Clinical presentation and pre-mortem diagnosis of variant creutzfeldt-jakob disease associated with blood transfusion: a case report. Commentary
- Author
- WILSON, Kumanan (Commentator (written text))
1 ; RICKETTS, Maura N (Commentator (written text))
2 ; WADSWORTH, Jonathan D. F4 ; HEWITT, Patricia5 ; COLLINGE, John3 4 ; WROE, Stephen J3 4 ; PAL, Suvankar4 ; SIDDIQUE, Durrenajaf3 4 ; HYARE, Harpreet4 ; MACFARLANE, Rebecca3 4 ; JOINER, Susan4 ; LINEHAN, Facqueline M4 ; BRANDNER, Sebastian4
[1] Toronto General Hospital, University Health Network, Toronto, Ontario, M5G 2C4, Canada
[2] Public Health Agency of Canada, Ottawa, Ontario, Canada
[3] National Prion Clinic, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, United Kingdom
[4] MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, United Kingdom
[5] National Blood Service, London, United Kingdom - Source
Lancet (British edition). 2006, Vol 368, Num 9552 ; 2037-2039,2061-2067 [10 p.] ; ref : 58 ref
- CODEN
- LANCAO
- ISSN
- 0140-6736
- Scientific domain
- General medicine general surgery
- Publisher
- Lancet, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Association Diagnostic Encéphalopathie spongiforme Creutzfeldt Jakob Etude cas Génotype Médecine Prion Sang Symptomatologie Transfusion Variabilité génétique Variant Encéphale pathologie Infection Maladie dégénérative Prion maladie Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Association Diagnosis Creutzfeldt Jakob disease Case study Genotype Medicine Prion Blood Symptomatology Transfusion Genetic variability Variant Cerebral disorder Infection Degenerative disease Prion disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Asociación Diagnóstico Encefalopatía espongiforme Creutzfeldt Jakob Estudio caso Genotipo Medicina Prion Sangre Sintomatología Transfusión Variabilidad genética Variante Encéfalo patología Infección Enfermedad degenerativa Prion enfermedad Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Generalities in medical sciences Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18331546
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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