Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis
Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis
About this item
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Author / Creator
Fusilli, Caterina , Migliore, Simone , Mazza, Tommaso , Consoli, Federica , De Luca, Alessandro , Barbagallo, Gaetano , Ciammola, Andrea , Gatto, Emilia Mabel , Cesarini, Martin , Etcheverry, Jose Luis , Parisi, Virginia , Al-Oraimi, Musallam , Al-Harrasi, Salma , Al-Salmi, Qasem , Marano, Massimo , Vonsattel, Jean-Paul Gerard , Sabatini, Umberto , Landwehrmeyer, Georg Bernhard and Squitieri, Ferdinando
Publisher
England: Elsevier Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: Elsevier Ltd
Subjects
More information
Scope and Contents
Contents
Huntington's disease is a rare, neurodegenerative disease caused by an expanded CAG repeat mutation in the huntingtin gene. Compared with adult-onset Huntington's disease, juvenile Huntington's disease (onset ≤20 years) is even rarer and has not been studied extensively. We aimed to further characterise juvenile Huntington's disease by examining th...
Alternative Titles
Full title
Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis
Authors, Artists and Contributors
Author / Creator
Migliore, Simone
Mazza, Tommaso
Consoli, Federica
De Luca, Alessandro
Barbagallo, Gaetano
Ciammola, Andrea
Gatto, Emilia Mabel
Cesarini, Martin
Etcheverry, Jose Luis
Parisi, Virginia
Al-Oraimi, Musallam
Al-Harrasi, Salma
Al-Salmi, Qasem
Marano, Massimo
Vonsattel, Jean-Paul Gerard
Sabatini, Umberto
Landwehrmeyer, Georg Bernhard
Squitieri, Ferdinando
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2111747802
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2111747802
Other Identifiers
ISSN
1474-4422
E-ISSN
1474-4465
DOI
10.1016/S1474-4422(18)30294-1
