Surgical Treatment of Dyskinesia in Parkinson’s Disease

por Munhoz, Renato P., Cerasa, Antonio, Okun, Michael S.
Publicado 2014

Deep brain stimulation for dystonia

por Santyr, Brendan, Munhoz, Renato P., Lozano, Andres M.
Publicado 2023

Tardive Akathisia with Asymmetric and Upper-body Presentation: Report of Two Cases and Literature Review

por Shahidi, Gholamali, Rohani, Mohammad, Munhoz, Renato Puppi, Akhoundi, Fahimeh H.
Publicado 2018

TNR Gene Mutation in Familial Parkinson’s Disease: Possible Implications for Essential Tremor

por Sáenz-Farret, Michel, Munhoz, Renato Puppi, Fasano, Alfonso, Zúñiga-Ramírez, Carlos
Publicado 2021

Chorea as the First Manifestation of Cerebral Infarction

por Hernandez Fustes, Otto Jesus, Puppi Munhoz, Renato, Arteaga Rodriguez, Carlos, Hernandez Fustes, Olga Judith
Publicado 2020

Follow-Up of Advanced Parkinson's Disease Patients after Clinical or Surgical Emergencies: A Practical Approach

por Teive, Hélio A. G., Ferreira, Matheus Gomes, Camargo, Carlos Henrique F., Munhoz, Renato P.
Publicado 2020

Deep brain stimulation in Parkinson’s disease: state of the art and future perspectives

por França, Carina, Carra, Rafael Bernhart, Diniz, Juliete Melo, Munhoz, Renato Puppi, Cury, Rubens Gisbert
Publicado 2022

Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)

por Dias, Francisco A, Munhoz, Renato P, Raskin, Salmo, Werneck, Lineu César, Teive, Hélio A G
Publicado 2011

New-Onset Movement Disorders Associated with COVID-19

por Brandão, Pedro Renato P., Grippe, Talyta C., Pereira, Danilo A., Munhoz, Renato P., Cardoso, Francisco
Publicado 2021

Thomas Willis’ legacy on the 400(th) anniversary of his birth

por Teive, Hélio Afonso Ghizoni, Coutinho, Léo, Camargo, Carlos Henrique Ferreira, Munhoz, Renato Puppi, Walusinski, Olivier
Publicado 2022

Nonmotor symptoms in spinocerebellar ataxias (SCAs)

por Moro, Adriana, Moscovich, Mariana, Farah, Marina, Camargo, Carlos Henrique F., Teive, Hélio A. G., Munhoz, Renato P.
Publicado 2019

Classification and Characteristics of Pain Associated with Parkinson's Disease

por Young Blood, Marcelo Rezende, Ferro, Marcelo Machado, Munhoz, Renato Puppi, Teive, Hélio Afonso Ghizoni, Camargo, Carlos Henrique Ferreira
Publicado 2016

Moyamoya disease and syndrome: a review

por Demartini Jr., Zeferino, Teixeira, Bernardo CA., Koppe, Gelson Luis, Gatto, Luana A. Maranha, Roman, Alex, Munhoz, Renato Puppi
Publicado 2022

Spinocerebellar ataxias – genotype-phenotype correlations in 104 Brazilian families

por Teive, Hélio A. G., Munhoz, Renato P., Arruda, Walter O., Lopes-Cendes, Iscia, Raskin, Salmo, Werneck, Lineu C., Ashizawa, Tetsuo
Publicado 2012

Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in Canada

por Alshimemeri, Sohaila, Abo Alsamh, Danah, Zhou, Lily, Furtado, Sarah, Kraft, Scott, Bruno, Veronica, Duquette, Antoine, Brais, Bernard, Suchowersky, Oksana, Munhoz, Renato P., Slow, Elizabeth
Publicado 2023

Reply to: Glioblastoma, IDH‐Wildtype, CNS WHO Grade 4, Associated with Deep Brain Stimulation in a Patient with Essential Tremor: Report of a Case with Molecular Characterization a...

por Balachandar, Arjun, Boutet, Alexandre, Vetkas, Artur, Germann, Jurgen, Chan, Ian Y.M., Mikulis, David, Munhoz, Renato P., Fasano, Alfonso, Kalia, Suneil K., Lozano, Andres M.
Publicado 2023

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

por Orlacchio, Antonio, Babalini, Carla, Borreca, Antonella, Patrono, Clarice, Massa, Roberto, Basaran, Sarenur, Munhoz, Renato P., Rogaeva, Ekaterina A., St George-Hyslop, Peter H., Bernardi, Giorgio, Kawarai, Toshitaka
Publicado 2010

Levodopa Versus Dopamine Agonist after Subthalamic Stimulation in Parkinson's Disease

por Picillo, Marina, Phokaewvarangkul, Onanong, Poon, Yu‐Yan, McIntyre, Cameron C., Beylergil, Sinem Balta, Munhoz, Renato P., Kalia, Suneil K., Hodaie, Mojgan, Lozano, Andres M., Fasano, Alfonso
Publicado 2020

Psychogenic Facial Movement Disorders: Clinical Features and Associated Conditions

por Fasano, Alfonso, Valadas, Anabela, Bhatia, Kailash P, Prashanth, LK, Lang, Anthony E, Munhoz, Renato P, Morgante, Francesca, Tarsy, Daniel, Duker, Andrew P, Girlanda, Paolo, Bentivoglio, Anna Rita, Espay, Alberto J
Publicado 2012

Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome

por Qaiser, Farah, Sadoway, Tara, Yin, Yue, Zulfiqar Ali, Quratulain, Nguyen, Charlotte M, Shum, Natalie, Backstrom, Ian, Marques, Paula T, Tabarestani, Sepideh, Munhoz, Renato P, Krings, Timo, Pearson, Christopher E, Yuen, Ryan K C, Andrade, Danielle M
Publicado 2021