Electrical storm treated successfully in a patient with TANGO2 gene mutation and long QT syndrome: A case report

Tekijä Scuotto, Frederico, Silva Jardim, Maria Fernanda, Piazzon, Flávia Balbo, Marcos de Moraes Albertini, Caio, Assad, Renato Samy, Fenelon, Guilherme, Cirenza, Claudio
Julkaisussa HeartRhythm Case Rep (2020)

Biochemical profile in an infant with neonatal hemochromatosis shows evidence of impairment of mitochondrial long-chain fatty acid oxidation

Tekijä Bastos, Karina Lucio de Medeiros, Quaio, Caio Robledo, Lima, Fabiana Roberto, Araújo, Iana Manuelle, Araújo, Candice Alves Tavares, Piazzon, Flávia Balbo, da Silva, Ismael Dale Cotrim Guerreiro, Benevides, Gabriel Nuncio, Tannuri, Ana Cristina, Tannuri, Uenis, Azevedo, Ramiro Anthero, Kim, Chong Ae
Julkaisussa Clin Mol Hepatol (2019)

Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience

Tekijä Zanardo, Évelin Aline, Dutra, Roberta Lelis, Piazzon, Flavia Balbo, Dias, Alexandre Torchio, Novo-Filho, Gil Monteiro, Nascimento, Amom Mendes, Montenegro, Marília Moreira, Damasceno, Jullian Gabriel, Madia, Fabrícia Andreia Rosa, da Costa, Thaís Virgínia Moura Machado, Melaragno, Maria Isabel, Kim, Chong Ae, Kulikowski, Leslie Domenici
Julkaisussa Clinics (Sao Paulo) (2017)