Zobrazeno 1 - 10
of 185
pro vyhledávání: '"Carlos Severo Dutra Filho"'
Autor:
Marcos Franken, Fabio Carlos Alves Lima, Priscila Nicolao Mazzola, Jocelito Bijoldo Martins, Bruno Costa Teixeira, Carlos Severo Dutra Filho, Flávio Antônio de Souza Castro
Publikováno v:
Revista Brasileira de Ciências do Esporte, Vol 36, Iss 2, Pp 353-368 (2014)
O estudo avaliou, na intensidade de 100% da velocidade crítica (VC), o comportamento de concentração de lactato sanguíneo ([LA]), esforço percebido (EP), frequência cardíaca (FC), concentrações plasmáticas de triptofano [TRP], de prolactina
Externí odkaz:
https://doaj.org/article/3dcc1fd45c1e480b8391f7bb1e508812
Autor:
Priscila Nicolao Mazzola, Bruno Costa Teixeira, Gabriel Henrique Schirmbeck, Alvaro Reischak-Oliveira, Terry G.J. Derks, Francjan J. van Spronsen, Carlos Severo Dutra-Filho, Ida Vanessa Doederlein Schwartz
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 55-59 (2015)
Background: In phenylketonuria, dietary treatment prevents most of the severe brain disease. However, patients have to follow a diet restricted in several natural components, what may cause decreased bone density and obesity. Exercise is known to imp
Externí odkaz:
https://doaj.org/article/2a4d9acf1cc94d7ba950cbfb48254186
Autor:
Caroline Paula Mescka, Fernanda Poletto, Bruna Donida, Andrea Pereira Rosa, Camila Vieira Pinheiro, Esteban Alberto Gonzalez, Felipe Maciel Catarino, Carlos Severo Dutra-Filho, Guilherme Baldo, Angela Sitta, Daniella de Moura Coelho, Carmen Regla Vargas
Publikováno v:
Metabolic Brain Disease. 36:1015-1027
Maple syrup urine disease (MSUD) is a genetic disorder that leads the accumulation of branched-chain amino acids (BCAA) leucine (Leu), isoleucine, valine and metabolites. The symptomatology includes psychomotor delay and mental retardation. MSUD ther
Publikováno v:
Metabolic brain disease. 36(4)
Phenylketonuria (PKU) is one of the commonest inborn error of amino acid metabolism. Before mass neonatal screening was possible, and the success of introducing diet therapy right after birth, the typical clinical finds in patients ranged from intell
Autor:
Belisa Parmeggiani, Guilhian Leipnitz, Marina Rocha Frusciante, Nevton Teixeira da Rosa-Junior, Carlos Severo Dutra Filho, Leonardo de Moura Alvorcem, Nícolas Manzke Glänzel, Moacir Wajner
Publikováno v:
Biochimie.
High urinary excretion and tissue accumulation of 3-methylglutaric acid (MGA) are observed in patients affected by 3-hydroxy-3-methylglutaric (HMGA) and 3-methylglutaconic (MGTA) acidurias. The pathomechanisms underlying the hepatic dysfunction commo
Autor:
Flávio Antônio de Souza Castro, Priscila Nicolao Mazzola, Carlos Severo Dutra-Filho, Marcos Franken
Publikováno v:
Sport Sciences for Health. 14:633-638
The objective of this study was to compare blood lactate concentration (LAC), heart rate (HR), rating of perceived exertion (RPE), tryptophan (TRP), prolactin (PRL), nonesterified fatty acids (NEFA), branched-chain amino acids (BCAAs) plasma concentr
Autor:
Carlos Severo Dutra-Filho, Denise Bertin Rojas, Moacir Wajner, Gabriel H. Schirmbeck, Clovis Milton Duval Wannmacher, Cláudia Funchal, Rodrigo Binkowski de Andrade, Ângela Zanatta, Tanise Gemelli
Publikováno v:
Molecular Neurobiology. 55:5101-5110
β-Alanine occurs naturally in the human central nervous system and performs different functions. It can act as either a neurotransmitter or a neuromodulator, depletion of taurine levels and competitive antagonist of γ-aminobutyric acid (GABA). The
Autor:
Terry G J Derks, Francjan J. van Spronsen, Priscila Nicolao Mazzola, Alvaro Reischak-Oliveira, Bruno Costa Teixeira, Ida Vanessa Doederlein Schwartz, Gabriel H. Schirmbeck, Carlos Severo Dutra-Filho
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular genetics and metabolism reports, 5, 55-59. ELSEVIER SCIENCE BV
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 55-59 (2015)
Molecular genetics and metabolism reports, 5, 55-59. ELSEVIER SCIENCE BV
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 55-59 (2015)
Background In phenylketonuria, dietary treatment prevents most of the severe brain disease. However, patients have to follow a diet restricted in several natural components, what may cause decreased bone density and obesity. Exercise is known to impr
Autor:
Carmen Regla Vargas, Jéssica Lamberty Faverzani, Tatiane Grazieli Hammerschmidt, Gilian Guerreiro, Carlos Alberto Yasin Wayhs, Carlos Severo Dutra-Filho, Vanusa Mandredini, Moacir Wajner, Daniella de Moura Coelho, Caroline Paula Mescka
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 775:43-47
Maple syrup urine disease (MSUD) is an inherited disorder caused by severe deficient activity of the branched-chain α-keto acid dehydrogenase complex involved in the degradation pathway of branched-chain amino acids (BCAAs) and their α-ketoacid der
Autor:
Bruna Donida, Carlos Severo Dutra-Filho, Angela Sitta, Gilian Guerreiro, Moacir Wajner, Desirèe Padilha Marchetti, Carmen Regla Vargas, Daniella de Moura Coelho, Jéssica Lamberty Faverzani, Tatiane Grazieli Hammerschmidt, Caroline Paula Mescka
Publikováno v:
International Journal of Developmental Neuroscience. 42:10-14
Maple syrup urine disease (MSUD) is a disorder of branched-chain amino acids (BCAA). The defect in the branched-chain α-keto acid dehydrogenase complex activity leads to an accumulation of these compounds and their corresponding α-keto-acids and α