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The Genetic Basis of Cognitive Impairment and Dementia in Parkinson's DiseaseNeuroprotective and Therapeutic Strategies against Parkinson's Disease: Recent PerspectivesInduced pluripotent stem cells in Parkinson's disease: scientific and clinical challengesNeuropsychiatric characteristics of GBA-associated Parkinson disease.The Monoamine Brainstem Reticular Formation as a Paradigm for Re-Defining Various Phenotypes of Parkinson's Disease Owing Genetic and Anatomical Specificity.LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian populationNonmotor symptoms in LRRK2 G2019S associated Parkinson's diseaseDepression and Parkinson's disease: current knowledge.Gender differences in the risk of familial parkinsonism: beyond LRRK2?Genetic LRRK2 models of Parkinson's disease: Dissecting the pathogenic pathway and exploring clinical applicationsParkinson's disease therapeutics: new developments and challenges since the introduction of levodopa.Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium.Cognitive impairment and dementia in Parkinson's disease: clinical features, diagnosis, and management.Evaluation and management of the non-motor features of Parkinson's disease.Neurobiology of cognitive impairment in Parkinson's disease.Nonmotor symptoms in sporadic versus familial forms of Parkinson's disease.Neuropathobiology of non-motor symptoms in Parkinson disease.Non-motor features of Parkinson disease.The neurotransmitter serotonin interrupts α-synuclein amyloid maturation.Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease.Phenotype analysis in patients with early onset Parkinson's disease with and without parkin mutations.Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease.Normal 'heart' in Parkinson's disease: is this a distinct clinical phenotype?Associations of specific psychiatric disorders with isolated focal dystonia, and monogenic and idiopathic Parkinson's disease.Cohort Profile: a population-based cohort to study non-motor symptoms in parkinsonism (EPIPARK).A population-based study on combined markers for early Parkinson's disease.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Nonmotor symptoms in genetic Parkinson disease.
@en
Nonmotor symptoms in genetic Parkinson disease.
@nl
type
label
Nonmotor symptoms in genetic Parkinson disease.
@en
Nonmotor symptoms in genetic Parkinson disease.
@nl
prefLabel
Nonmotor symptoms in genetic Parkinson disease.
@en
Nonmotor symptoms in genetic Parkinson disease.
@nl
P2093
P1433
P1476
Nonmotor symptoms in genetic Parkinson disease.
@en
P2093
Alexander Schmidt
Alfredo Ramirez
Carsten Buhmann
Ferdinand Binkofski
Heiner Raspe
Johann Hagenah
Joyce van der Vegt
Lena Kertelge
Maria Isabel Behrens
Meike Kasten
P304
P356
10.1001/ARCHNEUROL.67.6.670
P577
2010-06-01T00:00:00Z