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1. Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations. (14th March 2017)

2. Clinical dissection of early onset absence epilepsy in children and prognostic implications. Issue 10 (27th August 2013)

3. Coexistence of childhood absence epilepsy and benign epilepsy with centrotemporal spikes: A case series. (May 2017)

4. Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study. (19th November 2018)

7. Focal Cortical Dysplasia IIIa in Hippocampal Sclerosis-Associated Epilepsy: Anatomo-Electro-Clinical Profile and Surgical Results From a Multicentric Retrospective Study. (18th December 2021)

8. Focal Cortical Dysplasia IIIa in Hippocampal Sclerosis-Associated Epilepsy: Anatomo-Electro-Clinical Profile and Surgical Results From a Multicentric Retrospective Study. (18th November 2021)

9. Focal Cortical Dysplasia IIIa in Hippocampal Sclerosis-Associated Epilepsy: Anatomo-Electro-Clinical Profile and Surgical Results From a Multicentric Retrospective Study. (18th November 2021)

10. Focal Cortical Dysplasia IIIa in Hippocampal Sclerosis-Associated Epilepsy: Anatomo-Electro-Clinical Profile and Surgical Results From a Multicentric Retrospective Study. Issue 2 (13th January 2021)