Genetic Identification in Early Onset Parkinsonism among Norwegian Patients

EK Gustavsson; J Trinh; M McKenzie; S Bortnick; MS Petersen; MJ Farrer; JO Aasly

doi:10.1002/mdc3.12501

Genetic Identification in Early Onset Parkinsonism among Norwegian Patients

EK Gustavsson, J Trinh, M McKenzie, S Bortnick, MS Petersen, MJ Farrer, JO Aasly

Deildin fyri heilsu- og sjúkrarøktarvísindi - Faculty of Health Sciences

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

Abstract

BackgroundAn initial diagnosis of Parkinson's disease (PD) is challenging, especially in patients who have early onset and atypical disease. A genetic etiology for parkinsonism, when established, ends that diagnostic odyssey and may inform prognosis and therapy. The objective of this study was to elucidate the genetic etiology of parkinsonism in patients with early onset disease (age at onset

Original language	English
Pages (from-to)	499-508
Number of pages	10
Journal	Movement Disorders Clinical Practice
Volume	4
Issue number	4
DOIs	https://doi.org/10.1002/mdc3.12501
Publication status	Published - Jul 2017

Keywords

age at onset
early onset Parkinson's disease
mutation
parkinsonism
glut1 deficiency syndrome
deep brain-stimulation
clinical-diagnosis
movement-disorders
lewy body
disease
mutations
accuracy
variants
dementia

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10.1002/mdc3.12501

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abstract = "BackgroundAn initial diagnosis of Parkinson's disease (PD) is challenging, especially in patients who have early onset and atypical disease. A genetic etiology for parkinsonism, when established, ends that diagnostic odyssey and may inform prognosis and therapy. The objective of this study was to elucidate the genetic etiology of parkinsonism in patients with early onset disease (age at onset ",

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T1 - Genetic Identification in Early Onset Parkinsonism among Norwegian Patients

AU - Gustavsson, EK

AU - Trinh, J

AU - McKenzie, M

AU - Bortnick, S

AU - Petersen, MS

AU - Farrer, MJ

AU - Aasly, JO

PY - 2017/7

Y1 - 2017/7

N2 - BackgroundAn initial diagnosis of Parkinson's disease (PD) is challenging, especially in patients who have early onset and atypical disease. A genetic etiology for parkinsonism, when established, ends that diagnostic odyssey and may inform prognosis and therapy. The objective of this study was to elucidate the genetic etiology of parkinsonism in patients with early onset disease (age at onset

AB - BackgroundAn initial diagnosis of Parkinson's disease (PD) is challenging, especially in patients who have early onset and atypical disease. A genetic etiology for parkinsonism, when established, ends that diagnostic odyssey and may inform prognosis and therapy. The objective of this study was to elucidate the genetic etiology of parkinsonism in patients with early onset disease (age at onset

KW - age at onset

KW - early onset Parkinson's disease

KW - mutation

KW - parkinsonism

KW - glut1 deficiency syndrome

KW - deep brain-stimulation

KW - clinical-diagnosis

KW - movement-disorders

KW - lewy body

KW - disease

KW - mutations

KW - accuracy

KW - variants

KW - dementia

UR - http://dx.doi.org/10.1002/mdc3.12501

U2 - 10.1002/mdc3.12501

DO - 10.1002/mdc3.12501

M3 - Article

SN - 2330-1619

VL - 4

SP - 499

EP - 508

JO - Movement Disorders Clinical Practice

JF - Movement Disorders Clinical Practice

IS - 4

ER -

Genetic Identification in Early Onset Parkinsonism among Norwegian Patients

Abstract

Keywords

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