Investigação clínica e citogenética molecular em pacientes com atraso de desenvolvimento neuropsicomotor associado à malformação congênita

by Flavia Balbo Piazzon
Published 2016

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

by Frederico Scuotto, MD, CEPS-AC, Maria Fernanda Silva Jardim, MD, Flávia Balbo Piazzon, MD, PhD, Caio Marcos de Moraes Albertini, MD, PhD, Renato Samy Assad, MD, PhD, Guilherme Fenelon, MD, PhD, Claudio Cirenza, MD, PhD
Published 2020-05-01

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

by Karina Lucio de Medeiros Bastos, Caio Robledo Quaio, Fabiana Roberto Lima, Iana Manuelle Araújo, Candice Alves Tavares Araújo, Flávia Balbo Piazzon, Ismael Dale Cotrim Guerreiro da Silva, Gabriel Nuncio Benevides, Ana Cristina Tannuri, Uenis Tannuri, Ramiro Anthero Azevedo, Chong Ae Kim
Published 2019-03-01

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

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