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Departments Of Child Neurology National Center Hospital For Neurology And Psychiatry National Center | 論文
- Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms
- Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
- Surgical Treatment of a Case of Early Infantile Epileptic Encephalopathy with Suppression-Bursts Associated with Focal Cortical Dysplasia
- Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria
- Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability : Coexistence of auditory neuropathy and cochlear hearing loss
- Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
- II C12 Treatment of intractable epilepsies with supratherapeutic levels of phenobarbital
- Mechanical ventilation care in severe childhood neurological disorders
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
- A severely brain-damaged case of 3-hydroxyisobutyric aciduria
- Paroxysmal discharges on EEG in young autistic patients are frequent in frontal regions
- Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings
- Otoacoustic emission in patients with neurological disorders who have auditory brainstem response abnormality
- Transient seizure disappearance due to bilateral striatal necrosis in a patient with intractable epilepsy
- Characteristics of Bacillus subtilis Isolated from Composts Suppressing Phytopathogenic Microorganisms
- Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications
- Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
- Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children
- Postnatal evolution of cortical malformation in the "non-affected" hemisphere of hemimegalencephaly
- Hemifacial seizures due to ganglioglioma of cerebellum