Resultats de la cerca - Mário Campos
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Associations between single nucleotide polymorphisms in vitamin D metabolic pathway genes and serum 25(OH)D concentrations in Brazilian adults: the Pró‐Saúde Study per Flávia Fioruci Bezerra, Ana Carolina Proença da Fonseca, Verônica Marques Zembrzuski, Mário Campos, Pedro Hernán Cabello, Eduardo Faerstein
Publicat 2017Artigo -
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Next-Generation Sequencing for Molecular Diagnosis of Cystic Fibrosis in a Brazilian Cohort per Cambraia, Amanda, Junior, Mario Campos, Zembrzuski, Verônica Marques, Junqueira, Ricardo Magrani, Cabello, Pedro Hernán, de Cabello, Giselda Maria Kalil
Publicat 2021Text -
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Genetic, sociodemographic and lifestyle factors associated with serum 25-hydroxyvitamin D concentrations in Brazilian adults: the Pró-Saúde Study per Flávia Fioruci Bezerra, Paula Normando, Ana Carolina Proença da Fonseca, Verônica Marques Zembrzuski, Mário Campos, Pedro Hernán Cabello, Eduardo Faerstein
Publicat 2022Artigo -
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The first case of NEUROD1‐MODY reported in Latin America per Gabriella de Medeiros Abreu, Roberta Magalhães Tarantino, Pedro Hernán Cabello, Verônica Marques Zembrzuski, Ana Carolina Proença da Fonseca, Melanie Rodacki, Lenita Zajdenverg, Mário Campos
Publicat 2019Artigo -
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Ductal carcinoma in situ of the breast: Evaluation of main presentations on magnetic resonance imaging compared with findings on mammogram and histology per Gustavo Machado Badan, Décio Roveda Júnior, Sebastião Paito, Eduardo de Faria Castro Fleury, Bianca Maragno, Mario Campos, Carlos Alberto Pecci Ferreira, Felipe Augusto Trocoli Ferreira
Publicat 2016Artigo -
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MODY probability calculator for GCK and HNF1A screening in a multiethnic background population per Roberta Magalhães Tarantino, Gabriella de Medeiros Abreu, Ana Carolina Proença De Fonseca, Rosane Kupfer, Maria de Fátima Carvalho Pereira, Mário Campos, Lenita Zajdenverg, Melanie Rodacki
Publicat 2019Artigo -
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A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay per Cíntia Barros Santos-Rebouças, Natalia Fintelman‐Rodrigues, Lars Riff Jensen, Andreas W. Kuß, Márcia Gonçalves Ribeiro, Mário Campos, Jussara Mendonça dos Santos, Márcia Mattos Gonçalves Pimentel
Publicat 2011Artigo -
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Diagnostic underestimation of atypical ductal hyperplasia and ductal carcinoma in situ at percutaneous core needle and vacuum-assisted biopsies of the breast in a Brazilian referen... per Gustavo Machado Badan, Décio Roveda Júnior, Sebastião Piato, Eduardo de Faria Castro Fleury, Mario Campos, Carlos Alberto Ferreira Pecci, Felipe Augusto Trocoli Ferreira, Camila D'Ávila
Publicat 2016Artigo -
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Levels of mannose-binding lectin in individuals with visceral leishmaniasis in the northeast region of Brazil per E.L. da Silva, Mário Campos, Sílvio Gomes Monteiro, Graciomar Conceição Costa, A.L.P. Magalhães, Max Diêgo Cruz Santos, A.J.M. Caldas, Márcia Mattos Gonçalves Pimentel
Publicat 2015Artigo -
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Exon Dosage Variations in Brazilian Patients with Parkinson’s Disease: Analysis of<i>SNCA</i>,<i>PARKIN</i>,<i>PINK1</i>and<i>DJ-1</i>Genes per Karla Cristina Vasconcelos Moura, Mário Campos, Ana Lúcia Zuma de Rosso, Denise Hack Nicaretta, João Santos Pereira, Delson José Silva, Cíntia Barros Santos-Rebouças, Márcia Mattos Gonçalves Pimentel
Publicat 2012Artigo -
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Positive predictive values of Breast Imaging Reporting and Data System (BI-RADS®) categories 3, 4 and 5 in breast lesions submitted to percutaneous biopsy per Gustavo Machado Badan, Décio Roveda Júnior, Carlos Alberto Pecci Ferreira, Felipe Augusto Trocoli Ferreira, Eduardo de Faria Castro Fleury, Mario Campos, Rodrigo de Oliveira Seleti, Hélio da Cruz Júnior
Publicat 2013Artigo -
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Exon Dosage Variations in Brazilian Patients with Parkinson’s Disease: Analysis of SNCA, PARKIN, PINK1 and DJ-1 Genes per Moura, Karla Cristina Vasconcelos, Junior, Mário Campos, de Rosso, Ana Lúcia Zuma, Nicaretta, Denise Hack, Pereira, João Santos, Silva, Delson José, Santos-Rebouças, Cíntia Barros, Pimentel, Márcia Mattos Gonçalves
Publicat 2012Text -
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<p>The association of the fat mass and obesity-associated gene (FTO) rs9939609 polymorphism and the severe obesity in a Brazilian population</p> per Ana Carolina Proença da Fonseca, Gabriella de Medeiros Abreu, Verônica Marques Zembrzuski, Mário Campos, João Régis Ivar Carneiro, José Firmino Nogueira Neto, Giselda Maria Kalil de Cabello, Pedro Hernán Cabello
Publicat 2019Artigo -
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Identification of a novel large deletion and other copy number variations in the<i>CFTR</i>gene in patients with Cystic Fibrosis from a multiethnic population per Raisa da Silva Martins, Mário Campos, Aline dos Santos Moreira, Verônica Marques Zembrzuski, Ana Carolina Proença da Fonseca, Gabriella de Medeiros Abreu, Pedro Hernán Cabello, Giselda Maria Kalil de Cabello
Publicat 2019Artigo -
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Replicative Study in Performance-Related Genes of Brazilian Elite Soccer Players Highlights Genetic Differences from African Ancestry and Similarities between Professional and U20... per Tane Kanope, Caleb Guedes Miranda dos Santos, Feliciana Marinho, Gustavo Monnerat, Mário Campos, Ana Carolina Proença da Fonseca, Verônica Marques Zembrzuski, Miller Gomes de Assis, Michael W. Pfaffl, Eduardo Mendonça Pimenta
Publicat 2023Artigo -
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Genetic Variants in the Activation of the Brown-Like Adipocyte Pathway and the Risk for Severe Obesity per Ana Carolina Proença da Fonseca, Guilherme Proença da Fonseca, Bruna Marchesini, D Voigt, Mário Campos, Verônica Marques Zembrzuski, João Régis Ivar Carneiro, José Firmino Nogueira Neto, Pedro Hernán Cabello, Giselda Maria Kalil de Cabello
Publicat 2020Artigo
Eines de cerca:
Matèries relacionades
Medicine
Biology
Genetics
Internal medicine
Gene
Endocrinology
Mutation
Obesity
Disease
Pathology
Body mass index
Environmental health
Missense mutation
Allele
Diabetes mellitus
Population
Breast cancer
Cancer
Cohort
Genotype
Sanger sequencing
Biopsy
Exon
Gene expression
HNF1A
Insulin resistance
LRRK2
Parkinson's disease
Pediatrics
Phenotype