Valerija Dobričić
University of Lübeck(DE)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments, Neurological disorders and treatments, Neurological diseases and metabolism, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice(2013)326 cited
- → Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans(2017)60 cited
- → Metabolic syndrome in patients with myotonic dystrophy type 1(2014)43 cited
- → Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2(2014)37 cited
- → C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome(2014)36 cited
- Multidimensional aspects of pain in myotonic dystrophies.(2015)
- → Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients(2017)26 cited
- → Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited(2015)23 cited
- → Transcranial sonography in patients with myotonic dystrophy type 1(2014)19 cited
- → Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations(2013)18 cited