-
Hypophosphatasia presenting as parkinsonism with compound heterozygous mutations in ALPL gene
-
Hyposmia as a marker of (non-)motor disease progression in Parkinson’s disease
-
Hypothalamic functional connectivity correlates with autonomic symptom burden in patients with Multiple System Atrophy
-
Identification and Characterization of Selective and High Affinity Small Molecules as Positron Emission Tomography (PET) Imaging Tracers for Pathological Alpha-Synuclein
-
Identification of aberrant circulating miRNAs in Parkinson’s disease plasma samples
-
Identification of candidates for device-assisted therapy in Parkinson’s disease using Artificial Neural Networks
-
Identification of genetic alterations and SNCA mutation in Parkinson’s disease patients of Coimbatore Population, India
-
Identification of modifier genes related to G proteins pathways on the motor capacity of a Drosophila melanogaster model of Friedreich’s ataxia
-
Identification of potential new genes involved in autosomal recessive forms of Parkinson’s disease
-
Identification of protein biomarker/s in CSF of Parkinson’s disease (PD) with cognitive impairment
- « Previous Page
- 1
- …
- 97
- 98
- 99
- 100
- 101
- …
- 217
- Next Page »