Katrin S. Lindenberg

Ulm, BW 89081, Germany

Last Updated: 09/26/2026

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Found 17 publications

Challenging or less challenging oral diadochokinetic tasks-what works best in Huntington disease? A cross-sectional study.

Challenging or less challenging oral diadochokinetic tasks-what works best in Huntington disease? A cross-sectional study.

Journal: Journal of neurology
Published: June 07, 2025

General loss of proteostasis links Huntington disease to Cockayne syndrome.

General loss of proteostasis links Huntington disease to Cockayne syndrome.

Journal: Neurobiology of disease
Published: April 29, 2024

Establishing normative data for the evaluation of cognitive performance in Huntington's disease considering the impact of gender, age, language, and education.

Establishing normative data for the evaluation of cognitive performance in Huntington's disease considering the impact of gender, age, language, and education.

Journal: Journal of neurology
Published: February 03, 2023

Speech biomarkers in Huntington's disease: A cross-sectional study in pre-symptomatic, prodromal and early manifest stages.

Speech biomarkers in Huntington's disease: A cross-sectional study in pre-symptomatic, prodromal and early manifest stages.

Journal: European journal of neurology
Published: December 07, 2022

Disease-modifying treatment approaches in Huntington disease : Past and future

Disease-modifying treatment approaches in Huntington disease : Past and future

Journal: Der Nervenarzt
Published: October 06, 2021

HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease.

HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease.

Journal: Neurobiology of disease
Published: February 08, 2021

Monitoring the Motor Phenotype in Huntington's Disease by Analysis of Keyboard Typing During Real Life Computer Use.

Monitoring the Motor Phenotype in Huntington's Disease by Analysis of Keyboard Typing During Real Life Computer Use.

Journal: Journal of Huntington's disease
Published: January 18, 2021

Gene-selective treatment approaches for Huntington's disease

Gene-selective treatment approaches for Huntington's disease

Journal: Der Nervenarzt
Published: March 18, 2020

Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models.

Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models.

Journal: Frontiers in molecular neuroscience
Published: February 06, 2017

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function.

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function.

Journal: PloS one
Published: December 20, 2016

Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease.

Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease.

Journal: PloS one
Published: June 30, 2016

ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues.

ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues.

Journal: Neurobiology of disease
Published: May 12, 2016
Showing 1-12 of 17

Last Updated: 09/26/2026