Dissecting the Phenotype and Genotype of PLA2G6 ‐Related Parkinsonism (original) (raw)

PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism

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Tremor and other hyperkinetic movements (New York, N.Y.), 2016

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Severe early-onset parkinsonian syndrome caused by PLA2G6 heterozygous variants

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Early-Onset Parkinson's Disease Caused by PLA2G6 Compound Heterozygous Mutation, a Case Report and Literature Review

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Frontiers in Neurology, 2019

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PLA2G6-associated Dystonia-Parkinsonism: Case Report and Literature Review

Ruth Walker, Gholam-Ali Shahidi

Tremor and other hyperkinetic movements (New York, N.Y.), 2015

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R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family

Coro Paisán-Ruiz

European Journal of Neurology, 2009

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Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations

Abi Li

Neurobiology of Aging, 2010

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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients

Sareh Hosseinpour

Orphanet Journal of Rare Diseases

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Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes

Maria Pellecchia

Movement Disorders Clinical Practice, 2016

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PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progression

RAFAEL CAMINO LEÓN

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Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

Arun Taly

PloS one, 2016

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Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

Coro Paisán-Ruiz, Petra Schwingenschuh

Movement Disorders, 2010

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PLA2G6-associated neurodegeneration: Lessons from neurophysiological findings

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European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2018

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Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson’s disease with brain iron accumulation through pseudo-exon activation

Alessia Nasca

Neurogenetics, 2021

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Parkinson disease: Insights in clinical, genetic and pathological features of monogenic disease subtypes

Christine Van Broeckhoven

Journal of Chemical Neuroanatomy, 2011

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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Jon Stoessl

Neuron, 2004

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Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis

Carlotta Spagnoli

Brain and Development, 2017

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Update on Genetics of Parkinsonism

Zbigniew Wszolek

Neurodegenerative Diseases, 2012

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No association between common POLG1 variants and sporadic idiopathic Parkinson's disease

Gavin Hudson

Movement Disorders, 2009

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Oculogyric crises in PLA2G6 associated neurodegeneration

Babak Behnam

Parkinsonism & related disorders, 2018

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Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder

Michael Schlossmacher

Neurology, 2007

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Parkinson's Disease: From Genetics to Clinical Practice

Jaime Kulisevsky

Current Genomics, 2014

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Overexpressing PLA2G6 mutations cause symptoms of young–onset dystonia–parkinsonism type 14 and reduction in DHA levels in zebrafish model

Chin-song Lu

2020

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Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene

Reetta Hinttala

Parkinsonism & Related Disorders, 2008

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Clinical and Genetic Aspects in Patients with Idiopathic Parkinson Disease

Marija Milanovska

Neuroimaging for Clinicians - Combining Research and Practice, 2011

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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Samuel Pascual

Clinical Genetics, 2017

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The genetics of Parkinson’s disease: review of current and emerging candidates

Andrea Carmine Belin

Journal of Parkinsonism and Restless Legs Syndrome, 2014

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POLG1-related levodopa-responsive parkinsonism

P. Barros, Miguel Gago

Clinical Neurology and Neurosurgery, 2014

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Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes

Marek Godava

Medicine, 2016

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Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset

Ferdinando Squitieri

Annals of Neurology, 2002

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