Sinem Tunc

Ratzeburger Allee 160
Luebeck, SH 23538, Germany

Last Updated: 09/26/2026

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Found 25 publications

POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the Literature.

POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the Literature.

Journal: Cerebellum (London, England)
Published: April 05, 2023

In Vivo Investigation of Glucose Metabolism in Idiopathic and PRKN-Related Parkinson's Disease.

In Vivo Investigation of Glucose Metabolism in Idiopathic and PRKN-Related Parkinson's Disease.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 18, 2022

Time estimation and arousal responses in dopa-responsive dystonia.

Time estimation and arousal responses in dopa-responsive dystonia.

Journal: Scientific reports
Published: November 23, 2021

Atypical Parkinsonism with Pathological Dopamine Transporter Imaging in Neuronal Ceroid Lipofuscinosis Type 5.

Atypical Parkinsonism with Pathological Dopamine Transporter Imaging in Neuronal Ceroid Lipofuscinosis Type 5.

Journal: Movement disorders clinical practice
Published: November 20, 2021

Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias.

Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias.

Journal: Brain communications
Published: October 28, 2021

Altered homodimer formation and increased iron accumulation in VAC14-related disease: Case report and review of the literature.

Altered homodimer formation and increased iron accumulation in VAC14-related disease: Case report and review of the literature.

Journal: Parkinsonism & related disorders
Published: May 31, 2020

Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity.

Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity.

Journal: Movement disorders clinical practice
Published: March 05, 2020

"Twitching" and Stiffness in POLG1 Mutation Carriers: Red Flag or Red Herring?

"Twitching" and Stiffness in POLG1 Mutation Carriers: Red Flag or Red Herring?

Journal: Movement disorders clinical practice
Published: July 16, 2019

Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia--A neurophysiology study.

Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia--A neurophysiology study.

Journal: NeuroImage. Clinical
Published: July 04, 2019

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.

Journal: Cerebellum (London, England)
Published: May 22, 2019

Temporal discrimination threshold and blink reflex recovery cycle in cervical dystonia - two sides of the same coin?

Temporal discrimination threshold and blink reflex recovery cycle in cervical dystonia - two sides of the same coin?

Journal: Parkinsonism & related disorders
Published: March 10, 2019

A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia.

A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia.

Journal: Journal of the neurological sciences
Published: October 12, 2018
Showing 1-12 of 25

Last Updated: 09/26/2026