Browsing "Artigos e Materiais de Revistas Científicas - FM/MNE" by Title
Showing results 3 to 22 of 1444
< previous
next >
| Issue Date | Title | Author(s) |
|---|---|---|
| 2011 | A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia | FANGANIELLO, R. D.; KIMONIS, V. E.; CORTE, C. C.; NITRINI, R.; PASSOS-BUENO, M. R. |
| 2018 | A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation | SHINJO, Samuel Katsuyuki; OBA-SHINJO, Sueli Mieko; LERARIO, Antonio Marcondes; MARIE, Suely Kazue Nagahashi |
| 2017 | A Bug in the Brain and the Future of Neurosciences | FIGUEIREDO, Eberval Gadelha; WELLING, Leonardo C.; WELLING, Mariana S.; TEIXEIRA, Manoel J. |
| 2018 | A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome | ESTEPHAN, Eduardo de Paula; SOBREIRA, Claudia Ferreira da Rosa; SANTOS, Andre Cleriston Jose dos; TOMASELLI, Pedro Jose; MARQUES JR., Wilson; ORTEGA, Roberta Paiva Magalhes; COSTA, Marcela Camara Machado; SILVA, Andre Macedo Serafim da; MENDONCA, Rodrigo Holanda; CALDAS, Vitor Marques, et al |
| 2014 | A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G) | VIEIRA, Natassia M.; NASLAVSKY, Michel S.; LICINIO, Luciana; KOK, Fernando; SCHLESINGER, David; VAINZOF, Mariz; SANCHEZ, Nury; KITAJIMA, Joao Paulo; GAL, Lihi; CAVACANA, Natale, et al |
| 2016 | A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability | FIGUEIREDO, T.; MELO, U. S.; PESSOA, A. L. S.; NOBREGA, P. R.; KITAJIMA, J. P.; RUSCH, H.; VAZ, F.; LUCATO, L. T.; ZATZ, M.; KOK, F., et al |
| 2018 | A novel complex neurological phenotype due to a homozygous mutation in FDX2 | GURGEL-GIANNETTI, Juliana; LYNCH, David S.; PAIVA, Anderson Rodrigues Brandao de; LUCATO, Leandro Tavares; YAMAMOTO, Guilherme; THOMSEN, Christer; BASU, Somsuvro; FREUA, Fernando; GIANNETTI, Alexandre Varella; ASSIS, Bruno Della Ripa de, et al |
| 2016 | A novel GFAP mutation in a type II (late-onset) Alexander disease patient | PAIVA, Anderson Rodrigues Brandao de; FREUA, Fernando; LUCATO, Leandro Tavares; PARMERA, Jacy; DORIA, Denise; NOBREGA, Paulo Ribeiro; OLAVIO, Thiago Rosa; MACEDO-SOUZA, Lucia Ines; KOK, Fernando |
| 2015 | A patient with a long history of relapsing psychosis and mania presenting with anti-NMDA receptor encephalitis ten years after first episode | SIMABUKURO, Mateus Mistieri; FREITAS, Christian Henrique de Andrade; CASTRO, Luiz Henrique Martins |
| 2011 | A practical approach to the lateral cutaneous nerve of the thigh: An anatomical study | MARTINS, R. S.; SIQUEIRA, M. G.; SILVA JR., F. C.; HEISE, C. O.; TEIXEIRA, M. J. |
| 2013 | A Prospective Study Comparing Single and Double Fascicular Transfer to Restore Elbow Flexion After Brachial Plexus Injury | MARTINS, Roberto Sergio; SIQUEIRA, Mario Gilberto; HEISE, Carlos Otto; FORONI, Luciano; TEIXEIRA, Manoel Jacobsen |
| 2015 | A Research Design for the Quantification of the Neuropeptides Substance P and Calcitonin Gene-Related Peptide in Rat Skin Using Western Blot Analysis | LAPIN, Guilherme Abbud Franco; HOCHMAN, Bernardo; NISHIOKA, Michele Akemi; MAXIMINO, Jessica Ruivo; CHADI, Gerson; FERREIRA, Lydia Masako |
| 2018 | A SEVERE PHENOTYPE OF KENNEDY DISEASE ASSOCIATED WITH A VERY LARGE CAG REPEAT EXPANSION | MADEIRA, Joao L. O.; SOUZA, Alexandre B. C.; CUNHA, Flavia S.; BATISTA, Rafael L.; GOMES, Nathalia L.; RODRIGUES, Andresa S.; JORGE, Frederico Mennucci de Haidar; CHADI, Gerson; CALLEGARO, Dagoberto; MENDONCA, Berenice B., et al |
| 2016 | A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels | NETO, Osorio Abath; SILVA, Marina Rodrigues e; MARTINS, Cristiane de Araujo; OLIVEIRA, Acary de Souza Bulle; REED, Umbertina Conti; BIANCALANA, Valerie; PESQUERO, Joao Bosco; LAPORTE, Jocelyn; ZANOTELI, Edmar |
| 2011 | A Useful and Brief Cognitive Assessment for Advanced Dementia in a Population with Low Levels of Education | SALES, Manuela V. C.; SUEMOTO, Claudia K.; NITRINI, Ricardo; JACOB-FILHO, Wilson; MORILLO, Lilian S. |
| 2016 | A Window on the Study of Aversive Instrumental Learning: Strains, Performance, Neuroendocrine, and Immunologic Systems | OLIVEIRA, Caroline C. de; GOUVEIA, Flavia V.; CASTRO, Marina C. de; KUROKI, Mayra A.; SANTOS, Lennon C. T. dos; FONOFF, Erich T.; TEIXEIRA, Manoel J.; OTOCH, Jose P.; MARTINEZ, Raquel C. R. |
| 2022 | Aberrant Protein Glycosylation in Brain Cancers, with Emphasis on Glioblastoma | ROSA-FERNANDES, L.; OBA-SHINJO, S. M.; MACEDO-DA-SILVA, J.; MARIE, S. K. N.; PALMISANO, G. |
| 2017 | Ablative surgery for Parkinson's disease: Is there still a role for pallidotomy in the deep brain stimulation era? | SPINDOLA, Bruno; LEITE, Marco Antonio; ORSINI, Marco; FONOFF, Erich; LANDEIRO, Jose Alberto; PESSOA, Bruno Lima |
| 2023 | Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related <i>RYR1</i> mutations | SONNE, Alexander; ANTONOVIC, Anna Katarina; MELHEDEGAARD, Elise; AKTER, Fariha; ANDERSEN, Jesper L.; JUNGBLUTH, Heinz; WITTING, Nanna; VISSING, John; ZANOTELI, Edmar; FORNILI, Arianna, et al |
| 2012 | Abnormal sensory integration affects balance control in hemiparetic patients within the first year after stroke (vol 66, pg 2043, 2011) | OLIVEIRA, Clarissa B.; MEDEIROS, Italo R. T.; GRETERS, Mario G.; FROTA, Norberto A. F.; LUCATO, Leandro Tavares; MilbertoScaff; CONFORTO, Adriana B. |