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1. Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline. (25th October 2013)

2. De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. Issue 2 (8th July 2009)

3. Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factor. (23rd April 2015)