F-waves in neonates : increased spinal anterior horn motor neuron excitability
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-01-01
著者
-
Yasumoto Sawa
Department of Pediatrics, Faculty of Medicine, Fukuoka University
-
Yasumoto Sawa
Department Of Pediatrics Faculty Of Medicine Fukuoka University
-
Yasumoto Sawa
Department Of Pediatrics School Of Medicine Fukuoka University
-
MITSUDOME Akihisa
Department of Pediatrics, School of Medicine, Fukuoka University
-
Mitsudome Akihisa
Department Of Pediatrics School Of Medicine Fukuoka University
関連論文
- 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)
- II F10 A case of parietal lobe epilepsy with ictal smile
- Ictal Midline Epileptiform Discharges in Benign Familial Neonatal Convulsions
- Genetics of Idiopathic Epilepsies
- The genetics of febrile seizures and related epilepsy syndromes
- 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
- Japanese monozygotic twins with Rett syndrome
- F-waves in neonates : increased spinal anterior horn motor neuron excitability
- Symptomatic Chiari Malformation and Associated Pathophysiology in Pediatric and Adult Patients without Myelodysplasia
- 術後口蓋裂児における裂型によることばの発達の差異
- Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome
- Effect of aging on autonomic function in individuals with severe motor and intellectual disabilities
- Developmental changes in KCNQ2 and KCNQ3 expression in human brain : Possible contribution to the age-dependent etiology of benign familial neonatal convulsions
- Application of rapid random stimulation (RRS) to visual evoked potentials in children
- X-Linked mental retardation and epilepsy : pathogenetic significance of ARX mutations
- Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan
- Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies
- Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication