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You searched for: Author/Creator Howell, Katherine B.

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1. A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy. (11th May 2018)

3. Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions. Issue 1 (21st November 2013)

4. Complications of Influenza A or B Virus Infection in Individuals With SCN1A-Positive Dravet Syndrome. (24th January 2023)

5. Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome. (21st September 2020)

6. Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy. (8th November 2016)

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

9. Epileptic spasms are a feature of DEPDC5 mTORopathy. (August 2015)

10. Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice. (14th June 2022)