Jürgen Sperner
Publications by Year
Research Areas
Neurological disorders and treatments, Epilepsy research and treatment, Metabolism and Genetic Disorders, Vagus Nerve Stimulation Research, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes(2013)437 cited
- → Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation(2004)322 cited
- → Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood(2010)230 cited
- → A De Novo Mutation in the β-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum(2013)192 cited
- → Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia(2002)161 cited
- New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.(2002)
- → Operative and Technical Complications of Vagus Nerve Stimulator Implantation(2010)102 cited
- → Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region(2010)101 cited
- → FLIP&FLAP—A training programme for children and adolescents with epilepsy, and their parents(2009)88 cited
- → MR-Imaging Findings in Children with Sturge-Weber Syndrome(1990)60 cited