Significados de idiopathic pd en inglés

In many patients, the phenotype is indistinguishable from that of idiopathic PD.

Comprehensive metabolomic profiling revealed variations in urinary signatures associated with severity of idiopathic PD.

Conclusions: This study adds strong evidence that OPs are implicated in the aetiology of idiopathic PD.

Methods: One hundred and fifty patients with idiopathic PD (IPD) were recruited in this study.

LRRK2 mutations may lead to a clinical phenotype closely resembling idiopathic PD with a puzzling variety in neuropathology.

PD caused by parkin gene mutations is distinct from idiopathic PD on molecular grounds but has similar clinical and PET findings.

Although the idiopathic PD fingerprint was different from that of genetic PD, the molecular pathways deregulated converged between all PD subtypes.

A total of 109 parkinsonism patients were independently ascertained, of whom 62 presented late-onset, idiopathic PD.

Genealogical research showed that 45 index cases with idiopathic PD were linked to a common ancestor, indicating familiar clustering among the patients.

Study investigated urinary metabolic profiles of patients with idiopathic PD as compared to healthy controls (HC) to identify the potential biomarkers.

Data on mortality and comorbidity profile was gathered in a cohort of 190 individuals with idiopathic PD referred to a Movement Disorders Clinic.

We recruited 10 patients with frontal gait disorders, 10 patients with idiopathic PD and 10 age-matched healthy control participants.

Methods: Data was obtained from "Jönköping Parkinson Registry" database on routine care visits of 314 people with idiopathic PD in southern Sweden.

Genes contributing to rare mendelian forms of PD have been identified, but the genes involved in the more common idiopathic PD are not well understood.

The authors studied the accuracy of clinical diagnosis of idiopathic PD (IPD) in 100 consecutive clinically diagnosed cases that came to neuropathological examination.