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Issue DateTitleAuthor(s)
2016Nemaline myopathy related to HIV infection with a good response to immunosuppressionSILVA, A.; MENDONCA, R.; ESTEPHAN, E.; MORENO, C.; CARVALHO, M.; ZANOTELI, E.
2021NEUROMODULATION IN ACUTE ISCHEMIC STROKE: A SYSTEMATIC REVIEW AND META-ANALYSISPELLEGRINO, M.; SALLES, I.; SHINOSAKI, J.; REIS, S.; NOGUEIRA, R.; CONFORTO, A.
2015Non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder, chorea and dementia associated with antibodies to IgLON5: Case reportSIMABUKURO, M. M.; SABATER, L.; ADONI, T.; CURY, R. G.; HADDAD, M. S.; MOREIRA, C. H.; OLIVEIRA, L.; ALVES, R. C.; SOSTER, L. A.; NOGUEIRA, R. A., et al
2021Orbicularis Oculi Muscle morphometry alterations in Hemifacial SpasmGAMEIRO, Gustavo; OSAKI, Midori H.; OSAKI, Teissy; SCHOR, Paulo; MARIE, Suely Kazue Nagahashi; OSAKI, Tammy H.
2012Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Dermatomyositis Muscle Biopsies Is Correlated to Hypoxia and Perifascicular AtrophySHINJO, Samuel K.; OBA-SHINJO, Sueli M.; UNO, Miyuki; MARIE, Suely K. N.
2014Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia.SHINJO, Samuel Katsuyuki; OBA-SHINJO, Sueli Mieko; UNO, Miyuki; MARIE, Suely Kazue Nagahashi
2018The p.N88K mutation in the RAPSN gene in Brazilian patients with congenital myasthenic syndromeESTEPHAN, E.; ZAMBON, A.; MARCHIORI, P.; SILVA, A.; MORENO, C.; REED, U.; TOPF, A.; LOCHMUELLER, H.; ZANOTELIL, E.
2014Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein geneSMID, J.; LANDEMBERGER, M. C.; MARTINS, V. R.; SCHULTZ, R. R.; ROSEMBERG, S.; CHIMELLI, L.; NITRINI, R.
2021PRESERVATION OF QUALITY OF ACUTE STROKE CARE DURING THE COVID-19 PANDEMIC IN THE LARGEST SOUTH AMERICAN HOSPITALANDRADE, J.; FONSECA, B.; MORAES JR., A. A.; CONFORTO, A.
2015Prevalence of cognitive impairment in tremembe, BrazilCESAR, K. G.; BRUCKI, S. M. D.; TAKADA, L. T.; OLIVEIRA, M. O.; PORTO, F. H. G.; SENAHA, M. L. H.; BAHIA, V. S.; SILVA, T. B. L.; CECCHINI, M. A.; CASSIMIRO, L., et al
2014Prodromal transient ischemic attack or minor stroke and outcome in basilar artery occlusionCONFORTO, A. B.; FREITAS, G. R.; SCHONEWILLE, W. J.; ALGRA, A.
2012Proffered Paper: PTEN Phosphorylation by Fibroblast Growth Factor Receptors and SRC Mediates Resistance to Epidermal Growth Factor Receptor Inhibitors in GlioblastomaFURNARI, F.; FENTON, T.; ZHOU, H.; MARIE, S.; MISCHEL, P.; CAVENEE, W.
2018PROPOSING OF A LESS COSTLY STRATEGY FOR MOLECULAR DIAGNOSIS OF CONGENITAL MYASTHENIC SYNDROME IN BRAZIL.ESTEPHAN, E. P.; SILVA, M. A. S.; ZAMBON, A. A.; REED, U. C.; TOPF, A.; LOCHMUELLER, H.; ZANOTELI, E.
2013Quantitative proteomic analysis reveals a molecular triad signature as biomarker candidates for astrocytomas and oligodendrogliomasROSA, Jose Cesar; MARIE, Suely K. N.; OBA-SHINJO, Sueli; GIMENEZ, Marcela
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.