Listar Ciencias de la Salud por autor "Wajner, Moacir"
Mostrando ítems 1-8 de 8
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Clinical and biochemical findings in 7 patients with X-linked adrenoleukodystrophy treated with Lorenzo's oil
Vargas, Carmen Regla; Barschak, Alethea Gatto; Coelho, Daniela de Moura; Furlanetto, Vivian; Souza, Carolina Fischinger Moura de; Karam, Simone de Menezes; Jardim, Laura Bannach; Wajner, Moacir; Giugliani, Roberto (2000) [Artículo de periódico]A adrenoleucodistrofia ligada ao X (X-ALD) é uma desordem hereditária do metabolismo peroxissomal, bioquimicamente caracterizada pelo acúmulo de ácidos graxos de cadeia muito longa (‘very long chain fatty acids”- VLCFA) ... -
DNA damage in homocystinuria : 8-oxo-, 8-dihydro-2’-deoxyguanosine levels in cystathionine-β-synthase deficient patients and the in vitro protective effect of N-acetyl-L-cysteine
Vanzin, Camila Simioni; Mescka, Caroline Paula; Marchetti, Desirèe Padilha; Donida, Bruna; Deon, Marion; Jacques, Carlos Eduardo Diaz; Hauschild, Tatiane Cristina; Faverzani, Jéssica Lamberty; Hauschild, Tatiane Cristina; Moura, Dinara Jaqueline; Saffi, Jenifer; Coelho, Daniella de Moura; Wajner, Moacir; Wyse, Angela Terezinha de Souza; Vargas, Carmen Regla (2018) [Artículo de periódico]Introduction: Homocysteine (Hcy) tissue accumulation occurs in a metabolic disease characterized biochemically by cystathionine β-synthase (CBS) deficiency and clinically by mental retardation, vascular problems, and ... -
Inhibition of mitogen-activated proliferation of human lymphocytes "in vitro" by high concentrations of glutamine
Wajner, Moacir; Sommer, Marcia Helena; Fialho, Marcelo B.; Jobim, Luiz Fernando Job; Wannmacher, Clovis Milton Duval (1995) [Artículo de periódico]We investigated the influence of high concentrations of glutamine and asparagine on "in vitro" cellular growth of lymphocytes stimulated with phytohaemagglutinin (PHA), concanavalin A (Con A) and pokeweed mitogen (PWM), a ... -
Investigação de erros inatos do metabolismo
Wajner, Moacir; Vargas, Carmen Regla; Burin, Maira Graeff; Giugliani, Roberto; Coelho, Janice Carneiro (2001) [Artículo de periódico]Os erros inatos do metabolismo são doenças metabólicas hereditárias individualmente raras, mas que em seu conjunto apresentam uma incidência aproximada de pelo menos 1 caso para cada mil nascimentos. O presente trabalho ... -
Monitoring of phenylalanine levels in patients with phenylketonuria using dried blood spots : a comparison of two methods
Sebastião, Fernanda Medeiros; Burin, Maira Graeff; Civallero, Gabriel Eduardo Santiago; Tirelli, Kristiane Michelin; Sitta, Angela; Coelho, Daniella de Moura; Vargas, Carmen Regla; Wajner, Moacir; Giugliani, Roberto; Bitencourt, Fernanda Hendges de; Schwartz, Ida Vanessa Doederlein (2020) [Artículo de periódico]Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsible for the conversion of phenylalanine (Phe) to tyrosine (Tyr). Monitoring of patients with PKU requires the measurement ... -
Nova era da medicina genômica
Wajner, Moacir; Giugliani, Roberto (2001) [Texto de presentación/conclusión]Resumo não disponível -
Plinia trunciflora extract administration prevents HI-induced oxidative stress, inflammatory response, behavioral impairments, and tissue damage in rats
Carvalho, Andrey Vinicios Soares; Ribeiro, Rafael Teixeira; Duran Carabali, Luz Elena; Martini, Ana Paula Rodrigues; Hoeper, Eduarda de Souza; Sanches, Eduardo Farias; Konrath, Eduardo Luis; Dalmaz, Carla; Wajner, Moacir; Netto, Carlos Alexandre (2022) [Artículo de periódico]The disruption of redox homeostasis and neuroinflammation are key mechanisms in the pathogenesis of brain hypoxia–ischemia (HI); medicinal plants have been studied as a therapeutic strategy, generally associated with the ... -
Screening for organic acidurias and aminoacidopathies in high-risk Brazilian patients : eleven-year experience of a reference center
Wajner, Moacir; Sitta, Angela; Kayser, Aline; Deon, Marion; Groehs, Ana Carolina; Coelho, Daniella de Moura; Vargas, Carmen Regla (2019) [Artículo de periódico]Organic acidurias and aminoacidopathies are groups of frequent inborn errors of metabolism (IEMs), which are caused by mutations in specific genes that lead to loss of protein/enzyme or transport function with important ...