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Current Treatment Strategies and Future Treatment Options for Dravet Syndrome

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Daniela Chieffo et al.

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Domenica Battaglia et al.

EPILEPSY RESEARCH (2016)

Article Clinical Neurology

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Monica S. Cooper et al.

EPILEPSY RESEARCH (2016)

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Adam Wallace et al.

PEDIATRIC DRUGS (2016)

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MOLECULAR GENETICS & GENOMIC MEDICINE (2016)

Article Pediatrics

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Yvonne W. Wu et al.

PEDIATRICS (2015)

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Linda Dalic et al.

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Andreas Brunklaus et al.

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Rima Nabbout et al.

ORPHANET JOURNAL OF RARE DISEASES (2013)

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Jill M. Rodda et al.

ARCHIVES OF NEUROLOGY (2012)

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Berten Ceulemans et al.

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Nicola Specchio et al.

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Ellen M. Welch et al.

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M Isaac

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L Claes et al.

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Topiramate in the treatment of severe myoclonic epilepsy in infancy

M Nieto-Barrera et al.

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