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Issue DateTitleAuthor(s)
2017Biallelic mutation in FDXIL leads to a complex phenotype: optic atrophy, reversible leukoencephalopathy, metabolic myopathy and axonal polyneuropathyGURGEL-GIANNETTI, J.; LYNCH, D.; PAIVA, A.; YAMAMOTO, G.; LUCATO, L.; AMORIM, S.; FREUA, F.; GIANNETTI, A.; RIPA, B.; MONTI, F., et al
2018Brachio-cervical inflammatory myopathy with lymphoid follicle-like structures in a patient with sclerodermaSILVA, A.; VIANNA, M.; MENDONCA, R.; ZANOTELI, E.
2016Brain atrophy and major depression in the elderly: results from a large autopsy studyNUNES, P. V.; SUEMOTO, C. K.; LEITE, R. P.; FERRETTI-REBUSTINI, R. E.; PASQUALUCCI, C. A.; NITRINI, R.; BRENTANI, H. P.; FARFEL, J. M.; OLIVEIRA, K. C.; GRINBERG, L. T., et al
2022Brain Health Signature in Superagers: A Multimodal Brain MRI StudyGODOY, Laiz de; STUDART-NETO, Adalberto; NITRINI, Ricardo; JAGER, Rolf; BISDAS, Sotirios; LEITE, Claudia da Costa
2019A Brain PET staging system using Amyloid and Neurodegeneration Biomarkers for Individual Assessment in the Context of the 2018 NIA-AA Research Framework: an approach exploring clinical-biomarker mismatches and socio-demographic parametersCOUTINHO, A. M. N.; PORTO, F.; FARIA, D. de Paula; ONO, C. R.; GARCEZ, A. T.; SQUARZONI, P.; DURAN, F. L. S.; OLIVEIRA, M. O.; TRES, E. S.; BUCKI, S. M. D., et al
2019Brain transcriptome analysis of Japanese population living in BrazilMARIE, Suely Kazue Nagahashi; LERARIO, Antonio Marcondes; SHINJO, Sueli Mieko Oba; NASCIMENTO, Camila; LEITE, Renata; SUEMOTO, Claudia; PASQUALUCCI, Carlos Augusto; MURAYAMA, Shigeo
2016C9orf72 repeat expansions and TARDBP mutations in two Brazilian dementia research centersTAKADA, L.; BAHIA, V.; GUIMARAES, H.; SOUZA, L.; COSTA, T.; VALE, T.; RODRIGUEZ, R.; PORTO, F.; MACHADO, J.; BEATO, R., et al
2018Case report: CMT2D with intermediate pattern. an expanding phenotype?ESTEPHAN, E.; SAMPAIO, P.; SOUZA, F.; ROCHA, M.; ZANOTELI, E.; MARQUES JR., W.
2018CD99 expression in astrocytomas and functional analysis in glioblastoma cell lineCARDOSO, Lais Cavalca; MARIE, Suely Kazue; SOARES, Roseli Silva; OBA-SHINJO, Sueli M.
2015CD99 functional analysis in glioblastoma by RNAseqOBA-SHINJO, Sueli M.; CARDOSO, Lais C.; SILVA, Roseli da; LERARIO, Antonio M.; UNO, Miyuki; MARIE, Suely S. K.
2017CD99 plays an important role in glioblastoma cell migrationCARDOSO, Lais C.; LERARIO, Antonio M.; MARIE, Suely K.; SOARES, Roseli S.; OBA-SHINJO, Sueli M.
2018CD99 role in glioblastoma cell migrationCARDOSO, Cavalca; LERARIO, Antonio Marcondes; BRANTIS, Carlos Eduardo de Carvalho; FREITAS, Vanessa Galdeno; SOARES, Roseli da Silva; MARIE, Suely Kazue Nagahashi; OBA-SHINJO, Sueli Mieko
2017Central nervous system germinoma presenting as progressive cerebral hemiatrophy and pituitary enhancementGUEDES, B.; BARBOSA, B.; KUBOTA, G. T.; SOUZA, M. N.; FRASSETO, F.; ONO, C.; LUCATO, L.; NITRINI, R.; SIMABUKURO, M.
2012Centronuclear and myotubular myopathies: Clinical, histological and molecular findings in a large series of Brazilian patientsABATH, O.; SILVA, M. R.; PESQUERO, J. B.; OLIVEIRA, A. S. B.; CARVALHO, M.; CHADI, G.; REED, U. C.; ZANOTELI, E.
2018CHARACTERIZATION OF CHRONIC HEADACHE IN THE LATE PHASE OF CENTRAL VENOUS THROMBOSISBOSSONI, A.; PERES, M. F. P.; CONFORTO, A. Bastos
2018Characterization 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
2017CHARCOT-MARIE-TOOTH 2W. A NEW MUTATION?FREITAS, M. de; DIAS, J.; VIDAL, C.; SZKLARZ, D.; NASCIMENTO, O.; KOK, F.
2021Childhood Amyotrophic Lateral Sclerosis Caused by Excess Sphingolipid SynthesisMOHASSEL, 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
2017Clinical and genetic characterisation of adult onset leukoencephalopathyLYNCH, David; PAIVA, Anderson Rodrigues Brandao de; ZHANG, Wei Jia; LAKSHMANAN, Rahul; DAVAGNANAM, Indran; FOX, Nick; MURPHY, Elaine; KOK, Fernando; CHATAWAY, Jeremy; HOULDEN, Henry
2021Clinical and genetic spectrum of a large cohort of delta-sarcoglycan muscular dystrophyALONSO-PEREZ, J.; GONZALEZ-QUEREDA, L.; BRUNO, C.; PANICUCCI, C.; ALAVI, A.; ZANOTELI, E.; MUELAS, N.; VILCHEZ, J.; DOURADO, E.; KADEM, N., et al