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Unraveling the Complex Interplay between Alpha-Synuclein and Epigenetic Modification

International journal of molecular sciences, 2023-04, Vol.24 (7), p.6645

2023

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VPS35 dysfunction impairs lysosomal degradation of α-synuclein and exacerbates neurotoxicity in a Drosophila model of Parkinson's disease

Neurobiology of disease, 2014-11, Vol.71, p.1-13

2014

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DnaJ/Hsp40 Family and Parkinson's Disease

Frontiers in neuroscience, 2018-01, Vol.11, p.743-743

2018

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The Immediate Onset of Isolated and Unilateral Abducens Nerve Palsy Associated with COVID-19 Infection: A Case Report and Literature Review

Internal Medicine, 2022/06/01, Vol.61(11), pp.1761-1765

2022

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Parkinson’s disease-linked DNAJC13 mutation aggravates alpha-synuclein-induced neurotoxicity through perturbation of endosomal trafficking

Human molecular genetics, 2018-03, Vol.27 (5), p.823-836

2018

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Membrane Trafficking Illuminates a Path to Parkinson’s Disease

The Tohoku Journal of Experimental Medicine, 2017, Vol.242(1), pp.63-76

2017

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Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan

Journal of human genetics, 2020-09, Vol.65 (9), p.771-781

2020

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The AAA-ATPase VPS4 regulates extracellular secretion and lysosomal targeting of α-synuclein

PloS one, 2011-12, Vol.6 (12), p.e29460-e29460

2011

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High prevalence of serum anti-NH2-terminal of α-enolase antibodies in patients with multiple system atrophy and corticobasal syndrome

Journal of neurology, 2021-11, Vol.268 (11), p.4291-4295

2021

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Adult-onset Leigh Syndrome with a m.9176T>C Mutation Manifested As Reversible Cerebral Vasoconstriction Syndrome

Internal Medicine, 2023/07/01, Vol.62(13), pp.1995-1998

2023

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ESCRT-0 dysfunction compromises autophagic degradation of protein aggregates and facilitates ER stress-mediated neurodegeneration via apoptotic and necroptotic pathways

Scientific reports, 2016-04, Vol.6 (1), p.24997, Article 24997

2016

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Reply to the Letter "Reversible Vasoconstriction Syndrome Is a Complication of SARS-CoV-2 Infection/Vaccination Rather than That of Leigh Syndrome"

Internal Medicine, 2023/07/15, Vol.62(14), pp.2159-2160

2023

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Suppression of dynamin GTPase decreases α-synuclein uptake by neuronal and oligodendroglial cells: a potent therapeutic target for synucleinopathy

Molecular neurodegeneration, 2012-08, Vol.7 (1), p.38-38, Article 38

2012

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Case Report: Guitarist's cramp as the initial manifestation of dopa-responsive dystonia with a novel heterozygous GCH1 mutation [version 1; peer review: 2 approved, 1 approved with reservations]

F1000 research, 2021, Vol.10, p.361

2021

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Girdle Sensation Caused by Radiculitis due to Neurosarcoidosis

Internal Medicine, 2015, Vol.54(12), pp.1567-1568

2015

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18F-THK5351 Positron Emission Tomography Imaging in Neurodegenerative Tauopathies

Frontiers in aging neuroscience, 2021-11, Vol.13, p.761010-761010

2021

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Olfactory dysfunction and dementia in Parkinson's disease

Journal of Parkinson's disease, 2014, Vol.4 (2), p.181

2014

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Asymmetric basal ganglia lesion in hypertensive encephalopathy

Neurology and clinical neuroscience, 2020-05, Vol.8 (3), p.167-168

2020

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Brain Metabolic Changes of Cervical Dystonia with Spinocerebellar Ataxia Type 1 after Botulinum Toxin Therapy

Internal Medicine, 2016/07/15, Vol.55(14), pp.1919-1922

2016

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Postural leg tremor in X-linked spinal and bulbar muscular atrophy

Journal of clinical neuroscience, 2014-05, Vol.21 (5), p.799-802

2014

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A case of inflammatory myopathy with anti‐PM/Scl antibodies myopathologically presenting as polymyositis with mitochondrial pathology

Neurology and clinical neuroscience, 2020-09, Vol.8 (5), p.335-339

2020

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A case of neuralgic amyotrophy presented Vernet syndrome and suprascapular nerve palsy

Neurology and clinical neuroscience, 2019-05, Vol.7 (3), p.127-128

2019

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Late-onset Charcot–Marie–Tooth disease type 1B due to a novel mutation in the extracellular disulfide bridge of MPZ gene

Clinical neurology and neurosurgery, 2013-02, Vol.115 (2), p.208-209

2013

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PEG‐J tube breakage in a patient with Parkinson's disease receiving levodopa–carbidopa intestinal gel therapy

Neurology and clinical neuroscience, 2018-11, Vol.6 (6), p.197-198

2018

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Role of Neu4L sialidase and its substrate ganglioside GD3 in neuronal apoptosis induced by catechol metabolites

FEBS letters, 2007-02, Vol.581 (3), p.406-412

2007

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Unraveling the Complex Interplay between Alpha-Synuclein and Epigenetic Modification

VPS35 dysfunction impairs lysosomal degradation of α-synuclein and exacerbates neurotoxicity in a Drosophila model of Parkinson's disease

DnaJ/Hsp40 Family and Parkinson's Disease

The Immediate Onset of Isolated and Unilateral Abducens Nerve Palsy Associated with COVID-19 Infection: A Case Report and Literature Review

Parkinson’s disease-linked DNAJC13 mutation aggravates alpha-synuclein-induced neurotoxicity through perturbation of endosomal trafficking

Membrane Trafficking Illuminates a Path to Parkinson’s Disease

Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan

The AAA-ATPase VPS4 regulates extracellular secretion and lysosomal targeting of α-synuclein

High prevalence of serum anti-NH2-terminal of α-enolase antibodies in patients with multiple system atrophy and corticobasal syndrome

Adult-onset Leigh Syndrome with a m.9176T>C Mutation Manifested As Reversible Cerebral Vasoconstriction Syndrome

ESCRT-0 dysfunction compromises autophagic degradation of protein aggregates and facilitates ER stress-mediated neurodegeneration via apoptotic and necroptotic pathways

Reply to the Letter "Reversible Vasoconstriction Syndrome Is a Complication of SARS-CoV-2 Infection/Vaccination Rather than That of Leigh Syndrome"

Suppression of dynamin GTPase decreases α-synuclein uptake by neuronal and oligodendroglial cells: a potent therapeutic target for synucleinopathy

Case Report: Guitarist's cramp as the initial manifestation of dopa-responsive dystonia with a novel heterozygous GCH1 mutation [version 1; peer review: 2 approved, 1 approved with reservations]

Girdle Sensation Caused by Radiculitis due to Neurosarcoidosis

18F-THK5351 Positron Emission Tomography Imaging in Neurodegenerative Tauopathies

Olfactory dysfunction and dementia in Parkinson's disease

Asymmetric basal ganglia lesion in hypertensive encephalopathy

Brain Metabolic Changes of Cervical Dystonia with Spinocerebellar Ataxia Type 1 after Botulinum Toxin Therapy

Postural leg tremor in X-linked spinal and bulbar muscular atrophy

A case of inflammatory myopathy with anti‐PM/Scl antibodies myopathologically presenting as polymyositis with mitochondrial pathology

A case of neuralgic amyotrophy presented Vernet syndrome and suprascapular nerve palsy

Late-onset Charcot–Marie–Tooth disease type 1B due to a novel mutation in the extracellular disulfide bridge of MPZ gene

PEG‐J tube breakage in a patient with Parkinson's disease receiving levodopa–carbidopa intestinal gel therapy

Role of Neu4L sialidase and its substrate ganglioside GD3 in neuronal apoptosis induced by catechol metabolites

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