Hirose Shinichi | Department Of Pediatrics School Of Medicine Fukuoka University

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著作論文

A Case of West Syndrome Associated with Neonatal Hypoglycemic Brain Injury
最近15年間に当科で経験した乳児脳腫瘍の予後と晩期障害
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
Ictal Midline Epileptiform Discharges in Benign Familial Neonatal Convulsions
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
IV B13 Sodium channel genes in patients following febrile seizures plus
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
The effectiveness of clonazepam on the Rolandic discharges
I-IMP SPECT findings in mitochondrial encephalomyopathies
Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome
Estimation of the relationship between caspase-3 expression and clinical outcome of Burkitt's and Burkitt-like lymphoma
High-grade mature B-cell lymphoma with Burkitt-like morphology : Results of a clinicopathological study of 72 Japanese patients
Developmental changes in KCNQ2 and KCNQ3 expression in human brain : Possible contribution to the age-dependent etiology of benign familial neonatal convulsions
Phenotype for activated tissue macrophages in histiocytic necrotizing lymphadenitis
Histological characteristics of 21 Papua New Guinean children with high-grade B-cell lymphoma, which is frequently associated with EBV infection
Estimation of apoptosis and cell proliferation in histiocytic necrotizing lymphadenitis using immunohistochemical double staining
Hepatocellular apoptosis associated with cytotoxic T/natural killer-cell infiltration in chronic active EBV infection
X-Linked mental retardation and epilepsy : pathogenetic significance of ARX mutations
Positive association between benign familial infantile convulsions and LGI4
Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan
Autosomal dominant nocturnal frontal lobe epilepsy : a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation
Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies

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