Search Results - "Hama, Yuka"
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Identification of plasma microRNA expression changes in multiple system atrophy and Parkinson's disease
Published in Molecular brain (14-05-2019)“…MicroRNAs (miRNAs) are endogenous small (18-25 nt), single-stranded, non-coding RNAs that play key roles in post-transcriptional gene expression regulation…”
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Identification of plasma microRNAs as a biomarker of sporadic Amyotrophic Lateral Sclerosis
Published in Molecular brain (24-10-2015)“…Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease, which leads to the loss of upper and lower motor neurons, with a currently unknown…”
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SCA42 mutation analysis in a case series of Japanese patients with spinocerebellar ataxia
Published in Journal of human genetics (01-09-2017)“…Spinocerebellar ataxia (SCA) is a group of dominantly inherited heterogeneous disorders in which 43 subtypes have been identified to date. Recently, Japanese…”
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Influences of Folate Supplementation on Homocysteine and Cognition in Patients with Folate Deficiency and Cognitive Impairment
Published in Nutrients (14-10-2020)“…Although folate deficiency was reported to be associated with hyperhomocysteinemia, influence of folate supplementation on cognition remains controversial…”
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Circulating miRNome profiling in Moyamoya disease-discordant monozygotic twins and endothelial microRNA expression analysis using iPS cell line
Published in BMC medical genomics (29-08-2018)“…Background Moyamoya disease (MMD) is characterized by progressive stenosis of intracranial arteries in the circle of Willis with unknown etiology even after…”
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Imaging Mass Spectrometry Reveals the Changes in the Taurine Conjugates of Dihydroxycholanoic Acid During Hepatic Warm Ischemia and Reperfusion in a Rat Model
Published in Transplantation proceedings (01-07-2020)“…Warm ischemia and reperfusion injury (IRI) is a prognostic factor in donation after cardiac death donor transplantation. However, a reliable method to predict…”
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Dynamic molecular network analysis of iPSC-Purkinje cells differentiation delineates roles of ISG15 in SCA1 at the earliest stage
Published in Communications biology (09-04-2024)“…Better understanding of the earliest molecular pathologies of all neurodegenerative diseases is expected to improve human therapeutics. We investigated the…”
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Carotid Ultrasonography Can Identify Stroke Patients Ineligible for Intravenous Thrombolysis Therapy due to Acute Aortic Dissection
Published in Journal of neuroimaging (01-07-2015)“…ABSTRACT Acute aortic dissection is the most common acute aortic condition requiring urgent surgical therapy. Due to lack of typical symptoms, it is sometimes…”
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Genomic copy number variation analysis in multiple system atrophy
Published in Molecular brain (29-11-2017)“…Genomic variation includes single-nucleotide variants, small insertions or deletions (indels), and copy number variants (CNVs). CNVs affect gene expression by…”
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Slowly progressive Lemierre's syndrome with orbital pain and exophthalmos
Published in Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy (01-01-2016)“…Abstract Lemierre's syndrome is an oropharyngeal bacterial infection characterized by rapidly progressive septic thrombophlebitis of the internal jugular vein…”
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Lidocaine injections and neck corset wearing improve dropped head syndrome in Parkinson's disease and related disorders
Published in Clinical parkinsonism & related disorders (01-01-2019)“…Patients with Parkinson's disease and related disorders (PDRD) may exhibit dropped head syndrome (DHS), which does not yet have an effective treatment. To…”
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Antibody to Varicella-Zoster Virus Immediate-Early Protein 62 Augments Allodynia in Zoster via Brain-Derived Neurotrophic Factor
Published in Journal of Virology (01-02-2010)“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Childhood-onset anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (anti-HMGCR) necrotizing myopathy needs to be distinguished from muscular dystrophy: A case study
Published in Rinsho shinkeigaku = Clinical neurology (27-10-2017)“…A 24-year-old woman visited our hospital with a complaint of walking disability. She had no family history of consanguineous marriage, and her developmental…”
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Clinical Characteristics of Transient Ischemic Attack Patients with Atrial Fibrillation: Analyses of a Multicenter Retrospective Study
Published in Cerebrovascular diseases extra (09-07-2015)“…Background: Atrial fibrillation (AF) is an important risk factor for transient ischemic attack (TIA). However, little is known about the characteristics of TIA…”
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MicroRNA expression profiles of neuron-derived extracellular vesicles in plasma from patients with amyotrophic lateral sclerosis
Published in Neuroscience letters (24-08-2019)“…•We extracted neuron-derived extracellular vesicles (EVs) in plasma from patients with ALS.•MicroRNA expression profiles of neuron-derived EVs were analyzed.•A…”
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Evaluation of relative potency of calibrated ciguatoxin congeners by near-infrared fluorescent receptor binding and neuroblastoma cell-based assays
Published in Toxicon (Oxford) (01-07-2023)“…Ciguatera fish poisoning (CFP) is a foodborne illness affecting > 50,000 people worldwide annually. It is caused by eating marine invertebrates and fish that…”
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Plasma matrix metalloproteinase-3 correlates with the clinical severity in men with multiple system atrophy
Published in Neurology and clinical neuroscience (01-03-2013)Get full text
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18F-THK5351 positron emission tomography imaging for Gerstmann-Sträussler-Scheinker disease
Published in Journal of the neurological sciences (15-10-2022)Get full text
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A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity
Published in Cerebellum (London, England) (01-12-2023)“…Early-onset ataxias are often difficult to diagnose due to the genetic and phenotypic heterogeneity of patients. Whole exome sequencing (WES) is a powerful…”
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Correction: A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity
Published in Cerebellum (London, England) (01-12-2023)Get full text
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