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Diagnosis of autism spectrum disorder based on functional brain networks and machine learning

Scientific reports, 2023-05, Vol.13 (1), p.8072-8072, Article 8072

2023

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Brain connectivity in patients with dystonia during motor tasks

Journal of neural engineering, 2020-10, Vol.17 (5), p.056039-056039

2020

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DYT‐TUBB4A (DYT4 Dystonia): Clinical Anthology of 11 Cases and Systematized Review

Movement disorders clinical practice (Hoboken, N.J.), 2022-07, Vol.9 (5), p.659-675

2022

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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

Neurological sciences, 2022-02, Vol.43 (2), p.1061-1065

2022

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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) study

Neurophotonics (Print), 2020-10, Vol.7 (4), p.045004-045004

2020

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Analysis of functional connectivity using machine learning and deep learning in different data modalities from individuals with schizophrenia

Journal of neural engineering, 2023-10, Vol.20 (5), p.56025

2023

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Classification and genetics of dystonia

Lancet neurology, 2002-09, Vol.1 (5), p.316-325

2002

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PINK1 polymorphism IVS1−7 A→G, exposure to environmental risk factors and anticipation of disease onset in Brazilian patients with early-onset Parkinson's Disease

Neuroscience letters, 2010-01, Vol.469 (1), p.155-158

2010

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Task-related brain activity in upper limb dystonia revealed by simultaneous fNIRS and EEG

Clinical neurophysiology, 2024-03, Vol.159, p.1-12

2024

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PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients

Movement disorders, 2009-08, Vol.24 (11), p.1693-1696

2009

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Novel compound heterozygous mutations in PRKRA cause pure dystonia

Movement disorders, 2015-05, Vol.30 (6), p.877-878

2015

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DYT-TUBB4A (DYT4 Dystonia): New Clinical and Genetic Observations

Neurology, 2021-04, Vol.96 (14), p.e1887

2021

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Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites

American journal of medical genetics. Part A, 2007-09, Vol.143A (18), p.2098-2105

2007

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Omics profile of iPSC-derived astrocytes from Progressive Supranuclear Palsy (PSP) patients

Parkinsonism & related disorders, 2023-11, Vol.116, p.105847-105847, Article 105847

2023

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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

Journal of the neurological sciences, 2010-04, Vol.291 (1), p.64-68

2010

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The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATPIA3 gene

Brain (London, England : 1878), 2007-03, Vol.130, p.828-835

2007

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The prevalence of PRKRA mutations in idiopathic dystonia

Parkinsonism & related disorders, 2018-03, Vol.48, p.93-96

2018

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Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients

Cerebellum (London, England), 2016-06, Vol.15 (3), p.306-313

2016

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Neuropsychological and clinical heterogeneity of cognitive impairment in patients with multiple system atrophy

Clinical neurology and neurosurgery, 2018-01, Vol.164, p.121-126

2018

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Milestones in Friedreich ataxia: more than a century and still learning

Neurogenetics, 2015-07, Vol.16 (3), p.151-160

2015

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Predictable variables for short- and long-term botulinum toxin treatment response in patients with cervical dystonia

Neurological sciences, 2009-08, Vol.30 (4), p.291-294

2009

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Neuroleptic-induced tardive cervical dystonia: clinical series of 20 patients

Canadian journal of neurological sciences, 2009-03, Vol.36 (2), p.222

2009

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Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK

Biochimica et biophysica acta. Molecular basis of disease, 2018-05, Vol.1864 (5), p.1896-1903

2018

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Mutations in NPC1 in two Brazilian patients with Niemann-Pick disease type C and progressive supranuclear palsy-like presentation

Movement disorders, 2006-12, Vol.21 (12), p.2270-2272

2006

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Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function

Journal of neurology, 2016-04, Vol.263 (4), p.665-668

2016

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Diagnosis of autism spectrum disorder based on functional brain networks and machine learning

Brain connectivity in patients with dystonia during motor tasks

DYT‐TUBB4A (DYT4 Dystonia): Clinical Anthology of 11 Cases and Systematized Review

High prevalence of self-reported non-motor symptoms and lack of correlation with motor severity in adult patients with idiopathic isolated dystonia

Task-related brain activity and functional connectivity in upper limb dystonia: a functional magnetic resonance imaging (fMRI) and functional near-infrared spectroscopy (fNIRS) study

Analysis of functional connectivity using machine learning and deep learning in different data modalities from individuals with schizophrenia

Classification and genetics of dystonia

PINK1 polymorphism IVS1−7 A→G, exposure to environmental risk factors and anticipation of disease onset in Brazilian patients with early-onset Parkinson's Disease

Task-related brain activity in upper limb dystonia revealed by simultaneous fNIRS and EEG

PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients

Novel compound heterozygous mutations in PRKRA cause pure dystonia

DYT-TUBB4A (DYT4 Dystonia): New Clinical and Genetic Observations

Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites

Omics profile of iPSC-derived astrocytes from Progressive Supranuclear Palsy (PSP) patients

Evaluation of patients with Clinically Unclear Parkinsonian Syndromes submitted to brain SPECT imaging using the technetium-99m labeled tracer TRODAT-1

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATPIA3 gene

The prevalence of PRKRA mutations in idiopathic dystonia

Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients

Neuropsychological and clinical heterogeneity of cognitive impairment in patients with multiple system atrophy

Milestones in Friedreich ataxia: more than a century and still learning

Predictable variables for short- and long-term botulinum toxin treatment response in patients with cervical dystonia

Neuroleptic-induced tardive cervical dystonia: clinical series of 20 patients

Metabolic studies of a patient harbouring a novel S487L mutation in the catalytic subunit of AMPK

Mutations in NPC1 in two Brazilian patients with Niemann-Pick disease type C and progressive supranuclear palsy-like presentation

Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function

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