Search Results - "Tsujikawa, Koyo"
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Clinical implication of denervation in sporadic inclusion body myositis
Published in Journal of the neurological sciences (15-08-2022)“…Sporadic inclusion body myositis (sIBM) is often accompanied by signs suggestive of denervation on electromyography (EMG), which mimics neurogenic disorders…”
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Distinctive distribution of brain volume reductions in MELAS and mitochondrial DNA A3243G mutation carriers: A voxel-based morphometric study
Published in Mitochondrion (01-09-2016)“…The aim of this study was to investigate the clinically latent brain atrophy of patients with mitochondrial encephalopathy, lactic acidosis, and stroke-like…”
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HMGCR antibody-associated myopathy as a paraneoplastic manifestation of esophageal carcinoma
Published in Neurology (23-08-2016)“…Immune-mediated myopathies with antibodies may be triggered by statin exposure, but some patients with these disorders are statin-naive; thus, there are…”
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Clinicopathological features of graft versus host disease‐associated myositis
Published in Annals of clinical and translational neurology (01-02-2024)“…Background and Objective Chronic graft versus host disease (GVHD)‐associated myositis targeting skeletal muscle is a relatively rare but potentially…”
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Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology
Published in Science advances (27-05-2022)“…While amyloid-β lies upstream of tau pathology in Alzheimer's disease, key drivers for other tauopathies, including progressive supranuclear palsy (PSP), are…”
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Metabolome and transcriptome analysis on muscle of sporadic inclusion body myositis
Published in Annals of clinical and translational neurology (01-10-2022)“…Objective Sporadic inclusion body myositis (sIBM) is the most common acquired myopathy in patients older than 50 years of age. sIBM is hardly responds to any…”
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Effectiveness of midazolam for L-arginine-resistant headaches during stroke-like episodes in MELAS: a case report
Published in Rinsho shinkeigaku = Clinical neurology (2014)“…A 14-year-old girl was referred to us with severe migraine-like headaches associated with vomiting and right homonymous hemianopsia. On admission, MRI…”
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Dysregulation of Aldh1a2 underlies motor neuron degeneration in spinal muscular atrophy
Published in Neuroscience research (01-09-2023)“…Lower motor neuron degeneration is the pathological hallmark of spinal muscular atrophy (SMA), a hereditary motor neuron disease caused by loss of the SMN1…”
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Chronological changes of 123I-MIBG myocardial scintigraphy and clinical features of Parkinson's disease
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2015)“…ObjectivesThe aim of this study was to investigate chronological changes of 123I-meta-iodobenzylguanidine (MIBG) myocardial scintigraphy and its relation to…”
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Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia
Published in Clinical immunology (Orlando, Fla.) (01-08-2021)“…Early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH) is a neurodegenerative disorder caused by mutation in the aprataxin (APTX)-coding gene…”
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Chronological changes of 123 I-MIBG myocardial scintigraphy and clinical features of Parkinson's disease
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2015)Get full text
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Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis
Published in Neurology (23-03-2021)“…Objective To assess long-term (2 years) effects of bimagrumab in participants with sporadic inclusion body myositis (sIBM). Methods Participants (aged 36–85…”
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Elderly-onset familial myasthenia gravis in two siblings
Published in Neuromuscular disorders : NMD (01-06-2016)“…Highlights • We report two siblings' cases of elderly-onset MG sharing the common HLA haplotypes. • These cases indicate that elderly-onset MG can occur in a…”
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