Saito Kayoko | Department Of Neuropsychiatry School Of Medicine Hirosaki University

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著作論文

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
Mutation screening of AP3M2 in Japanese epilepsy patients
Genetics of Idiopathic Epilepsies
The genetics of febrile seizures and related epilepsy syndromes
IV D6 How SCN1A mutations contribute to Dravet syndrome : a comparison of clinical and EEG features between Dravet syndrome with and without SCN1A mutations
Genetics of epilepsy : current status and perspectives
Molecular Genetics of Human Familial Epilepsy Syndromes
Genetic abnormalities underlying familial epilepsy syndromes
Electroclinical Picture of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Japanese Family
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
Co-localization of β-peptide and phosphorylated tau in astrocytes in a patient with corticobasal degeneration
Surgical Indication for Refractory Childhood Epilepsy
Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy
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
Study on surgical treatment of intractable childhood epilepsy
Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus
Thalamic lesions in a long-surviving child with spinal muscular atrophy type I : MRI and EEG findings
A 1-year-old infant with McArdle disease associated with hyper-creatine kinase-emia during febrile episodes
Creatine monohydrate therapy in a Leigh syndrome patient with A8344G mutation
Beta-Blocker Therapy for Cardiac Dysfunction in Patients With Muscular Dystrophy
Polymorphism analysis of Fukuyama type congenital muscular dystrophy(FCMD) siblings with different phenotypes
Bibliography of congenital muscular dystrophies : Series V (2001)
Benign Familial Infantile Convulsions : Linkage to Chromosome 16p12-q12 in 14 Families
Positive association between benign familial infantile convulsions and LGI4
Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
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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