Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Zumira A, Carneiro"'
Autor:
Isadora Andrade, River Ribeiro, Zumira A. Carneiro, Roberto Giugliani, Catarina Pereira, Claudia Cozma, Daniel Grinberg, Lluïsa Vilageliu, Charles M. Lourenco
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Mucopolysaccharidosis VI, or Maroteaux–Lamy disease, is an autosomal recessive disease characterized by deficiency of the enzyme arylsulfatase B in the lysosomal catabolism of glycosaminoglycans. Due to reduced (or even null) en
Externí odkaz:
https://doaj.org/article/6ddbc9dc239d45769128ef2220eba000
Autor:
Charles Marques Lourenço, Janaina Dovidio, Isabela F. Lopes, Laís C. Silva, Marcela Almeida, Laura Vagnini, Jacqueline Fonseca, Zumira A. Carneiro, Beat Thöny
Publikováno v:
JIMD Reports, Vol 61, Iss 1, Pp 19-24 (2021)
Abstract Tetrahydrobiopterin (BH4) is a cofactor that participates in the biogenesis reactions of a variety of biomolecules, including l‐tyrosine, l‐3,4‐dihydroxyphenylalanine, 5‐hydroxytryptophan, nitric oxide, and glycerol. Dihydropteridine
Externí odkaz:
https://doaj.org/article/7b828b4eb5b847499bedf6164e4f39a5
Autor:
Gabriela Cabrera Garbuio, Jéssica Rezende Mio, Letícia Cassaro Feltrin, Marina Soccal Silva, Zumira Aparecida Carneiro, Charles Marques Lourenço
Publikováno v:
Medicina, Vol 54, Iss 3 (2021)
A Hemiplegia Alternante da Infância é um distúrbio neurológico grave e uma doença rara (1 em cada 100.000 recém-nascidos), caracterizado por ataques repetidos transitórios de hemiplegia episódica ou tetraplegia que podem durar minutos a horas
Externí odkaz:
https://doaj.org/article/7a9bc1c0c82547da9cb6f04608984e65
Autor:
Maria Cecília de Mattos Alves Silva, Thayane Rosas Batista Rezende, Zumira A. Carneiro, Charles Marques Lourenço
Publikováno v:
Clinical and Biomedical Research, Vol 41, Iss 1 (2021)
Neurodegeneration with brain iron accumulation (NBIA) is a complex group of hereditary progressive neurodegenerative diseases characterized by deposition of iron in the basal ganglia. Twelve genetic forms of this disorder have been identified in prev
Externí odkaz:
https://doaj.org/article/fc07c5a7e9fc4feeb7bda39e34e2c184
Autor:
Drielly A. Paixão, Carla D. Lopes, Zumira A. Carneiro, Luana M. Sousa, Leticia P. de Oliveira, Norberto P. Lopes, Marcos Pivatto, Joana Darc S. Chaves, Mauro V. de Almeida, Javier Ellena, Mariete B. Moreira, Adelino V.G. Netto, Ronaldo J. de Oliveira, Silvana Guilardi, Sérgio de Albuquerque, Wendell Guerra
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 109, Iss , Pp 157-166 (2019)
In order to improve the previously observed antichagasic activity of Cu(II) complexes containing 2-chlorobenzhydrazide (2-CH), we report herein the synthesis and anti-Trypanosoma cruzi activity of novel copper complexes containing 2-methoxybenzhydraz
Externí odkaz:
https://doaj.org/article/6556df07ab6246f0b61cfa4933a4ad4d
Autor:
Giulianna Baldini, José Fernando Palmejiani, João Pedro Bonevechio Sant'Anna, Zumira Aparecida Carneiro, Roberto Giugliani, Catarina Pereira, Claudia Cozma, Cara O’Neill, Charles M. Lourenco
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 8 (2020)
Abstract Sanfilippo syndrome or mucopolysaccharidosis III (MPS III), includes a group of four autosomal recessive lysosomal storage disorders caused by deficient activity of enzymes involved in the catabolism of heparan sulfate. The four types of MPS
Externí odkaz:
https://doaj.org/article/c349fbc6e12d44179aa0a778c4c81d07
Autor:
Samilly Oliveira, Elias Machado, Fabricio Fóla, Zumira Aparecida Carneiro, Charles Marques Lourenço
Publikováno v:
Medicina, Vol 53, Iss 3 (2020)
Também denominada síndrome cerebrohepatorenal, a síndrome de Zellweger é uma doença autossômica recessiva rara, pertencente ao espectro de erros inatos do metabolismo que afetam os peroxissomos. São causados principalmente por mutações
Externí odkaz:
https://doaj.org/article/d1b9242173c44ede924262f7bb24a68e
Autor:
Drielly A. Paixão, Leticia P. de Oliveira, Pedro Ivo da S. Maia, Victor M. Deflon, Zumira A. Carneiro, Katia Júlia de Almeida, Norberto P. Lopes, Marcos Pivatto, Joana Darc S. Chaves, Sérgio de Albuquerque, Mauro V. de Almeida, Silvana Guilardi, Wendell Guerra
Publikováno v:
Journal of Saudi Chemical Society, Vol 22, Iss 7, Pp 809-815 (2018)
We report here the characterization of two new polymeric copper(II) complexes containing 2-chlorobenzhydrazide (2-CH) and two N,N-donor ligands, namely, 1,10-phenanthroline (phen) and 4-4′-dimethoxy-2-2′-bipyridine (dmb). The structure of a new p
Externí odkaz:
https://doaj.org/article/50a25a530dff40b9b162054267f5a88a
Autor:
Ana Paula Morguete Ferreira, Fabrícia Belloni dos Santos Vieira, Felipe Rezende Giacomelli, Tânia Aparecida Bernardes Page, Viviane Romano Moraes, Zumira Aparecida Carneiro
Publikováno v:
HU Revista, Vol 43, Iss 3 (2018)
O citomegalovírus pertence à família do Herpes vírus, e está presente na maior parte da população. A citomegalovirose no período neonatal pode estar associada à transmissão intra-útero por via transplacentária, ou ainda, perinatal. No cas
Externí odkaz:
https://doaj.org/article/b4a638e6f0294da883b5b82201da8ab2
Autor:
Beat Thöny, Zumira Aparecida Carneiro, Marcela Almeida, Isabela F. Lopes, Laura Vagnini, Laís C. Silva, Jacqueline Fonseca, Charles Marques Lourenço, Janaina Dovidio
Publikováno v:
JIMD Reports
JIMD Reports, Vol 61, Iss 1, Pp 19-24 (2021)
JIMD Reports, Vol 61, Iss 1, Pp 19-24 (2021)
Tetrahydrobiopterin (BH4) is a cofactor that participates in the biogenesis reactions of a variety of biomolecules, including l‐tyrosine, l‐3,4‐dihydroxyphenylalanine, 5‐hydroxytryptophan, nitric oxide, and glycerol. Dihydropteridine reductas