Underlying neurologic disorders and recurrence rates of status epilepticus in childhood

スポンサーリンク

概要

• 論文の詳細を見る
• 2008-11-01

著者

• OHNO Kousaku

  Division of Child Neurology, Faculty of Medicine, Tottori University

• OKANISHI Tohru

  Department of Pediatrics, Seirei-Mikatahara Hospital

• TOGARI Hajime

  Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences

• Ohno Kousaku

  鳥取大学医学部附属脳幹性疾患研究施設 脳神経小児科

• 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

• MAEGAKI Yoshihiro

  Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori Univer

• 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

• Togari Hajime

  Department Of Pediatrics And Neonatology Nagoya City University Graduate School Of Medical Sciences

• Maegaki Yoshihiro

  Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit

• Ohno Kousaku

  Department Of Neurobiology School Of Life Sciences Tottori University Faculty Of Medicine

• Ohno Kousaku

  Department Of Pediatric Neurology School Of Life Sciences Tottori University Faculty Of Medicine

• Ohtani Kyoichi

  Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit

• Okanishi Tohru

  Department Of Pediatrics Seirei-mikatahara General Hospital

• Togari Hajime

  Department Of Pediatrics Neonatology And Congenital Disorders Nagoya City University Graduate School

• Ohno Kousaku

  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

• Maegaki Yoshihiro

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

• OKANISHI Tohru

  Department of Child Neurology, Seirei Hamamatsu General Hospital

• MAEGAKI Yoshihiro

  Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University

関連論文

• Frontal behavioral syndromes in Prader-Willi syndrome
• 早産児における急性期離脱後一過性循環不全と後期脳室周囲白質軟化症の関係
• 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?
• IL-10 and RANTES are Elevated in Nasopharyngeal Secretions of Children with Respiratory Syncytial Virus Infection
• High postnatal oxidative stress in neonatal cystic periventricular leukomalacia
• Prevalence and features of migraine in Japanese junior high school students aged 12-15yr
• Cardiac Vagal Activation by Adrenocorticotropic Hormone Treatment in Infants with West Syndrome
• Periventricular Leukomalacia with Late-Onset Circulatory Dysfunction of Premature Infants : Correlation with Severity of Magnetic Resonance Imaging Findings and Neurological Outcomes
• 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
• IS1-04 Oxidative stress subsides by time after living related liver transplantation in pediatric age(Liver and Biliary ductal system,Share Smiles with Sick Children, Dreams and Innovation for Pediatric Surgery)
• Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
• Disappearance of frontal N30 component of median nerve stimulated SSEPs in two young children with abnormal striatal lesions
• Intracraninal calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report
• Sensorineural deafness in siblings with adenosine deaminase deficiency
• 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
• Nitric oxide further attenuates pulmonary hypertension in magnesium-treated piglets
• Nitric oxide inhalation and nitric oxide synthase inhibitor supplement for endotoxin-induced hypotension
• A prospective clinical study on inhaled nitric oxide therapy for neonates in Japan
• Reduction in cerebral blood flow volume in infants complicated with hypoxic ischemic encephalopathy resulting in cerebral palsy
• Protective Effect of Neurotropin Against Lipopolysaccharide-Induced Hypotension and Lethality Linked to Suppression of Inducible Nitric Oxide Synthase Induction
• Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics
• Interleukin-1β induces the expression of lipocortin 1 mRNA in cultured rat cortical astrocytes
• Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency
• Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter
• Automated determination of 5-fluorouracil and its metabolite in urine by high-performance liquid chromatography with column switching
• Frequency of the Prader-Willi syndrome in the San-in district, Japan
• Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis
• Alteration of Ammonia and Carnitine Levels in Short-Term Treatment with Pivalic Acid-Containing Prodrug
• Hereditary Orotic Aciduria Heterozygotes Accompanied with Neurological Symptoms
• 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
• A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy
• Long follow up of betaine therapy in two Japanese siblings with cystathionine β-synthase deficiency
• Novel mutations in the cytochrome P450 2C19 gene : a pitfall of the PCR-RFLP method for identifying a common mutation
• A Simple Quantitative Assay for Urinary Adenosine Using Column-Switching High-Performance Liquid Chromatography
• Urinary uracil in female patients with ornithine transcarbamylase deficiency
• Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency
• Multiple sclerosis with onset of cerebellar ataxia in an 18-month-old girl
• Urinary pyrimidine analysis in healthy newborns, infants, children, adults and patients with congenital metabolic diseases
• Vitamin B_6-Responsive Ornithine Aminotransferase Deficiency with a Novel Mutation G237D
• Pontine hypoplasia in a child with sensorineural deafiness
• Polymorphisms of the Factor VII Gene Associated with the Low Activities of Vitamin K-Dependent Coagulation Factors in One-Month-Old Infants
• Detection of PHKA2 Gene Mutation in Four Japanese Patients with Hepatic Phosphorylase Kinase Deficiency
• Screening for Pyrimidine Metabolism Disorders Using Dried Filter-Paper Urine Samples : Method Development and a Pilot Study in Nagoya City, Japan
• Correlation between Magnetic Resonance Imaging and Clinical Profiles of Periventricular Leukomalacia
• National survey of periventricular leukomalacia in Japan
• Dopamine penetrates to the central nervous system in developing rats
• Optical imaging reveals cation-Cl^- cotransporter-mediated transient rapid decrease in intracellular Cl^- concentration induced by oxygen-glucose deprivation in rat neocortical slices
• Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
• Unique Electroencephalographic Change of Acute Encephalopathy in Glutaric Aciduria Type 1
• Apoptosis Involved in Density-dependent Regulation of Rat Fibroblastic 3Y1 CellCulture
• Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
• MOLECULAR EPIDEMIOLOGY OF TUBEROUS SCLEROSIS
• Reappearance of visual and somatosensory evoked potentials in a patient with childhood adrenoleukodystrophy after bone marrow transplantation and dietary erucic acid therapy
• Delayed gyration with pontocerebellar hypoplasia type 1
• Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy : Two sibling cases
• Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency : A case report
• Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis
• Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
• Determination of 3-hydroxyisovalerylcarnitine and other acylcarnitine levels using liquid chromatography-tandem mass spectrometry in serum and urine of a patient with multiple carboxylase deficiency
• Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
• 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
• A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish
• IS2-05 Children undergoing LRLTx for treatment of Inherited-Metabolic Diseases are prone to higher oxidative stress and complement activity
• Evaluation of valproate effects on acylcarnitine in epileptic children by LC-MS/MS
• Kunihiko Suzuki and sphingolipidoses
• Pontocerebellar hypoplasia type 3 with tetralogy of Fallot

もっと見る 閉じる

スポンサーリンク