Search Results - "de Marco, Luiz Armando"

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    PTEN expression in patients with carcinoma of the cervix and its association with p53, Ki-67 and CD31 by Loures, Luciano Fernandes, Cândido, Eduardo Batista, Vidigal, Paula Vieira Teixeira, Seabra, Mariana Ataydes Leite, Marco, Luiz Armando Cunha de, Silva-Filho, Agnaldo Lopes da

    “…To investigate protein expression and mutations in phosphatase and tensin homolog (PTEN) in patients with stage IB cervical squamous cell carcinoma (CSCC) and…”
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    Journal Article
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    Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract by Reis, Geisilaine Soares dos, Simões e Silva, Ana Cristina, Freitas, Izabella Silva, Heilbuth, Thiago Ramos, Marco, Luiz Armando de, Oliveira, Eduardo Araújo, Miranda, Débora Marques

    Published in Jornal de pediatria (01-01-2014)
    “…to determine the frequency of different phenotypes for congenital anomalies of the kidney and urinary tract (CAKUT) in a Brazilian sample, and to evaluate the…”
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    Genetic Variations in AMPK , FOXO3A , and POMC Increase the Risk of Extreme Obesity by Santana, Cinthia Vila Nova, Magno, Luiz Alexandre Viana, Ramos, Adauto Versiani, Rios, Maria Angélica, Sandrim, Valéria Cristina, De Marco, Luiz Armando, de Miranda, Débora Marques, Romano-Silva, Marco Aurélio

    Published in Journal of obesity (2024)
    “…Genetic variability significantly impacts metabolism, weight gain, and feeding behaviors, predisposing individuals to obesity. This study explored how…”
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    Whole-exome sequencing as a diagnostic tool for distal renal tubular acidosis by Pereira, Paula Cristina Barros, Melo, Flávia Medeiros, De Marco, Luiz Armando Cunha, Oliveira, Eduardo Araújo, Miranda, Débora Marques, Simões e Silva, Ana Cristina

    Published in Jornal de pediatria (01-11-2015)
    “…Distal renal tubular acidosis (dRTA) is characterized by metabolic acidosis due to impaired renal acid excretion. The aim of this study was to demonstrate the…”
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    Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obsessive-compulsive disorder by Rocha, Felipe Filardi da, Alvarenga, Nathália Bueno, Lage, Naira Vassalo, Romano-Silva, Marco Aurélio, Marco, Luiz Armando de, Corrêa, Humberto

    Published in Revista brasileira de psiquiatria (01-06-2011)
    “…A substantial body of evidence suggests that obsessive-compulsive disorder has a genetic component, and substantial candidate genes for the disorder have been…”
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    Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract by Reis, Geisilaine Soares dos, Silva, Ana Cristina Simões e, Freitas, Izabella Silva, Heilbuth, Thiago Ramos, Marco, Luiz Armando de, Oliveira, Eduardo Araújo, Miranda, Débora Marques

    “…To determine the frequency of different phenotypes for congenital anomalies of the kidney and urinary tract (CAKUT) in a Brazilian sample, and to evaluate the…”
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    Journal Article
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    Importance of genetic polymorphisms in the response to age-related macular degeneration treatment by Carlos Eduardo dos Reis Veloso, Luciana Negrão Frota de Almeida, Luiz Armando De Marco, Raul Nunes Galvarro Vianna, Márcio Bittar Nehemy

    Published in Revista Brasileira de Oftalmologia (01-06-2012)
    “…Age-related macular degeneration (AMD) is a degenerative disorder that affects the central retina and involves the Bruch's membrane, the retinal pigment…”
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    Analysis of KRAS, BRAF, and EGFR mutational status in respiratory epithelial adenomatoid hamartoma (REAH) by Guimarães, Letícia Martins, Vieira, Tamara da Silva, De Marco, Luiz Armando, Thompson, Lester D. R., Gomes, Carolina Cavalieri

    Published in Journal of oral pathology & medicine (01-07-2023)
    “…Background Respiratory epithelial adenomatoid hamartoma (REAH) is a sinonasal glandular overgrowth arising from the surface respiratory epithelium and…”
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    Journal Article
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