Laryngeal dystonia in a case of severe motor and intellectual disabilities due to Japanese encephalitis sequelae
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-08-01
著者
-
HAYASHI Masaharu
Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neuroscience
-
KURATA Kiyoko
Department of Pediatrics Tokyo Metropolitan Fuchu Medical Center for Severely Handicapped
-
KUMADA Satoko
Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neuroscience
-
Kumada Satoko
Department Of Neuropediatrics Tokyo Metropolitan Neurological Hospital
-
濱野 喜美子
Department Of Pediatrics Tokyo Metropolitan Fuchu Medical Center For Disabled
-
HAMANO Kimiko
Department of Pediatrics, Metropolitan Fuchu Medical Center for Severe Motor and Intellectual Disabi
-
UCHIYAMA Akira
Department of Pediatrics, Metropolitan Fuchu Medical Center for Severe Motor and Intellectual Disabi
-
NAITO Rie
Department of Neurootology, Tokyo Metropolitan Neurological Hospital
-
HAYASHIDA Tetsuro
Department of Neurootology, Tokyo Metropolitan Neurological Hospital
-
Hayashi Masaharu
Department Of Clinical Neuropathology Tokyo Metropolitan Institute For Neuroscience
-
Naito Rie
Department Of Neuro-otology Tokyo Metropolitan Neurological Hospital
-
Naito Rie
Department Of Neurootology Tokyo Metropolitan Neurological Hospital
-
Kurata Kiyoko
Department Of Pediatrics Tokyo Metropolitan Fuchu Medical Center For The Disabled
-
Uchiyama Akira
Department Of Pediatrics Tokyo Metropolitan Fuchu Medical Center For Disabled
-
Uchiyama Akira
Department Of Gastroenterology Juntendo University Nerima Hospital
-
Hayashida Tetsuro
Department Of Neurootology Tokyo Metropolitan Neurological Hospital
-
HAYASHI Masaharu
Department of Brain Development and Neural Regeneration, Tokyo Metropolitan Institute of Medical Science
関連論文
- 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
- Oxidative stress and disturbed glutamate transport in spinal muscular atrophy
- II F9 A neuropathological study on the limbic system in dentatorubral-pallidoluysian atrophy
- 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
- Analysis of the influence of diurnal variation in maternal movements on fetal heart rate acceleration
- 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
- A Variant Form of Nasogastric Tube Syndrome
- 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
- Nine-year-old girl presenting familial occurrence of progressive developmental abnormalities with the white matter lesions
- 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
- Radiofrequency ablation of hepatocellular carcinoma : The feasibility of magnetic resonance imaging with gadolinium ethoxybenzyl diethylene triamine pentaacetic acid for evaluating the ablative margin
- 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
- Oxidative stress and disturbed glutamate transport in spinal muscular atrophy