Search Results - "Silva, Helena Matos"

  • Showing 1 - 10 results of 10
Refine Results
  1. 1
  2. 2
  3. 3
  4. 4

    Congenital erythrocytosis – discover of a new mutation in the EGLN1 gene by Barradas, João, Rodrigues, Catarina Dantas, Ferreira, Gisela, Rocha, Paula, Constanço, Conceição, Andrade, Maria Reis, Bento, Celeste, Silva, Helena Matos

    Published in Clinical case reports (01-06-2018)
    “…Key Clinical Message Congenital erythrocytosis is a hereditary disorder due to an increase in red cell mass that can be caused by mutations in proteins…”
    Get full text
    Journal Article
  5. 5

    Syphilis in pregnancy and adverse birth outcomes: A nationwide longitudinal study in Brazil by Silva, Helena Benes Matos, Cássia Ribeiro‐Silva, Rita, Junior, Elzo Pereira Pinto, Barreto, Maurício L., Paixão, Enny S., Ichihara, Maria Yury

    “…Objective The present study aimed to evaluate the association between syphilis in pregnancy and low birth weight, small for gestational age, and preterm birth…”
    Get full text
    Journal Article
  6. 6
  7. 7
  8. 8

    Factors associated with body image dissatisfaction in a Brazilian university sample during the COVID-19 pandemic by Cunha, Carla de Magalhães, Pereira, Emile Miranda, Souto, Maria Clara Reis, de Sá, Laís Barbosa, da Silva, Helena Benes Matos, de Brito, Edleide, de Santana, Mônica Leila Portela

    Published in Frontiers in education (Lausanne) (14-03-2023)
    “…We investigated the prevalence of body image dissatisfaction (BID) and associated factors among professors and undergraduate students in Brazil during the…”
    Get full text
    Journal Article
  9. 9
  10. 10

    Congenital erythrocytosis - discover of a new mutation in the EGLN1 gene by Barradas, João, Rodrigues, Catarina Dantas, Ferreira, Gisela, Rocha, Paula, Constanço, Conceição, Andrade, Maria Reis, Bento, Celeste, Silva, Helena Matos

    Published in Clinical case reports (01-06-2018)
    “…Congenital erythrocytosis is a hereditary disorder due to an increase in red cell mass that can be caused by mutations in proteins involved in HIF-α pathway,…”
    Get full text
    Report