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Brain & Development|August 11, 2020
Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsyLuciana Midori Inuzuka, Lucia Inês Macedo-Souza, Bruno Della-Ripa, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2020
ATP6V1B2-related epileptic encephalopathyLuciana Midori Inuzuka, Lúcia Inês Macedo-Souza, Bruno Della-Rippa, et al.Brain & Development|November 4, 2019
Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literatureLuciana Midori Inuzuka, Lúcia Inês Macedo-Souza, Bruno Della-Ripa, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 8, 2006
Outcome of hemispheric surgeries for refractory epilepsy in pediatric patientsVera Cristina Terra-Bustamante, Luciana Midori Inuzuka, Regina Maria França Fernandes, et al.Arquivos De Neuro-Psiquiatria|June 28, 2023
Ketogenic therapy in childhood and adolescence: recommendations of the Brazilian experts groupLetícia Pereira de Brito Sampaio, Adélia Maria de Miranda Henriques-Souza, Katia Lin, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 16, 2021
MECP2-related conditions in males: A systematic literature review and 8 additional casesLuciana Midori Inuzuka, Matheus Guerra-Peixe, Lúcia Inês Macedo-Souza, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Pageof 1