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2. A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Issue 4 (9th September 2016)

4. Assessing seizure burden in pediatric epilepsy using an electronic medical record–based tool through a common data element approach. (2nd June 2021)

6. Atypical Vitamin B6 Deficiency: A Rare Cause of Unexplained Neonatal and Infantile Epilepsies. (May 2014)

7. Biological concepts in human sodium channel epilepsies and their relevance in clinical practice. (23rd February 2020)

8. Broad Phenotypic Heterogeneity due to a Novel SCN1A Mutation in a Family With Genetic Epilepsy With Febrile Seizures Plus. (February 2014)

10. Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID‐19 pandemic. (16th September 2022)