Molecular pathology of human cerebral malformations
スポンサーリンク
概要
著者
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Mizuguchi Masashi
Department Of Pediatrics Jichi Medical School
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Mizuguchi Masashi
Department Of Developmental Medical Sciences Graduate School Of Medicine The University Of Tokyo
関連論文
- Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS method
- High concentration of serum nitrite/nitrate obtained from patients with influenza-associated encephalopathy
- Immunochemical and immunohistochemical localization of Bcl-x protein in the rat central nervous system
- A 2-year-old boy with hypoactivity of neonatal onset and profound developmental delay
- An 11-month-old girl with arrested psychomotor development and lactic acidosis
- Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus
- Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
- Developmental and aging changes in the expression of amyloid precursor protein in Down syndrome brains
- Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
- Delirious behavior in children with acute necrotizing encephalopathy
- NEUROLOGICAL ASPECTS OF TUBEROUS SCLEROSIS
- Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
- Transient cheiro-oral syndrome due to a ruptured intracranial dermoid cyst
- Acute disseminated encephalomyelitis after live rubella vaccination
- Ras シグナル伝達系の遺伝子変異による重複症候群の遺伝子解析
- Neuronal migration disorder: Expression of gene products in the neocortex
- Neuropathology of tuberous sclerosis
- Acute necrotizing encephalopathy : A comparison between influenza and non-influenza cases
- Imaging and pathology in pediatric neurological disorders
- Congenital infection-like syndrome with intracranial calcification
- Reply to the letter : "Arima syndrome and bilateral retinoblastoma in interstitial deletion of 13q14.13-q32.3" : Where is the molar tooth sign?
- Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma
- Differential development of the human cerebellar vermis: immunohistochemical and morphometrical evaluation
- Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases
- Acute necrotizing encephalopathy of childhood:a novel form of acute encephalopathy prevalent in Japan and Taiwan
- Molecular pathology of human cerebral malformations
- A 35-year-old female with growth and developmental retardation, progressive ataxia, dementia and visual loss
- Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1 : Is it useful?
- Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes