Randomized Trial of Botulinum Toxin Type A in Hereditary Spastic Paraplegia — The SPASTOX Trial by Diniz de Lima, Fabricio, Faber, Ingrid, Servelhere, Katiane R., Bittar, Maria Fernanda R., Martinez, Alberto R.M., Piovesana, Luiza G., Martins, Melina P., Martins, Carlos Roberto, Benaglia, Tatiana, Sá Carvalho, Benilton, Nucci, Anamarli, França, Marcondes C.

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Neonatal screening for spinal muscular atrophy: A pilot study in Brazil by Oliveira Netto, Alice Brinckmann, Brusius-Facchin, Ana Carolina, Lemos, Júlia F, Pasetto, Fernanda B, Brasil, Carolina S, Trapp, Franciele B, Saute, Jonas Alex Morales, Donis, Karina Carvalho, Becker, Michele Michelin, Wiest, Paloma, Coutinho, Vivian L S, Castro, Simone, Ferreira, Juliana, Silveira, Cynthia, Bittar, Maria Fernanda R, Wang, Cristina, Lana, Janaina M, França Junior, Marcondes Cavalcante, Giugliani, Roberto

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Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients by Borsatto, Taciane, Sperb-Ludwig, Fernanda, Lima, Samyra E, S Carvalho, Maria R, S Fonseca, Pablo A, S Camelo, Jr, José, M Ribeiro, Erlane, F V de Medeiros, Paula, M Lourenço, Charles, F M de Souza, Carolina, Boy, Raquel, Félix, Têmis M, M Bittar, Camila, L C Pinto, Louise, C Neto, Eurico, J Blom, Henk, D Schwartz, Ida V

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Correction: Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients by Borsatto, Taciane, Sperb-Ludwig, Fernanda, Lima, Samyra E, Carvalho, Maria R S, Fonseca, Pablo A S, Camelo, Jr, José S, Ribeiro, Erlane M, de Medeiros, Paula F V, Lourenço, Charles M, de Souza, Carolina F M, Boy, Raquel, Félix, Têmis M, Bittar, Camila M, Pinto, Louise L C, Neto, Eurico C, Blom, Henk J, Schwartz, Ida V D

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Neutrophil activation and circulating neutrophil extracellular traps are increased in venous thromboembolism patients for at least one year after the clinical event by Zapponi, Kiara C. S., Orsi, Fernanda A., Cunha, José Luiz R., de Brito, Ingrid R., Romano, Anna Virginia C., Bittar, Luis Fernando, De Paula, Erich Vinicius, Penteado, Carla F., Montalvão, Silmara, Annichino-Bizzacchi, Joyce Maria

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Screening of RB1 alterations in Brazilian patients with retinoblastoma and relatives with retinoma: phenotypic and genotypic associations by Barbosa, Raquel H, Aguiar, Fernanda C C, Silva, Morgana F L, Costa, Regis A, Vargas, Fernando R, Lucena, Evandro, Carvalho de Souza, Mírian, de Almeida, Liz Maria, Bittar, Camila, Ashton Prolla, Patrícia, Bonvicino, Cibele R, Seuánez, Héctor N

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