E. R. Brunt
University Medical Center Groningen(NL)University of Groningen(NL)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological disorders and treatments, Parkinson's Disease Mechanisms and Treatments, DNA Repair Mechanisms
Most-Cited Works
- → Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome(2001)992 cited
- → Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1(1994)775 cited
- → Brain pathology of spinocerebellar ataxias(2012)405 cited
- → Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions(2012)262 cited
- → Spinocerebellar ataxias in the Netherlands(2002)254 cited
- → Polarised Asymmetric Inheritance of Accumulated Protein Damage in Higher Eukaryotes(2006)244 cited
- → New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado–Joseph disease)