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Issue DateTitleAuthor(s)
2019214th ENMC International Workshop: Establishing an international consortium for gene discovery and clinical research for Congenital Muscle Disease, Heemskerk, the Netherlands, 6-18 October 2015DONKERVOORT, Sandra; DOWLING, James J.; LAPORTE, Jocelyn; MACARTHUR, Daniel; BONNEMANN, Carsten G.; BEGGS, Alan; BONNE, Gisele; BONNEMANN, Carsten; DONKERVOORT, Sandra; DOWLING, James, et al
20133D Preoperative Planning in the ER with OsiriX (R): When There is No Time for NeuronavigationMANDEL, Mauricio; AMORIM, Robson; PAIVA, Wellingson; PRUDENTE, Marcelo; TEIXEIRA, Manoel Jacobsen; ANDRADE, Almir Ferreira de
2011A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaFANGANIELLO, R. D.; KIMONIS, V. E.; CORTE, C. C.; NITRINI, R.; PASSOS-BUENO, M. R.
2018A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutationSHINJO, Samuel Katsuyuki; OBA-SHINJO, Sueli Mieko; LERARIO, Antonio Marcondes; MARIE, Suely Kazue Nagahashi
2017A Bug in the Brain and the Future of NeurosciencesFIGUEIREDO, Eberval Gadelha; WELLING, Leonardo C.; WELLING, Mariana S.; TEIXEIRA, Manoel J.
2018A common CHRNE mutation in Brazilian patients with congenital myasthenic syndromeESTEPHAN, 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
2014A 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
2016A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disabilityFIGUEIREDO, 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
2018A novel complex neurological phenotype due to a homozygous mutation in FDX2GURGEL-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
2016A novel GFAP mutation in a type II (late-onset) Alexander disease patientPAIVA, 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
2015A patient with a long history of relapsing psychosis and mania presenting with anti-NMDA receptor encephalitis ten years after first episodeSIMABUKURO, Mateus Mistieri; FREITAS, Christian Henrique de Andrade; CASTRO, Luiz Henrique Martins
2011A practical approach to the lateral cutaneous nerve of the thigh: An anatomical studyMARTINS, R. S.; SIQUEIRA, M. G.; SILVA JR., F. C.; HEISE, C. O.; TEIXEIRA, M. J.
2013A Prospective Study Comparing Single and Double Fascicular Transfer to Restore Elbow Flexion After Brachial Plexus InjuryMARTINS, Roberto Sergio; SIQUEIRA, Mario Gilberto; HEISE, Carlos Otto; FORONI, Luciano; TEIXEIRA, Manoel Jacobsen
2015A Research Design for the Quantification of the Neuropeptides Substance P and Calcitonin Gene-Related Peptide in Rat Skin Using Western Blot AnalysisLAPIN, Guilherme Abbud Franco; HOCHMAN, Bernardo; NISHIOKA, Michele Akemi; MAXIMINO, Jessica Ruivo; CHADI, Gerson; FERREIRA, Lydia Masako
2018A SEVERE PHENOTYPE OF KENNEDY DISEASE ASSOCIATED WITH A VERY LARGE CAG REPEAT EXPANSIONMADEIRA, 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
2016A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic LevelsNETO, 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
2011A Useful and Brief Cognitive Assessment for Advanced Dementia in a Population with Low Levels of EducationSALES, Manuela V. C.; SUEMOTO, Claudia K.; NITRINI, Ricardo; JACOB-FILHO, Wilson; MORILLO, Lilian S.
2016A Window on the Study of Aversive Instrumental Learning: Strains, Performance, Neuroendocrine, and Immunologic SystemsOLIVEIRA, 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.
2017Ablative 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
2012Abnormal 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.