Search Results - "Ribeiro, Georgina S"

A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil by Oliveira, Raimundo Antonio G, Oshiro, Marilena, Hirata, Mario H, Hirata, Rosario D C, Ribeiro, Georgina S, Medeiros, Tereza M D, de O Barretto, Orlando C

“…In this study, we used red cell glucose-6-phosphate dehydrogenase (G6PD) activity to screen for G6PD-deficient individuals in 373 unrelated asymptomatic adult…”
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Heart failure patients with B1-adrenoreceptor polymorphisms have augmented carvedilol response as detected by cardiac I123-MIBG scintigraphy by Miranda, Sandra Marina R, Moscavitch, Samuel Datum, Pereira, Sabrina B, de Azevedo, Jader C, Messias, Leandro R, Rodrigues, Ronaldo C, Mesquita, Evandro T, Ribeiro, Georgina S, Mesquita, Claudio T

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ASSOCIATION BETWEEN ADRENERGIC RECEPTOR GENOTYPES AND BETA-BLOCKER TREATMENT RESPONSE IN HEART FAILURE PATIENTS: ANALYSIS BY CARDIAC 123I-MIBG SCINTIGRAPHY by Mesauita, Claudio Tinoco, Miranda, Sandra M, Moscavitch, Samuel, Rodrigues, Ronaldo, Pereira, Sabrina B, Messias, Leandro, Ribeiro, Georgina S, Azevedo, Jader C, Santos, Marcus Vinicus J, Mesquita, Evandro T

“…Inclusion criteria were: presence of Heart Failure by Framinghan Criteria, NYHA class I-IV, age 30-80 years, left ventricular ejection fraction <45% (Simpson…”
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Effect of the 894G>T polymorphism of the endothelial nitric oxide synthase on vascular reactivity following maximal dynamic exercise by Neves, Fabricia J, Silva, Bruno M, Rocha, Natália G, Sales, Allan RK, Ribeiro, Georgina S, Nóbrega, Antonio C

“…BACKGROUNDConsidering that the role of nitric oxide as a vasodilator is increased after an acute bout of exercise and that the 894G>T polymorphism of the…”
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Beta-Adrenergic Receptor Polymorphisms in Susceptibility, Response to Treatment and Prognosis in Heart Failure by Pereira, Sabrina B, Veloso, Monica W, Chermont, Sergio, Quintao, Monica, Andrade, Wolney, Villacorta, Humberto, Contarato, Luiza, Rosa, Maria Luiza G, Nobrega, Antonio Claudio L, Mesquita, Evandro T, Ribeiro, Georgina S

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Dietary iron supplementation does not aggravate experimental malaria in young rats by Cardoso, M A, Ferreira, M U, Ribeiro, G S, Penteado, M D, Andrade Júnior, H F

“…The hypotheses that iron-deficient hosts are less susceptible to severe malaria and that iron supplementation aggravates infection have been supported by some…”
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Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria by Gonzaga, Ana Denise Gomes, Amorim, Lidia Maria da Fonte, Fonseca, Ana Beatriz Monteiro, Nogueira, Tatiana Lucia Santos, Pereira, Olga Maria Diniz, Nagai, Maria Aparecida, Oliveira Barretto, Orlando Cesar, Ribeiro, Georgina Severo

“…Summary Acute intermittent porphyria (AIP), an autosomal dominant disorder, is caused by a deficiency of hydroxymethylbilane synthase (HMBS). In the present…”
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Impact Of Maximal Dynamic Exercise On Blood Flow In Subjects With Enos Gene Polymorphism (894G>T): 1420 Board #22 May 27 11:00 AM - 12:30 PM by Neves, Fabricia J., Silva, Bruno M., Rocha, Natália G., Sales, Allan R.K., Stelet, Vinícius N., Gonçalves, Rodrigo J.P., Ribeiro, Georgina S., Souza, Márcio N., Nóbrega, Antonio C.L.

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The frequency of β-globin gene haplotypes, α-thalassemia and genetic polymorphisms of methylenetetrahydrofolate reductase, factor V Leiden and prothrombin genes in children with sickle cell disease in Rio de Janeiro, Brazil by Silva Filho, Isaac L., Ribeiro, Georgina S., Pimenta-Bueno, Leíse M., Serpa, Maria José A.

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The frequency of β-globin gene haplotypes, α-thalassemia and genetic polymorphisms of methylenetetrahydrofolate reductase, factor V Leiden and prothrombin genes in children with sickle cell disease in Rio de Janeiro, Brazil Frequência dos haplótipos da globina beta, da talassemia alfa e dos polimorfismos genéticos dos genes da metilenotetrahidrofolato redutase, do fator V Leiden e da protrombina em crianças com doença falciforme no Rio de Janeiro, Brasil by Isaac L. Silva Filho, Georgina S. Ribeiro, Leíse M. Pimenta-Bueno, Maria José A. Serpa

“…A freqüência dos haplótipos beta S e beta C do gene da globina e a prevalência de talassemia alfa e de mutações nos genes da metilenotetrahidrofolato redutase…”
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