FAQ

PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE

Known as: Dystonia-Parkinsonism, Adult-Onset, PARK14 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2010-2017
02420102017

Related topics

Related topics

16 relations
Abnormality of extrapyramidal motor functionAggressive behaviorAutosomal recessive inheritanceBradykinesia
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Broader (3)

Dystonia DisordersParkinsonian Disordersgroup VI phospholipase A2

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE
Muscle Rigidity
Tremor
Autosomal recessive inheritance
Impaired cognition
Muscle Spasticity

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
PLA2G6 accumulates in Lewy bodies in PARK14 and idiopathic Parkinson's disease.
The histopathological hallmark of Parkinson's disease (PD) and dementia with Lewy bodies (DLB) is the occurrence of insoluble… (More)
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2017
2017
Alteration of mitochondrial protein PDHA1 in Lewy body disease and PARK14.
The histopathological hallmark of Parkinson's disease (PD) and dementia with Lewy bodies (DLB) is the occurrence of insoluble… (More)
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2017
2017
Expanded phenotype and hippocampal involvement in a novel compound heterozygosity of adult PLA2G6 associated neurodegeneration (PARK14).
 
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2017
2017
PARK14 PLA2G6 mutants are defective in preventing rotenone-induced mitochondrial dysfunction, ROS generation and activation of mitochondrial apoptotic pathway
Mutations in the gene encoding Ca2+-independent phospholipase A2 group 6 (PLA2G6) cause the recessive familial type 14 of… (More)
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Review
2012
Review
2012
Autosomal recessive parkinsonism.
Several forms of autosomal recessive parkinsonism are known. In three forms, caused by mutations in parkin (PARK2), PINK1 (PARK6… (More)
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2011
2011
PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort.
OBJECTIVE Mutations in the PLA2G6 gene at the PARK14 locus have been reported in complicated parkinsonism. To assess the… (More)
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Review
2010
Review
2010
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
Seven autosomal recessive genes associated with juvenile and young-onset Levodopa-responsive parkinsonism have been identified… (More)
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