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Issue DateTitleAuthor(s)
2020RAINBOWFISH: A study of risdiplam (RG7916) in infants with presymptomatic spinal muscular atrophy (SMA)SERVAIS, L.; BERTINI, E.; AL-MUHAIZEA, M.; NELSON, L.; PRUFER, A.; VLODAVETS, D.; WANG, Y.; ZANOTELI, E.; BURKE, L.; EL-KHAIRI, M., et al
2021RAINBOWFISH: A study of risdiplam in infants with presymptomatic SMABERTINI, E.; AL-MUHAIZEA, M.; FARRAR, M.; NELSON, L.; ARAUJO, A. Prufer de Q. C.; SERVAIS, L.; WANG, Y.; ZANOTELI, E.; EL-KHAIRI, M.; GERBER, M., et al
2021RAINBOWFISH: A study of risdiplam in infants with presymptomatic spinal muscular atrophy (SMA)SERVAIS, L.; AL-MUHAIZEA, M.; FARRAR, M.; NELSON, L.; PRUFER, A.; FINKEL, R.; WANG, Y.; ZANOTELI, E.; EL-KHAIRI, M.; GERBER, M., et al
2021RAINBOWFISH: A Study of Risdiplam in Newborns with Presymptomatic Spinal Muscular Atrophy (SMA)FINKEL, Richard S.; AL-MUHAIZEA, Mohammad; FARRAR, Michelle A.; NELSON, Leslie; PRUFER, Alexandra; SERVAIS, Laurent; WANG, Yi; ZANOTELI, Edmar; PALFREEMAN, Laura; EL-KHAIRI, Muna, et al
2015Rapidly progressive dementia in a neurologic unit of a tertiary hospital in BrazilSTUDART NETO, A.; SOARES NETO, H.; SIMABUKURO, M.; GONCALVES, M.; FORTINI, I. D. A.; CASTRO, L.; NITRINI, R.
2018Recessive congenital fiber type disproportion caused by TPM3 mutationMORENO, C.; ESTEPHAN, E.; ABATH NETO, O.; CAMELO, C.; SILVA, A.; REED, U.; BONNEMANN, C.; ZANOTELI, E.
2021REPETITIVE PERIPHERAL SENSORY STIMULATION AS AN ADD-ON INTERVENTION FOR UPPER LIMB REHABILITATION IN STROKE: A RANDOMIZED TRIALCONFORTO, A.; MACHADO, A.; RIBEIRO, N.; PLOW, E.; LIEW, S-L; LEITE, C. Da Costa; ZAVALIANGOS-PETROPULU, A.; MENEZES, I.; ANJOS, S. Dos; LUCCAS, R., et al
2018Repetitive Peripheral Sensory Stimulation in Stroke: a Systematic Review and Meta-AnalysisCONFORTO, Adriana B.; ANJOS, Sarah; SILVA, Arnaldo; CONTI, Juliana; MACHADO, Andre G.; COHEN, Leonardo G.
2014Retrospective analysis of prognostic factors in patients undergoing surgical resection for multiple brain metastasesPETITTO, Carlos; LAGE, Liana Valente; CAIRES, Inacelli Queiroz De Souza; SOUZA, Karla T.; FEDE, Angelo Bezerra de Souza; FEHER, Olavo; HOFF, Paulo M.; CAMARGO, Verldlana; MENCARINI, Ana; MUNHOZ, Rodrigo Ramella, et al
2020RNA-SEQ and Microarray Analysis Reveal the Interplay between Hub Genes and Developmental Pathways in MedulloblastomaSILVA, A. Martins Da; BARONI, M.; SALOMAO, K.; CHAGAS, P. Ferreira Das; BONFIM-SILVA, R.; GERON, L.; CRUZEIRO, G. Veiga; SILVA JR., W. Da; QUEIROZ, R.; MARIE, S., et al
2018Role of MELK, STMN1, and FANCC in human astrocytoma.SR., Fernanda Oliveira Serachi; SR., Sueli Mieko Oba Shinjo
2015RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challengesGARDINER, A.; SCALCO, R.; PARTON, M.; HANNA, M.; PITCEATHLY, R.; ZANOTELI, E.; MURPHY, E.; TREVES, S.; HOULDEN, H.; WILMSHURST, J., et al
2015Safety of pregnancy following cerebral venous thrombosis (ISCVT2-PREGNANCY)SOUSA, D. Aguiar de; CANHAO, P.; CRASSARD, I.; COUTINHO, J.; ARAUZ, A.; CONFORTO, A.; GIROUD, M.; FERRO, J. M. M. C.
2019SENSITIVITY OF NEUROPHYSIOLOGIC TESTS REGARDING THE NEUROMUSCULAR JUNCTION IN PATIENTS WITH CONGENITAL MYASTHENIC SYNDROMESCALDAS, Vitor Marques; ESTEPHAN, Eduardo de Paula; SILVA, Andre Macedo Serafim da; MENDONCA, Rodrigo de Holanda; HEISE, Carlos Otto; ZANOTELI, Edmar
2016Severe axial muscular involvement in Laing distal myopathy with a thumbprint finding on MRIDABAJ, I.; MORENO, C. Araujo Martins; ABATH NETO, O.; BERTINI, E.; CASTIGLIONI, C.; GUIMARAES, J. Brandao; REED, U. Conti; MESROB, L.; LECHNER, D.; FIORILLO, C., et al
2019Silencing of GLSiso2 (GAC) decreases cell proliferation and induces cell death in glioblastoma cell lineFRANCO, Yollanda Moreira; SOARES, Roseli Silva; OBA-SHINJO, Sueli M.; MARIE, Suely Kazue Nagahashi
2014Slowly progressive dementia in adult-onset subacute sclerosing panencephalitisNETO, A. S.; NOBREGA, P. R.; CASTRO, L. H. M.; NITRINI, R.; DUARTE, M. I. S.; LUCATO, L. T.
2013SPINAL LESIONS DUE TO TOPHACEOUS GOUT - A DIFFERENTIAL DIAGNOSIS NOT RELATED TO SYMPTOMSMELLO, F. M.; GOLDENSTEIN-SCHAINBERG, C.; FULLER, R.; HALPERN, A. S.
2015SQSTM1 AND VCP MUTATIONS IN A SERIES OF 205 INCLUSION BODY MYOSITIS CASESGANG, Q.; BETTENCOURT, C.; BRADY, S.; HOLTON, J. L.; PITTMAN, A. M.; HUGHES, D.; HEALY, E.; PARTON, M.; HILTON-JONES, D.; SHIEH, P. B., et al
2014Stathmin is involved in the maternal embryonic leucine zipper kinase pathway and impacts in the outcome of glioblastomaUNO, Miyuki; OBA-SHINJO, Sueli Mieko; SILVA, Roseli; GIMENEZ, Marcela; ROSA, Jose Cesar; MARIE, Suely Kazue Nagahashi