Browsing "Comunicações em Eventos - LIM/15" by Title
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Issue Date | Title | Author(s) |
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2020 | FDG-PET degeneration patterns predict amyloid deposition in Corticobasal Syndrome | PARMERA, J.; COUTINHO, A.; NETO, A.; ONO, C.; ARANHA, M.; BUCHPIGUEL, C.; NITRINI, R.; BARBOSA, E.; BRUCKI, S. |
2021 | FIREFISH Part 2: 24-month Efficacy and Safety of Risdiplam in Infants with Type 1 Spinal Muscular Atrophy (SMA) | DARRAS, Basil T.; MASSON, Ricardo z; MAZURKIEWICZ-BELDZINSKA, Maria; ROSE, Kristy; XIONG, Hui; ZANOTELI, Edmar; BARANELLO, Giovanni; VLODAVETS, Dmitry; DODMAN, Angela; EL-KHAIRI, Muna, et al |
2020 | FIREFISH Part 2: Efficacy and safety of risdiplam (RG7916) in infants with Type 1 spinal muscular atrophy (SMA) | BARANELLO, Giovanni; SERVAIS, Laurent; MASSON, Riccardo; MAZURKIEWICZ-BELDZINSKA, Maria; ROSE, Kristy; VLODAVETS, Dmitry; XIONG, Hui; ZANOTELI, Edmar; EL-KHAIRI, Muna; FUERST-RECKTENWALD, Sabine, et al |
2020 | FIREFISH Part 2: Efficacy and safety of risdiplam (RG7916) in infants with Type 1 spinal muscular atrophy (SMA) | SERVAIS, L.; BARANELLO, G.; MASSON, R.; MAZURKIEWICZ-BELDZINSKA, M.; ROSE, K.; VLODAVETS, D.; XIONG, H.; ZANOTELI, E.; EL-KHAIRI, M.; FUERST-RECKTENWALD, S., et al |
2020 | FIREFISH Part 2: Efficacy and Safety of Risdiplam (RG7916) in Infants with Type 1 Spinal Muscular Atrophy (SMA) | SERVAIS, Laurent; BARANELLO, Giovanni; MASSON, Riccardo; MAZURKIEWICZ-BELDZINSKA, Maria; ROSE, Kristy; VLODAVETS, Dmitry; XIONG, Hui; ZANOTELI, Edmar; EL-KHAIRI, Muna; FUERST-RECKTENWALD, Sabine, et al |
2020 | FIREFISH Parts 1 and 2: 12-month pooled safety and efficacy outcomes of risdiplam (RG7916) in infants with Type 1 spinal muscular atrophy (SMA) | SERVAIS, L.; BLOESPFLUG-TANGUY, O.; DARRAS, B.; DAY, J.; DECONINCK, N.; KLEIN, A.; MASSON, R.; MAZURKIEWICZ-BELDZINSKA, M.; MERCURI, E.; ROSE, K., et al |
2021 | FIREFISH Parts 1 and 2: 24-Month Safety and Efficacy of Risdiplam in Type 1 SMA | MASSON, R.; BOESPFLUG-TANGUY, O.; DARRAS, B. T.; DAY, J. W.; DECONINCK, N.; KLEIN, A.; MAZURKIEWICZ-BEDZISKA, M.; MERCURI, E.; ROSE, K.; SERVAIS, L., et al |
2017 | First results from the international LMNA-related congenital and childhood onset muscular dystrophy retrospective natural history study | YAOU, R. Ben; DABAJ, I.; YUN, P.; NORATO, G.; XIONG, H.; NASCIMENTO, A.; MAGGI, L.; SARKOZY, A.; MONGES, S.; BERTOLI, M., et al |
2016 | GABAa - Receptor and LGI1 Antibody Encephalitis in a Patient with Thymoma | SIMABUKUROZ, Mateus; PETIT-PEDROL, Mar; LUCATO, Leandro; CASTRO, Luiz; NITRINI, Ricardo |
2016 | Gordon Syndrome in the differencial diagnosis of kidneytubular acidosis-Case report and literature review | SOUZA, A. M. C.; QUEIROZ, A. F.; VAISBICH, M. H.; CARDOSO, R. L.; KOK, F. |
2015 | Haploidentical stem cell transplantation with post-transplant Cyclophosphamide for patients with X-Linked Adrenoleukodystrophy and severe aplastic anemia: retrospective analysis | ESTEVES, I.; FERNANDES, J.; RIBEIRO, A.; SANTOS, F.; KONDO, A.; BONFIM, C.; KOK, F.; VARGAS, J.; MANTOVANI, L. Fernando; RODRIGUES, M., et al |
2016 | Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Patients with X-linked Adrenoleukodystrophy: expanding the donor pool in an urgent situation | FERNANDES, J.; BONFIM, C.; KERBAUY, F.; RODRIGUES, M.; ALMEIDA, A.; ESTEVES, I.; LOTH, G.; KUWAHARA, C.; BUENO, C.; KONDO, A., et al |
2018 | High frequency of manifesting carriers in the recessive X-linked myotubular myopathy | SOUZA, L.; ALMEIDA, C.; SILVA, L.; PAVANELLO, R.; GURGEL-GIANNETI, J.; ZANOTELI, E.; ZATZ, M.; OTTO, P.; VAINZOF, M. |
2015 | High Frequency Stimulation of the Subthalamic Nucleus Improves Graft Survival and Behavioural Outcome in a Rat Model of Parkinson's Disease | FURLANETTI, Luciano L.; CORDEIRO, Joacir G.; CORDEIRO, Karina K.; GARCIA, Joanna A.; WINKLER, Christian; LEPSKI, Guilherme; COENEN, Volker A.; DOEBROESSY, Mate D. |
2017 | High resolution vessel wall magnetic resonance imaging in HIV associated vasculopathy | KUBOTA, G. Taricani; FERREIRA, R. de Faria; FIGUEIREDO, T. Rocha; SANTOS, G. Titoneli dos; MORAIS, L. Martins Tavares Scianni; BARBOSA, B. J. Alencar Pires; YAMAMOTO, F. Iuji; GUEDES, B. Fukelmann; CONFORTO, A. Bastos |
2018 | Higher expression of lysyl oxidase family in GBM mesenchymal subtype and the clinical impact of LOXL3 | SOARES, Roseli Silva; LAURENTINO, Talita Sousa; MARIE, Suely Kazue Nagahashi; OBA-SHINJO, Sueli Mieko |
2015 | Human microglia transcriptome and cross-species analysis | GALATRO, T. F. de A.; HOLTMAN, I. R.; BROUWER, N.; SOLA, P.; REIS, G. N.; VAINCHTEIN, I. D.; VERAS, M.; PEREIRA, T.; PASQUALUCCI, C.; SOGAYAR, M. C., et al |
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. |
2018 | Hypercontractile congenital muscle stiffness | CAMELO, C.; SILVA, A. Da; REED, U.; BONNEMANN, C.; ZANOTELI, E. |
2015 | Hypertension Severity is Associated With Impaired Cognitive Performance | MUELA, Henrique C.; COSTA-HONG, Valeria A.; MACHADO, Michel F.; MORAES, Natalia C.; MEMORIA, Claudia M.; YASSUDA, Monica S.; SHU, Edson B.; NOGUEIRA, Ricardo C.; MASSARO, Ayrton R.; FEITOSA, Raul R., et al |