Analysis of national coverage of neonatal cystic fibrosis screening in Brazil from 2008 to 2017

Author:

Sadigurschi Gabriela1ORCID,Vaz Micherino Bianca1,Assunção Mendes da Cunha Maria Beatriz2,Antão Paiva Carmen Lucia3,da Silva e Sá Gloria Regina4

Affiliation:

1. Escola de Medicina e Cirurgia do Rio de Janeiro, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

2. Departamento de Métodos Quantitativos, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

3. Programa de Pós Graduação em Biologia Molecular e Celular, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

4. Instituto de Saúde Coletiva, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. Early Decline of Pancreatic Function in Cystic Fibrosis Patients with Class 1 or 2 CFTR Mutations

2. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients

3. Genetic ancestry, admixture and health determinants in Latin America

4. Brazilian guidelines for the diagnosis and treatment of cystic fibrosis

5. Horizonte B. Diagnóstico Situacional do Programa Nacional de Triagem Neonatal nos Estados Brasileiros [Situational Diagnosis of the National Neonatal Screening Program in Brazilian States] [Internet]. 2013. [cited 2020 Aug 24]. Available from: www.nupad.medicina.ufmg.br.

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