Thora Lohnau
Ratzeburger Allee 160
Luebeck, SH 23538, Germany
Luebeck, SH 23538, Germany
Last Updated: 09/26/2026
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Found 9 publications
Ceramide accumulation induces mitophagy and impairs β-oxidation in PINK1 deficiency.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: September 14, 2021
The role of mutations in COL6A3 in isolated dystonia.
Journal: Journal of neurology
Published: November 24, 2015
Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency.
Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency.
Journal: The Journal of cell biology
Published: November 11, 2015
THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression.
Journal: Biochimica et biophysica acta
Published: May 11, 2014
Mutations in GNAL: a novel cause of craniocervical dystonia.
Journal: JAMA neurology
Published: February 19, 2014
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.
Journal: Journal of neurology
Published: July 18, 2013
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.
Journal: Annals of neurology
Published: September 19, 2012
Exome sequencing in a family with restless legs syndrome.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 28, 2012
Autosomal dominant Parkinson's disease in a large German pedigree.
Journal: Acta neurologica Scandinavica
Published: November 24, 2011
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Last Updated: 09/26/2026