Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rui Felipe de Oliveira, Cardozo"'
Autor:
Angela T. S. Wyse, Clovis Milton Duval Wannmacher, Moacir Wajner, Paula Karine Barcelos Dornelles, Rui Felipe de Oliveira Cardozo, Carmen Pilla, Carlos Severo Dutra-Filho
Publikováno v:
International Journal of Developmental Neuroscience. 21:145-151
Maple syrup urine disease (MSUD) is a metabolic disorder biochemically characterized by the accumulation of branched-chain alpha-amino acids (BCAA) and their branched-chain alpha-keto acids (BCKA) in blood and tissues. Neurological dysfunction is usu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa6343a66d993d4ba6381613e3641f5
https://doi.org/10.1016/s0736-5748(03)00028-5
https://doi.org/10.1016/s0736-5748(03)00028-5
Autor:
Carmen Pilla, Clovis Milton Duval Wannmacher, Moacir Wajner, Carlos Severo Dutra-Filho, Rui Felipe de Oliveira Cardozo, Angela T. S. Wyse
Publikováno v:
Neurochemical Research. 28:675-679
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=doi_________::144e594012854cab2b152725e0d660f4
https://doi.org/10.1023/a:1022876130038
https://doi.org/10.1023/a:1022876130038
Autor:
Moacir Wajner, Rui Felipe de Oliveira Cardozo, Clovis Milton Duval Wannmacher, Angela T. S. Wyse, Carmen Pilla, Carlos Severo Dutra-Filho
Publikováno v:
Metabolic Brain Disease. 18:17-25
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=doi_________::288f7d362e2a52c25ca0d66521a9266e
https://doi.org/10.1023/a:1021974517837
https://doi.org/10.1023/a:1021974517837
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