Hand Stereotypies in Rett Syndrome

por Ferreira, Matheus G., Teive, Hélio A. G.
Publicado 2020

“Copromessaging”: a new feature of Tourette’s syndrome?

por Franklin, Gustavo L., Teive, Hélio A.G.
Publicado 2020

Brazilian Academy of Neurology: 60 Years

por Massaro, Ayrton, Teive, Hélio A. G., Caramelli, Paulo
Publicado 2022

Cognitive dysfunction and dementia in movement disorders

por Barbosa, Egberto Reis, Teive, Hélio A. G., Tumas, Vitor
Publicado 2016

Comment on Clinical Profile of Genetically Proven Huntington's Disease Patients From Eastern India

por Franklin, Gustavo L., Camargo, Carlos Henrique, Meira, Alex T., Teive, Hélio A. G.
Publicado 2021

Comment on: “Investigation of intermediate CAG alleles of the HTT in the general population of Rio de Janeiro, Brazil, in comparison with a sample of Huntington disease‐affected fa...

por Franklin, Gustavo L., Meira, Alex T., Camargo, Carlos H. F., Teive, Hélio A. G.
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

Arquivos de Neuro-Psiquiatria: 80 years

por Massaro, Ayrton, Teive, Hélio A. G., Livramento, Jose Antônio, Machado, Luis dos Ramos, Caramelli, Paulo
Publicado 2023

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

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

Evaluation of Patients with Parkinson's Disease in Intensive Care Units: A Cohort Study

por Réa-Neto, Álvaro, Dal Vesco, Bruna C., Bernardelli, Rafaella S., Kametani, Aline M., Oliveira, Mirella C., Teive, Hélio A. G.
Publicado 2021

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

T2-hyperintensity in the internal globus pallidus in Machado-Joseph disease

por Meira, Alex T., Araruna, Jorge E. D., Araujo, Lais Vieira, Leite, Raíssa N. L. F., Franklin, Gustavo L., Nepomuceno, Adriana M. T., Teive, Hélio A. G.
Publicado 2023

Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry

por Bushara, Khalaf, Bower, Matthew, Liu, Jilin, McFarland, Karen N., Landrian, Ivette, Hutter, Diane, Teive, Hélio A. G., Rasmussen, Astrid, Mulligan, Connie J., Ashizawa, Tetsuo
Publicado 2013

Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10

por Hashem, Vera, Tiwari, Anjana, Bewick, Brittani, Teive, Helio A. G., Moscovich, Mariana, Schüele, Birgitt, Bushara, Khalaf, Bower, Matt, Rasmussen, Astrid, Tsai, Yu-Chih, Clark, Tyson, McFarland, Karen, Ashizawa, Tetsuo
Publicado 2020

Correction: Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10

por Hashem, Vera, Tiwari, Anjana, Bewick, Brittani, Teive, Helio A. G., Moscovich, Mariana, Schüle, Birgitt, Bushara, Khalaf, Bower, Matt, Rasmussen, Astrid, Tsai, Yu-Chih, Clark, Tyson, McFarland, Karen, Ashizawa, Tetsuo
Publicado 2020

Movement disorders in hereditary spastic paraplegias

por Pedroso, Jose Luiz, Vale, Thiago Cardoso, Freitas, Julian Letícia de, Araújo, Filipe Miranda Milagres, Meira, Alex Tiburtino, Neto, Pedro Braga, França, Marcondes C., Tumas, Vitor, Teive, Hélio A. G., Barsottini, Orlando G. P.
Publicado 2023

Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10

por White, Misti C., Gao, Rui, Xu, Weidong, Mandal, Santi M., Lim, Jung G., Hazra, Tapas K., Wakamiya, Maki, Edwards, Sharon F., Raskin, Salmo, Teive, Hélio A. G., Zoghbi, Huda Y., Sarkar, Partha S., Ashizawa, Tetsuo
Publicado 2010

Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn

por Efthymiou, Stephanie, Novis, Luiz E., Koutsis, Georgios, Koniari, Chrysoula, Maroofian, Reza, Turchetti, Valentina, Velonakis, Georgios, Vasconcellos, Luiz F., Raskin, Salmo, Srinivasan, Varunvenkat M., Pagnamenta, Alistair T., Arun, Yaramanchanahalli B., Kinhal, Uddhava V., Gowda, Vykuntaraju K., Teive, Helio A. G., Houlden, Henry
Publicado 2023

Is Ataxia an Underestimated Symptom of Huntington's Disease?

por Franklin, Gustavo L., Camargo, Carlos Henrique F., Meira, Alex T., Pavanelli, Giovana M., Milano, Sibele S., Germiniani, Francisco B., Lima, Nayra S. C., Raskin, Salmo, Barsottini, Orlando Graziani Povoas, Pedroso, José Luiz, Maggi, Fernanda Aparecida, Tumas, Vitor, de Carvalho, Pedro Manzke, de Oliveira, Ana Carolina, Braga, Bárbara, Souza, Laura Cristina, Guimarães, Rachel Paes, Piovesana, Luiza Gonzaga, Lopes-Cendes, Íscia Teresinha, de Azevedo, Paula Christina, França, Marcondes Cavalcante, Martinez, Alberto Rolim Muro, Teive, Hélio A. G.
Publicado 2020