Dravet syndrome (severe myoclonic epilepsy in infancy)
C Dravet, H Oguni�- Handbook of clinical neurology, 2013 - Elsevier
Severe myoclonic epilepsy in infancy (SMEI) is a rare disease, characterized by febrile and
afebrile, generalized and unilateral, clonic or tonic–clonic seizures that occur in the first year�…
afebrile, generalized and unilateral, clonic or tonic–clonic seizures that occur in the first year�…
Dravet syndrome (severe myoclonic epilepsy in infancy)
C Dravet, H Oguni�- Handbook of clinical neurology, 2013 - pubmed.ncbi.nlm.nih.gov
Severe myoclonic epilepsy in infancy (SMEI) is a rare disease, characterized by febrile and
afebrile, generalized and unilateral, clonic or tonic-clonic seizures that occur in the first year�…
afebrile, generalized and unilateral, clonic or tonic-clonic seizures that occur in the first year�…
Dravet syndrome (severe myoclonic epilepsy in infancy).
C Dravet, H Oguni�- Handbook of Clinical Neurology, 2013 - europepmc.org
Severe myoclonic epilepsy in infancy (SMEI) is a rare disease, characterized by febrile and
afebrile, generalized and unilateral, clonic or tonic-clonic seizures that occur in the first year�…
afebrile, generalized and unilateral, clonic or tonic-clonic seizures that occur in the first year�…
[CITATION][C] Dravet syndrome (severe myoclonic epilepsy in infancy)
C Dravet, H Oguni�- Handbook of Clinical Neurology, 2013 - cir.nii.ac.jp