Paulo Emidio Lobão Cunha
2PUBLICATIONS
8CO-AUTHORS
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Publications (2)
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|Jul 29, 2024
Rett syndrome due to mutation in the MECP2 gene and electroencephalographic findings.Marta Rodrigues de Carvalho, Thiago Toscano Cavalcante, Pedro Sudbrack Oliveira
|Oct 27, 2021
Nodular heterotopia: a rare finding in patients with epilepsy and SCN1A mutation.Matheus Rocha Pereira Klettenberg, Victor Alves Rodrigues, Diógenes Diego de Carvalho Bispo
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Frequent Collaborators
1 joint publications
Matheus Rocha Pereira Klettenberg
1 joint publications
Victor Alves Rodrigues
1 joint publications
Diógenes Diego de Carvalho Bispo
1 joint publications
Lisiane Seguti Ferreira
1 joint publications
Marta Rodrigues de Carvalho
1 joint publications
Thiago Toscano Cavalcante
1 joint publications
Pedro Sudbrack Oliveira
1 joint publications
Pedro Vicente Ferreira Naves
