897 resultados para Gil González, Antonio
Resumo:
Defeza dos cidadãos Antonio Carlos Ribeiro de Andrada Machado e Silva e Martin Francisco Ribeiro de Andrada Contém as acusações feitas a estes deputados e apresenta a peça de defesa produzida por Saturnino, que, na qualidade de advogado dos réus, refuta a existência dos crimes de sedição e conspiração de que são acusados e defende a liberdade de expressão. Ao fim do trabalho, é apresentada a sentença que os inocenta das acusações.
Resumo:
Antônio Galvão, filho de Duarte Galvão, excedeu em fama e imaginação a se pai e a seu avô, Rui Galvão. Nasceu na Índia Oriental, em 1490, e morreu em 1557.
Resumo:
XX1 CUIEET - Congreso Universitario de Innovación Educativa en las Enseñanzas Técnicas, Valencia, 2013.
Resumo:
A indicação de responsabilidade aparece abreviada no v.1, mas por extenso nos demais vs.
Resumo:
Referência: Library of Congress - Online Catalog.
Resumo:
1 carta (mecanografiada) ; 210x290mm. Ubicación: Caja 1 - Carpeta 5
Resumo:
7 cartas (mecanografiadas) ; entre 215x286mm y 157x215mm. Ubicación: Caja 1 - Carpeta 10
Resumo:
9 p.
Resumo:
Apenas empresas nacionais poderão explorar mineração em áreas de fronteiras, estratégicas e em territórios indígenas. Também foram discutidas outras emendas que propõem a nacionalização total do subsolo brasileiro serão decididas no voto. Lei complementar definirá as áreas estratégicas. Empresas nacionais terão preferência no transporte de cabotagem e no transporte marítimo internacional. O governo brasileiro deverá comprar navios nos estaleiros brasileiros. É função do Estado incentivar a organização dos garimpeiros em cooperativas. Lei Ordinária disporá sobre a política tarifária de serviços públicos. A seguir foi votada o artigo 205. Estabelece que jazidas, minas, recursos minerais e potenciais recursos energia hidráulica são propriedades da União.
Resumo:
Background: Primary distal renal tubular acidosis (dRTA) caused by mutations in the genes that codify for the H+ -ATPase pump subunits is a heterogeneous disease with a poor phenotype-genotype correlation. Up to now, large cohorts of dRTA Tunisian patients have not been analyzed, and molecular defects may differ from those described in other ethnicities. We aim to identify molecular defects present in the ATP6V1B1, ATP6V0A4 and SLC4A1 genes in a Tunisian cohort, according to the following algorithm: first, ATP6V1B1 gene analysis in dRTA patients with sensorineural hearing loss (SNHL) or unknown hearing status. Afterwards, ATP6V0A4 gene study in dRTA patients with normal hearing, and in those without any structural mutation in the ATP6V1B1 gene despite presenting SNHL. Finally, analysis of the SLC4A1 gene in those patients with a negative result for the previous studies. Methods: 25 children (19 boys) with dRTA from 20 families of Tunisian origin were studied. DNAs were extracted by the standard phenol/chloroform method. Molecular analysis was performed by PCR amplification and direct sequencing. Results: In the index cases, ATP6V1B1 gene screening resulted in a mutation detection rate of 81.25%, which increased up to 95% after ATP6V0A4 gene analysis. Three ATP6V1B1 mutations were observed: one frameshift mutation (c.1155dupC; p.Ile386fs), in exon 12; a G to C single nucleotide substitution, on the acceptor splicing site (c.175-1G > C; p.?) in intron 2, and one novel missense mutation (c. 1102G > A; p. Glu368Lys), in exon 11. We also report four mutations in the ATP6V0A4 gene: one single nucleotide deletion in exon 13 (c.1221delG; p. Met408Cysfs* 10); the nonsense c.16C > T; p.Arg6*, in exon 3; and the missense changes c.1739 T > C; p.Met580Thr, in exon 17 and c.2035G > T; p.Asp679Tyr, in exon 19. Conclusion: Molecular diagnosis of ATP6V1B1 and ATP6V0A4 genes was performed in a large Tunisian cohort with dRTA. We identified three different ATP6V1B1 and four different ATP6V0A4 mutations in 25 Tunisian children. One of them, c.1102G > A; p.Glu368Lys in the ATP6V1B1 gene, had not previously been described. Among deaf since childhood patients, 75% had the ATP6V1B1 gene c. 1155dupC mutation in homozygosis. Based on the results, we propose a new diagnostic strategy to facilitate the genetic testing in North Africans with dRTA and SNHL.
Resumo:
Antonio Duplá Ansuategui, Piedad Frías Nogales e Iban Zaldúa (editores)
Resumo:
Background: Patients with chronic obstructive pulmonary disease (COPD) often experience exacerbations of the disease that require hospitalization. Current guidelines offer little guidance for identifying patients whose clinical situation is appropriate for admission to the hospital, and properly developed and validated severity scores for COPD exacerbations are lacking. To address these important gaps in clinical care, we created the IRYSS-COPD Appropriateness Study. Methods/Design: The RAND/UCLA Appropriateness Methodology was used to identify appropriate and inappropriate scenarios for hospital admission for patients experiencing COPD exacerbations. These scenarios were then applied to a prospective cohort of patients attending the emergency departments (ED) of 16 participating hospitals. Information was recorded during the time the patient was evaluated in the ED, at the time a decision was made to admit the patient to the hospital or discharge home, and during follow-up after admission or discharge home. While complete data were generally available at the time of ED admission, data were often missing at the time of decision making. Predefined assumptions were used to impute much of the missing data. Discussion: The IRYSS-COPD Appropriateness Study will validate the appropriateness criteria developed by the RAND/UCLA Appropriateness Methodology and thus better delineate the requirements for admission or discharge of patients experiencing exacerbations of COPD. The study will also provide a better understanding of the determinants of outcomes of COPD exacerbations, and evaluate the equity and variability in access and outcomes in these patients.
Resumo:
9 cartas (mecanografiadas) ; 207x300mm. Ubicación: Caja 1 - Carpeta 36
Resumo:
Presentado en el 13th WSEAS International Conference on Automatic Control, Modelling and Simulation, ACMOS'11