Search Results - "Nélio Januário, José"

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    Impact of Lowering TSH Cut-Off on Neonatal Screening for Congenital Hypothyroidism in Minas Gerais, Brazil by Teixeira Palla Braga, Nathalia, Vilela Antunes, Jáderson Mateus, Colosimo, Enrico Antônio, Alves Dias, Vera Maria, Januário, José Nélio, Novato Silva, Ivani

    “…A higher incidence of primary congenital hypothyroidism (CH) has been related to increased sensitivity in neonatal screening tests. The benefit of treatment in…”
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    Journal Article
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    Comparison of HPV genotyping by type-specific PCR and sequencing by Carvalho, Nara de Oliveira, del Castillo, Dora Méndez, Perone, Carlos, Januário, José Nélio, Melo, Victor Hugo de, Brasileiro Filho, Geraldo

    Published in Memórias do Instituto Oswaldo Cruz (01-02-2010)
    “…Human papillomavirus (HPV) infection is the most common sexually transmitted disease worldwide and there is a strong link between certain high-risk viral types…”
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    Mortality of children with sickle cell disease: a population study by Fernandes, Ana Paula Pinheiro Chagas, Januário, José Nélio, Cangussu, Camila Blanco, Macedo, Daniela Lino de, Viana, Marcos Borato

    Published in Jornal de pediatria (01-07-2010)
    “…To describe the deaths of children with sickle cell disease (SCD) in Minas Gerais, Brazil, and followed up at the Fundação Hemominas. Cohort of children…”
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    High prevalence of genotype 1 in individuals with hepatitis C in Belo Horizonte, MG by Perone, Carlos, Del Castillo, Dora Mendez, Pereira, Gilsimary Lessa, Carvalho, Nara de Oliveira, Januário, José Nélio, Teixeira, Rosângela

    “…The hepatitis C virus is characterized by significant genetic heterogeneity. It is currently classified into six main genotypes and several subtypes…”
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    Journal Article
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    The time has come: a new scene for PKU treatment by Santos, Luciana Lara dos, Magalhães, Myrian de Castro, Januário, José Nélio, Aguiar, Marcos José Burle de, Carvalho, Maria Raquel Santos

    Published in Genetics and molecular research (31-03-2006)
    “…Phenylketonuria (PKU) is one of the few genetic diseases in which mental retardation can be prevented. Hence, diagnosis and treatment must be established…”
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