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  • Gislaine Zilli Réus, Giselli Scaini, Gabriela C. Jeremias, Camila Brulezi Furlanetto, Emilio Luiz Streck
  • Biology, Medicine
  • Brain Research
  • 2014 (First Publication: 1 October 2014)
  • Methylphenidate (MPH) is commonly prescribed for children who have been diagnosed with attention deficit hyperactivity disorder (ADHD); however, the action mechanisms of methylphenidate have not beenContinue Reading
  • Emilio Luiz Streck, Cinara Ludvig Gonçalves, Camila Brulezi Furlanetto, Giselli Scaini, Felipe Dal-Pizzol, João Quevedo
  • Psychology, Medicine
  • Revista brasileira de psiquiatria
  • 2014 (First Publication: 15 April 2014)
  • INTRODUCTION Mitochondrial dysfunction has been postulated to participate in the development of many neuropsychiatric disorders, but there is no consensus as to its role. The aim of this paper is toContinue Reading
  • Giselli Scaini, Lis Mairá Mello-Santos, +8 authors Emilio Luiz Streck
  • Medicine
  • Molecular Neurobiology
  • 2013 (First Publication: 1 December 2013)
  • Maple syrup urine disease (MSUD) is a neurometabolic disorder caused by deficiency of the activity of the mitochondrial enzyme complex branched-chain α-keto acid dehydrogenase leading to accumulationContinue Reading
  • Samira S Valvassori, Wilson R. Resende, +8 authors João Quevedo
  • Biology, Medicine
  • Current neurovascular research
  • 2015 (First Publication: 31 October 2015)
  • The aim of the present study was to evaluate the effects of sodium butyrate on depressive-like behavior and mitochondrial alteration parameters in animal models of depression induced by maternalContinue Reading
  • Kellen Ronçani Simon, Rosane Maria Souza dos Santos, +10 authors Patricia Fernanda Schuck
  • Chemistry, Medicine
  • Biochemistry and cell biology = Biochimie et…
  • 2013 (First Publication: 1 October 2013)
  • Phenylketonuria (PKU) is a disease caused by a deficiency of phenylalanine hydroxylase (PAH), resulting in an accumulation of phenylalanine (Phe) in the brain tissue, cerebrospinal fluid, and otherContinue Reading
  • Ândrea C. Ramos, Gabriela Kozuchovski Ferreira, Milena Carvalho-Silva, Camila Brulezi Furlanetto, Emilio Luiz Streck
  • Medicine, Biology
  • International Journal of Developmental…
  • 2013 (First Publication: 1 August 2013)
  • Tyrosinemia type II is an inborn error of metabolism caused by mutations in the gene that encodes tyrosine aminotransferase, which leads to increased blood tyrosine levels. Considering that tyrosineContinue Reading