Elisabeth Stögmann
Medical University of Vienna(AT)
Publications by Year
Research Areas
Dementia and Cognitive Impairment Research, Alzheimer's disease research and treatments, Genetic Associations and Epidemiology, Genomics and Rare Diseases, Epilepsy research and treatment
Most-Cited Works
- → Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A(2013)196 cited
- → Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy(2004)168 cited
- → A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy(2002)109 cited
- → Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2(2013)84 cited
- → Clinical Seizure Lateralization in Frontal Lobe Epilepsy(2007)77 cited
- → Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations(2006)70 cited
- → Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer’s Disease(2015)70 cited
- [Sex differences in Alzheimer's disease].(2008)
- → A novel mutation in the VCP gene (G157R) in a german family with inclusion‐body myopathy with paget disease of bone and frontotemporal dementia(2009)62 cited
- → Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder(2008)59 cited