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Jornal De Pediatria|February 21, 2012
Mental retardation in Duchenne muscular dystrophyFlávia Nardes, Alexandra P Q C Araújo, Márcia Gonçalves Ribeiro
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 25, 2024
Similar disease progression in nonsense Duchenne muscular dystrophy boys as general natural history: Single Brazilian center 15 years registry viewFlávia Nardes, Alexandra Prufer de Queiroz Campos Araújo, Sofia Russi, et al.
Arquivos De Neuro-Psiquiatria|October 13, 2024
Why should a 5q spinal muscular atrophy neonatal screening program be started?Michele Michelin Becker, Flávia Nardes, Tamara Dangouloff, et al.
Critical Care (London, England)|August 18, 2004
Performance of six severity-of-illness scores in cancer patients requiring admission to the intensive care unit: a prospective observational studyMárcio Soares, Flávia Fontes, Joana Dantas, et al.
Arquivos De Neuro-Psiquiatria|November 6, 2024
Type-1 spinal muscular atrophy cohort before and after disease-modifying therapiesBrenda Klemm Arci Mattos de Freitas Alves, Alexandra Prufer de Queiroz Campos Araujo, Flávia Nardes Dos Santos, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 31, 2025
Is late diagnosis of Duchenne muscular dystrophy still a reality?Michele Michelin Beckerq, Juliana Gurgel-Giannetti, Alexandra Prufer de Queiroz Campos Araujo, et al.
Arquivos De Neuro-Psiquiatria|February 5, 2024
Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophyEdmar Zanoteli, Alexandra Prufer de Queiróz Campos Araujo, Michele Michelin Becker, et al.
Neurology. Genetics|October 16, 2020
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophyRodrigo de Holanda Mendonça, Ciro Matsui, Graziela Jorge Polido, et al.
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