Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum

Author:

Vicente-Pascual Mikel123ORCID,Rossi Marcello4,Gámez Josep5,Lladó Albert1,Valls Josep1,Grau-Rivera Oriol2,Ávila Polo Rainiero6,Llorens Franc78,Zerr Inga7,Ferrer Isidre9,Nos Carlos10,Parchi Piero411ORCID,Sánchez-Valle Raquel12,Gelpí Ellen212ORCID

Affiliation:

1. Department of Neurology; Hospital Clínic de Barcelona; Barcelona Spain

2. Neurological Tissue Bank of the Biobanc-Hospital Clínic; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS); Barcelona Spain

3. Department of Neurology; Hospital Universitari Arnau de Vilanova; Lérida Spain

4. IRCCS Institute of Neurological Sciences; Bellaria Hospital; Bologna Italy

5. Department of Neurology; Hospital Vall d'Hebrón; Barcelona Spain

6. Department of Pathology; Complejo Hospitalario Regional Virgen Del Rocío; Sevilla Spain

7. Department of Neurology; University Medical Center; Göttingen Germany

8. CIBERNED (Network center for biomedical research of neurodegenerative diseases); Institute Carlos III, Ministry of Health; Madrid Spain

9. Institute of Neuropathology; Hospital Universitari de Bellvitge (IDIBELL); Barcelona Spain

10. General Subdirectorate of Surveillance and Response to Emergencies in Public Health; Department of Public Health in Catalonia; Barcelona Spain

11. Department of Experimental, Diagnostic and Specialty Medicine (DIMES); University of Bologna; Bologna Italy

12. Institute of Neurology; Medical University of Vienna; Vienna Austria

Funder

Department of Public Health Generalitat de Catalunya

Spanish “Ministerio de Economía y Competitividad, Subprograma Técnicos de Apoyo 2014”

Spanish Fondo de Investigaciones Sanitarias

Spanish Ministry of Health - Instituto Carlos III

Fundació la Marató de TV3

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Reference11 articles.

1. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein;Zou;Ann Neurol,2010

2. Creutzfeldt-Jakob disease with amyotrophy and demyelinating polyneuropathy;Kovács;Arch Neurol,2002

3. Amyotrophic form of Creutzfeldt-Jakob disease with rapid course in 82-year-old man;Nowacki;Folia Neuropathol,2000

4. A patient with Creutzfeldt-Jakob disease presenting with amyotrophy: a case report;Panegyres;J Med Case Rep Journal of Medical Case Reports,2013

5. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph Lateral Scler Other Motor Neuron Disord,2001

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