The evolving MR imaging appearance of lissencephaly : A case report

スポンサーリンク

概要

• 論文の詳細を見る
• 2007-09-01

著者

• Tada Hiroko

  Department Of Pediatrics Kameda Medical Center

• Tada Hiroko

  Department Of Bioscience And Biotechnology Faculty Of Engineering Graduate School Of Natural Science

• BARKOVICH A.

  Department of Radiology, University of California at San Francisco

• Barkovich A.

  Department Of Radiology University Of California At San Francisco

• Barkovich A.

  Neuroradiology Section University Of California

• Fujii Katsunori

  Department Of Pediatrics Chiba University Graduate School Of Medicine

• Fujii Katsunori

  Department Of Pediatrics Graduate School Of Medicine Chiba University

• Takanashi Jun-ichi

  Department Of Pediatrics Chiba University School Of Medicine

• Fujii Katsunori

  Department Of Health Science General Education A Ichi Institute Of Technology

関連論文

• Intracellular Delivery of Glutathione S-transferase-fused Proteins into Mammalian Cells by Polyethylenimine-Glutathione Conjugates
• Protein Transduction Assisted by Polyethylenimine-Cationized Carrier Proteins
• Intracellular Delivery of Proteins into Mammalian Living Cells by Polyethylenimine-Cationization
• Immunohistochemical Localization of Betacellulin a New Member of the EGF Family in Normal Human Pancreas and lslet Tumor Cells
• PJ-759 Equivalent Inhibitory Effects of 4.0-mm-Diameter Bare Metal Stent with 3.5-mm-Diameter Drug-eluting Stent to Prevent Restenosis after Percutaneous Coronary Intervention(Coronary revascularization, PCI-22, The 71st Annual Scientific Meeting of the J
• Encephalopathy with a reversible splenial lesion is associated with hyponatremia
• Two newly proposed infectious encephalitis/encephalopathy syndromes
• Anti-tumor effect in an in vivo model by human-derived pancreatic RNase with basic fibroblast growth factor insertional fusion protein through antiangiogenic properties
• FRS-068 Deletion of Endogenous Erythropoietin System in Non-Hematopoietic Cells Impairs Development of Coronary Angiogenesis and Enhances Susceptibility to Pressure-Overload-Induced Heart Failure(Heart Failure, Cardiac Remodeling and Cardiomyopathy 1, The
• The Expression of Erythropoietin-receptor on Stem Cells might Play Crucial Roles in the Protection of Cardiac Muscle under Ischemic-or Hypoxic-condition(Myocardial Ischemia-reperfusion, Basic 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Cir
• The Erythropoietin-Erythropoietin Receptor System is Crucial for Mobilization of Endothelial Progenitor Cells in Hypoxia-Induced Pulmonary Hypertension(Angiogenesis 3 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• Endogenous Plasma Erythropoietin May Limit Infarct Size by Preventing Apoptosis Through Erythropoietin-Erythropoietin Receptor Signaling in Non-hematopoietic Lineage(Myocardial Ischemia-reperfusion, Basic 1 (IHD), The 69th Annual Scientific Meeting of the
• RNase 3(ECP) Is an Extraordinarily Stable Protein among Human Pancreatic-Type RNases
• OJ-245 Molecular Mechanism for the Protective Effect of Endogenous Erythropoietin-Erythropoietin Receptor System against Myocardial Ischemia/Reperfusion Injury(Myocardial ischemia-reperfusion, basic/clinical-2 (M) OJ41,Oral Presentation (Japanese),The 70t
• OJ-184 Impaired Mobilization and Incorporation of Progenitor Cells into the Ischemic/Hypoxic Tissues in Erythropoietin Receptor-Knockout Mice(Regeneration (angionenesis/myocardial regeneration)-3 (M) OJ31,Oral Presentation (Japanese),The 70th Anniversary
• OJ-168 Important Protective Role of Endogenous Erythropoietin System in Ischemic Cardiovascular Disease(Endothelium-2 (H) OJ28,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• OE-130 Important Protective Role of Endogenous Erythropoietin System against Pressure Overload-Induced Left Ventricular Dysfunction in Mice in Vivo(Heart failure, basic-1 (M) OE22,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting
• 2 Deficiency of Erythropoietin Receptor Gene in Non-hematopoietic Lineage Deteriorates Cardiac Function and Survival in Ventricular Pressure Overload in Mice(Molecular Mechanism of Hypertensive Heart Failure,Symposium 5 (SY5) (H),The 70th Anniversary Annu
• OJ-295 Endogenous Erythropoietin May Protect Myocardium in Patients with Acute Myocardial Infarction Subjected to Successful Percutaneous Coronary Intervention(Acute Myocardial Infarction, Clinical (Pathophysiology) 5 (IHD) : OJ35)(Oral Presentation (Japa
• FRS-167 Absence of Erythropoietin Receptor Gene in Non-hematopoietic lineage Deteriorates Left Ventricular Remodeling after Myocardial Ischemia and Reperfusion(Coronary Heart Disease : Basic Science (IHD) : FRS20)(Featured Research Session (English))
• Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency
• Transient Cell Proliferation with Polyethylenimine-Cationized N-Terminal Domain of Simian Virus 40 Large T-Antigen(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
• Optimum Modification for the Highest Cytotoxicity of Cationized Ribonuclease
• Srabilization of Human RNase 1 by Introduction of a Disulfide Bond between Residues 4 and 118
• Convenient and Efficient In Vitro Folding of Disulfide-Containing Globular Protein from Crude Bacterial Inclusion Bodies^1
• 3 Roles of Anemia and Erythropoietin in the Development of Heart Failure : Important Aspects of Cardiorenal Syndrome(Cardiorenal Syndrome and Hypertensive Heart Diseases, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• Abnormal DNA synthesis induction in X-ray-irradiated Gorlin fibroblast cells
• Intradural spinal meningioma in a 5-year-old female
• Retrocerebellar arachnoid cysts in siblings with mental retardation and undescended testis
• Empty sella syndrome in nevoid basal cell carcinoma syndrome
• γ-Irradiation Deregulates Cell Cycle Control and Apoptosis in Nevoid Basal Cell Carcinoma Syndrome-derived Cells
• A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible : A case report
• Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom
• Delirious behavior in influenza is associated with a reversible splenial lesion
• Optimum Onset Period for Training Based on Maximum Peak Velocity of Height by Wavelet Interpolation Method in Japanese High School Athletes
• Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome
• U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites
• Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes
• Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum
• Slit ventricle syndrome after cyst-peritoneal shunting for temporal arachnoid cyst in children-a clinical entity difficult to detect on neuroimaging study
• A posterior fossa lipoma extending into the cervical spine and subcutaneous space via a cranium bifidum
• Angiogenesis In Vitro : Vascular Tube Formation From the Differentiation of Neural Stem Cells
• Models for Cooperative Mechanism in Proteins Composed of Subunits
• Malformations of cortical development and epilepsy
• The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusion
• Magnetic resonence imaging : role in the understanding of cerebral malformations
• The evolving MR imaging appearance of lissencephaly : A case report
• Moyamoya disease in children
• Wide range of CNS manifestations of rotavirus infection
• Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases
• Genetic diagnosis and acetazolamide treatment of familial hemiplegic migraine
• Pontine hypoplasia in 5p-syndrome : A key MRI finding for a diagnosis
• Oxidative stress in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS)
• Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome
• Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes
• Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations
• Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome
• Lesions in the central tegmental tract in autopsy cases of developmental brain disorders

もっと見る 閉じる

スポンサーリンク