最近15年間に当科で経験した乳児脳腫瘍の予後と晩期障害

スポンサーリンク

概要

• 論文の詳細を見る
• 2009-06-01

著者

• Fukushima Takeo

  Departments of Neurosurgery, Faculty of Medicine, Fukuoka University

• Hirose Shinichi

  Department of Pediatrics, Faculty of Medicine, Fukuoka University

• Yasumoto Sawa

  Department of Pediatrics, Faculty of Medicine, Fukuoka University

• Inoue Takahito

  Department of Pediatrics, Faculty of Medicine, Fukuoka University

• 野村 優子

  Department Of Pediatrics School Of Medicine Fukuoka University

• YANAI Fumio

  Department of Pediatrics, School of Medicine, Fukuoka University

• AKIYOSHI Hidetaka

  Department of Pediatrics, School of Medicine, Fukuoka University

• NIBU Keiko

  Department of Pediatrics, School of Medicine, Fukuoka University

• TSUGU Hitoshi

  Department of Neurosurgery, School of Medicine, Fukuoka University

• Nibu Keiko

  Department Of Pediatrics School Of Medicine Fukuoka University

• Nibu Keiko

  Department Of Pediatrics Fukuoka University

• Yanai Fumio

  Department Of Pediatrics School Of Medicine Fukuoka University

• Yanai Fumio

  Department Of Pediatrics Fukuoka University

• Tsugu Hitoshi

  Department Of Neurosurgery School Of Medicine Fukuoka University

• Akiyoshi Hidetaka

  Department Of Pediatrics School Of Medicine Fukuoka University

• Yasumoto Sawa

  Department Of Pediatrics Faculty Of Medicine Fukuoka University

• Hirose Shinichi

  Department Of Pediatrics Faculty Of Medicine Fukuoka University

• Hirose Shinichi

  福岡大学 医学部小児科

• Inoue Takahiro

  Department Of Pediatrics Faculty Of Medicine Fukuoka University

• Fujita Takako

  Department Of Pediatrics Faculty Of Medicine Fukuoka University

• Hirose Shinichi

  Department Of Pediatrics School Of Medicine Fukuoka University

• Fukushima Takeo

  Department Of Neurosurgery Fukuoka University

• Inoue Takahito

  Department Of Molecular Pharmacology Faculty Of Pharmaceutical Science Kyoto University

• Hirose Shinichi

  Department Of Biomolecular Engineering Graduate School Of Bioscience And Biotechnology Tokyo Institu

• Shiraishi Hideyuki

  Department Of Pediatrics Kyoto University Faculty Of Medicine

• Tsugu Hitoshi

  Department Of Neurosurgery Faculty Of Medicine Fukuoka University

• Fukushima Takeo

  Department Of Neurosurgery Faculty Of Medicine Fukuoka University

関連論文

• Reperfusion Injury as a Complication Associated with Peripherally Inserted Central Catheters
• A New Liquid Embolic Material, a 2-Hydroxyethyl Methacrylate-co-Methyl Methacrylate : a Safty Study in a Swine Endovascular Embolization Model
• A Case of West Syndrome Associated with Neonatal Hypoglycemic Brain Injury
• 最近15年間に当科で経験した乳児脳腫瘍の予後と晩期障害
• A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
• Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
• II F10 A case of parietal lobe epilepsy with ictal smile
• Mutation screening of AP3M2 in Japanese epilepsy patients
• Ictal Midline Epileptiform Discharges in Benign Familial Neonatal Convulsions
• Genetics of Idiopathic Epilepsies
• The genetics of febrile seizures and related epilepsy syndromes
• IV D6 How SCN1A mutations contribute to Dravet syndrome : a comparison of clinical and EEG features between Dravet syndrome with and without SCN1A mutations
• IV B13 Sodium channel genes in patients following febrile seizures plus
• Genetics of epilepsy : current status and perspectives
• Molecular Genetics of Human Familial Epilepsy Syndromes
• Genetic abnormalities underlying familial epilepsy syndromes
• Electroclinical Picture of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Japanese Family
• The effectiveness of clonazepam on the Rolandic discharges
• I-IMP SPECT findings in mitochondrial encephalomyopathies
• Japanese monozygotic twins with Rett syndrome
• F-waves in neonates : increased spinal anterior horn motor neuron excitability
• Long-Term Outcome of Treatment With Protocols AL841, AL851, and ALHR88 in Children With Acute Lymphoblastic Leukemia: Results Obtained by the Kyushu-Yamaguchi Children's Cancer Study Group
• Primary Yolk Sac Tumor Within the Lateral Ventricle : Case Report
• Ruptured Tectal Arteriovenous Malformation Demonstrated Angiographically After Removal of an Unruptured Occipital Lobe Arteriovenous Malformation
• Complication Caused by Use of Fibrin Glue in Vessel Transposition for Trigeminal Neuralgia
• Ruptured Aneurysm of the Distal Anterior Cerebral Artery : Clinical Features and Surgical Strategies
• Squamous Cell Carcinoma Arising in an Intracranial Dermoid Cyst : Case Report
• Cerebellar Gliomas with Exophytic Growth : Three Case Reports
• Symptomatic Chiari Malformation and Associated Pathophysiology in Pediatric and Adult Patients without Myelodysplasia
• Ultrasound screening for renal and urinary tract anomalies in healthy infants
• Evaluation of the Factors Predicting the Outcome of Transsphenoidal Microsurgery in Patients with Premenopausal Microprolactinoma
• Genome-wide identification of febrile seizure and related epilepsy phenotype loci
• Surgical Results of Brain Metastasis from Lung Cancer : Prognostic Factors
• Expression of Nuclear Factor-kB, Tumor Necrosis Factor Receptor Type 1, and c-Myc in Human Astrocytomas
• Intracranial Cavernous Angioma Manifesting as Subarachnoid Hemorrhage : Case Report
• Treatment of Bacterial Brain Abscess by Repeated Aspiration : Follow up by Serial Computed Tomography
• Direct Approach to the Ventrolateral Medulla for Cavernous Malformation : Case Report
• Cavernous Malformation of the Ventral Midbrain Successfully Removed Via a Transsylvian-Transpeduncular Approach
• Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome
• Hemangioblastoma Mimicking Tentorial Meningioma : Preoperative Embolization of the Meningeal Arterial Blood Supply : Case Report
• B-35. Air Embolism during Neurosurgical Operation in the Sitting Position
• A Post-Traumatic Ligamentum Flavum Progressive Hematoma : A Case Report
• Pineocytoma with Neuronal Differentiation : Case Report
• 遅発型オルニチントランスカルバミラーゼ欠損症男性患者における予後因子と血漿アミノ酸プロフィールの特徴
• Estimation of the relationship between caspase-3 expression and clinical outcome of Burkitt's and Burkitt-like lymphoma
• High-grade mature B-cell lymphoma with Burkitt-like morphology : Results of a clinicopathological study of 72 Japanese patients
• Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus
• Developmental changes in KCNQ2 and KCNQ3 expression in human brain : Possible contribution to the age-dependent etiology of benign familial neonatal convulsions
• Radiological Features of Choroid Plexus Papillomas in Childhood
• Variation in Appearance of Glioma on Serial Thallium-201 Single Photon Emission Computed Tomography : Case Report
• Calcifying Pseudotumor of the Neural Axis : Case Report
• Endoscopic Management of a Traumatic Meningo-encephalocele Through a Planum Sphenoidale Defect : Case Report
• Subependymoma With Prominent Rosenthal Fiber Formation : Case Report
• Spinal cord blood flow decreases following microinjection of sodium nitroprusside into the nucleus tractus solitarii of anesthetized rats
• Immunoreactive Transforming Growth Factor β1, Its Receptor, bcl-2 Protein, and p53 Protein in Colorectal Adenomas
• IGF-1 Induces Growth, Survival and Morphological Change of Primary Hepatocytes on a Galactose-bared Polymer through both MAPK and B-catenin Pathways
• S4-4 Genetics of idiopathic epilepsies
• Apoptosis of cultured microglia by the deprivation of macrophage colony-stimulating factor
• Participation of cAMP and cAMP-dependent protein kinase in β-adrenoceptor-mediated interleukin-1β mRNA induction in cultured microglia
• Comparison of Clinical Outcomes of Intraventricular Hematoma Between Neuroendoscopic Removal and Extraventricular Drainage
• Phenotype for activated tissue macrophages in histiocytic necrotizing lymphadenitis
• Histological characteristics of 21 Papua New Guinean children with high-grade B-cell lymphoma, which is frequently associated with EBV infection
• Estimation of apoptosis and cell proliferation in histiocytic necrotizing lymphadenitis using immunohistochemical double staining
• Hepatocellular apoptosis associated with cytotoxic T/natural killer-cell infiltration in chronic active EBV infection
• Regional excitatory and inhibitory amino acid concentrations in pentylenetetrazol kindling and kindled rat brain
• X-Linked mental retardation and epilepsy : pathogenetic significance of ARX mutations
• Positive association between benign familial infantile convulsions and LGI4
• Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan
• Clinical features of Wilson disease : Analysis of 10 cases
• Intracerebral Hemorrhage Despite Prophylactic Administration of Vitamin K in Infants : Two Case Reports
• Radiation-Induced Astrocytoma With Rapid Malignant Transformation : Case Report
• Endoscopic Management of a Traumatic Meningo-encephalocele Through a Planum Sphenoidale Defect : —Case Report—
• Determinants of surgical repair of patent ductus arteriosus in low-birth-weight infants
• Direct Approach to the Ventrolateral Medulla for Cavernous Malformation : Case Report
• Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
• Autosomal dominant nocturnal frontal lobe epilepsy : a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation
• Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies
• Ruptured Tectal Arteriovenous Malformation Demonstrated Angiographically After Removal of an Unruptured Occipital Lobe Arteriovenous Malformation : Case Report
• Properties of a Novel GABAA Receptor γ2 Subunit Mutation Associated With Seizures
• Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes
• Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication
• Prenatal Diagnosis of High Grade Atrioventricular Block with Polymorphic Ventricular Premature Contractions due to Congenital Long QT Syndrome Using Doppler Flow Recording
• A boy with a severe phenotype of succinic semialdehyde dehydrogenase deficiency
• Four-year experience with prenatal diagnosis of congenital heart defects at a single referral center in Japan with focus on inaccurately diagnosed cases
• A Case of Tetrasomy 18p with Tracheomalacia
• A Novel Mutation of Human Liver Alanine:Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1: Immunohistochemical Quantification and Subcellular Distribution
• Fatal Hemorrhage of a Supratentorial Extraventricular Anaplastic Ependymoma in an Elderly Patient
• e-21. Application of Carcinostatic Agents into the Cerebrospinal Fluid Space: Experimental and Clinical Studies
• Triple Spinal Dysraphic Lesions
• Properties of a Novel GABA_A Receptor γ_2 Subunit Mutation Associated With Seizures
• Newborn screening for Fabry disease in Japan : prevalence and genotypes of Fabry disease in a pilot study

もっと見る 閉じる

スポンサーリンク