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Issue Date	Title	Author(s)
2017	Surveillance of human prion diseases in Brazil data from 2005 to 2017	LANDEMBERGER, M. C.; MACHADO, C. F.; SMID, J.; GOMES, H. R.; CHIMELLI, L.; CANEDO, N. H.; ROSEMBERG, S.; NITRINI, R.; MARTINS, V. R.
2022	Laboratory proactivity can solve non-diagnostic whole exome sequencing: Probing new genes in old data	VEDOVATO-DOS-SANTOS, Juliana Heather; KITAJIMA, Joao P.; JORDAO, Juliana; FREITAS, Erika L.; RIBEIRO, Mara D. O.; SALOMAO, Julia G.; RAMOS, Luiza L. P.; COSTA, Larissa A.; BISPO, Luciana; MONTI, Fernanda; FREITAS, Caroline; MONTEIRO, Fabiola Paoli; KOK, Fernando
2020	Inositol monophosphatase 1 (IMPA1) mutation in intellectual disability patients impairs neurogenesis but not gliogenesis	FIGUEIREDO, T.; MENDES, A.; KOBAYASHI, G.; MOREIRA, D.; OLIVEIRA, D.; GOULART, E.; STERN, S.; KOK, F.; MARCHETTO, M.; SANTOS, R.; GAGE, F.; ZATZ, M.
2014	Cerebral autoregulation in fulminant hepatic failure	NOGUEIRA, Ricardo; MENDES, Fernando; PACHECO, Marcelo; LINS, Karla; TEIXEIRA, Manoel; BOR-SENG-SHU, Edson
2015	Human prion diseases in brazil	LANDEMBERGER, M. C.; MACHADO, C.; SMID, J.; GOMES, H.; CHIMELLI, L.; CANEDO, N.; ROSEMBERG, S.; NITRINI, R.; MARTINS, V.
2016	Cross-cultural Adaptation and Validity of the Brazilian version of the Clinical staging scale and disease progression in frontotemporal dementia	SILVA, T. Bento Lima da; BAHIA, V.; CECCHINI, M. Amore; CASSIMIRO, L.; CARVALHO, V. Amaral; GUIMARAES, H. Cerqueira; CARAMELLI, P.; BALTHAZAR, M.; DAMASCENO, B.; BOTTINO, C.; BRUCKI, S.; SOUZA, L. Cruz de; MIOSHI, E.; NITRINI, R.; YASSUDA, M.
2016	C9orf72 repeat expansions and TARDBP mutations in two Brazilian dementia research centers	TAKADA, L.; BAHIA, V.; GUIMARAES, H.; SOUZA, L.; COSTA, T.; VALE, T.; RODRIGUEZ, R.; PORTO, F.; MACHADO, J.; BEATO, R.; CESAR, K.; SMID, J.; BRUCKI, S.; MAXIMINO, J.; CAMARGOS, S.; CHADI, G.; CARAMELLI, P.; NITRINI, R.

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