HAYASHI Masaharu | Department of Brain Development and Neural Regeneration, Tokyo Metropolitan Institute of Medical Science

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著作論文

Peculiar form of cerebral microdysgenesis characterized by white matter neurons with perineuronal and perivascular glial satellitosis: A study using a variety of human autopsied brains
Immunohistological study of globoid cell leukodystrophy
Neurodegenerative features in developmental brain disorders
Immunohistochemical analysis of brainstem lesions in infantile spasms
Neurodegeneration in hereditary nucleotide repair disorders
Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosis
Dissociative brain stem lesions in cephalothoracopagus twins
Analysis of the hypothalamus in a case of X-linked lissencephaly with abnormal genitalia (XLAG)
Pathological study of bronchospasms/tracheomalasia in patients with severe motor and intellectual disabilities
Thalamic lesions in a long-surviving child with spinal muscular atrophy type I : MRI and EEG findings
重症心身障害児(者)における気管動脈瘻出血についての検討
An autopsy case of caudate nucleus lobulation accompanied with diaphragmatic eventration
Laryngeal dystonia in a case of severe motor and intellectual disabilities due to Japanese encephalitis sequelae
Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survival
Neurofibrillary tangles and deposition of oxidative products in the brain in cases of myotonic dystrophy
Arthrogryposis multiplex congenita with callosal agenesis and dentato-olivary dysplasia
Zonisamide eradicated paroxysmal headache with EEG abnormalities triggered by hypertensive encephalopathy due to purpura nephritic syndrome
Protracted juvenile neuronal ceroid lipofuscinosis : An autopsy report and immunohistochemical analysis
Neuropathological analysis of the brainstem and cerebral cortex lesions on epileptogenesis in hereditary dentatorubral-pallidoluysian atrophy
Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome
Sleep development in children with congenital and acquired hypothyroidism
An autopsy case presenting repetitive hypoglycemia and unique cortical dysplasia
Bilirubin encephalopathy : A study of neuronal subpopulations and neurodegenerative mechanisms in 12 autopsy cases
Hypoglossal hypoplasia and hyperplasia of the area postrema following perinatal hypoxic brain damage
Is developmental neuropathology of the motor neurons the key to resolving the mystery in motor neuron diseases?
Oxidative stress in developmental brain disorders
Effect of dietary Lorenzo's oil and docosahexaenoic acid treatment for Zellweger syndrome
Low-dose levodopa is effective for laryngeal dystonia in xeroderma pigmentosum group A
The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusion
Oxidative stress as a biomarker of respiratory disturbance in patients with severe motor and intellectual disabilities
Idiopathic torsion bystonia and writing tremor within a family
Systemic growth hormone corrects sleep disturbance in Smith-Magenis syndrome
An 11-year-old boy showing rapid psychomotor regression and diffuse cerebral white matter lesions
A 5-year-old girl with muscle atrophy lacking motor developments after spontaneous sitting
Severe gastrointestinal dysmotility in a patient with congenital myopathy : causal relationship to decrease of interstitial cells of Cajal
Neuropathology of the limbic system and brainstem in West syndrome
The pedunculopontine nucleus in developmental disorders of the basal ganglia
Oxidative stress in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS)
Lesions of cortical GABAergic interneurons and acetylcholine neurons in xeroderma pigmentosum group A
Focal encephalopathy with recurrent episodes of epileptic status and cluster mimicking hemiconvulsion-hemiplegia-epilepsy syndrome
Oxidative stress markers and phosphorus magnetic resonance spectroscopy in a patient with GLUT1 deficiency treated with modified Atkins diet
Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination
Lesions in the central tegmental tract in autopsy cases of developmental brain disorders

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