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Cognitive impairment in myotonic dystrophy type 1 is associated with white matter damage

PloS one, 2014-08, Vol.9 (8), p.e104697-e104697

2014

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Longitudinal brain connectivity changes and clinical evolution in Parkinson's disease

Molecular psychiatry, 2021-09, Vol.26 (9), p.5429-5440

2021

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Tracking Cortical Changes Throughout Cognitive Decline in Parkinson's Disease

Movement disorders, 2020-11, Vol.35 (11), p.1987-1998

2020

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Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

Movement disorders, 2014-06, Vol.29 (7), p.857-867

2014

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Brain structural and functional connectivity in Parkinson's disease with freezing of gait

Human brain mapping, 2015-12, Vol.36 (12), p.5064-5078

2015

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Efficient neuroplasticity induction in chronic stroke patients by an associative brain-computer interface

Journal of neurophysiology, 2016-03, Vol.115 (3), p.1410-1421

2016

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Are there two different forms of functional dystonia? A multimodal brain structural MRI study

Molecular psychiatry, 2020-12, Vol.25 (12), p.3350-3359

2020

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The topography of brain damage at different stages of Parkinson's disease

Human brain mapping, 2013-11, Vol.34 (11), p.2798-2807

2013

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Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Movement disorders, 2016-04, Vol.31 (4), p.436-457

2016

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Longitudinal White Matter Damage Evolution in Parkinson's Disease

Movement disorders, 2022-02, Vol.37 (2), p.315-324

2022

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Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study

Journal of neurology, 2014-08, Vol.261 (8), p.1575-1583

2014

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Role of habenula and amygdala dysfunction in Parkinson disease patients with punding

Neurology, 2017-06, Vol.88 (23), p.2207

2017

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Longitudinal clinical, cognitive, and neuroanatomical changes over 5 years in GBA-positive Parkinson’s disease patients

Journal of neurology, 2022-03, Vol.269 (3), p.1485-1500

2022

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Progressive brain atrophy and clinical evolution in Parkinson’s disease

NeuroImage clinical, 2020-01, Vol.28, p.102374-102374, Article 102374

2020

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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

Nature genetics, 2013-09, Vol.45 (9), p.1077-1082

2013

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Breakdown of the affective‐cognitive network in functional dystonia

Human brain mapping, 2020-08, Vol.41 (11), p.3059-3076

2020

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The Profile and Evolution of Neuropsychiatric Symptoms in Multiple System Atrophy: Self- and Caregiver Report

The journal of neuropsychiatry and clinical neurosciences, 2021-05, Vol.33 (2), p.124-131

2021

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Cognitive impairment and structural brain damage in multiple system atrophy-parkinsonian variant

Journal of neurology, 2020, Vol.267 (1), p.87-94

2020

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Functional MRI connectivity of the primary motor cortex in functional dystonia patients

Journal of neurology, 2022-06, Vol.269 (6), p.2961-2971

2022

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DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery

Neurogenetics, 2024-04, Vol.25 (2), p.141-147

2024

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Why is nitric oxide important for our brain?

Functional neurology, 2015-07, Vol.30 (3), p.159-163

2015

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Cerebro-cerebellar motor networks in clinical subtypes of Parkinson’s disease

NPJ Parkinson's Disease, 2022-09, Vol.8 (1), p.113-113, Article 113

2022

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Neurogenetic traits outline vulnerability to cortical disruption in Parkinson’s disease

NeuroImage clinical, 2022-01, Vol.33, p.102941-102941, Article 102941

2022

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Multiparametric MRI to distinguish early onset Alzheimer's disease and behavioural variant of frontotemporal dementia

NeuroImage clinical, 2017-01, Vol.15, p.428-438

2017

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Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment

Journal of neurology, 2023-07, Vol.270 (7), p.3492-3498

2023

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Cognitive impairment in myotonic dystrophy type 1 is associated with white matter damage

Longitudinal brain connectivity changes and clinical evolution in Parkinson's disease

Tracking Cortical Changes Throughout Cognitive Decline in Parkinson's Disease

Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

Brain structural and functional connectivity in Parkinson's disease with freezing of gait

Efficient neuroplasticity induction in chronic stroke patients by an associative brain-computer interface

Are there two different forms of functional dystonia? A multimodal brain structural MRI study

The topography of brain damage at different stages of Parkinson's disease

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Longitudinal White Matter Damage Evolution in Parkinson's Disease

Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study

Role of habenula and amygdala dysfunction in Parkinson disease patients with punding

Longitudinal clinical, cognitive, and neuroanatomical changes over 5 years in GBA-positive Parkinson’s disease patients

Progressive brain atrophy and clinical evolution in Parkinson’s disease

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

Breakdown of the affective‐cognitive network in functional dystonia

The Profile and Evolution of Neuropsychiatric Symptoms in Multiple System Atrophy: Self- and Caregiver Report

Cognitive impairment and structural brain damage in multiple system atrophy-parkinsonian variant

Functional MRI connectivity of the primary motor cortex in functional dystonia patients

DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery

Why is nitric oxide important for our brain?

Cerebro-cerebellar motor networks in clinical subtypes of Parkinson’s disease

Neurogenetic traits outline vulnerability to cortical disruption in Parkinson’s disease

Multiparametric MRI to distinguish early onset Alzheimer's disease and behavioural variant of frontotemporal dementia

Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment

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