Maegaki Yoshihiro | Division Of Child Neurology Department Of Brain And Neurosciences Faculty Of Medicine Tottori University

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概要

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著作論文

Underlying neurologic disorders and recurrence rates of status epilepticus in childhood
Lower brainstem dysfunction in an infant with persistent primitive trigeminal artery
Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin : A new syndrome?
Intracraninal calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report
Sensorineural deafness in siblings with adenosine deaminase deficiency
Associated factors in neonatal hypoglycemic brain injury
Late-onset, unusual neurological symptoms in children with mycoplasma infection
Bilateral middle cerebral artery infarctions following mild varicella infection : A case report
Transient encephalopathy with reversible white matter lesions : A case report
Laminar cortical necrosis in adrenal crisis : Sequential changes on MRI
Congenital ocular motor apraxia : Clinical and neuroradiological findings, and long-term intellectual prognosis
A patient with simplified gyral pattern followed by progressive brain atrophy
Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy
Delayed neuropsychiatric syndrome in a child following carbon monoxide poisoning
Acute encephalitis with refractory, repetitive partial seizures : Case reports of this unusual post-encephalitic epilepsy
Forced mouth opening reaction : A primitive reflex released from cortical inhibition
Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter
Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
Reappearance of visual and somatosensory evoked potentials in a patient with childhood adrenoleukodystrophy after bone marrow transplantation and dietary erucic acid therapy
Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
Sequential neuroradiological and neurophysiological studies in a Japanese girl with merosin-deficient congenital muscular dystrophy
A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish

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