NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms von Zanette, Vanessa, do Valle, Daniel, Telles, Bruno Augusto, Robinson, Alan J., Monteiro, Vaneisse, Santos, Mara Lucia S. F., Souza, Ricardo Lehtonen R., Beninca, Cristiane

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Neurological, neurobehavioral, and radiological alterations in patients with mucopolysaccharidosis III (Sanfilippo's syndrome) in Brazil von Valle, Daniel Almeida do, Santos, Mara Lúcia Schmitz Ferreira, Telles, Bruno Augusto, Cordeiro, Mara L.

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Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations von Dutra, Lívia Almeida, Silva, Pedro Victor de Castro, Ferreira, João Henrique Fregadolli, Marques, Alexandre Coelho, Toso, Fabio Fieni, Vasconcelos, Claudia Cristina Ferreira, Brum, Doralina Guimarães, Pereira, Samira Luisa Dos Apóstolos, Adoni, Tarso, Rocha, Leticia Januzi de Almeida, Sampaio, Leticia Pereira de Brito, Sousa, Nise Alessandra de Carvalho, Paolilo, Renata Barbosa, Pizzol, Angélica Dal, Costa, Bruna Klein da, Disserol, Caio César Diniz, Pupe, Camila, Valle, Daniel Almeida do, Diniz, Denise Sisterolli, Abrantes, Fabiano Ferreira de, Schmidt, Felipe da Rocha, Cendes, Fernando, Oliveira, Francisco Tomaz Meneses de, Martins, Gabriela Joca, Silva, Guilherme Diogo, Lin, Katia, Pinto, Lécio Figueira, Santos, Mara Lúcia Schimtz Ferreira, Gonçalves, Marcus Vinícius Magno, Krueger, Mariana Braatz, Haziot, Michel Elyas Jung, Barsottini, Orlando Graziani Povoas, Nascimento, Osvaldo José Moreira do, Nóbrega, Paulo Ribeiro, Proveti, Priscilla Mara, Castilhos, Raphael Machado do, Daccach, Vanessa, Glehn, Felipe von

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Pediatric Anti-N-methyl-D-aspartate Receptor Encephalitis Mimicking Glutaric Aciduria Type 1: A Case Report von do Valle, Daniel Almeida, Santos, Mara Lucia Schmitz Ferreira, Zeny, Michelle Silva, Cordeiro, Mara L.

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Psychobehavioral factors and family functioning in mucopolysaccharidosis: preliminary studies von do Valle, Daniel Almeida, Bara, Tiago Dos Santos, Furlin, Vanessa, Santos, Mara Lúcia Schmitz Ferreira, Cordeiro, Mara L

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Neurodevelopmental disorder associated with gene ARF3: A case report von Santos Henrique, Suelen, França, Mariana Jordão, Silva Junior, Rui Carlos, Santos, Mara Lúcia Schmitz Ferreira, Valle, Daniel Almeida

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MUCOPOLYSACARIDOSIS TYPE IIIB MISDIAGNOSED AS AN AUTISTIC SPECTRUM DISORDER: A CASE REPORT AND LITERATURE REVIEW von Irigonhê, Alan Tibério Dalpiaz, Moreira, Angélica Malman Thomazine, Valle, Daniel Almeida do, Santos, Mara Lúcia Schmitz Ferreira

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BRPF1‐associated syndrome: A patient with congenital ptosis, neurological findings, and normal intellectual development von Souza, Josiane, Valle, Daniel Almeida, Santos, Mara Lucia Schmidt Ferreira, Colomé, Fernanda Bonilla, Teive, Helio Afonso Ghizoni, da Silva Freitas, Renato, Herai, Roberto Hirochi

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Predictive factors of genetic diagnosis and real-life impact of next-generation sequencing for children with epilepsy von Pinto, Gustavo Moura da Mata Machado Ferreira, Fidalski, Solena Ziemer Kusma, Santos, Mara Lúcia Schmidt Ferreira, de Souza, Josiane, do Valle, Daniel Almeida

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Characteristics of Opsoclonus-Myoclonus Syndrome in Patients of the Largest Pediatric Hospital in Latin America von Zeny, Michelle Silva, do Valle, Daniel Almeida, Santos, Mara Lúcia Schmitz Ferreira, Bara, Tiago S., Cordeiro, Mara L.

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GABAA receptor encephalitis associated with human parvovirus B19 virus infection: Case report von Valle, Daniel Almeida do, Santos, Mara Lúcia S. Ferreira, Spinosa, Mônica J., Telles, Bruno A., Prando, Carolina, Cordeiro, Mara L.

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Clinical variability of children with anti-N-methyl-d-aspartate receptor encephalitis in southern Brazil: a cases series and review of the literature von do Valle, Daniel Almeida, Galeazzi, Joselainy Stela Pires, Machado, Mayara de Rezende, dos Santos, Vanessa Catarine Silva Abreu Ribeiro, da Silva, Alcir Francisco, Lohr Júnior, Alfredo, Santos, Mara Lúcia Schmitz Ferreira, Scola, Rosana Herminia

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Petrogenesis and tectonic significance of two bimodal volcanic stages from the Ediacaran Campo Alegre-Corupá Basin (Brazil): Record of metacratonization during the consolidation of... von Martins Lino, Lucas, Quiroz-Valle, Francy Roxana, Stipp Basei, Miguel Ângelo, Farias Vlach, Silvio Roberto, Hueck, Mathias, Willbold, Matthias, Brandolise Citroni, Sérgio, do Valle Lemos-Santos, Daniel

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Neurological Characteristics of Pediatric Glycogen Storage Disease von Muzetti, Julio Henrique, do Valle, Daniel Almeida, Santos, Mara L. S. Ferreira, Telles, Bruno Augusto, Cordeiro, Mara L.

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Carbamazepine-responsive chorea in a toddler with semilobar holoprosencephaly: Case report von Oliveira, Leonardo, Silveira, Izabela, Silva, Thiago, Valle, Daniel

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The role of human adenoviruses type 41 in acute diarrheal disease in Minas Gerais after rotavirus vaccination von Reis, Thaís Aparecida Vieira, Assis, Andrêssa Silvino Ferreira, do Valle, Daniel Almeida, Barletta, Vívian Honorato, de Carvalho, Iná Pires, Rose, Tatiana Lundgren, Portes, Silvana Augusta Rodrigues, Leite, José Paulo Gagliardi, da Rosa e Silva, Maria Luzia

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General overview of urea cycle disorders (UCDs) in Brazil von Schwartz, Ida Vanessa Doederlein, dos Santos, Mariana Lopes, Fink, Isabela Alicia, de Bitencourt, Fernanda Fernanda Hendges, Sperb-Ludwig, Fernanda, Refosco, Lilia Farret, de Souza, Carolina Fischinger Moura, Poswar, Fabiano Oliveira, Vieira, Marta Wey, Moretzsohn, Monica, Curiati, Marco Antonio, Santos, Mara Lúcia Schmitz Ferreira, do Valle, Daniel Almeida, Menezes, Ana Cecília, da Silva Baptista Arpini, Luana, Heredia, Romina Soledad, da Silva, Luiz Carlos Santana, de Camargo Pinto, Louise Lapagesse, de Rosso Giuliani, Liane, Adjuto, Giselle Maria Araujo Felix, de Distúrbios do Ciclo da Uréia, Grupo Brasileiro

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Enzyme Replacement Therapy Decreases Left Ventricular Mass Index in Patients with Hunter Syndrome? von do Valle, Daniel Almeida, Cirino, Raphael Henrique Déa, Santos, Mara Lúcia Schmitz Ferreira, Pellissari, Eliana Costa, Scola, Rosana Herminia

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GABA(A) receptor encephalitis associated with human parvovirus B19 virus infection Case report von Valle, Daniel Almeida do, Santos, Mara Lucia S. Ferreira, Spinosa, Monica J., Telles, Bruno A., Prando, Carolina, Cordeiro, Mara L.

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Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations von Zanette, Vanessa, Reyes, Aurelio, Johnson, Mark, do Valle, Daniel, Robinson, Alan J., Monteiro, Vaneisse, Telles, Bruno Augusto, L.R. Souza, Ricardo, S.F. Santos, Mara L, Benincá, Cristiane, Zeviani, Massimo

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