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CP C. Painous
SP S. Pascual-Diaz
EM E. Muñoz-Moreno
VS V. Sánchez
JP JC. Pariente
AP A. Prats-Galino
MS M. Soto
MF M. Fernández
AP A. Pérez-Soriano
AC A. Camara
EM E. Muñoz
FV F. Valldeoriola
NC N. Caballol
CP C. Pont-Sunyer
NM N. Martin
MB M. Basora
MT M. Tio
JR J. Rios
MM MJ. Martí
NB N. Bargalló
YC Y. Compta
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Movement disorders specialized neurologists (Y.C., C.P., A.P.) collected the following demographic and clinical variables of all participants: age at disease onset, sex and age and disease duration at the time of the study procedures. Cognition was assessed by means of the MoCa [24] (except Mini Mental test (MMSE) [30] in MSA as part of an independent protocol [23]). Motor assessments were based on the Unified Multiple System Atrophy Rating Scale (UMSARS) [31] in MSA patients, the PSP Rating Scale (PSPRS) [32] in PSP, and the subscale of the Unified Parkinson’s Disease Rating Scale (UPDRS part III) [33] in all subjects except in MSA subjects. Hoehn and Yahr classification (HY) [34] was obtained for all the participants. Disability assessment was based on the Schwab and England Activities of Daily Living (SEADL) scale [35].

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