Lista de obras -

A case series of PLS patients with frontotemporal dementia and overview of the literature

artículo científico publicado en 2017

A systematic review of behavioural changes in motor neuron disease ⬇️

artículo científico publicado el 16 de marzo de 2012

Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis

scientific article published on 07 March 2019

Brain imaging in myotonic dystrophy type 1: A systematic review

artículo científico publicado en 2017

Characterization of EEG-based functional brain networks in myotonic dystrophy type 1

artículo científico publicado en 2020

Cognitive and behavioral status in Japanese ALS patients: a multicenter study

artículo científico publicado en 2020

Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophy

artículo científico publicado en 2010

Combined N-of-1 trials to investigate mexiletine in non-dystrophic myotonia using a Bayesian approach; study rationale and protocol.

artículo científico publicado en 2015

De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects

artículo científico publicado en 2020

Diagnostic value of additional histopathological fascia examination in idiopathic inflammatory myopathies

artículo científico publicado en 2019

Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials

artículo científico publicado en 2018

Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative study

artículo científico publicado en 2018

Exploring the fitness hypothesis in ALS: a population-based case-control study of parental cause of death and lifespan

artículo científico publicado en 2017

Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases

article

High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective study

scientific article published on 28 August 2019

Inclusion body myositis in patients with spinocerebellar ataxia types 3 and 6

artículo científico publicado en 2020

Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study

artículo científico publicado en 2020

Is the Frontal Assessment Battery reliable in ALS patients? ⬇️

artículo científico publicado el 13 de agosto de 2012

Ischemic stroke mimicking acute myocardial infarction, a diagnostic dilemma

artículo científico publicado en 2006

Japanese version of the ALS-FTD-Questionnaire (ALS-FTD-Q-J).

artículo científico publicado en 2016

Long-Term Air Pollution Exposure and Amyotrophic Lateral Sclerosis in Netherlands: A Population-based Case–control Study.

artículo científico publicado en 2017

Long-Term Exposure To Traffic Related Air Pollution Is Associated With An Increased Risk Of Amyotrophic Lateral Sclerosis ⬇️

scholarly article

Meet and eat, an interdisciplinary group intervention for patients with myotonic dystrophy about healthy nutrition, meal preparation, and consumption: a feasibility study

scientific article published on 20 November 2018

Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis

artículo científico publicado en 2017

No association between gluten sensitivity and amyotrophic lateral sclerosis

artículo científico publicado en 2017

Numb cheek syndrome as the first manifestation of anti-Hu paraneoplastic neuronopathy

artículo científico publicado en 2005

OptimisAtion of Diagnostic Accuracy in idioPathic inflammaTory myopathies (ADAPT study): a protocol for a prospective diagnostic accuracy study of multimodality testing in patients suspected of a treatable idiopathic inflammatory myopathy

artículo científico publicado en 2021

Prefrontal involvement related to cognitive impairment in progressive muscular atrophy

artículo científico publicado en 2014

Progression of cognitive and behavioural impairment in early amyotrophic lateral sclerosis

artículo científico publicado en 2020

Reader response: ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS

scientific article published on 01 July 2019

Response to the letter to editor about "Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis"

artículo científico publicado en 2019

Response to ‘Exploring limits of neuropsychological screening in ALS: The FAB problem’ ⬇️

artículo científico publicado el 4 de enero de 2013

Structural white matter networks in myotonic dystrophy type 1.

artículo científico publicado en 2018

Tau Rather than TDP-43 Proteins are Potential Cerebrospinal Fluid Biomarkers for Frontotemporal Lobar Degeneration Subtypes: A Pilot Study.

artículo científico publicado en 2016

The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALS.

artículo científico publicado en 2012

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

artículo científico publicado en 2012

The cognitive profile of ALS: a systematic review and meta-analysis update

artículo científico publicado en 2015

The cognitive profile of amyotrophic lateral sclerosis: A meta-analysis

artículo científico publicado en 2010

The cognitive profile of behavioural variant FTD and its similarities with ALS: a systematic review and meta-analysis

artículo científico publicado en 2018

The cognitive profile of myotonic dystrophy type 1: A systematic review and meta-analysis.

artículo científico publicado en 2017

The frontotemporal syndrome of ALS is associated with poor survival

scientific article published on 26 September 2016

The verbal fluency index: Dutch normative data for cognitive testing in ALS.

artículo científico publicado en 2014

West Nile virus poliomyelitis after a holiday in Egypt

artículo científico publicado el 1 de enero de 2012

[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]

scientific article published on 01 January 2010

Lista de obras de

A case series of PLS patients with frontotemporal dementia and overview of the literature

A systematic review of behavioural changes in motor neuron disease ⬇️

Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis

Brain imaging in myotonic dystrophy type 1: A systematic review

Characterization of EEG-based functional brain networks in myotonic dystrophy type 1

Cognitive and behavioral status in Japanese ALS patients: a multicenter study

Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophy

Combined N-of-1 trials to investigate mexiletine in non-dystrophic myotonia using a Bayesian approach; study rationale and protocol.

De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects

Diagnostic value of additional histopathological fascia examination in idiopathic inflammatory myopathies

Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials

Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative study

Exploring the fitness hypothesis in ALS: a population-based case-control study of parental cause of death and lifespan

Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases

High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective study

Inclusion body myositis in patients with spinocerebellar ataxia types 3 and 6

Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study

Is the Frontal Assessment Battery reliable in ALS patients? ⬇️

Ischemic stroke mimicking acute myocardial infarction, a diagnostic dilemma

Japanese version of the ALS-FTD-Questionnaire (ALS-FTD-Q-J).

Long-Term Air Pollution Exposure and Amyotrophic Lateral Sclerosis in Netherlands: A Population-based Case–control Study.

Long-Term Exposure To Traffic Related Air Pollution Is Associated With An Increased Risk Of Amyotrophic Lateral Sclerosis ⬇️

Meet and eat, an interdisciplinary group intervention for patients with myotonic dystrophy about healthy nutrition, meal preparation, and consumption: a feasibility study

Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis

No association between gluten sensitivity and amyotrophic lateral sclerosis

Numb cheek syndrome as the first manifestation of anti-Hu paraneoplastic neuronopathy

OptimisAtion of Diagnostic Accuracy in idioPathic inflammaTory myopathies (ADAPT study): a protocol for a prospective diagnostic accuracy study of multimodality testing in patients suspected of a treatable idiopathic inflammatory myopathy

Prefrontal involvement related to cognitive impairment in progressive muscular atrophy

Progression of cognitive and behavioural impairment in early amyotrophic lateral sclerosis

Reader response: ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS

Response to the letter to editor about "Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis"

Response to ‘Exploring limits of neuropsychological screening in ALS: The FAB problem’ ⬇️

Structural white matter networks in myotonic dystrophy type 1.

Tau Rather than TDP-43 Proteins are Potential Cerebrospinal Fluid Biomarkers for Frontotemporal Lobar Degeneration Subtypes: A Pilot Study.

The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALS.

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

The cognitive profile of ALS: a systematic review and meta-analysis update

The cognitive profile of amyotrophic lateral sclerosis: A meta-analysis

The cognitive profile of behavioural variant FTD and its similarities with ALS: a systematic review and meta-analysis

The cognitive profile of myotonic dystrophy type 1: A systematic review and meta-analysis.

The frontotemporal syndrome of ALS is associated with poor survival

The verbal fluency index: Dutch normative data for cognitive testing in ALS.

West Nile virus poliomyelitis after a holiday in Egypt

[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]