Progressive Supranuclear Palsy-Like Phenotype in a
GBA
E326K Mutation Carrier
Mov Disord Clin Pract
.
2016 Jul 27;4(3):444-446.
doi: 10.1002/mdc3.12406.
eCollection 2017 May-Jun.
Authors
Marina Picillo
1
,
Simona Petrucci
2
,
Enza Maria Valente
1
,
Sabina Pappatà
3
,
Fiorenzo Squame
4
,
Monia Ginevrino
1
,
Leonardo Pace
5
,
Paolo Barone
1
,
Maria Teresa Pellecchia
1
Affiliations
1
Center for Neurodegenerative Diseases (CEMAND) Department of Medicine and Surgery Neuroscience section University of Salerno Salerno Italy.
2
Department of Neurology and Psychiatry "Sapienza" University of Rome Rome Italy.
3
Institute of Biostructure and Bioimaging CNR Naples Italy.
4
Nuclear Medicine A.O.U. San Giovanni di Dio e Ruggi d'Aragona Salerno Italy.
5
Department of Medicine and Surgery University of Salerno Salerno Italy.
PMID:
30838276
PMCID:
PMC6353524
DOI:
10.1002/mdc3.12406
No abstract available
Keywords:
GBA; PSP; glucocerebrosidase; parkinsonism.
Publication types
Case Reports