Okada M | Division Of Neuroscience Graduate School Of Medicine Mie University

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著作論文

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
Mutation screening of AP3M2 in Japanese epilepsy patients
Genetics of Idiopathic Epilepsies
The genetics of febrile seizures and related epilepsy syndromes
Genetics of epilepsy : current status and perspectives
Molecular Genetics of Human Familial Epilepsy Syndromes
Genetic abnormalities underlying familial epilepsy syndromes
IV D7 Reciprocal release profile between hippocampal monoamines and acetylcholine releases in a novel spontaneous epilepsy model, mu3B deficient mice
NS-5 Behavioral and electroencephalographical analysis of epileptogenesis in μ3B knockout mouse
NS-4 Epileptic seizure in mice deficient in μ3B subunit of AP-3B complex
Hyperactivity of Endoplasmic Reticulum Associated Exocytosis Mechanism Contributes to Acute Phencyclidine Intoxication
IV F3 Effects of carbamazepine on cAMP-dependent protein kinase related exocytosis
II F16 A case of familial paroxysmal hypnogenic dyskinesia and sick sinus syndrome with severe abnormality of potassium-conductance in peripheral nerve
II C22 Two-dimensional monitoring of effects of carbamazepine on propagation of neuronal excitability using multiple-electrode dish with high-speed fluorescence CCD system.
Impaired M-Current and Neuronal Excitability
Genetic Identifiers of Epilepsy
Different patterns of dipole source localization in gelastic seizure with or without a sense of mirth
Sociomedical aspects of epileptic patients : Their employment and marital status
Prognosis and clinical features of intractable epilepsy : A prospective study
Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies
Hyperpolarization-activated cyclic nucleotide gated channels: a potential molecular link between epileptic seizures and Aβ generation in Alzheimer's disease

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