Lista de obras -

Accuracy and Reliability of the Kinect Version 2 for Clinical Measurement of Motor Function.

artículo científico publicado en 2016

Accuracy and repeatability of two methods of gait analysis - GaitRite™ und Mobility Lab™ - in subjects with cerebellar ataxia

artículo científico publicado en 2016

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

scholarly article by Daniela Berg et al published 2005 in Movement Disorders

Altered Coupling of Psychological Relaxation and Regional Volume of Brain Reward Areas in Multiple Sclerosis

artículo científico publicado en 2020

An update on inherited ataxias

artículo científico publicado en 2008

Association Between Fatigue and Motor Exertion in Patients With Multiple Sclerosis-a Prospective Study

artículo científico publicado en 2020

Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression

Brain networks modulated by subthalamic nucleus deep brain stimulation.

artículo científico publicado en 2016

Bright light therapy in Parkinson's disease: a pilot study

artículo científico publicado en 2007

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency

artículo científico publicado en 2015

Clozapine: acquittal of the usual suspect

artículo científico publicado en 2009

Comparison of three clinical rating scales in Friedreich ataxia (FRDA).

artículo científico publicado en 2009

Connectivity Predicts deep brain stimulation outcome in Parkinson disease

artículo científico publicado en 2017

Depression comorbidity in spinocerebellar ataxia

artículo científico publicado en 2011

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

artículo científico publicado en 2008

Effects of subthalamic nucleus deep brain stimulation on emotional working memory capacity and mood in patients with Parkinson's disease

artículo científico publicado en 2017

Falls in spinocerebellar ataxias: Results of the EuroSCA Fall Study

artículo científico publicado en 2010

Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1

artículo científico publicado en 2020

Instability of syllable repetition in patients with spinocerebellar ataxia and Parkinson's disease

scientific article published on 22 November 2011

Instrumental Assessment of Stepping in Place Captures Clinically Relevant Motor Symptoms of Parkinson's Disease

scientific article published on 23 September 2020

Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14

scientific article published on 27 April 2020

Less Is More - Estimation of the Number of Strides Required to Assess Gait Variability in Spatially Confined Settings

article by Daniel Kroneberg et al published 2018 in Frontiers in Aging Neuroscience

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

artículo científico publicado en 2015

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias

MRI Markers and Functional Performance in Patients With CIS and MS: A Cross-Sectional Study

Maximum walking speed in multiple sclerosis assessed with visual perceptive computing

artículo científico publicado en 2017

Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1

artículo científico publicado en 2020

Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.

artículo científico publicado en 2010

Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6.

artículo científico publicado en 2015

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.

artículo científico publicado en 2014

Ranking of Dystonia Severity by Pairwise Video Comparison

artículo científico publicado en 2016

Rationale and design of the prevention of paclitaxel-related neurological side effects with lithium trial – Protocol of a multicenter, randomized, double-blind, placebo- controlled proof-of-concept phase-2 clinical trial

artículo científico publicado en 2022

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients

artículo científico publicado en 2006

Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients

artículo científico publicado en 2007

Self-rated health status in spinocerebellar ataxia--results from a European multicenter study

artículo científico publicado en 2010

Spinal cord lesions and atrophy in NMOSD with AQP4-IgG and MOG-IgG associated autoimmunity

artículo científico publicado en 2018

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds

artículo científico publicado en 2010

Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features

artículo científico publicado en 2011

Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings

artículo científico publicado en 2012

Subjective and objective assessment of physical activity in multiple sclerosis and their relation to health-related quality of life

artículo científico publicado en 2017

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study

artículo científico publicado en 2018

Validity of visual perceptive computing for static posturography in patients with multiple sclerosis

artículo científico publicado en 2016

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

artículo científico publicado en 2009

Lista de obras de

Accuracy and Reliability of the Kinect Version 2 for Clinical Measurement of Motor Function.

Accuracy and repeatability of two methods of gait analysis - GaitRite™ und Mobility Lab™ - in subjects with cerebellar ataxia

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

Altered Coupling of Psychological Relaxation and Regional Volume of Brain Reward Areas in Multiple Sclerosis

An update on inherited ataxias

Association Between Fatigue and Motor Exertion in Patients With Multiple Sclerosis-a Prospective Study

Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression

Brain networks modulated by subthalamic nucleus deep brain stimulation.

Bright light therapy in Parkinson's disease: a pilot study

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency

Clozapine: acquittal of the usual suspect

Comparison of three clinical rating scales in Friedreich ataxia (FRDA).

Connectivity Predicts deep brain stimulation outcome in Parkinson disease

Depression comorbidity in spinocerebellar ataxia

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

Effects of subthalamic nucleus deep brain stimulation on emotional working memory capacity and mood in patients with Parkinson's disease

Falls in spinocerebellar ataxias: Results of the EuroSCA Fall Study

Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1

Instability of syllable repetition in patients with spinocerebellar ataxia and Parkinson's disease

Instrumental Assessment of Stepping in Place Captures Clinically Relevant Motor Symptoms of Parkinson's Disease

Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14

Less Is More - Estimation of the Number of Strides Required to Assess Gait Variability in Spatially Confined Settings

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias

MRI Markers and Functional Performance in Patients With CIS and MS: A Cross-Sectional Study

Maximum walking speed in multiple sclerosis assessed with visual perceptive computing

Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1

Neuropsychological features of patients with spinocerebellar ataxia (SCA) types 1, 2, 3, and 6.

Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6.

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6.

Ranking of Dystonia Severity by Pairwise Video Comparison

Rationale and design of the prevention of paclitaxel-related neurological side effects with lithium trial – Protocol of a multicenter, randomized, double-blind, placebo- controlled proof-of-concept phase-2 clinical trial

Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients

Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients

Self-rated health status in spinocerebellar ataxia--results from a European multicenter study

Spinal cord lesions and atrophy in NMOSD with AQP4-IgG and MOG-IgG associated autoimmunity

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds

Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features

Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings

Subjective and objective assessment of physical activity in multiple sclerosis and their relation to health-related quality of life

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study

Validity of visual perceptive computing for static posturography in patients with multiple sclerosis

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.