Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families

Predictors of cognitive impairment in an early stage Parkinson's disease cohort

(2014) Michele T. M. Hu et al.   MOVEMENT DISORDERS

Effects of stimulation of the subthalamic nucleus on naming and reading nouns and verbs in Parkinson's disease

(2012) Maria Caterina Silveri et al.   NEUROPSYCHOLOGIA

Autosomal recessive parkinsonism

(2011) Vincenzo Bonifati   PARKINSONISM & RELATED DISORDERS

Dysexecutive syndrome: Diagnostic criteria and validation study

(2010) Olivier Godefroy et al.   ANNALS OF NEUROLOGY

PINK1-linked parkinsonism is associated with Lewy body pathology

(2010) Lluís Samaranch et al.   BRAIN

Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease

(2010) Lena Kertelge et al.   MOVEMENT DISORDERS

Systematic review of levodopa dose equivalency reporting in Parkinson's disease

(2010) Claire L. Tomlinson et al.   MOVEMENT DISORDERS

Clinical and demographic characteristics of PINK1 mutation carriers-A meta-analysis

(2010) Meike Kasten et al.   MOVEMENT DISORDERS

Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficit

(2010) C. Eggers et al.   NEUROLOGY

Somatosensory processing in a German family with PINK1 mutations: its potential role in Parkinson disease

(2009) J Gierthmuhlen et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Impulse control disorders in Parkinson's disease: prevalence and possible risk factors

(2009) Daniel Weintraub   PARKINSONISM & RELATED DISORDERS

Evaluation of PINK1 variants in Indian Parkinson's disease patients

(2009) Arindam Biswas et al.   PARKINSONISM & RELATED DISORDERS

Limbic and Frontal Cortical Degeneration Is Associated with Psychiatric Symptoms in PINK1 Mutation Carriers

(2008) Kathrin Reetz et al.   BIOLOGICAL PSYCHIATRY

PINK1heterozygous rare variants: prevalence, significance and phenotypic spectrum

(2008) Roberta Marongiu et al.   HUMAN MUTATION

Subclinical sensory abnormalities in unaffected PINK1 heterozygotes

(2008) M. Fiorio et al.   JOURNAL OF NEUROLOGY

The Sydney multicenter study of Parkinson's disease: The inevitability of dementia at 20 years

(2008) Mariese A. Hely et al.   MOVEMENT DISORDERS

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype

(2008) B.F.L. van Nuenen et al.   NEUROLOGY