Diagnosis of autism spectrum disorder based on functional brain networks and machine learning von Alves, Caroline L., Toutain, Thaise G. L. de O., de Carvalho Aguiar, Patricia, Pineda, Aruane M., Roster, Kirstin, Thielemann, Christiane, Porto, Joel Augusto Moura, Rodrigues, Francisco A.

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Brain connectivity in patients with dystonia during motor tasks von Baltazar, Carlos Arruda, Machado, Birajara Soares, de Faria, Danilo Donizete, Paulo, Artur José Marques, Silva, Sonia Maria Cezar Azevedo, Ferraz, Henrique Ballalai, Aguiar, Patrícia de Carvalho

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Analysis of functional connectivity using machine learning and deep learning in different data modalities from individuals with schizophrenia von Alves, Caroline L, Toutain, Thaise G L de O., Porto, Joel Augusto Moura, Aguiar, Patrícia Maria de Carvalho, de Sena, Eduardo Pondé, Rodrigues, Francisco A, Pineda, Aruane M, Thielemann, Christiane

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High prevalence of self-reported non-motor symptoms and lack of correlation with motor severity in adult patients with idiopathic isolated dystonia von da Silva-Júnior, Francisco Pereira, dos Santos Alves, Camila Oliveira, Silva, Sônia Maria Cesar Azevedo, Borges, Vanderci, Ferraz, Henrique Ballalai, Rocha, Maria Sheila Guimarães, Limongi, João Carlos Papaterra, Barbosa, Egberto Reis, de Carvalho Aguiar, Patrícia

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Task-related brain activity and functional connectivity in upper limb dystonia: a functional magnetic resonance imaging (fMRI) and functional near-infrared spectroscopy (fNIRS) stu... von de Faria, Danilo Donizete, Paulo, Artur José Marques, Balardin, Joana, Sato, João Ricardo, Junior, Edson Amaro, Baltazar, Carlos Arruda, Lucca, Renata Prôa Dalle, Borges, Vanderci, Silva, Sonia Maria Cesar Azevedo, Ferraz, Henrique Ballalai, de Carvalho Aguiar, Patrícia

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Classification and genetics of dystonia von de Carvalho Aguiar, Patricia M, Ozelius, Laurie J

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Task-related brain activity in upper limb dystonia revealed by simultaneous fNIRS and EEG von Marques Paulo, Artur José, Sato, João Ricardo, de Faria, Danilo Donizete, Balardin, Joana, Borges, Vanderci, de Azevedo Silva, Sonia Maria, Ballalai Ferraz, Henrique, de Carvalho Aguiar, Patrícia

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DYT-TUBB4A (DYT4 Dystonia): New Clinical and Genetic Observations von Bally, Julien F., Camargos, Sarah, Oliveira dos Santos, Camila, Kern, Drew S., Lee, Teresa, Pereira da Silva-Junior, Francisco, Puga, Renato David, Cardoso, Francisco, Barbosa, Egberto Reis, Yadav, Rachita, Ozelius, Laurie J., de Carvalho Aguiar, Patricia, Lang, Anthony E.

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Novel compound heterozygous mutations in PRKRA cause pure dystonia von de Carvalho Aguiar, Patricia, Borges, Vanderci, Ferraz, Henrique Ballalai, Ozelius, Laurie Jean

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Omics profile of iPSC-derived astrocytes from Progressive Supranuclear Palsy (PSP) patients von Ravagnani, Felipe G., Valerio, Hellen P., Maués, Jersey H.S., de Oliveira, Arthur N., Puga, Renato D., Griesi-Oliveira, Karina, Picosse, Fabíola R., Ferraz, Henrique B., Catharino, Rodrigo R., Ronsein, Graziella E., de Carvalho Aguiar, Patrícia

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Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites von Saunders-Pullman, Rachel, Raymond, Deborah, Senthil, Geetha, Kramer, Patricia, Ohmann, Erin, Deligtisch, Amanda, Shanker, Vicki, Greene, Paul, Tabamo, Rowena, Huang, Neng, Tagliati, Michele, Kavanagh, Patricia, Soto-Valencia, Jeannie, Aguiar, Patricia de Carvalho, Risch, Neil, Ozelius, Laurie, Bressman, Susan

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The prevalence of PRKRA mutations in idiopathic dystonia von dos Santos, Camila Oliveira, da Silva-Júnior, Francisco Pereira, Puga, Renato David, Barbosa, Egberto Reis, Azevedo Silva, Sonia Maria Cesar, Borges, Vanderci, Limongi, João Carlos Papaterra, Rocha, Maria Sheila Guimarães, Ferraz, Henrique Ballalai, de Carvalho Aguiar, Patricia

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Multiclass classification of Autism Spectrum Disorder, attention deficit hyperactivity disorder, and typically developed individuals using fMRI functional connectivity analysis von Alves, Caroline L, Martinelli, Tiago, Sallum, Loriz Francisco, Rodrigues, Francisco Aparecido, Toutain, Thaise G L de O, Porto, Joel Augusto Moura, Thielemann, Christiane, Aguiar, Patrícia Maria de Carvalho, Moeckel, Michael

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Milestones in Friedreich ataxia: more than a century and still learning von Abrahão, Agessandro, Pedroso, José Luiz, Braga-Neto, Pedro, Bor-Seng-Shu, Edson, de Carvalho Aguiar, Patricia, Barsottini, Orlando Graziani Povoas

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PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients von Godeiro-Junior, Clecio, de Carvalho-Aguiar, Patricia M., Felício, Andre C., Barsottini, Orlando G.P., Silva, Sonia M.A., Borges, Vanderci, Andrade, Luiz Augusto F., Ferraz, Henrique Ballalai

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Neuropsychological and clinical heterogeneity of cognitive impairment in patients with multiple system atrophy von Barcelos, Lorena Broseghini, Saad, Flávia, Giacominelli, Carla, Saba, Roberta Arb, de Carvalho Aguiar, Patrícia Maria, Silva, Sonia Maria Azevedo, Borges, Vanderci, Bertolucci, Paulo Henrique Ferreira, Ferraz, Henrique Ballalai

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Evaluation of patients with Clinically Unclear Parkinsonian Syndromes submitted to brain SPECT imaging using the technetium-99m labeled tracer TRODAT-1 von Felicio, Andre C, Godeiro-Junior, Clecio, Shih, Ming C, Borges, Vanderci, Silva, Sônia M.A, Aguiar, Patrícia de Carvalho, Hoexter, Marcelo Q, Barsottini, Orlando G.P, Andrade, Luiz A.F, Bressan, Rodrigo A, Ferraz, Henrique B

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Mutations in NPC1 in two Brazilian patients with Niemann-Pick disease type C and progressive supranuclear palsy-like presentation von Godeiro-Júnior, Clécio, Jun Inaoka, Riguel, Rocha Barbosa, Marcelo, Regis Silva, Maria Regina, de Carvalho Aguiar, Patrícia, Barsottini, Orlando

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Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK von Arita, Juliana Harumi, Barros, Mário H., Ravagnani, Felipe Gustavo, Ziosi, Marcello, Sanches, Lívia Rentas, Picosse, Fabíola Rosa, Lopes, Tania Oliveira, de Carvalho Aguiar, Patrícia, Macabelli, Carolina Habermann, Chiaratti, Marcos R., Pedroso, José Luiz, Quinzii, Catarina M., Barsottini, Orlando Graziani Póvoas, Ferreiro-Barros, Claudia Cristina

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Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function von dos Santos, Camila Oliveira, Masuho, Ikuo, da Silva-Júnior, Francisco Pereira, Barbosa, Egberto Reis, Silva, Sonia Maria Cesar Azevedo, Borges, Vanderci, Ferraz, Henrique Ballalai, Rocha, Maria Sheila Guimarães, Limongi, João Carlos Papaterra, Martemyanov, Kirill A., de Carvalho Aguiar, Patricia

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