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Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
Hermann, Peter; Appleby, Brian; Brandel, Jean-Philippe; Caughey, Byron; Collins, Steven; Geschwind, Michael D; Green, Alison; Haïk, Stephane; Kovacs, Gabor G; Ladogana, Anna; Llorens, Franc; Mead, Simon; Nishida, Noriyuki; Pal, Suvankar; Parchi, Piero; Pocchiari, Maurizio; Satoh, Katsuya; Zanusso, Gianluigi; Zerr, Inga.
Afiliação
  • Hermann P; National Reference Center for Transmissible Spongiform Encephalopathies, Department of Neurology, University Medical Center Göttingen, Göttingen, Germany. Electronic address: peter.hermann@med.uni-goettingen.de.
  • Appleby B; National Prion Disease Pathology Surveillance Center, Case Western Reserve University, Cleveland, OH, USA; Departments of Neurology, Psychiatry, and Pathology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH, USA.
  • Brandel JP; Cellule Nationale de Référence des Maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière, Paris, France; Institut du Cerveau et de la Moelle épinière, Sorbonne Université, Paris, France.
  • Caughey B; Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.
  • Collins S; Australian National Creutzfeldt-Jakob disease Registry, Florey Institute of Neuroscience and Mental Health and Department of Medicine, University of Melbourne, Parkville, VIC, Australia.
  • Geschwind MD; Department of Neurology, University of California, San Francisco, CA, USA.
  • Green A; National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Haïk S; Cellule Nationale de Référence des Maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière, Paris, France; Institut du Cerveau et de la Moelle épinière, Sorbonne Université, Paris, France.
  • Kovacs GG; Tanz Centre for Research in Neurodegenerative Disease and Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada; Laboratory Medicine Program, University Health Network, Toronto, ON, Canada.
  • Ladogana A; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
  • Llorens F; National Reference Center for Transmissible Spongiform Encephalopathies, Department of Neurology, University Medical Center Göttingen, Göttingen, Germany; Network Center For Biomedical Research Of Neurodegenerative Diseases, Institute Carlos III, L'Hospitalet de Llobregat, Barcelona, Spain; Bellvitg
  • Mead S; National Prion Clinic, University College London Hospitals NHS Foundation Trust, London, UK; Medical Research Council Prion Unit at University College London, Institute of Prion Diseases, London, UK.
  • Nishida N; Department of Molecular Microbiology and Immunology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Pal S; National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Parchi P; Istituto di Ricovero e Cura e Carattere Scientifico, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
  • Pocchiari M; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
  • Satoh K; Department of Locomotive Rehabilitation Science, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Zanusso G; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Zerr I; National Reference Center for Transmissible Spongiform Encephalopathies, Department of Neurology, University Medical Center Göttingen, Göttingen, Germany; German Center for Neurodegenerative Diseases, Göttingen, Germany.
Lancet Neurol ; 20(3): 235-246, 2021 03.
Article em En | MEDLINE | ID: mdl-33609480

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Síndrome de Creutzfeldt-Jakob Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Síndrome de Creutzfeldt-Jakob Idioma: En Ano de publicação: 2021 Tipo de documento: Article