(Q48034191)

7 February 2018

title

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

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8

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Anna Rita Bentivoglio

10

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Laura Serra

object named as

Laura Serra

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Enza Maria Valente

object named as

Enza Maria Valente

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author name string

Lucia Ricciardi

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7 February 2018

Simona Petrucci

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Arianna Guidubaldi

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Tamara Ialongo

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Alessandro Ferraris

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Barbara Spanò

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language of work or name

English

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publication date

27 August 2014

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7 February 2018

published in

Movement Disorders

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volume

29

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issue

12

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page(s)

1561-1566

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Hereditary early-onset Parkinson's disease caused by mutations in PINK1

cites work

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Autosomal recessive parkinsonism

21 January 2018

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PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum

21 January 2018

1 reference

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations

21 January 2018

1 reference

Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations.

21 January 2018

1 reference

PINK1-linked parkinsonism is associated with Lewy body pathology.

21 January 2018

1 reference

Subclinical sensory abnormalities in unaffected PINK1 heterozygotes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study

21 January 2018

1 reference

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

21 January 2018

1 reference

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

21 January 2018

1 reference

Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families

21 January 2018

1 reference

Diagnostic criteria for Parkinson disease

21 January 2018

1 reference

The metric properties of a novel non-motor symptoms scale for Parkinson's disease: Results from an international pilot study.

21 January 2018

1 reference

The Parkinson's disease sleep scale: a new instrument for assessing sleep and nocturnal disability in Parkinson's disease

21 January 2018

1 reference

The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment

21 January 2018

1 reference

Reliability, validity, and clinical correlates of apathy in Parkinson's disease

21 January 2018

1 reference

The assessment of anxiety states by rating

21 January 2018

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

21 January 2018

1 reference

Atrophy of medial temporal lobes on MRI in "probable" Alzheimer's disease and normal ageing: diagnostic value and neuropsychological correlates

21 January 2018

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Qualitative assessment of cerebral atrophy on MRI: inter- and intra-observer reproducibility in dementia and normal aging.

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical and demographic characteristics of PINK1 mutation carriers--a meta-analysis.

21 January 2018

1 reference

Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers

21 January 2018

1 reference

Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients

21 January 2018

1 reference

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism

21 January 2018

1 reference

Evaluation of PINK1 variants in Indian Parkinson's disease patients.

21 January 2018

1 reference

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

21 January 2018

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Dysexecutive syndrome: diagnostic criteria and validation study.

21 January 2018

1 reference

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

21 January 2018

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Evidence for a possible neuroanatomical basis for lexical processing of nouns and verbs

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/MDS.25994

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7 February 2018

release_qrouxdqi7ncbbazbhhglu3oumy

Fatcat ID

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7 February 2018