Monday, September 23, 2019
- 1:45pm-3:15pm
-
Neurofascin is a novel gene associated with autosomal recessive spastic and polyneuropathy
Genetics · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neurological Wilson Disease: Clinical Aspects and Evolution in 10 Cases
Rare Genetic and Metabolic Diseases · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neuromelanin MRI detects monoaminergic cell loss in Huntington Disease Expansion Gene Carriers.
Huntington’s Disease · Agora 3 West, Level 3
- 1:45pm-3:15pm
-
Neuropathological findings in a SPG4 gene mutation carrier
Other · Agora 2 West, Level 2
- 1:45pm-3:15pm
-
Neuropathology in a case of HD-like syndrome caused by mutations in RNF216
Rare Genetic and Metabolic Diseases · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neuroprotective and neurotrophic efficacy of Ginkgo biloba extracts against 3-nitropropionic acid-induced oxidative stress in a rat model of Huntington’s disease
Huntington’s Disease · Agora 3 West, Level 3
- 1:45pm-3:15pm
-
Neuropsychiatric clusters in patients with Parkinson’s disease and their clinical and demographic correlates
Psychiatric Manifestations · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neuropsychiatric manifestations in Parkinson’s disease
Psychiatric Manifestations · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neuropsychological and behavioral profile of patients with isolated REM sleep behaviour disorders (iRBD) and patients with RBD associated with Parkinson’s Disease (PDRBD)
Restless Leg Syndrome, RBD and Other Sleep Disorders · Les Muses Terrace, Level 3
- 1:45pm-3:15pm
-
Neuropsychological profile of patients with functional movement disorders
Functional (Psychogenic) Movement Disorders · Les Muses Terrace, Level 3
- «Previous Page
- 1
- …
- 44
- 45
- 46
- 47
- 48
- …
- 75
- Next Page»