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You searched for: Author/Creator Bennett, Mark F.

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1. Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus. (4th May 2021)

2. Cutting edge approaches to detecting brain mosaicism associated with common focal epilepsies: implications for diagnosis and potential therapies. (2nd November 2021)

3. Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania. Issue 3 (22nd July 2019)

4. Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy. (25th February 2022)

5. Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy. (February 2022)

6. Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP. Issue 7 (18th May 2021)

8. Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting. Issue 12 (6th September 2022)

9. Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes. (6th December 2022)

10. SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy. (8th January 2019)