UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Validation of enhanced kinect sensor based motion capturing for gait assessment

PloS one, 2017-04, Vol.12 (4), p.e0175813-e0175813

2017

Volltextzugriff (PDF)

Cerebellar tDCS Does Not Improve Learning in a Complex Whole Body Dynamic Balance Task in Young Healthy Subjects

PloS one, 2016-09, Vol.11 (9), p.e0163598-e0163598

2016

Volltextzugriff (PDF)

Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity

Movement disorders, 2016-12, Vol.31 (12), p.1891-1900

2016

Volltextzugriff (PDF)

Long-term effects of coordinative training in degenerative cerebellar disease

Movement disorders, 2010-10, Vol.25 (13), p.2239-2246

2010

Volltextzugriff (PDF)

Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: A rater-blinded, intra-individually controlled trial

Parkinsonism & related disorders, 2017-06, Vol.39, p.80-84

2017

Volltextzugriff (PDF)

The SSTeP-KiZ System-Secure Real-Time Communication Based on Open Web Standards for Multimodal Sensor-Assisted Tele-Psychotherapy

Sensors (Basel, Switzerland), 2022-12, Vol.22 (24), p.9589

2022

Volltextzugriff (PDF)

Spatiotemporal tuning of the facilitation of biological motion perception by concurrent motor execution

The Journal of neuroscience, 2011-03, Vol.31 (9), p.3493-3499

2011

Volltextzugriff (PDF)

Interacting Learning Processes during Skill Acquisition: Learning to control with gradually changing system dynamics

Scientific reports, 2017-10, Vol.7 (1), p.13191-13, Article 13191

2017

Volltextzugriff (PDF)

Dysfunctional neuro-muscular mechanisms explain gradual gait changes in prodromal spastic paraplegia

Journal of neuroengineering and rehabilitation, 2023-07, Vol.20 (1), p.90-90, Article 90

2023

Volltextzugriff (PDF)

Predicting Perturbed Human Arm Movements in a Neuro-Musculoskeletal Model to Investigate the Muscular Force Response

Frontiers in bioengineering and biotechnology, 2020-04, Vol.8, p.308-308

2020

Volltextzugriff (PDF)

Motor expertise facilitates the accuracy of state extrapolation in perception

PloS one, 2017-11, Vol.12 (11), p.e0187666-e0187666

2017

Volltextzugriff (PDF)

Multifeature quantitative motor assessment of upper limb ataxia including drawing and reaching

Annals of clinical and translational neurology, 2024-05, Vol.11 (5), p.1097-1109

2024

Volltextzugriff (PDF)

Gait ataxia-specific cerebellar influences and their rehabilitation

Movement disorders, 2013-09, Vol.28 (11), p.1566-1575

2013

Volltextzugriff (PDF)

4-Aminopyridine improves real-life gait performance in SCA27B on a single-subject level: a prospective n-of-1 treatment experience

Journal of neurology, 2023-11, Vol.270 (11), p.5629-5634

2023

Volltextzugriff (PDF)

Real-life gait assessment in degenerative cerebellar ataxia: Toward ecologically valid biomarkers

Neurology, 2020-09, Vol.95 (9)

2020

Volltextzugriff (PDF)

Reduced Age‐Dependent Penetrance of a Large FGF14 GAA Repeat Expansion in a 74‐Year‐Old Woman from a German Family with SCA27B

Movement disorders, 2024-07

2024

Volltextzugriff (PDF)

Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia

Movement disorders, 2022-05, Vol.37 (5), p.1047-1058

2022

Volltextzugriff (PDF)

Video game-based coordinative training improves ataxia in children with degenerative ataxia

Neurology, 2012-11, Vol.79 (20), p.2056-2060

2012

Volltextzugriff (PDF)

Digital Gait Biomarkers Allow to Capture 1‐Year Longitudinal Change in Spinocerebellar Ataxia Type 3

Movement disorders, 2022-11, Vol.37 (11), p.2295-2301

2022

Volltextzugriff (PDF)

Digital Gait Outcomes for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Discriminative, Convergent, and Ecological Validity in a Multicenter Study (PROSPAX)

Movement disorders, 2024-06

2024

Volltextzugriff (PDF)

Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity

Movement disorders, 2016-12, Vol.31 (12), p.1891-1900

2016

Volltextzugriff (PDF)

Specific influences of cerebellar dysfunctions on gait

Brain (London, England : 1878), 2007-03, Vol.130 (3), p.786-798

2007

Volltextzugriff (PDF)

Digital Gait Measures Capture 1‐Year Progression in Early‐Stage Spinocerebellar Ataxia Type 2

Movement disorders, 2024-05, Vol.39 (5), p.788-797

2024

Volltextzugriff (PDF)

CNS-associated T-lymphocytes in a mouse model of Hereditary Spastic Paraplegia type 11 (SPG11) are therapeutic targets for established immunomodulators

Experimental neurology, 2022-09, Vol.355, p.114119-114119, Article 114119

2022

Volltextzugriff (PDF)

Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3

Brain (London, England : 1878), 2023-10, Vol.146 (10), p.4132-4143

2023

Volltextzugriff (PDF)

1 – 25 von 69

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(63)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(47)
Life Sciences & Biomedicine
(32)
Neurosciences & Neurology
(30)
Humans
(22)
Clinical Neurology
(20)
Neurosciences
(20)
Male
(15)
Ataxia
(13)
Cerebellum
(13)
Female
(13)
Neurology
(13)
Adult
(12)
Cerebellar Ataxia
(12)
Technology
(12)
Gait
(11)
Middle Aged
(9)
Movement Disorders
(8)
Psychomotor Performance - Physiology
(8)
Young Adult
(8)
Adolescent
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Movement Disorders
(11)
Cerebellum
(4)
Angewandte Chemie
(3)
Neurology
(3)
Plos One
(3)
Annals Of Clinical And Translational Neurology
(2)
Brain
(2)
Journal Of Neurology
(2)
Robotics And Autonomous Systems
(2)
The Journal Of Neuroscience
(2)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Validation of enhanced kinect sensor based motion capturing for gait assessment

Cerebellar tDCS Does Not Improve Learning in a Complex Whole Body Dynamic Balance Task in Young Healthy Subjects

Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity

Long-term effects of coordinative training in degenerative cerebellar disease

Individualized exergame training improves postural control in advanced degenerative spinocerebellar ataxia: A rater-blinded, intra-individually controlled trial

The SSTeP-KiZ System-Secure Real-Time Communication Based on Open Web Standards for Multimodal Sensor-Assisted Tele-Psychotherapy

Spatiotemporal tuning of the facilitation of biological motion perception by concurrent motor execution

Interacting Learning Processes during Skill Acquisition: Learning to control with gradually changing system dynamics

Dysfunctional neuro-muscular mechanisms explain gradual gait changes in prodromal spastic paraplegia

Predicting Perturbed Human Arm Movements in a Neuro-Musculoskeletal Model to Investigate the Muscular Force Response

Motor expertise facilitates the accuracy of state extrapolation in perception

Multifeature quantitative motor assessment of upper limb ataxia including drawing and reaching

Gait ataxia-specific cerebellar influences and their rehabilitation

4-Aminopyridine improves real-life gait performance in SCA27B on a single-subject level: a prospective n-of-1 treatment experience

Real-life gait assessment in degenerative cerebellar ataxia: Toward ecologically valid biomarkers

Reduced Age‐Dependent Penetrance of a Large FGF14 GAA Repeat Expansion in a 74‐Year‐Old Woman from a German Family with SCA27B

Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia

Video game-based coordinative training improves ataxia in children with degenerative ataxia

Digital Gait Biomarkers Allow to Capture 1‐Year Longitudinal Change in Spinocerebellar Ataxia Type 3

Digital Gait Outcomes for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Discriminative, Convergent, and Ecological Validity in a Multicenter Study (PROSPAX)

Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity

Specific influences of cerebellar dysfunctions on gait

Digital Gait Measures Capture 1‐Year Progression in Early‐Stage Spinocerebellar Ataxia Type 2

CNS-associated T-lymphocytes in a mouse model of Hereditary Spastic Paraplegia type 11 (SPG11) are therapeutic targets for established immunomodulators

Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3

Suchergebnisse filtern