Attention deficit disorder/hyperactivity: a scientific overview

por Polanczyk, Guilherme V., Casella, Erasmo Barbante, Miguel, Euripedes Constantino, Reed, Umbertina Conti
Publicado 2012

Phenotypic and immunohistochemical characterization of sarcoglycanopathies

por Ferreira, Ana F. B., Carvalho, Mary S., Resende, Maria Bernadete D., Wakamatsu, Alda, Reed, Umbertina Conti, Marie, Suely Kazue Nagahashi
Publicado 2011

Air stacking: effects on pulmonary function in patients with spinal muscular atrophy and in patients with congenital muscular dystrophy,

por Marques, Tanyse Bahia Carvalho, Neves, Juliana de Carvalho, Portes, Leslie Andrews, Salge, João Marcos, Zanoteli, Edmar, Reed, Umbertina Conti
Publicado 2014

DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy

por Abath, Osorio, Martins, Cristiane de Araújo, Carvalho, Mary, Chadi, Gerson, Seitz, Katia Werneck, Oliveira, Acary Souza Bulle, Reed, Umbertina Conti, Laporte, Jocelyn, Zanoteli, Edmar
Publicado 2015

Cognitive performance of children with spinal muscular atrophy: A systematic review

por Polido, Graziela Jorge, de Miranda, Mariana Mangini Vaz, Carvas, Nelson, Mendonça, Rodrigo de Holanda, Caromano, Fátima Aparecida, Reed, Umbertina Conti, Zanoteli, Edmar, Voos, Mariana Callil
Publicado 2019

Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation

por Camelo, Clara Gontijo, Artilheiro, Mariana Cunha, Martins Moreno, Cristiane Araújo, Ferraciolli, Suely Fazio, Serafim Silva, André Macedo, Fernandes, Tatiana Ribeiro, Lucato, Leandro Tavares, Rocha, Antônio José, Reed, Umbertina Conti, Zanoteli, Edmar
Publicado 2023

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