المؤلفون: 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: s.mead@prion.ucl.ac.uk.

المصدر: The Lancet. Neurology [Lancet Neurol] 2020 Oct; Vol. 19 (10), pp. 840-848. Date of Electronic Publication: 2020 Sep 16.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1474-4465 (Electronic) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE

مواضيع طبية MeSH: 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

المؤلفون: Balendra R; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Uphill J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Collinson C; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Druyeh R; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Adamson G; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Hummerich H; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Zerr I; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany.; German Center for Neurodegenerative Diseases, Gottingen, Germany., Gambetti P; Department of Pathology, Case Western Reserve University, Cleveland, OH, 44060, USA., Collinge J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Mead S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK. s.mead@prion.ucl.ac.uk.

المصدر: BMC medical genetics [BMC Med Genet] 2016 Apr 07; Vol. 17, pp. 28. Date of Electronic Publication: 2016 Apr 07.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Creutzfeldt-Jakob Syndrome/*genetics , Phosphoinositide Phospholipase C/*genetics, Creutzfeldt-Jakob Syndrome/diagnosis ; Exons ; Genetic Loci ; Genome-Wide Association Study ; Genotyping Techniques ; Germany ; Humans ; Linkage Disequilibrium ; Prion Proteins ; Prions/genetics ; Prions/metabolism ; Risk Factors ; United States

SCR Disease Name: Creutzfeldt-Jakob Disease, Sporadic

المؤلفون: Thompson AG; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Uphill J; MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK., Lowe J; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Porter MC; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Lukic A; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Carswell C; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Rudge P; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., MacKay A; NHS Highland Mental Health Services, Argyll and Bute Hospital, Lochgilphead, Argyll, UK., Collinge J; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK., Mead S; 1] MRC Prion Unit, Department of Neurodegenerative Disease, University College London (UCL) Institute of Neurology, London, UK [2] NHS National Prion Clinic, National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, UK.

المصدر: Translational psychiatry [Transl Psychiatry] 2015 Apr 21; Vol. 5, pp. e552. Date of Electronic Publication: 2015 Apr 21.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101562664 Publication Model: Electronic Cited Medium: Internet ISSN: 2158-3188 (Electronic) Linking ISSN: 21583188 NLM ISO Abbreviation: Transl Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Creutzfeldt-Jakob Syndrome/*genetics , Mood Disorders/*genetics , Psychotic Disorders/*genetics, Ankyrins/genetics ; Argonaute Proteins/genetics ; Bipolar Disorder/genetics ; Carrier Proteins/genetics ; Case-Control Studies ; Chromosomes, Human, Pair 6/genetics ; Cohort Studies ; Creutzfeldt-Jakob Syndrome/psychology ; Delusions/genetics ; Delusions/psychology ; Depression/genetics ; Depression/psychology ; Depressive Disorder, Major/genetics ; Genome-Wide Association Study ; Hallucinations/genetics ; Hallucinations/psychology ; Humans ; Mood Disorders/psychology ; Nerve Tissue Proteins/genetics ; Phosphotransferases (Alcohol Group Acceptor)/genetics ; Polymorphism, Single Nucleotide ; Prion Diseases/genetics ; Prion Diseases/psychology ; Prion Proteins ; Prions/genetics ; Psychotic Disorders/psychology ; RNA-Binding Proteins ; Schizophrenia/genetics ; United Kingdom

المؤلفون: Mead S; Medical Research Council Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London, UK., Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J

المصدر: The Lancet. Neurology [Lancet Neurol] 2009 Jan; Vol. 8 (1), pp. 57-66.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.

بيانات الدورية: Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Print ISSN: 1474-4422 (Print) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Creutzfeldt-Jakob Syndrome/*epidemiology , Creutzfeldt-Jakob Syndrome/*genetics, Adult ; Age of Onset ; Aged ; Alleles ; Chromosomes, Human/genetics ; DNA/genetics ; Data Interpretation, Statistical ; Female ; Genome-Wide Association Study ; Genotype ; Humans ; Kuru/epidemiology ; Linkage Disequilibrium/genetics ; Male ; Membrane Proteins/genetics ; Middle Aged ; Papua New Guinea/epidemiology ; Polymorphism, Single Nucleotide ; Population Surveillance ; Prion Proteins ; Prions/genetics ; Quality Control ; Risk Factors ; Stathmin ; United Kingdom/epidemiology

المؤلفون: Beck JA; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Campbell TA, Adamson G, Poulter M, Uphill JB, Molou E, Collinge J, Mead S

المصدر: Journal of medical genetics [J Med Genet] 2008 Dec; Vol. 45 (12), pp. 813-7. Date of Electronic Publication: 2008 Sep 19.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Alleles*, Creutzfeldt-Jakob Syndrome/*genetics , Nerve Tissue Proteins/*genetics, Creutzfeldt-Jakob Syndrome/metabolism ; GPI-Linked Proteins ; Genetic Predisposition to Disease ; Genetic Variation ; Humans ; Nerve Tissue Proteins/metabolism

المؤلفون: Gabor G. Kovacs, Stephanie A. Booth, Sebastian Brandner, Penny Norsworthy, Anna Ladogana, Akin Nihat, Herbert Budka, Saima Zafar, Helen Speedy, Antonio Salas, Parvin Ahmed, Holger Hummerich, Gerard H. Jansen, Tze How Mok, Michael D. Geschwind, Beata Sikorska, Maurizio Pocchiari, Christiane Stehmann, Sabina Capellari, Jean-Louis Laplanche, Sven J. van der Lee, Emma Jones, Jean-Charles Lambert, Olga Calero, Pierluigi Gambetti, Ewa Golanska, Serena Aneli, Richard Knight, Giuseppe Matullo, Pawel P. Liberski, Athanasios Dimitriadis, Jerome Whitfield, Hata Karamujić-Čomić, Federico Martinón-Torres, Emmanuelle Viré, Jiri G. Safar, Tracy Campbell, Pascual Sánchez-Juan, Katie Glisic, Anna Bartoletti-Stella, Carla A. Ibrahim-Verbaas, Adriano Aguzzi, Anna Poleggi, Aili Golubjatnikov, Karl Frontzek, Jean Phillipe Brandel, Phillipe Amouyel, Parmjit S. Jat, Zane Jaunmuktane, Simon Mead, Steven J. Collins, Inga Zerr, Liam Quinn, Piero Parchi, Janis Blevins, Elodie Bouaziz-Amar, Brian S. Appleby, Shannon Sarros, Jacqueline M. Linehan, Miguel Calero, Michael B. Coulthart, Stéphane Haïk, John Collinge, James Uphill, Cornelia M. van Duijn

المساهمون: Diseases, Network Centre for Biomedical Research in Neurodegenerative, Jones E., Hummerich H., Vire E., Uphill J., Dimitriadis A., Speedy H., Campbell T., Norsworthy P., Quinn L., Whitfield J., Linehan J., Jaunmuktane Z., Brandner S., Jat P., Nihat A., How Mok T., Ahmed P., Collins S., Stehmann C., Sarros S., Kovacs G.G., Geschwind M.D., Golubjatnikov A., Frontzek K., Budka H., Aguzzi A., Karamujic-Comic H., van der Lee S.J., Ibrahim-Verbaas C.A., van Duijn C.M., Sikorska B., Golanska E., Liberski P.P., Calero M., Calero O., Sanchez-Juan P., Salas A., Martinon-Torres F., Bouaziz-Amar E., Haik S., Laplanche J.-L., Brandel J.-P., Amouyel P., Lambert J.-C., Parchi P., Bartoletti-Stella A., Capellari S., Poleggi A., Ladogana A., Pocchiari M., Aneli S., Matullo G., Knight R., Zafar S., Zerr I., Booth S., Coulthart M.B., Jansen G.H., Glisic K., Blevins J., Gambetti P., Safar J., Appleby B., Collinge J., Mead S., Universidad de Cantabria, Neurology, Amsterdam Neuroscience - Neurodegeneration, Epidemiology

المصدر: The lancet / Neurology 19(10), 840-848 (2020). doi:10.1016/S1474-4422(20)30273-8
Lancet Neurol 2020; 19: 840?48
UCrea Repositorio Abierto de la Universidad de Cantabria
instname
Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
The Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, G G, Geschwind, M D, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, S J, Ibrahim-Verbaas, C A, van Duijn, C M, Sikorska, B, Golanska, E, Liberski, P P, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M, Aneli, S, Matullo, G, Knight, R, Zafar, S, Zerr, I, Booth, S, Coulthart, M B, Jansen, G H, Glisic, K, Blevins, J, Gambetti, P, Safar, J, Appleby, B, Collinge, J & Mead, S 2020, ' Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease : a genome-wide association study ', Lancet Neurology, vol. 19, no. 10, pp. 840-848 . https://doi.org/10.1016/S1474-4422(20)30273-8

مصطلحات موضوعية: 0301 basic medicine, epidemiology [Creutzfeldt-Jakob Syndrome], Tau protein, Single-nucleotide polymorphism, Genome-wide association study, diagnosis [Creutzfeldt-Jakob Syndrome], Disease, genetics [Genetic Loci], methods [Genome-Wide Association Study], Polymorphism, Single Nucleotide, Creutzfeldt-Jakob Syndrome, PRNP, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Humans, Genetic Predisposition to Disease, ddc:610, genetics [Genetic Predisposition to Disease], Genotyping, Exome sequencing, Genetics, biology, Odds ratio, genetics [Creutzfeldt-Jakob Syndrome], 030104 developmental biology, Genetic Loci, epidemiology [Genetic Predisposition to Disease], biology.protein, genetics [Polymorphism, Single Nucleotide], Neurology (clinical), 030217 neurology & neurosurgery, Genome-Wide Association Study, Human

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7233c1ef4905578810d4be7f91aaa40