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Publications by authors named "Paulo Emidio Lobao Cunha"
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Rett syndrome due to mutation in the MECP2 gene and electroencephalographic findings.
Marta Rodrigues de Carvalho
Thiago Toscano Cavalcante
Pedro Sudbrack Oliveira
Pedro Vicente Ferreira Naves
Paulo Emidio Lobão Cunha
Arq Neuropsiquiatr
August 2024
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Nodular heterotopia: a rare finding in patients with epilepsy and SCN1A mutation.
Matheus Rocha Pereira Klettenberg
Victor Alves Rodrigues
Diógenes Diego de Carvalho Bispo
Paulo Emidio Lobão Cunha
Lisiane Seguti Ferreira
Arq Neuropsiquiatr
October 2021
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