スポンサーリンク
Department Of Child Neurology National Center Hospital For Mental Nervous And Disorders National Cen | 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 early-infantile epileptic encephalopathy with suppression-bursts associated with focal cortical dysplasia
- Surgical Treatment of a Case of Early Infantile Epileptic Encephalopathy with Suppression-Bursts Associated with Focal Cortical Dysplasia
- Tremor and seizures associated with chronic manganese intoxication
- Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy
- A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
- Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
- 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
- Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
- A case of intraneural perineurioma presenting with monomelic atrophy in a child
- Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy
- Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome
- CD4^+ CD25^ regulatory T cell in childhood ocular myasthenia gravis
- Effects of low-dose hydrochlorothiazide on urolithiasis and bone metabolism in severely disabled individuals : A pilot study
- Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
- Decreased resting energy expenditure in patients with Duchenne muscular dystrophy
- A case of congenital axonal neuropathy associated with West syndrome