Found: 14
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Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.
- Published in:
- Movement Disorders, 2000, v. 15, n. 1, p. 120, doi. 10.1002/1531-8257(200001)15:1<120::AID-MDS1019>3.0.CO;2-S
- By:
- Publication type:
- Article
Leber’s hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
- Published in:
- Multiple Sclerosis Journal, 2011, v. 17, n. 6, p. 763, doi. 10.1177/1352458511404033
- By:
- Publication type:
- Article
Breadsticks Flavoured with Olives and Onions: One-Year Shelf Life.
- Published in:
- Foods, 2023, v. 12, n. 9, p. 1798, doi. 10.3390/foods12091798
- By:
- Publication type:
- Article
Effects of Shortening Replacement with Extra Virgin Olive Oil on the Physical–Chemical–Sensory Properties of Italian Cantuccini Biscuits.
- Published in:
- Foods, 2022, v. 11, n. 3, p. 299, doi. 10.3390/foods11030299
- By:
- Publication type:
- Article
The neuroanatomical correlates of anxiety in a healthy population: differences between the State-Trait Anxiety Inventory and the Hamilton Anxiety Rating Scale.
- Published in:
- Brain & Behavior, 2014, v. 4, n. 4, p. 504, doi. 10.1002/brb3.232
- By:
- Publication type:
- Article
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer’s disease
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2011, v. 7, n. 6, p. 574, doi. 10.1016/j.jalz.2011.02.010
- By:
- Publication type:
- Article
P1-427: Depressive mood in patients with Alzheimer’s disease
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-427: Depressive mood in patients with Alzheimer’s disease
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Increased cerebellar gray matter volume in head chefs.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171457
- By:
- Publication type:
- Article
A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 1, p. 127, doi. 10.1007/s00415-008-0571-x
- By:
- Publication type:
- Article
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.
- Published in:
- Journal of Neurology, 2002, v. 249, n. 10, p. 1413, doi. 10.1007/s00415-002-0856-4
- By:
- Publication type:
- Article
DJ‐1 mutations and parkinsonism‐dementia‐amyotrophic lateral sclerosis complex.
- Published in:
- Annals of Neurology, 2005, v. 58, n. 5, p. 803
- By:
- Publication type:
- Article
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia.
- Published in:
- Annals of Neurology, 2002, v. 51, n. 6, p. 794, doi. 10.1002/ana.10185
- By:
- Publication type:
- Article