Lista de obras -

ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.

artículo científico publicado en 2014

Biomarkers of Parkinson's disease: 20 years later

scientific article published on 04 April 2019

Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis

artículo científico publicado en 2011

Early- and late-onset essential tremor patients represent clinically distinct subgroups

artículo científico publicado en 2016

Examination of Patients with Essential Tremor

artículo científico publicado en 2014

Four-repeat tauopathies

artículo científico publicado en 2019

Genetics of tremor

artículo científico publicado en 2018

Genome-wide association study in essential tremor identifies three new loci

artículo científico publicado en 2016

Gut microbiota in Parkinson disease in a northern German cohort.

artículo científico publicado en 2017

HTLV-1 associated myelopathy after renal transplantation

artículo científico publicado en 2015

Is essential tremor a single entity?

artículo científico publicado en 2017

Mobility Deficits Assessed With Mobile Technology: What Can We Learn From Brain Iron-Altered Animal Models?

scientific article published on 08 August 2019

Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor

scientific article published on 06 April 2020

Mutations in HTRA2 are not a common cause of familial classic ET.

artículo científico publicado en 2015

Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family

artículo científico publicado en 2015

Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features

artículo científico publicado en 2011

Progress of Pharmacological Approaches in Parkinson's Disease

artículo científico publicado en 2019

RAB39B mutations are a rare finding in Parkinson disease patients

artículo científico publicado en 2015

Rare Variants in Specific Lysosomal Genes Are Associated with Parkinson's Disease

scientific article published on 08 April 2020

Rare variants in ANO3 are not a susceptibility factor in essential tremor

artículo científico publicado en 2013

Rest tremor revisited: Parkinson's disease and other disorders.

artículo científico publicado en 2017

Serum neuronal exosomes predict and differentiate Parkinson's disease from atypical parkinsonism

scientific article published on 09 April 2020

Testing for alcohol sensitivity of tremor amplitude in a large cohort with essential tremor.

artículo científico publicado en 2015

The Co-Occurrence of Tricho-Rhino-Phalangeal Syndrome and Early-Onset Levodopa-Sensitive Parkinsonism

artículo científico publicado en 2014

The etiology of essential tremor: Genes versus environment.

artículo científico publicado en 2017

The impact of rare variants in FUS in essential tremor

artículo científico publicado en 2015

Topography of essential tremor.

artículo científico publicado en 2017

Use of β2-adrenoreceptor agonist and antagonist drugs and risk of Parkinson disease

artículo científico publicado en 2019

β-adrenoreceptors and the risk of Parkinson's disease

scientific article published on 27 January 2020

Lista de obras de

ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.

Biomarkers of Parkinson's disease: 20 years later

Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis

Early- and late-onset essential tremor patients represent clinically distinct subgroups

Examination of Patients with Essential Tremor

Four-repeat tauopathies

Genetics of tremor

Genome-wide association study in essential tremor identifies three new loci

Gut microbiota in Parkinson disease in a northern German cohort.

HTLV-1 associated myelopathy after renal transplantation

Is essential tremor a single entity?

Mobility Deficits Assessed With Mobile Technology: What Can We Learn From Brain Iron-Altered Animal Models?

Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor

Mutations in HTRA2 are not a common cause of familial classic ET.

Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family

Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features

Progress of Pharmacological Approaches in Parkinson's Disease

RAB39B mutations are a rare finding in Parkinson disease patients

Rare Variants in Specific Lysosomal Genes Are Associated with Parkinson's Disease

Rare variants in ANO3 are not a susceptibility factor in essential tremor

Rest tremor revisited: Parkinson's disease and other disorders.

Serum neuronal exosomes predict and differentiate Parkinson's disease from atypical parkinsonism

Testing for alcohol sensitivity of tremor amplitude in a large cohort with essential tremor.

The Co-Occurrence of Tricho-Rhino-Phalangeal Syndrome and Early-Onset Levodopa-Sensitive Parkinsonism

The etiology of essential tremor: Genes versus environment.

The impact of rare variants in FUS in essential tremor

Topography of essential tremor.

Use of β2-adrenoreceptor agonist and antagonist drugs and risk of Parkinson disease

β-adrenoreceptors and the risk of Parkinson's disease