, O., ... Jardim, L. B. (2018). Selective Forces Related to Spinocerebellar Ataxia Type 2. Cerebellum. https://doi.org/10.1007/s12311-018-0977-7
  4. Monte, T. L., Reckziegel, E. D. R., Augustin, M. C., Locks-Coelho, L. D., Santos, A. S. P., Furtado, G. V., ... Rede Neurogenética (2018). The progression rate of spinocerebellar ataxia type 2 changes with stage of disease. Orphanet journal of rare diseases, 13(1), [20]. https://doi.org/10.1186/s13023-017-0725-y
  5. 2017
  6. 2016
  7. Donis, K. C., Saute, J. A. M., Krum-Santos, A. C., Furtado, G. V., Mattos, E. P., Saraiva-Pereira, M. L., ... Jardim, L. B. (2016). Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence. Neurogenetics, 17(2), 107-113. https://doi.org/10.1007/s10048-016-0473-5
  8. 2015
  9. Preusser Mattos, E., Anjos da Silva, A., A. Magalhães, J. A., L. Leite, J. C., Leistner-Segal, S., Gus-Kessler, R., ... Vieira Sanseverino, M. T. (2015). Identification of a premature stop codon mutation in the PHGDH gene in severe Neu‐Laxova syndrome—evidence for phenotypic variability. American Journal of Medical Genetics. Part A, 167(6), 1323-1329. https://doi.org/10.1002/ajmg.a.36930
  10. 2014
  11. 2013
  12. 2008

ID: 16210861