Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marcondes C. França Junior"'
Autor:
Thiago J. R. Rezende, Brunno M. Campos, Johnny Hsu, Yue Li, Can Ceritoglu, Kwame Kutten, Marcondes C. França Junior, Susumu Mori, Michael I. Miller, Andreia V. Faria
Publikováno v:
Brain and Behavior, Vol 9, Iss 10, Pp n/a-n/a (2019)
Abstract Introduction The increasing use of large sample sizes for population and personalized medicine requires high‐throughput tools for imaging processing that can handle large amounts of data with diverse image modalities, perform a biologicall
Externí odkaz:
https://doaj.org/article/27e050d4019e480eabce465c59550879
Autor:
Raphael F. Casseb, Brunno M. de Campos, Alberto R.M. Martinez, Gabriela Castellano, Marcondes C. França Junior
Publikováno v:
NeuroImage: Clinical, Vol 21, Iss , Pp - (2019)
Sensory-motor integration models have been proposed aiming to explain how the brain uses sensory information to guide and check the planning and execution of movements. Sensory neuronopathy (SN) is a peculiar disease characterized by exclusive, sever
Externí odkaz:
https://doaj.org/article/bee6436adce0427dbeb8ff97f8e09519
Autor:
Alexandra P. Q. C. Araujo, Alzira A. S. de Carvalho, Eduardo B. U. Cavalcanti, Jonas Alex M. Saute, Elmano Carvalho, Marcondes C. França Junior, Alberto R. M. Martinez, Monica de M. M. Navarro, Anamarli Nucci, Maria Bernadete D. de Resende, Marcus Vinicius M. Gonçalves, Juliana Gurgel-Giannetti, Rosana H. Scola, Cláudia F. da R. Sobreira, Umbertina C. Reed, Edmar Zanoteli
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 8, Pp 589-599
ABSTRACT Significant advances in the understanding and management of Duchenne muscular dystrophy (DMD) took place since international guidelines were published in 2010. Our objective was to provide an evidence-based national consensus statement for m
Externí odkaz:
https://doaj.org/article/1ac683c8b5d2459b91290a1a85302f58
Autor:
André M. S. Silva, Antônio R. Coimbra-Neto, Paulo Victor S. Souza, Pablo B. Winckler, Marcus V. M. Gonçalves, Eduardo B. U. Cavalcanti, Alzira A. D. S. Carvalho, Cláudia F. D. R. Sobreira, Clara G. Camelo, Rodrigo D. H. Mendonça, Eduardo D. P. Estephan, Umbertina C. Reed, Marcela C. Machado-Costa, Mario E. T. Dourado-Junior, Vanessa C. Pereira, Marcelo M. Cruzeiro, Paulo V. P. Helito, Laís U. Aivazoglou, Leonardo V. D. Camargo, Hudson H. Gomes, Amaro J. S. D. Camargo, Wladimir B. V. D. R. Pinto, Bruno M. L. Badia, Luiz H. Libardi, Mario T. Yanagiura, Acary S. B. Oliveira, Anamarli Nucci, Jonas A. M. Saute, Marcondes C. França-Junior, Edmar Zanoteli
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1225-1238 (2019)
Abstract Objective ANO5‐related myopathy is an important cause of limb‐girdle muscular dystrophy (LGMD) and hyperCKemia. The main descriptions have emerged from European cohorts, and the burden of the disease worldwide is unclear. We provide a de
Externí odkaz:
https://doaj.org/article/9569ce804f2d459a98f49ce1fbcc02cb