Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Angela Terezinha Souza, Wyse"'
Autor:
Daniela Delwing, de Lima, Fábio, Delwing, José Geraldo Pereira, da Cruz, Angela Terezinha Souza, Wyse, Débora, Delwing-Dal Magro
Publikováno v:
Fundamentalclinical pharmacology. 26(2)
In this study, we investigated in vivo and in vitro effect of arginine on parameters of oxidative stress namely thiobarbituric acid-reactive substances (TBA-RS) and total radical-trapping antioxidant parameter (TRAP) in plasma and on the antioxidant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86854da5e9d4a8a5edce70f173f94f8c
https://pubmed.ncbi.nlm.nih.gov/21210846
https://pubmed.ncbi.nlm.nih.gov/21210846
Autor:
Adriana, Kessler, Elisa, Costabeber, Carlos Severo, Dutra-Filho, Angela Terezinha Souza, Wyse, Moacir, Wajner, Clóvis Milton Duval, Wannmacher
Publikováno v:
Neurochemical research. 28(8)
Type II hyperprolinemia is an inherited disorder caused by a deficiency of delta 1-pyrroline-5-carboxilic acid dehydrogenase, whose biochemical hallmark is proline accumulation in plasma and tissues. Although neurological symptoms occur in most patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e0ba97f6347827a535b5eb842176db29
https://pubmed.ncbi.nlm.nih.gov/12834256
https://pubmed.ncbi.nlm.nih.gov/12834256
Autor:
Adriana, Kessler, Elisa, Costabeber, Carlos Severo, Dutra-Filho, Angela Terezinha Souza, Wyse, Moacir, Wajner, Clovis Milton Duval, Wannmacher
Publikováno v:
Metabolic brain disease. 18(2)
Type II Hyperprolinemia is an inherited disorder caused by a deficiency of delta1-pyrroline-5-carboxilic acid dehydrogenase, whose biochemical hallmark is proline accumulation in plasma and tissues. Although neurologic symptoms occur in most patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32d3825840100732402d61b007354c6b
https://pubmed.ncbi.nlm.nih.gov/12822836
https://pubmed.ncbi.nlm.nih.gov/12822836
Autor:
Carmen, Pilla, Rui Felipe de Oliveira, Cardozo, Carlos Severo, Dutra-Filho, Angela Terezinha Souza, Wyse, Moacir, Wajner, Clóvis Milton Duval, Wannmacher
Publikováno v:
Neurochemical research. 28(5)
Maple syrup urine disease (MSUD) is an inherited metabolic disorder biochemically characterized by the accumulation of branched-chain amino acids (BCAAs) and their branched-chain keto acids (BCKAs) in blood and other tissues. Neurological dysfunction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fdb16b215c8fda41f7794de595e5265b
https://pubmed.ncbi.nlm.nih.gov/12716015
https://pubmed.ncbi.nlm.nih.gov/12716015
Autor:
Carmen, Pilla, Rui Felipe, de Oliveira Cardozo, Carlos Severo, Dutra-Filho, Angela Terezinha Souza, Wyse, Moacir, Wajner, Clóvis Milton Duval, Wannmacher
Publikováno v:
Metabolic brain disease. 18(1)
Maple syrup urine disease (MSUD) is a metabolic disorder biochemically characterized by the accumulation of branched-chain amino acids (BCAA) and their branched-chain keto acids (BCKA) in blood and tissues. Neurological dysfunction is usually present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a277116112898fa60a43beb9d253b46
https://pubmed.ncbi.nlm.nih.gov/12603079
https://pubmed.ncbi.nlm.nih.gov/12603079
Autor:
Luciane Rosa, Feksa, Andrea Renata, Cornelio, Virginia Cielo, Rech, Carlos Severo, Dutra-Filho, Angela Terezinha Souza, Wyse, Moacir, Wajner, Clóvis Milton Duval, Wannmacher
Publikováno v:
Neurochemical research. 27(9)
The mechanisms by which phenylalanine is toxic to the brain in phenylketonuria are not fully understood. Considering that brain glucose metabolism is reduced in these patients, our main objective was to determine pyruvate kinase activity in brain cor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d53a1ac86db9ae5006444c01e207cd4
https://pubmed.ncbi.nlm.nih.gov/12396106
https://pubmed.ncbi.nlm.nih.gov/12396106