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Akademický článek

Mild Diabetes Models and Their Maternal-Fetal Repercussions

Autor: D. C. Damasceno, Y. K. Sinzato, A. Bueno, A. O. Netto, B. Dallaqua, F. Q. Gallego, I. L. Iessi, S. B. Corvino, R. G. Serrano, G. Marini, F. Piculo, I. M. P. Calderon, M. V. C. Rudge

Publikováno v: Journal of Diabetes Research, Vol 2013 (2013)

The presence of diabetes in pregnancy leads to hormonal and metabolic changes making inappropriate intrauterine environment, favoring the onset of maternal and fetal complications. Human studies that explore mechanisms responsible for changes caused

Externí odkaz: https://doaj.org/article/08f6f5494ce84fc891bdd2edd74ff439

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Akademický článek

Quantification of lysosphingomyelin and lysosphingomyelin-509 for the screening of acid sphingomyelinase deficiency

Publikováno v: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)

Abstract Background Acid sphingomyelinase deficiency (ASMD) is a lysosomal disorder caused by deficiency of acid sphingomyelinase (ASM) leading to the accumulation of sphingomyelin (SM) in a variety of cell types. Lysosphingomyelin (LysoSM) is the de

Externí odkaz: https://doaj.org/article/1013ea20819c42278d1b94181b7a75d1

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Akademický článek

Measurement of sulfatides in the amniotic fluid supernatant: A useful tool in the prenatal diagnosis of metachromatic leukodystrophy

Autor: Francyne Kubaski, Zackary M. Herbst, Maira Graeff Burin, Kristiane Michelin‐Tirelli, Franciele B. Trapp, Rejane Gus, Alice B. O. Netto, Ana Carolina Brusius‐Facchin, Sandra Leistner‐Segal, Maria Teresa Sanseverino, Carolina Moura Fischinger de Souza, Matheus V. M. B. Wilke, Thiago Oliveira, Jose A. A. Magalhães, Roberto Giugliani

Publikováno v: JIMD Reports, Vol 63, Iss 2, Pp 162-167 (2022)

Abstract Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal disorder caused by deficiency of arylsulfatase A (ARSA), leading to an accumulation of sulfatides. Sulfatides have been quantified in urine, dried blood spots (DBS), and

Externí odkaz: https://doaj.org/article/cb2cd21c4abc442088c12a59965a6411

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Akademický článek

Capacidades para inovação em serviços: Análise bibliométrica e direções para pesquisas futuras / Capabilities for service innovation: Bibliometric analysis and directions for future research

Autor: Rafael T. Crispim, Carlai O. Netto, Guilherme F. Camboim, Felipe F. Camboim

Publikováno v: RAM. Revista de Administração Mackenzie, Vol 23, Iss 6 (2022)

RESUMO Objetivo: Este estudo tem como objetivo identificar como a literatura de estudos de inovação aborda o tema das capacidades para inovação em serviços e propor direções para futuras pesquisas nesse campo. Originalidade/valor: Existe u

Externí odkaz: https://doaj.org/article/2897051a317e4e39afe91e99438dcf06

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Akademický článek

Experience of the NPC Brazil Network with a Comprehensive Program for the Screening and Diagnosis of Niemann-Pick Disease Type C

Autor: Francyne Kubaski, Alberto Burlina, Giulia Polo, Danilo Pereira, Zackary M. Herbst, Camilo Silva, Franciele B. Trapp, Kristiane Michelin-Tirelli, Franciele F. Lopes, Maira G. Burin, Ana Carolina Brusius-Facchin, Alice B. O. Netto, Larissa Faqueti, Gabrielle D. Iop, Edina Poletto, Roberto Giugliani

Publikováno v: International Journal of Neonatal Screening, Vol 8, Iss 3, p 39 (2022)

Niemann-Pick disease type C (NPC) is a lysosomal disorder caused by impaired cholesterol metabolism. Levels of lysosphingomyelin 509 (LysoSM509) have been shown elevated in dried blood spots (DBS) of NPC and acid sphingomyelinase deficiency patients.

Externí odkaz: https://doaj.org/article/cce8ae4353fe4c76a53f67cf47819f02

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Akademický článek

Clinical and molecular characterization of patients fulfilling Chompret criteria for Li-Fraumeni syndrome in Southern Brazil.

Autor: Camila Matzenbacher Bittar, Yasminne Marinho de Araújo Rocha, Igor Araujo Vieira, Clévia Rosset, Tiago Finger Andreis, Ivaine Tais Sauthier Sartor, Osvaldo Artigalás, Cristina B O Netto, Barbara Alemar, Gabriel S Macedo, Patricia Ashton-Prolla

Publikováno v: PLoS ONE, Vol 16, Iss 9, p e0251639 (2021)

Li-Fraumeni syndrome (LFS) is an autosomal dominant cancer predisposition syndrome caused by pathogenic germline variants in the TP53 gene, characterized by a predisposition to the development of a broad spectrum of tumors at an early age. The core t

Externí odkaz: https://doaj.org/article/5faa01362f1d4910bee4c50e4ee2336c

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Akademický článek

Impact of different exercise intensities on pregnant rats and on their offspring

Autor: ALINE O. NETTO, NATHÁLIA C. DIAS MACEDO, FRANCIANE Q. GALLEGO, YURI K. SINZATO, GUSTAVO T. VOLPATO, ELENA ZAMBRANO, DÉBORA C. DAMASCENO

Publikováno v: Anais da Academia Brasileira de Ciências, Vol 92, Iss 4 (2020)

Abstract This study aimed at evaluating the levels of different maternal exercise intensities on maternal and fetal outcomes. Wistar rats were mated and the pregnant rats were distributed into four experimental groups (n = 13 animals/group): Control

Externí odkaz: https://doaj.org/article/af1e078ccf9a478dabacedd52f842dff

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Alocação de salas usando fluxo máximo de custo mínimo em grafos bipartidos

Autor: João O. Netto, Hebert Silva

Publikováno v: Anais da VIII Escola Regional de Informática de Goiás (ERI-GO 2020).

Este artigo apresenta uma solução para o problema de alocação de salas no âmbito da UFG. O problema consiste em, dado um conjunto de pedidos para uso de salas e um conjunto de salas disponíveis, otimizar a ocupação das salas garantindo que ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1501b284fb788e91495501cbb39fccab
https://doi.org/10.5753/erigo.2020.13867

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Akademický článek

Increased oxidative damage in carriers of the germline TP53 p.R337H mutation.

Autor: Gabriel S Macedo, Leonardo Lisbôa da Motta, Juliana Giacomazzi, Cristina B O Netto, Vanusa Manfredini, Camila S Vanzin, Carmen Regla Vargas, Pierre Hainaut, Fábio Klamt, Patricia Ashton-Prolla

Publikováno v: PLoS ONE, Vol 7, Iss 10, p e47010 (2012)

Germline mutations in TP53 are the underlying defect of Li-Fraumeni Syndrome (LFS) and Li-Fraumeni-like (LFL) Syndrome, autosomal dominant disorders characterized by predisposition to multiple early onset cancers. In Brazil, a variant form of LFS/LFL

Externí odkaz: https://doaj.org/article/2bd510bbc68a40c0a63d3e448cb1aeba

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Tuberculosis: a study of 111 cases in an area of high prevalence in the extreme south of Brazil

Autor: Marta Osório Ribeiro, Ivo Gomes de Mattos, Isabel Cristina de O. Netto, Pedro Alves d'Azevedo

Publikováno v: Brazilian Journal of Infectious Diseases v.10 n.3 2006
Brazilian Journal of Infectious Diseases
Brazilian Society of Infectious Diseases (BSID)
instacron:BSID
Brazilian Journal of Infectious Diseases, Volume: 10, Issue: 3, Pages: 194-198, Published: JUN 2006
Brazilian Journal of Infectious Diseases, Vol 10, Iss 3, Pp 194-198

Tuberculosis is an increasingly important public health problem in developing countries. We studied 111 tuberculosis patients confirmed by mycobacteria isolation between 1998 and 2000 in Rio Grande, in south Brazil. One-hundred-thirteen pulmonary and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd4361fcff897c3864ade6c0c902b1c5
https://doi.org/10.1590/s1413-86702006000300008

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