Inflammatory myopathies: an update for neurologists

por Silva, André Macedo Serafim, Campos, Eliene Dutra, Zanoteli, Edmar
Publicado 2022

Neuromyelitis optica: a challenging diagnosis at secondary hospital

por de Oliveira, Anna Paula Romero, Taranto, Patrícia, Herbst, Livia, Kirihara, Andre, Veras, Maira Letícia, Silva, André Macedo Serafim, Garcia, Marcio Ricardo Taveira, Lino, Angelina Maria Martins
Publicado 2013

A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms

por Sampedro Castañeda, Marisol, Zanoteli, Edmar, Scalco, Renata S, Scaramuzzi, Vinicius, Marques Caldas, Vitor, Conti Reed, Umbertina, da Silva, Andre Macedo Serafim, O’Callaghan, Benjamin, Phadke, Rahul, Bugiardini, Enrico, Sud, Richa, McCall, Samuel, Hanna, Michael G, Poulsen, Hanne, Männikkö, Roope, Matthews, Emma
Publicado 2018

Clinical Manifestation of Nebulin-Associated Nemaline Myopathy

por Moreno, Cristiane Araujo Martins, Artilheiro, Mariana Cunha, Fonseca, Alulin Tacio Quadros Santos Monteiro, Camelo, Clara Gontijo, de Medeiros, Gisele Chagas, Sassi, Fernanda Chiarion, de Andrade, Claudia Regina Furquim, Donkervoort, Sandra, Silva, Andre Macedo Serafim, Dalfior-Junior, Luiz, Abath-Neto, Osorio Lopes, Reed, Umbertina Conti, Bönnemann, Carsten, Zanoteli, Edmar
Publicado 2023

Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders

por Moreno, Cristiane Araujo Martins, Camelo, Clara Gontijo, Sampaio, Pedro Henrique Marte de Arruda, Fonseca, Alulin Tácio Quadros Santos Monteiro, Estephan, Eduardo de Paula, Silva, André Macedo Serafim, Pirola, Renann Nunes, Silva, Luiz Henrique Libardi, Lima, Karlla Danielle Ferreira, de Albuquerque, Marco Antônio Veloso, Camelo, Antonio Edvan, Marques, Marcos Vinícius Oliveira, Yanagiura, Mario Teruo, Cavalcante, Wagner Cid Palmeira, Matsui, Ciro, Isihi, Lucas Michielon de Augusto, Mendonça, Rodrigo Holanda, Pouza, Ana Flávia Pincerno, de Carvalho, Mary Souza, Reed, Umbertina Conti, Zanoteli, Edmar
Publicado 2022

Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy

por Mendonça, Rodrigo de Holanda, Matsui, Ciro, Polido, Graziela Jorge, Silva, André Macedo Serafim, Kulikowski, Leslie, Torchio Dias, Alexandre, Zanardo, Evelin Aline, Solla, Davi Jorge Fontoura, Gurgel-Giannetti, Juliana, de Moura, Ana Carolina Monteiro Lessa, Sampaio, Gabriela Palhares Campolina, Oliveira, Acary Souza Bulle, de Souza, Paulo Victor Sgobbi, Pinto, Wladimir Bocca Vieira de Rezende, Gonçalves, Eduardo Augusto, Farias, Igor Braga, Nardes, Flávia, Araújo, Alexandra Prufer de Queiroz Campos, Marques, Wilson, Tomaselli, Pedro José, Ribeiro, Mara Dell Ospedale, Kitajima, João Paulo, Paoli Monteiro, Fabíola, Saute, Jonas Alex Morales, Becker, Michele Michelin, Saraiva-Pereira, Maria Luiza, Brusius-Facchin, Ana Carolina, van der Linden, Vanessa, Florêncio, Rodrigo Neves, Barbosa, André Vinícius Soares, Machado-Costa, Marcela Camara, Pessoa, André Luiz Santos, Souza, Leticia Silva, Franca, Marcondes Cavalcante, Kok, Fernando, Reed, Umbertina Conti, Zanoteli, Edmar
Publicado 2020