MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-06-01
著者
-
HASHIZUME Yoshio
Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University
-
Hashizume Yoshio
Department Of Neuropathology Institute For Medical Science Of Aging Aichi Medical University
-
Sahashi Ko
Department Of Internal Medicine Division Of Neurology Aichi Medical University School Of Medicine
-
Kimura Seigo
Department Of Neurology Nagoya University Graduate School Of Medicine
-
Iwasaki Yasushi
Department Of Neurology Nagoya University Graduate School Of Medicine
-
Iwasaki Yasushi
Department Of Applied Chemistry Faculty Of Engineering Kyushu Institute Of Technology
-
Ibi Tohru
Department Of Internal Medicine Division Of Neurology Aichi Medical University School Of Medicine
-
Kimura Shinya
Department Of Biotechnology The University Of Tokyo
-
Izumi Masayuki
Department Of Internal Medicine Division Of Neurology Aichi Medical University School Of Medicine
-
Yoshida Mari
Department Of Chemistry For Materials Graduate School Of Engineering Mie University
-
Hoshino Akira
Department Of Neurology Aichi Medical University School Of Medicine
-
Kitamoto Tetsuyuki
Division Of Cjd Science And Technology Department Of Prion Research Center For Translational And Adv
-
Izumi Masayuki
Department Of Chemistry Graduate School Of Science Osaka University
-
HASHIZUME Yoshio
Department of Biochemistry, Institute for Developmental Research, Aichi Prefecture Colony
関連論文
- A Novel Technique for Removal of Permanent Pacemaker Leads
- Glucose Consumption and Rate Constants for ^<18>F-fluorodeoxyglucose in Human Gliomas
- Primary Angiitis of the Central Nervous System Mimicking Tumor-Like Lesion : —Case Report—
- Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease
- Anti-myeloma effect of homoharringtonine with concomitant targeting of the myeloma-promoting molecules, Mcl-1, XIAP, and β-catenin
- Antiproliferative Efficacy of the Third-Generation Bisphosphonate, Zoledronic Acid, Combined with Other Anticancer Drugs in Leukemic Cell Lines
- The Bcr-Abl tyrosine kinase inhibitor imatinib and promising new agents against Philadelphia chromosome-positive leukemias
- An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease)
- Cellular tau pathology and immunohistochemical study of tau isoforms in sporadic tauopathies
- Autophagy and autophagic cell death are next targets for elimination of the resistance to tyrosine kinase inhibitors
- A 65-year-old man with headaches and left homonymous hemianopsia
- Single-Step Purification and Characterization of MBP(Maltose Binding Protein)-DnaJ Fusion Protein and Its Utilization for Structure-Function Analysis
- Tetrathiapentalene Derivatives with Long Alkyl Chains
- OJ-304 Acute Effect of L-Arginine on Tricarboxylic Acid Cycle Metabolism Evaluated by C^ -Acetate Kinetics on PET in Mitochondrial Cardiomyopathy(Nuclear cardiology-1 (I) OJ51,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting
- RECS1 deficiency in mice induces susceptibility to cystic medial degeneration
- Ethylenedioxy-Containing Tetrathiapentalene Derivative with Ethylthio Chains, C_2TEO-TTP
- Selenium Analogs of Tetrathiapentalene Derivatives with Long Alkyl Chains
- Primary Ewing's Sarcoma of the Skull Base with Intracerebral Extension : Case Report
- p53-independent anti-tumor effects of the nitrogen-containing bisphosphonate zoledronic acid
- Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob disease
- Acute motor and sensory neuronopathy associated with small-cell lung cancer : A clinicopathological study
- β-Selective Glycosidation of a 5-Thioglucosamine Derivative
- Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement
- Direct Parasympathetic Pathway from Midbrain to Ciliary Muscles in Cats and Monkeys
- Regulatory Role of C-Terminal Residues of SUlA in Its Degradation by Lon Protease in Escherichia coli
- Autopsy case of Creutzfeldt-Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum
- May Plasma Brain (B-type) Natriuretic Peptide Concentration Reflect a Cardiac Sympathetic Function of Parkinson's Disease?
- A Large Scale Isolation of cDNAs Responsive to Shear Stress from Cultured Human Endothelial Cells
- Argyrophilic grain disease presenting with frontotemporal dementia : A neuropsychological and pathological study of an autopsied case with presenile onset
- Gastric Dysmotility Associated with Accumulation of Mitochondrial A3243G Mutation in the Stomach
- Extracranial Metastases of Malignant Ependymoma : Case Report
- Widespread spinal cord involvement in progressive supranuclear palsy
- 微生物由来のシアル酸転移酵素を利用した糖質合成
- Growth Hormone Insensitivity Syndrome Associated with Syringomyelia and Type I Chiari Malformation
- Histochemistry of muscular creatinephosphotokinase : The second report
- Neutrophil-mediated inflammation in respiratory syncytial viral bronchiolitis
- A Facile Synthesis of 5-Thio-L-fucose and 3-O-Allyl-L-fucose Triacetate from D- Arabinose
- En Bloc Surgery for Colon Cancer : Report of a Case
- Electron-stimulated Desorption of Kr2+ Ions from the Surface of Solid Kr (第32回真空に関する連合講演会プロシ-ディングス)
- Abnormal Myocardial Energy-Production State in Mitochondrial Cardiomyopathy and Acute Response to L-Arginine Infusion : C-11 Acetate Kinetics Revealed by Positron Emission Tomography
- Monitoring Global Gene Expression of Proteases and Improvement of Human Lysozyme Production in the nptB Gene Disruptant of Aspergillus oryzae
- Open Heart Surgery in a Paraplegic Patient
- Primary Angiitis of the Central Nervous System Mimicking Tumor-Like Lesion : Case Report
- Multiple system atrophy : α-synuclein and neuronal degeneration
- Early recovery in hemodynamics after direct hemoperfusion with polymyxin B-immobilized fibers may predict mortality rate in patients with septic shock
- Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease
- Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter
- Amyloid angiopathy in centenarians brain
- Pathological changes of the spinal cord in centenarians
- Pathology of spinal vascular disease
- INHIBITION OF DOPAMINE β-HYDROXYLASE IN BLOOD VESSELS BY PICOLINIC ACID DERIVATIVES IN VIVO AND THEIR ANTIHYPERTENSIVE EFFECTS
- A clinico-neuropathological study on brain death.
- An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein
- An autopsy case of diffuse neurofibrillary tangles with calcification : Early stage pathologic findings
- Neuropathological study of cerebellar degeneration in prion disease
- Distribution of Neuronal Cytoplasmic Inclusions in Multiple System Atrophy
- The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD)
- Creutzfeldt-Jakob disease with an M232R substitution : report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum
- Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology : An autopsy case showing typical clinical features of Creutzfeldt-Jakob disease
- Efficient Mannich Reaction Using Iminium Salts Generated from Glycine Derivatives
- A traceback phenomenon can reveal the origin of prion infection
- An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology
- Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy
- MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology
- Amyotrophic lateral sclerosis with dementia : The clinicopathological spectrum
- New Strategy for the Synthesis of Glycoprotein : A Single Expression Method of Two Peptide Segments Encoded as a Tandem Sequence in Plasmid and Its Conversion to Peptide-^αThioester
- Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy
- Demographic Features of Japanese Patients with Sporadic Inclusion Body Myositis: A Single-center Referral Experience
- Hypereosinophilic Syndrome Accompanied by Buerger's Disease-like Femoral Arterial Occlusions
- Neuropathological Studies of Patients with Possible Non-Herpetic Acute Limbic Encephalitis and So-called Acute Juvenile Female Non-Herpetic Encephalitis