Acute encephalitis with refractory, repetitive partial seizures (AERRPS)
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-01-01
著者
-
OHNO Kousaku
Division of Child Neurology, Faculty of Medicine, Tottori University
-
Ohno K
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Ohno Kousaku
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Ohno K
Department Of Neurobiology School Of Life Sciences Faculty Of Medicine Tottori University
-
Ohno Kousaku
Division Of Child Neurology Faculty Of Medicine Tottori University
-
Okanishi Tohru
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
SAITO Yoshiaki
Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori Univer
-
Ohno Kousaku
Department Of Neurobiology School Of Life Sciences Tottori University Faculty Of Medicine
-
Saito Yoshiaki
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Ohno Kousaku
Department Of Pediatric Neurology School Of Life Sciences Tottori University Faculty Of Medicine
-
Ohno Kousaku
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Saito Yoshiaki
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Ohno Kousaku
Division Of Child Neurology Department Of Brain And Neurosciences Faculty Of Medicine Tottori Univer
関連論文
- Frontal behavioral syndromes in Prader-Willi syndrome
- A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI
- Underlying neurologic disorders and recurrence rates of status epilepticus in childhood
- Accumulation of cholesterol and G_ ganglioside in cells cultured in the presence of progesterone:an implication for the basic defect in Niemann-Pick disease typc C
- Increased levels of GM_2 ganglioside in fibroblasts from a patient with juvenile Niemann - Pick disease type C
- 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?
- Galactonojirimycin derivatives restore mutant human β-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse
- Antisense suppression of TSC1 gene product, hamartin, enhances neurite outgrowth in NGF-treated PC12h cells
- Increased NPC1 mRNA in skin fibroblasts from Niemann-Pick disease type C patients
- Structural basis of the GM2 gangliosidosis B variant
- Novel TSC1 and TSC2 mutations in Japanese patients with tuberous sclerosis complex
- Progressive neuronal loss in the ventral posterior lateral and medial nuclei of thalamus in Niemann-Pick disease type C mouse brain
- Isolation of NPC1-Deficient Chinese Hamster Ovary Cell Mutants by Gene Trap Mutagenesis^1
- Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome
- Disappearance of frontal N30 component of median nerve stimulated SSEPs in two young children with abnormal striatal lesions
- Molecular and structural studies of the GM2 gangliosidosis O variant
- A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
- Associated factors in neonatal hypoglycemic brain injury
- Late-onset, unusual neurological symptoms in children with mycoplasma infection
- Acute encephalitis with refractory, repetitive partial seizures (AERRPS)
- 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
- Protective Effect of Neurotropin Against Lipopolysaccharide-Induced Hypotension and Lethality Linked to Suppression of Inducible Nitric Oxide Synthase Induction
- Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter
- Frequency of the Prader-Willi syndrome in the San-in district, Japan
- Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis
- Carbohydrate-deficient glycoprotein syndrome : electrophoretic study of multiple serum glycoproteins
- Familial limb pain in childhood : Unusual manifestation of migraine?
- Permanent Cardiac Pacing Following Surgery for Acquired Valvular Disease
- Pontine hypoplasia in a child with sensorineural deafiness
- Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
- Apoptosis Involved in Density-dependent Regulation of Rat Fibroblastic 3Y1 CellCulture
- MOLECULAR EPIDEMIOLOGY OF TUBEROUS SCLEROSIS
- Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
- Effects of selective serotonin re-uptake inhibitors on behavior in Kluver-Bucy syndrome during childhood
- Down 症候群剖検1514例における良性および悪性腫瘍の検討
- Sequential neuroradiological and neurophysiological studies in a Japanese girl with merosin-deficient congenital muscular dystrophy
- The effect of N-octyl-β-valienamine on β-glucosidase activity in tissues of normal mice
- Kunihiko Suzuki and sphingolipidoses