Internal Trapping of a Ruptured Vertebral Artery Dissecting Aneurysm Followed by Recanalization of the Trapped Vertebral Artery Without Aneurysm Recurrence : Case Report

スポンサーリンク

概要

• 論文の詳細を見る
• 2010-10-15

著者

• Fujita Takashi

  Department Of Cardiology Kanazawa University

• Oda Keiko

  Department Of Pediatrics And Child Health Kurume University School Of Medicine

• Oda Keiko

  Department Of Neurosurgery Ohta-nishinouchi Hospital

• ARAKI Shinobu

  Department of Neurosurgery, Ohta-Nishinouchi Hospital

• KAWAKAMI Masahisa

  Department of Neurosurgery, Ohta-Nishinouchi Hospital

• Araki Shinobu

  Department Of Neurosurgery Ohta-nishinouchi Hospital

• Araki Shinobu

  Department Of Mining Engineering Kyushu Institute Of Technology

• Kawakami Masahisa

  Department Of Neurosurgery Ohta-nishinouchi Hospital

• Fujita Takashi

  Department Of Breast Oncology Aichi Cancer Center Hospital

• Fujita Takashi

  Department Of Neurosurgery Ohta-nishinouchi Hospital

• Fujita Takashi

  Department Of Biochemistry The University Of Sydney

• Oda Keiko

  Department Of Neurosurgery Fukushima Medical University

• Fujita Takashi

  Department Of Anesthesiology Suwa Red Cross Hospital

関連論文

• FRS-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
• Pituitary Adenylate Cyclase-Activating Polypeptibe (PACAP) Receptor mRNA in the Rat Adrenal Gland: Localization by In Situ Hybridization and Identification of Splice Variants
• Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
• Failure of Follow-up Gallium Single-Photon Emission Computed Tomography and Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography to Predict the Deterioration of a Patient With Cardiac Sarcoidosis
• PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
• Gene mutations in adult Japanese patients with dilated cardiomyopathy
• OE-126 Angiotensin-Converting Enzyme D Allele is a Modifier Causing Left Ventricular Systolic Dysfunction in Genotyped Hypertrophic Cardiomyopathy : Results from Longitudinal Study(Heart failure, clinical(02)(M),Oral Presentation(English),The 72nd Annual
• FRS-034 Impact of Anglotensin II Type 1 Receptor A/C1166 Gene Ploymorphism on the Onset of Atrial Fibrillation in Genotyped Hypertrophic Cardiomyopathy(Molecular Determinants for the Development of Cardiomyopathy(M),Featured Research Session,The 72nd Annu
• PE-437 Progressive LV Remodeling and Adverse Cardiac Events in HCM Associated With Mutations in Cardiac Troponin Genes : Longitudinal 10 years Follow-up(Heart failure, basic-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• Internal Trapping of a Ruptured Vertebral Artery Dissecting Aneurysm Followed by Recanalization of the Trapped Vertebral Artery Without Aneurysm Recurrence : Case Report
• Distribution of QTc Values and Prevalence of Short QT Syndrome in the Japanese Population (ECG/Body Surface Potential Mapping/Holter 6 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Gene Mutations in Patients with Hypertrophic Cardiomyopathy Showing Mild Left Ventricular Hypertrophy(Cardiomyopathy, Clinical 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Differences in Diagnostic Value of Classic Electrocardiographic Voltage Criteria for Hypertrophic Cardiomyopathy in a Genotyped Population(Cardiomyopathy, Clinical 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Ankyrin-B Gene Mutation is a Rare Cause of Long QT Syndrome in Japan(Arrhythmia, Basic 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Long-Term Course of Patients with Cardiomyopathy Associated with Phospholamban Gene Mutations(Cardiomyopathy, Clinical 8 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Early Development of Dilated Cardiomyopathy in Subjects with Hypertrophic Cardiomyopathy Caused by Mutations of the Thin Filament Genes(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Angiotensin II Type 1 Receptor A/C1166 Gene Polymorphism and Left Ventricular Systolic Dysfunction in Hypertrophic Cardiomyopathy with Sarcomere Gene Mutations(Cardiomyopathy, Clinical 7 (M), The 69th Annual Scientific Meeting of the Japanese Circulation
• Impact of Bundle-Branch Block on Clinical Manifestation in Patients with Hypertrophic Cardiomyopathy : Analyses Based on Molecular Genetic Diagnoses(Cardiomyopathy, Clinical 6 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Cardiac Manifestations and Genotype-Phenotype Correlations in Carriers with the STA Gene Mutations(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Mutation of the β Myosin Heavy Chain Gene associated with Isolated Left Ventricular Noncompaction(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• The Effects of FLEXI-CUT DCA for the Presence of Calcified Lesions with IVUS
• The Study of Intimal Hyperplasia Concerned with Reference Diameter in Multi-Link Stenting : Late Loss Is Not Influenced by Reference Diameter
• PE-218 The Patients with Severe Heart Failure Present Respiratory Oscillation and the Abnormal Power Increase in Fractal Analysis during the Daytime(PE037,Obesity/SAS 1 (H),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circul
• Adenovirus-mediated Gene Transduction of IκB or IκB Plus Bax Gene Drastically Enhances Tumor Necrosis Factor (TNF)-induced Apoptosis in Human Gliomas
• Transactivation of Core Binding Factor α1 as a Basic Mechanism to Trigger Parathyroid Hormone-Induced Osteogenesis
• Incadronate and Etidronate Accelerate Phosphate-Primed Mineralization of MC4 Cells via ERK1/2-Cbfa1 Signaling Pathway in a Ras-Independent Manner: Further Involvement of Mevalonate-Pathway Blockade for Incadronate
• Phosphate Stimulates Differentiation and Mineralization of the Chondroprogenitor Clone ATDC5
• Bone-anabolic Effect of Salmon Calcitonin on Glucocorticoid-Induced Osteopenia in Rats
• Macrolide-resistant Mycoplasma pneumoniae in patients with community-acquired pneumonia
• Acute Results of Distal Protection Device (GuardWire Plus : GWP) for the Patients with Acute Coronary Syndrome
• A case of HER2-positive male breast cancer with lung metastases showing a good response to trastuzumab and paclitaxel treatment
• A variety of microbial components induce tolerance to lipopolysaccharide by differentially affecting MyD88-dependent and -independent pathways
• Sepsis in children
• The outbreak of mumps in a small island in Japan
• Expression of FTZ-F1α in transgenic Xenopus embryos and oocytes
• Determination of Second-Order Nonlinear Optical Susceptibility of GaN Films on Sapphire
• Structure of Mouse Interferon Stimulated Gene Factor 3γ (ISGF3γ/p48)cDNA and Chromosomal Localization of the Gene^1
• Mannose-binding Protein Recognizes Glioma Cells : In vitro Analysis of Complement Activation on Glioma Cells via the Lectin Pathway
• Impact of prophylactic pyridoxine on occurrence of hand-foot syndrome in patients receiving capecitabine for advanced or metastatic breast cancer
• MALDI Mass Spectrometry Using 2,4,6-Trihydroxyacetophenone and 2,4-Dihydroxyacetophenone with Cyclodextrins : Suppression of Matrix-related Ions in Low-molecular-weight Region
• Experimental Studies on Coal Dust Explosion : Propagation of Explosion Flame of Coal Dust Cloud
• Coloration Related to Nanostructure of Yttria-Stabilized Cubic Zirconia Single Crystal Implanted with Ag Ions
• Suppression of Matrix-related Ions Using Cyclodextrin in MALDI Mass Spectrometry
• Holoprosencephaly
• Autocrine Amplification of Type I Interferon Gene Expression Mediated by Interferon Stimulated Gene Factor 3 (ISGF3)
• Continuous positive airway pressure oxygenation during one-lung ventilation with 50% nitrous oxide and isoflurane in oxygen
• Green Light Drives Leaf Photosynthesis More Efficiently than Red Light in Strong White Light : Revisiting the Enigmatic Question of Why Leaves are Green
• 641 Measurement of variation in Young's modulus after large deformation and simulation of Its influence on Springback Characteristic during bending
• Shock melting origin of a troilite-rich clast in the Moorabiechondrite (L3)
• 29p-A-6 MODEL FOR THE ELASTIC FLEXIBILITY OF HUMAN SPECTRIN - THE MAJOR PROTEIN OF THE ERYTHROCYTE CYTOSKELETON
• Fe-Mg heteorogeneity in the low-Ca pyroxenes during metamorphism of the ordinary chondrites
• Combined Microsurgical and Endoscopic Removal of Extensive Suprasellar and Prepontine Epidermoid Tumors
• Origin of metal-troilite aggregates in six ordinary chondrites
• Analysis of Yeast Prion Aggregates with Amyloid-staining Compound In Vivo
• Radiation-Induced World Health Organization Grade II Meningiomas in Young Patients Following Prophylactic Cranial Irradiation for Acute Lymphoblastic Leukemia in Childhood : Three Case Reports
• High recurrence risk and use of adjuvant trastuzumab in patients with small, HER2-positive, node-negative breast cancers
• Optical Properties of Quartz Implanted with V Ions
• Microstructures and Optical Properties of LiNbO3 Sequentially Implanted with Ag and Cu Ions
• Aspergillus Osteomyelitis in a Child Who Has p67-phox-deficient Chronic Granulomatous Disease.
• Detection of Cytomegalovirus DNA in Urine from Newborns in NICU Using a Polymerase Chain Reaction.
• Internal Trapping of a Ruptured Vertebral Artery Dissecting Aneurysm Followed by Recanalization of the Trapped Vertebral Artery Without Aneurysm Recurrence -Case Report-:—Case Report—
• The post-operative pathological prognostic parameters of clear cell renal cell carcinoma in pT1a cases
• Structure of Mouse Interferon Stimulated Gene Factor 3.GAMMA. (ISGF3.GAMMA./p48) cDNA and Chromosomal Localization of the Gene.
• Autocrine Amplification of Type I Interferon Gene Expression Mediated by Interferon Stimulated Gene Factor 3 (ISGF3).
• Identification of the narrow lumen of the ureter using a Fogarty catheter during laparoscopic pyeloplasty

もっと見る 閉じる

スポンサーリンク