-
DYT16/PRKRA founder mutation causes childhood-onset generalized dystonia in a family from southern Italy
-
DYT2 dystonia – Too rare to be found?
-
E-counselling to movement disorder callers in Africa
-
E326K GBA polymorphism and Parkinson’s disease in Russian population
-
Early clinical features of paraneoplastic cerebellar degeneration: Diagnostic outcomes of adult onset cerebellar ataxia
-
Early grey matter changes in structural covariance networks in Huntington’s disease
-
Early retirement and loss of income among X linked dystonia parkinsonism (XDP / DYT3) patients in Capiz, Roxas City Philippines
-
Early stridor onset predicts survival in multiple system atrophy
-
EARLYSTIM: STN-DBS alleviates behavioural side effects of dopamine replacement therapy when compared to best medical treatment
-
EBM review on the diagnostic work-up of multiple system atrophy
- « Previous Page
- 1
- …
- 65
- 66
- 67
- 68
- 69
- …
- 207
- Next Page »