Genetics of Parkinson’s Disease - A Clinical Perspective

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. Ross OA, Braithwaite AT, Skipper LM, Kachergus

Although this syndrome seems to be associated with an increased risk of aggressive behavior, we hypothesize that a large set of vulnerability risk factors found in individuals

Although a reasonable number of studies on factors associated with sedentary behavior are available, little is known on the efectiveness of the interventions available to reduce

Association of cerebrospinal fluid beta-amyloid 1-42, T-tau, P-tau181, and alpha-synuclein levels with clinical features of drug-naive patients with early Parkinson disease.

In MKNF, this is not an issue, since these components are not kept separate; however, in dl-programs there is a strict distinction between the database part (the underlying

A) Perceber como/se estas organizações estão a trabalhar para maximizar o seu impacto social. Este tema apresenta-se como um objetivo central já que é ainda

When using SNPs in type II TA systems with a minimum number of genes (13 genes), all basic groups of M. tuberculosis can be represented, including those with clinical significance,

Here, we present a series of methods for identification of genetic variants and genotypes with clinical associations, phasing genetic data and using Mendelian inheritance for