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Wyszukujesz frazę ""Creutzfeldt-Jakob Syndrome"" wg kryterium: Temat


Tytuł :
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis.
Autorzy :
Norsworthy PJ; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Thompson AGB; National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Mok TH; National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Guntoro F; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Dabin LC; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Nihat A; National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Paterson RW; Dementia Research Centre, UCL Institute of Neurology, University College London, Queen Square, London, WC1N 3BG, UK.
Schott JM; Dementia Research Centre, UCL Institute of Neurology, University College London, Queen Square, London, WC1N 3BG, UK.
Collinge J; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.; National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
Mead S; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK. .; National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK. .
Viré EA; MRC Prion Unit at UCL, UCL Institute of Prion Diseases, Courtauld Building, 33 Cleveland Street, London, W1W 7FF, UK.
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Źródło :
Nature communications [Nat Commun] 2020 Aug 07; Vol. 11 (1), pp. 3960. Date of Electronic Publication: 2020 Aug 07.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Profiling*
Creutzfeldt-Jakob Syndrome/*blood
Creutzfeldt-Jakob Syndrome/*genetics
MicroRNAs/*blood
MicroRNAs/*genetics
Aged ; Alzheimer Disease/genetics ; Biomarkers/blood ; Cohort Studies ; Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/pathology ; Disease Progression ; Female ; Gene Expression Regulation ; Humans ; Longitudinal Studies ; Male ; Middle Aged ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; ROC Curve ; Reproducibility of Results
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Czasopismo naukowe
Tytuł :
Clinical Reasoning: A 57-year-old woman with progressive ataxia and falls.
Autorzy :
Badahdah A; From the Department of Medicine, Dalhousie University, Halifax, Canada; and Department of Medicine, University of Jeddah, Saudi Arabia. .
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Źródło :
Neurology [Neurology] 2020 Oct 06; Vol. 95 (14), pp. 650-656. Date of Electronic Publication: 2020 Aug 04.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Accidental Falls*
Cerebellar Ataxia/*etiology
Creutzfeldt-Jakob Syndrome/*complications
Creutzfeldt-Jakob Syndrome/*diagnosis
Demyelinating Diseases/*etiology
Creutzfeldt-Jakob Syndrome/pathology ; Female ; Humans ; Middle Aged
Czasopismo naukowe
Tytuł :
Creutzfeldt-Jakob disease in a man with COVID-19: SARS-CoV-2-accelerated neurodegeneration?
Autorzy :
Young MJ; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, United States. Electronic address: .
O'Hare M; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, United States.
Matiello M; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, United States.
Schmahmann JD; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, United States.
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Źródło :
Brain, behavior, and immunity [Brain Behav Immun] 2020 Oct; Vol. 89, pp. 601-603. Date of Electronic Publication: 2020 Jul 15.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Brain/*diagnostic imaging
Coronavirus Infections/*complications
Creutzfeldt-Jakob Syndrome/*complications
Pneumonia, Viral/*complications
Aged ; Betacoronavirus ; Brain/physiopathology ; COVID-19 ; Coronavirus Infections/immunology ; Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/immunology ; Creutzfeldt-Jakob Syndrome/physiopathology ; Disease Progression ; Electroencephalography ; Fluorodeoxyglucose F18 ; Humans ; Magnetic Resonance Imaging ; Male ; Pandemics ; Pneumonia, Viral/immunology ; Positron-Emission Tomography ; Radiopharmaceuticals ; SARS-CoV-2
Czasopismo naukowe
Tytuł :
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
Autorzy :
Jones E; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Hummerich H; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Viré E; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Uphill J; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Dimitriadis A; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Speedy H; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Campbell T; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Norsworthy P; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Quinn L; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Whitfield J; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Linehan J; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Jaunmuktane Z; Division of Neuropathology, University College London Hospitals National Health Service Foundation Trust, London, UK; Department of Clinical and Movement Neurosciences and Queen Square Brain Bank for Neurological Disorders, University College London Queen Square Institute of Neurology, London, UK.
Brandner S; Division of Neuropathology, University College London Hospitals National Health Service Foundation Trust, London, UK; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
Jat P; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Nihat A; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK; National Prion Clinic, University College London Hospitals National Health Service Foundation Trust, London, UK.
How Mok T; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK; National Prion Clinic, University College London Hospitals National Health Service Foundation Trust, London, UK.
Ahmed P; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK.
Collins S; Australian National Creutzfeldt-Jakob Disease Registry, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, VIC, Australia.
Stehmann C; Australian National Creutzfeldt-Jakob Disease Registry, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, VIC, Australia.
Sarros S; Australian National Creutzfeldt-Jakob Disease Registry, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, VIC, Australia.
Kovacs GG; Institute of Neurology, Medical University of Vienna, Vienna, Austria; Department of Laboratory Medicine and Pathobiology and Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, ON, Canada; Laboratory Medicine Program, Krembil Brain Institute, University Health Network, Toronto, ON, Canada.
Geschwind MD; University of California San Francisco Memory and Aging Center, Department of Neurology, University of California, San Francisco, CA, USA.
Golubjatnikov A; University of California San Francisco Memory and Aging Center, Department of Neurology, University of California, San Francisco, CA, USA.
Frontzek K; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.
Budka H; Institute of Neuropathology, University of Zurich, Zurich, Switzerland; Medical University Vienna, Vienna, Austria.
Aguzzi A; Institute of Neuropathology, University of Zurich, Zurich, Switzerland.
Karamujić-Čomić H; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, Netherlands.
van der Lee SJ; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, Netherlands.
Ibrahim-Verbaas CA; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, Netherlands.
van Duijn CM; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, Netherlands; Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Sikorska B; Department of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Golanska E; Department of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Liberski PP; Department of Molecular Pathology and Neuropathology, Medical University of Lodz, Lodz, Poland.
Calero M; Chronic Disease Programme (UFIEC-CROSADIS) and Network Centre for Biomedical Research in Neurodegenerative Diseases (CIBERNED), and Alzheimer Disease Research Unit, CIEN Foundation, Queen Sofia Foundation Alzheimer Centre, Instituto de Salud Carlos III, Madrid, Spain.
Calero O; Chronic Disease Programme (UFIEC-CROSADIS) and Network Centre for Biomedical Research in Neurodegenerative Diseases (CIBERNED), and Alzheimer Disease Research Unit, CIEN Foundation, Queen Sofia Foundation Alzheimer Centre, Instituto de Salud Carlos III, Madrid, Spain.
Sanchez-Juan P; Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, CIBERNED and IDIVAL, Santander, Spain.
Salas A; Unidade de Xenética, Instituto de Ciencias Forenses (INCIFOR), Facultade de Medicina, Universidade de Santiago de Compostela, and GenPoB Research Group, Instituto de Investigaciones Sanitarias (IDIS), Hospital Clínico Universitario de Santiago (SERGAS), Galicia, Spain.
Martinón-Torres F; Translational Paediatrics and Infectious Diseases, Department of Paediatrics, Hospital Clínico Universitario de Santiago de Compostela, Galicia, Spain.
Bouaziz-Amar E; Department of Biochemistry and Molecular Biology, Lariboisière Hospital, AP-HP, University of Paris, Paris, France.
Haïk S; Sorbonne Université, INSERM U1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, Paris, France; Cellule nationale de référence des maladies de Creutzfeldt-Jakob, AP-HP, University Hospital Pitié-Salpêtrière, Paris, France.
Laplanche JL; Department of Biochemistry and Molecular Biology, Lariboisière Hospital, AP-HP, University of Paris, Paris, France.
Brandel JP; Sorbonne Université, INSERM U1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, Paris, France; Cellule nationale de référence des maladies de Creutzfeldt-Jakob, AP-HP, University Hospital Pitié-Salpêtrière, Paris, France.
Amouyel P; INSERM, CHU Lille, Institut Pasteur de Lille, U1167-RID-AGE, Labex DISTALZ, University of Lille, Lille, France.
Lambert JC; INSERM, CHU Lille, Institut Pasteur de Lille, U1167-RID-AGE, Labex DISTALZ, University of Lille, Lille, France.
Parchi P; IRCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Experimental, Diagnostic, and Specialty Medicine, University of Bologna, Bologna, Italy.
Bartoletti-Stella A; IRCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Capellari S; IRCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Poleggi A; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
Ladogana A; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
Pocchiari M; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
Aneli S; Department of Medical Sciences, Università degli studi di Torino, Torino, Italy.
Matullo G; Department of Medical Sciences, Università degli studi di Torino, Torino, Italy.
Knight R; National Creutzfeldt-Jakob Disease Research and Surveillance Unit, Edinburgh, UK.
Zafar S; Department of Neurology, Clinical Dementia Centre and National Reference Centre for Creutzfeldt-Jakob Disease Surveillance, University Medical School, Göttingen, Germany; German Centre for Neurodegenerative Diseases (DZNE), Göttingen, Germany; Biomedical Engineering and Sciences Department, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology, Islamabad, Pakistan.
Zerr I; Department of Neurology, Clinical Dementia Centre and National Reference Centre for Creutzfeldt-Jakob Disease Surveillance, University Medical School, Göttingen, Germany; German Centre for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Booth S; Prion Disease Program, Public Health Agency of Canada, Winnipeg, MB, Canada.
Coulthart MB; Canadian Creutzfeldt-Jakob Disease Surveillance System, Public Health Agency of Canada, Ottawa, ON, Canada.
Jansen GH; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, ON, Canada.
Glisic K; Departments of Pathology and Neurology, Case Western Reserve University, Cleveland, OH, USA; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA.
Blevins J; Departments of Pathology and Neurology, Case Western Reserve University, Cleveland, OH, USA; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA.
Gambetti P; Departments of Pathology and Neurology, Case Western Reserve University, Cleveland, OH, USA; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA.
Safar J; Departments of Pathology and Neurology, Case Western Reserve University, Cleveland, OH, USA; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA.
Appleby B; Departments of Pathology and Neurology, Case Western Reserve University, Cleveland, OH, USA; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA.
Collinge J; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK; National Prion Clinic, University College London Hospitals National Health Service Foundation Trust, London, UK.
Mead S; Medical Research Council Prion Unit, University College London Institute of Prion Diseases, London, UK; National Prion Clinic, University College London Hospitals National Health Service Foundation Trust, London, UK. Electronic address: .
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Źródło :
The Lancet. Neurology [Lancet Neurol] 2020 Oct; Vol. 19 (10), pp. 840-848. Date of Electronic Publication: 2020 Sep 16.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*genetics
Genetic Loci/*genetics
Genetic Predisposition to Disease/*genetics
Genome-Wide Association Study/*methods
Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/epidemiology ; Genetic Predisposition to Disease/epidemiology ; Humans ; Polymorphism, Single Nucleotide/genetics ; Risk Factors
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Czasopismo naukowe
Tytuł :
A nationwide trend analysis in the incidence and mortality of Creutzfeldt-Jakob disease in Japan between 2005 and 2014.
Autorzy :
Nishimura Y; Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan. .
Harada K; Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan.
Koyama T; Department of Pharmaceutical Biomedicine, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, 7008558, Japan.
Hagiya H; Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan.
Otsuka F; Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan.
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Źródło :
Scientific reports [Sci Rep] 2020 Sep 23; Vol. 10 (1), pp. 15509. Date of Electronic Publication: 2020 Sep 23.
Typ publikacji :
Journal Article
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*epidemiology
Adult ; Age Factors ; Aged ; Aged, 80 and over ; Creutzfeldt-Jakob Syndrome/mortality ; Female ; Humans ; Incidence ; Japan/epidemiology ; Male ; Middle Aged ; Retrospective Studies ; Sex Factors
Czasopismo naukowe
Tytuł :
Long survival sporadic Creutzfeldt-Jakob disease.
Autorzy :
Liu XY; From the Department of Neurology (X.Y.L., G.W.), Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai; and National Institute for Viral Disease Control and Prevention (Q.S.), Chinese Center for Disease Control and Prevention, Beijing, China.
Shi Q; From the Department of Neurology (X.Y.L., G.W.), Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai; and National Institute for Viral Disease Control and Prevention (Q.S.), Chinese Center for Disease Control and Prevention, Beijing, China.
Wang G; From the Department of Neurology (X.Y.L., G.W.), Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai; and National Institute for Viral Disease Control and Prevention (Q.S.), Chinese Center for Disease Control and Prevention, Beijing, China. .
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Źródło :
Neurology [Neurology] 2020 Jul 14; Vol. 95 (2), pp. 87-88. Date of Electronic Publication: 2020 Jun 10.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Creutzfeldt-Jakob Syndrome*/diagnostic imaging
Creutzfeldt-Jakob Syndrome*/psychology
Dementia/etiology ; Diffusion Magnetic Resonance Imaging ; Disease Progression ; Electroencephalography ; Female ; Humans ; Middle Aged ; Prion Proteins/genetics
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Czasopismo naukowe
Tytuł :
Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure.
Autorzy :
Brandel JP; Assistance Publique-Hôpitaux de Paris, Paris, France.
Vlaicu MB; Groupe Hospitalier Nord-Essonne, Orsay, France.
Culeux A; INSERM Unité 1127, Paris, France.
Belondrade M; Etablissement Français du Sang, Montpellier, France.
Bougard D; Etablissement Français du Sang, Montpellier, France.
Grznarova K; INSERM Unité 1127, Paris, France.
Denouel A; INSERM Unité 1127, Paris, France.
Plu I; Assistance Publique-Hôpitaux de Paris, Paris, France.
Bouaziz-Amar E; Assistance Publique-Hôpitaux de Paris, Paris, France.
Seilhean D; Assistance Publique-Hôpitaux de Paris, Paris, France.
Levasseur M; Groupe Hospitalier Nord-Essonne, Orsay, France.
Haïk S; INSERM Unité 1127, Paris, France .
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Źródło :
The New England journal of medicine [N Engl J Med] 2020 Jul 02; Vol. 383 (1), pp. 83-85.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*etiology
Occupational Exposure/*adverse effects
Occupational Injuries/*complications
Prion Proteins/*analysis
Wounds, Stab/*complications
Accidents, Occupational ; Adult ; Animals ; Brain/diagnostic imaging ; Brain/pathology ; Brain Chemistry ; Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/transmission ; Fatal Outcome ; Female ; Humans ; Laboratory Personnel ; Magnetic Resonance Imaging ; Methionine/genetics ; Mice ; Mice, Transgenic ; Prion Proteins/blood ; Prion Proteins/cerebrospinal fluid
Raport
Tytuł :
A Case of Creutzfeldt-Jakob Disease with Stroke-Like Onset.
Autorzy :
Okamoto K; Department of Neurology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
Abe T; Department of Neurology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan. Electronic address: .
Itoh Y; Department of Neurology, Osaka City University Graduate School of Medicine, Osaka City, Osaka, Japan.
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Źródło :
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2020 Jun; Vol. 29 (6), pp. 104788. Date of Electronic Publication: 2020 Mar 28.
Typ publikacji :
Case Reports
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*complications
Paresis/*etiology
Stroke/*complications
Aged, 80 and over ; Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/physiopathology ; Diagnosis, Differential ; Fatal Outcome ; Female ; Humans ; Paresis/diagnosis ; Paresis/physiopathology ; Predictive Value of Tests ; Stroke/diagnosis ; Stroke/physiopathology
Raport
Tytuł :
Creutzfeldt-Jakob Disease: A single center experience and systemic analysis of cases in Turkey.
Autorzy :
Uslu FI; Bezmialem Vakif University, Department of Neurology, Istanbul, Turkey,Bezmialem Foundation University Hospital, Department of Neurology, Istanbul, Turkey.
Elif G; Bezmialem Vakif University, Department of Neurology, Istanbul, Turkey.
Gürsoy AE; Bezmialem Vakif University, Department of Neurology, Istanbul, Turkey.
Kolukisa M; Bezmialem Vakif University, Department of Neurology, Istanbul, Turkey.
Yildiz GB; Bezmialem Vakif University, Department of Neurology, Istanbul, Turkey.
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Transliterated Title :
CreutzfeldtJakob-kór: Egy neurológiai központ tapasztalatai és a törökországi esetek szisztematikus áttekintése.
Źródło :
Ideggyogyaszati szemle [Ideggyogy Sz] 2020 May 30; Vol. 73 (05-06), pp. 177-184.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Brain/*diagnostic imaging
Creutzfeldt-Jakob Syndrome/*diagnosis
Electroencephalography/*methods
Cerebrospinal Fluid ; Cognitive Dysfunction/etiology ; Creutzfeldt-Jakob Syndrome/cerebrospinal fluid ; Diagnosis, Differential ; Humans ; Magnetic Resonance Imaging/methods ; Turkey
Czasopismo naukowe
Tytuł :
Mitochondrial respiratory chain deficiency correlates with the severity of neuropathology in sporadic Creutzfeldt-Jakob disease.
Autorzy :
Flønes IH; Neuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021, Bergen, Norway.; Department of Clinical Medicine, University of Bergen, Pb 7804, 5020, Bergen, Norway.
Ricken G; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
Klotz S; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
Lang A; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
Ströbel T; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
Dölle C; Neuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021, Bergen, Norway.; Department of Clinical Medicine, University of Bergen, Pb 7804, 5020, Bergen, Norway.
Kovacs GG; Institute of Neurology, Medical University of Vienna, Vienna, Austria. .; Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Ontario, Canada. .; Laboratory Medicine Program, University Health Network, Toronto, Canada. .
Tzoulis C; Neuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021, Bergen, Norway. .; Department of Clinical Medicine, University of Bergen, Pb 7804, 5020, Bergen, Norway. .
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Źródło :
Acta neuropathologica communications [Acta Neuropathol Commun] 2020 Apr 16; Vol. 8 (1), pp. 50. Date of Electronic Publication: 2020 Apr 16.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
CA3 Region, Hippocampal/*metabolism
Creutzfeldt-Jakob Syndrome/*metabolism
Dentate Gyrus/*metabolism
Electron Transport Chain Complex Proteins/*deficiency
Mitochondria/*metabolism
Neurons/*metabolism
Temporal Lobe/*metabolism
CA3 Region, Hippocampal/pathology ; Case-Control Studies ; Cell Respiration ; Creutzfeldt-Jakob Syndrome/enzymology ; Creutzfeldt-Jakob Syndrome/pathology ; Dentate Gyrus/pathology ; Female ; Humans ; Male ; Mitochondria/enzymology ; Neurons/pathology ; Severity of Illness Index ; Temporal Lobe/pathology
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Czasopismo naukowe
Tytuł :
Metal homeostasis disturbances in neurodegenerative disorders, with special emphasis on Creutzfeldt-Jakob disease - Potential pathogenetic mechanism and therapeutic implications.
Autorzy :
Nakagawa Y; Center for Pharma-Food Research (CPFR), Division of Pharmaceutical Sciences, Graduate School of Integrative Pharmaceutical and Nutritional Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan. Electronic address: .
Yamada S; Center for Pharma-Food Research (CPFR), Division of Pharmaceutical Sciences, Graduate School of Integrative Pharmaceutical and Nutritional Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
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Źródło :
Pharmacology & therapeutics [Pharmacol Ther] 2020 Mar; Vol. 207, pp. 107455. Date of Electronic Publication: 2019 Dec 19.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*metabolism
Metals/*metabolism
Neurodegenerative Diseases/*metabolism
Animals ; Creutzfeldt-Jakob Syndrome/drug therapy ; Creutzfeldt-Jakob Syndrome/pathology ; Homeostasis ; Humans ; Neurodegenerative Diseases/drug therapy ; Neurodegenerative Diseases/pathology
Czasopismo naukowe
Tytuł :
[A patient with Creutzfeldt-Jakob disease presenting with a motoneurone disease].
Autorzy :
Pericot-Nierga I; Hospital de Santa Caterina. Institut d'Assistència Sanitària, Salt, España.
Turbau-Recio J; Hospital de Santa Caterina. Institut d'Assistència Sanitària, Salt, España.
Bragado I; Hospital de Santa Caterina. Institut d'Assistència Sanitària, Salt, España.
Hernández M; Hospital de Santa Caterina. Institut d'Assistència Sanitària, Salt, España.
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Transliterated Title :
Paciente con enfermedad de Creutzfeldt-Jakob que comenzó con una enfermedad de motoneurona.
Źródło :
Revista de neurologia [Rev Neurol] 2020 Feb 01; Vol. 70 (3), pp. 118.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*complications
Motor Neuron Disease/*etiology
Aged, 80 and over ; Brain/pathology ; Creutzfeldt-Jakob Syndrome/diagnosis ; Creutzfeldt-Jakob Syndrome/diagnostic imaging ; Creutzfeldt-Jakob Syndrome/pathology ; Cytoplasmic Granules/chemistry ; Cytoplasmic Granules/ultrastructure ; Dementia/etiology ; Diagnosis, Differential ; Female ; Humans ; Motor Neuron Disease/diagnostic imaging ; Motor Neuron Disease/pathology ; Prion Diseases/diagnosis
Raport
Tytuł :
Accumulation of Astrocytic Aquaporin 4 and Aquaporin 1 in Prion Protein Plaques.
Autorzy :
Sadashima S; Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.; Department of Neurology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Honda H; Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Suzuki SO; Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Shijo M
Aishima S; Department of Pathology, Saga University Hospital, Saga, Japan.
Kai K; Department of Pathology, Saga University Hospital, Saga, Japan.
Kira J; Department of Neurology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Iwaki T; Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
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Źródło :
Journal of neuropathology and experimental neurology [J Neuropathol Exp Neurol] 2020 Apr 01; Vol. 79 (4), pp. 419-429.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Aquaporin 1/*metabolism
Aquaporin 4/*metabolism
Astrocytes/*pathology
Brain/*pathology
Creutzfeldt-Jakob Syndrome/*pathology
Gerstmann-Straussler-Scheinker Disease/*pathology
Prion Proteins/*metabolism
Aged ; Aged, 80 and over ; Astrocytes/metabolism ; Brain/metabolism ; Creutzfeldt-Jakob Syndrome/metabolism ; Female ; Gerstmann-Straussler-Scheinker Disease/metabolism ; Humans ; Male ; Middle Aged ; Protein Aggregation, Pathological/metabolism ; Protein Aggregation, Pathological/pathology ; White Matter/metabolism ; White Matter/pathology
Czasopismo naukowe
Tytuł :
Posterior cortical ribboning in the Heidenhain variant of Creutzfeldt-Jakob Disease.
Autorzy :
Freitas CS; Instituto de Medicina Integral Prof. Fernando Figueira, Recife PE, Brazil.
Pinheiro MGM; Instituto de Medicina Integral Prof. Fernando Figueira, Recife PE, Brazil.
Fonte EJD; Instituto de Medicina Integral Prof. Fernando Figueira, Recife PE, Brazil.
Hazin AN; Instituto de Medicina Integral Prof. Fernando Figueira, Recife PE, Brazil.
Smid J; Universidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Grupo de Neurologia Cognitiva e do Comportamento, São Paulo SP, Brazil.
Barbosa BJAP; Instituto de Medicina Integral Prof. Fernando Figueira, Recife PE, Brazil.; Universidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Grupo de Neurologia Cognitiva e do Comportamento, São Paulo SP, Brazil.
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Źródło :
Arquivos de neuro-psiquiatria [Arq Neuropsiquiatr] 2020 Apr; Vol. 78 (4), pp. 241.
Typ publikacji :
Editorial
MeSH Terms :
Creutzfeldt-Jakob Syndrome*
Electroencephalography ; Humans ; Magnetic Resonance Imaging
Opinia redakcyjna
Tytuł :
Is sporadic Creutzfeldt-Jakob disease transfusion-transmissible?
Autorzy :
Saá P; Scientific Affairs, American Red Cross, Gaithersburg, MD, USA.
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Źródło :
Transfusion [Transfusion] 2020 Apr; Vol. 60 (4), pp. 655-658.
Typ publikacji :
Editorial
MeSH Terms :
Blood Transfusion*
Creutzfeldt-Jakob Syndrome/*etiology
Transfusion Reaction/*etiology
Creutzfeldt-Jakob Syndrome/transmission ; Humans ; Prions
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Opinia redakcyjna
Tytuł :
Factors Influencing the Incubation of an Infectious Form of Creutzfeldt-Jakob Disease.
Autorzy :
Peckeu L; Sorbonne Université, INSERM, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM.
Brandel JP; Sorbonne Université, INSERM, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM.; AP-HP, Cellule Nationale de Référence des maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière.
Welaratne A; Sorbonne Université, INSERM, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM.; AP-HP, Cellule Nationale de Référence des maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière.
Amar E; AP-HP, Hôpital Lariboisière, Service de Biochimie et Biologie Moléculaire, Université Paris Descartes, Paris, France.
Costagliola D; Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique.
Haïk S; Sorbonne Université, INSERM, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM.; AP-HP, Cellule Nationale de Référence des maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière.; AP-HP, Hôpital de la Pitié-Salpêtrière, Laboratoire de Neuropathologie R Escourolle.
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Źródło :
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America [Clin Infect Dis] 2020 Mar 17; Vol. 70 (7), pp. 1487-1490.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Communicable Diseases*
Creutzfeldt-Jakob Syndrome*/diagnosis
Prions*/genetics
Humans ; Iatrogenic Disease ; Prion Proteins/genetics
Czasopismo naukowe
Tytuł :
Co-existence of PrP types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics.
Autorzy :
Cali I; Department of Pathology, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.
Puoti G; Department of Advanced Medical and Surgical Sciences, University of Campania 'L. Vanvitelli', Caserta, 81100, Italy.
Smucny J; Department of Psychiatry, University of California, Davis, CA, 95616, USA.
Curtiss PM; New York University, School of Medicine, New York, NY, 10016, USA.
Cracco L; Department of Pathology, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.
Kitamoto T; Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, 980-8576, Japan.
Occhipinti R; Department of Physiology and Biophysics, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.
Cohen ML; Department of Pathology, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.
Appleby BS; Department of Neurology, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.; Department of Psychiatry, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA.
Gambetti P; Department of Pathology, Case Western Reserve University, School of Medicine, Cleveland, OH, 44106, USA. .
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Źródło :
Scientific reports [Sci Rep] 2020 Jan 30; Vol. 10 (1), pp. 1503. Date of Electronic Publication: 2020 Jan 30.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Creutzfeldt-Jakob Syndrome/*genetics
PrPSc Proteins/*genetics
Adult ; Aged ; Aged, 80 and over ; Brain/metabolism ; Brain/pathology ; Cohort Studies ; Creutzfeldt-Jakob Syndrome/metabolism ; Creutzfeldt-Jakob Syndrome/pathology ; Female ; Genetic Association Studies ; Humans ; Male ; Middle Aged ; PrPSc Proteins/chemistry ; PrPSc Proteins/classification ; Protein Conformation ; Protein Stability ; Tissue Distribution ; Valine/chemistry ; Valine/genetics
SCR Disease Name :
Creutzfeldt-Jakob Disease, Sporadic
Czasopismo naukowe
Tytuł :
Prion Problem: A Rapidly Progressive Dementia.
Autorzy :
Miller M; Department of Medicine, Denver Health Medical Center, University of Colorado School of Medicine, Denver. Electronic address: .
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Źródło :
The American journal of medicine [Am J Med] 2020 Jan; Vol. 133 (1), pp. 58-59. Date of Electronic Publication: 2019 Aug 13.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Brain/*diagnostic imaging
Creutzfeldt-Jakob Syndrome/*diagnostic imaging
Creutzfeldt-Jakob Syndrome/cerebrospinal fluid ; Creutzfeldt-Jakob Syndrome/physiopathology ; Electroencephalography ; Female ; Humans ; Magnetic Resonance Imaging ; Middle Aged
Czasopismo naukowe
Tytuł :
Creutzfeldt-Jakob disease: a systematic review of global incidence, prevalence, infectivity, and incubation.
Autorzy :
Uttley L; School of Health and Related Research, University of Sheffield, Sheffield, UK. Electronic address: .
Carroll C; School of Health and Related Research, University of Sheffield, Sheffield, UK.
Wong R; School of Health and Related Research, University of Sheffield, Sheffield, UK.
Hilton DA; Department of Neuropathology, University Hospitals Plymouth National Health Service Trust, Plymouth, UK.
Stevenson M; School of Health and Related Research, University of Sheffield, Sheffield, UK.
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Źródło :
The Lancet. Infectious diseases [Lancet Infect Dis] 2020 Jan; Vol. 20 (1), pp. e2-e10.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Systematic Review
MeSH Terms :
Infectious Disease Incubation Period*
Creutzfeldt-Jakob Syndrome/*epidemiology
Creutzfeldt-Jakob Syndrome/*pathology
Iatrogenic Disease/*epidemiology
Adult ; Aged ; Aged, 80 and over ; Creutzfeldt-Jakob Syndrome/transmission ; Female ; Humans ; Incidence ; Male ; Middle Aged ; Prevalence ; Risk Assessment ; Young Adult
Czasopismo naukowe
Tytuł :
Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC.
Autorzy :
Abu-Rumeileh S; Department of Biomedical and Neuromotor Sciences, University of Bologna, 40139, Bologna, Italy.
Baiardi S; Department of Biomedical and Neuromotor Sciences, University of Bologna, 40139, Bologna, Italy.
Polischi B; IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy.
Mammana A; IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy.
Franceschini A; IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy.
Green A; The National CJD Research and Surveillance Unit, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Capellari S; Department of Biomedical and Neuromotor Sciences, University of Bologna, 40139, Bologna, Italy.; IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy.
Parchi P; IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139, Bologna, Italy. .; Department of Experimental Diagnostic and Specialty Medicine, University of Bologna, 40139, Bologna, Italy. .
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Źródło :
Journal of neurology [J Neurol] 2019 Dec; Vol. 266 (12), pp. 3136-3143. Date of Electronic Publication: 2019 Sep 20.
Typ publikacji :
Journal Article
MeSH Terms :
Biological Assay/*standards
Creutzfeldt-Jakob Syndrome/*cerebrospinal fluid
Creutzfeldt-Jakob Syndrome/*diagnosis
Neurofilament Proteins/*cerebrospinal fluid
Prion Proteins/*cerebrospinal fluid
tau Proteins/*cerebrospinal fluid
Aged ; Biomarkers/cerebrospinal fluid ; Blotting, Western/standards ; Creutzfeldt-Jakob Syndrome/physiopathology ; Electroencephalography ; Enzyme-Linked Immunosorbent Assay/standards ; Female ; Follow-Up Studies ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Retrospective Studies ; Sensitivity and Specificity
Czasopismo naukowe

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