Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis

The Lancet Neurology - Tập 17 - Trang 986-993 - 2018
Caterina Fusilli1, Simone Migliore2, Tommaso Mazza1, Federica Consoli3, Alessandro De Luca3, Gaetano Barbagallo4, Andrea Ciammola5, Emilia Mabel Gatto6, Martin Cesarini6, Jose Luis Etcheverry6, Virginia Parisi6, Musallam Al-Oraimi7, Salma Al-Harrasi7, Qasem Al-Salmi7, Massimo Marano8, Jean-Paul Gerard Vonsattel9, Umberto Sabatini10, Georg Bernhard Landwehrmeyer11, Ferdinando Squitieri2
1Bioinformatics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy
2Huntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy
3Molecular Genetics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy
4Institute of Neurology, University Magna Græcia, Catanzaro, Italy
5Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy
6Departments of Movement Disorders, Instituto Neurociencias de Buenos Aires, and Neurology, Sanatorio de la Trinidad Mitre, Buenos Aires, Argentina
7National Genetic Centre, Royal Hospital, Ministry of Health, Muscat, Sultanate of Oman
8Italian League for Research on Huntington and Related Diseases Foundation, Rome, Italy
9The New York Brain Bank, Columbia University, New York, NY, USA
10Department of Neuroradiology, University Magna Graecia, Catanzaro, Italy
11Abteilung Neurologie, Universitätsklinik Ulm Ulm Germany

Tài liệu tham khảo

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