Browsing "Comunicações em Eventos - FM/MNE" by Title
Showing results 32 to 51 of 316
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| Issue Date | Title | Author(s) |
|---|---|---|
| 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., et al |
| 2015 | C9ORF72 repeated expansion in patients with familial amyotrophic lateral sclerosis from a Brazilian research center. A preliminary report | CHADI, G.; MAXIMINO, J. R.; JORGE, F. M. H.; CALLEGARO, D. |
| 2018 | Case report: CMT2D with intermediate pattern. an expanding phenotype? | ESTEPHAN, E.; SAMPAIO, P.; SOUZA, F.; ROCHA, M.; ZANOTELI, E.; MARQUES JR., W. |
| 2014 | Caudal zona incerta stimulation alleviates tremor and ataxia in a patient with fragile X-associated tremor/ataxia syndrome | GHILARDI, M. G. dos Santos; CURY, R. G.; ANGELOS, J. S. dos; BARBOSA, E. R.; TEIXEIRA, M. J.; FONOFF, E. T. |
| 2018 | CD99 expression in astrocytomas and functional analysis in glioblastoma cell line | CARDOSO, Lais Cavalca; MARIE, Suely Kazue; SOARES, Roseli Silva; OBA-SHINJO, Sueli M. |
| 2015 | CD99 functional analysis in glioblastoma by RNAseq | OBA-SHINJO, Sueli M.; CARDOSO, Lais C.; SILVA, Roseli da; LERARIO, Antonio M.; UNO, Miyuki; MARIE, Suely S. K. |
| 2017 | CD99 plays an important role in glioblastoma cell migration | CARDOSO, Lais C.; LERARIO, Antonio M.; MARIE, Suely K.; SOARES, Roseli S.; OBA-SHINJO, Sueli M. |
| 2018 | CD99 role in glioblastoma cell migration | CARDOSO, Cavalca; LERARIO, Antonio Marcondes; BRANTIS, Carlos Eduardo de Carvalho; FREITAS, Vanessa Galdeno; SOARES, Roseli da Silva; MARIE, Suely Kazue Nagahashi; OBA-SHINJO, Sueli Mieko |
| 2017 | Central nervous system germinoma presenting as progressive cerebral hemiatrophy and pituitary enhancement | GUEDES, B.; BARBOSA, B.; KUBOTA, G. T.; SOUZA, M. N.; FRASSETO, F.; ONO, C.; LUCATO, L.; NITRINI, R.; SIMABUKURO, M. |
| 2012 | Centronuclear and myotubular myopathies: Clinical, histological and molecular findings in a large series of Brazilian patients | ABATH, O.; SILVA, M. R.; PESQUERO, J. B.; OLIVEIRA, A. S. B.; CARVALHO, M.; CHADI, G.; REED, U. C.; ZANOTELI, E. |
| 2014 | Cerebral autoregulation in fulminant hepatic failure | NOGUEIRA, Ricardo; MENDES, Fernando; PACHECO, Marcelo; LINS, Karla; TEIXEIRA, Manoel; BOR-SENG-SHU, Edson |
| 2018 | Cerebral compliance assessment using Trancranial Doppler | BRASIL, S.; BOR-SENG-SHU, E.; DE-LIMA-OLIVEIRA, M.; NOGUEIRA, R.; SALINET, A.; PAIVA, W.; TEIXEIRA, M. |
| 2013 | Cerebral embolic activity in a patient during acute crisis of Takayasu's arteritis | NOGUEIRA, R. C.; BOR-SENG-SHU, E.; SANTOS, E.; TEIXEIRA, M. J. |
| 2014 | Characteristic activity pattern obtained by MER to demarcate the borders between the caudal zona incerta and STN for stereotactic treatment of post-traumatic tremor | FONOFF, E. T.; LOPEZ, W. O. Contreras; REIS, P. R.; NEVILLE, I.; NAVARRO, J.; JACOBSEN, M. T. |
| 2018 | Characterization of The Brazilian ARSACS Phenotype: Clinical, Ophthalmological, Neuroimaging, and Genetic Features of Fourteen Cases. | REZENDE FILHO, Flavio; PEDROSO, Jose Luiz; SALLUM, Juliana Maria; KOK, Fernando; FRANCA, Marcondes; VASCONCELLOS, Ingrid; MARQUES, Wilson; LOURENCO, Charles; GIUNTI, Paola; BARSOTTINI, Orlando |
| 2017 | CHARCOT-MARIE-TOOTH 2W. A NEW MUTATION? | FREITAS, M. de; DIAS, J.; VIDAL, C.; SZKLARZ, D.; NASCIMENTO, O.; KOK, F. |
| 2021 | Charge-Pump Circuit in 65nm CMOS for Neural Stimulation on Deep-Brain Stimulation | NORDI, Tiago Mateus; BARBOSA, V. M.; GOUNELLA, R. H.; ASAN, Godfred; LUPPE, Maximiliam; NAVARRO, Joao; JUNIOR, Soares; CARMO, J. P.; FONOFF, Erich Talamoni; COLOMBARI, Eduardo |
| 2021 | Childhood Amyotrophic Lateral Sclerosis Caused by Excess Sphingolipid Synthesis | MOHASSEL, Payam; DONKERVOORT, Sandra; LONE, Museer A.; NALLS, Matthew A.; GABLE, Kenneth; GUPTA, Sita D.; FOLEY, A. Reghan; HU, Ying; SAUTE, Jonas Alex Morales; MOREIRA, Ana Lucila, et al |
| 2017 | Clinical and genetic characterisation of adult onset leukoencephalopathy | LYNCH, David; PAIVA, Anderson Rodrigues Brandao de; ZHANG, Wei Jia; LAKSHMANAN, Rahul; DAVAGNANAM, Indran; FOX, Nick; MURPHY, Elaine; KOK, Fernando; CHATAWAY, Jeremy; HOULDEN, Henry |
| 2021 | Clinical and genetic spectrum of a large cohort of delta-sarcoglycan muscular dystrophy | ALONSO-PEREZ, J.; GONZALEZ-QUEREDA, L.; BRUNO, C.; PANICUCCI, C.; ALAVI, A.; ZANOTELI, E.; MUELAS, N.; VILCHEZ, J.; DOURADO, E.; KADEM, N., et al |