Search Results - "Shiraishi, Wataru"
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1
A Unilateral Bright Middle Cerebellar Peduncle Sign
Published in Internal Medicine (01-08-2021)Get full text
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2
Immunotherapy‐responsive brainstem lesion accompanied with anti‐galactocerebroside antibody
Published in Clinical & experimental neuroimmunology (01-05-2022)“…Background Brainstem lesions are a diagnostic challenge and clinicians have to differentiate between many diseases including acute disseminated…”
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3
Blood transfusion‐induced posterior reversible encephalopathy syndrome presenting severe brain atrophy: A report of two cases
Published in Clinical case reports (01-01-2022)“…Several cases of posterior reversible encephalopathy syndrome (PRES) after blood transfusion have been reported, but the long‐term prognosis is unknown. Here,…”
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4
Bright middle cerebellar peduncle sign in multiple system atrophy with predominant cerebellar ataxia is more apparent in double-inversion recovery imaging than in conventional imaging
Published in PloS one (13-11-2024)“…Multiple system atrophy (MSA) is a neurodegenerative disorder that presents as parkinsonism, cerebellar ataxia, and autonomic dysfunction. Magnetic resonance…”
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5
Clearance of peripheral nerve misfolded mutant protein by infiltrated macrophages correlates with motor neuron disease progression
Published in Scientific reports (12-08-2021)“…Macrophages expressing C–C chemokine receptor type 2 (CCR2) infiltrate the central and peripheral neural tissues of amyotrophic lateral sclerosis (ALS)…”
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6
A Case of Hyperglycemia-Induced Epileptic Homonymous Hemianopsia
Published in Curēus (Palo Alto, CA) (22-07-2024)“…Hyperglycemia sometimes initially presents with neurological manifestations, including seizures, visual hallucinations, choreoathetosis, hemiballismus,…”
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Identifying Hyperreflective Foci in Diabetic Retinopathy via VEGF-Induced Local Self-Renewal of CX3CR1+ Vitreous Resident Macrophages
Published in Diabetes (New York, N.Y.) (01-12-2022)“…Intraretinal hyperreflective foci (HRF) are significant biomarkers for diabetic macular edema. However, HRF at the vitreoretinal interface (VRI) have not been…”
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8
Hypothermia‐induced triphasic waves
Published in Neurology and clinical neuroscience (01-07-2021)“…A 79‐year‐old Japanese woman was admitted to our hospital with consciousness disturbance and difficulty in moving. On admission, her core temperature was 28°C…”
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9
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2
Published in Annals of neurology (01-04-2016)“…Objective The objective of this study was to identify new causes of Charcot–Marie–Tooth (CMT) disease in patients with autosomal‐recessive (AR) CMT. Methods To…”
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10
Bilateral Phrenic Nerve Palsy Associated With Neuralgic Amyotrophy
Published in Curēus (Palo Alto, CA) (11-04-2024)“…Neuralgic amyotrophy (NA) is a multifocal inflammatory neuropathy accompanied by acute pain and muscle atrophy. NA commonly affects the upper extremities, but…”
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Case Report: Paraneoplastic Tumefactive Demyelination Associated With Seminoma
Published in Frontiers in neurology (11-07-2022)“…Paraneoplastic tumefactive demyelination (TD) is a rare disorder of the central nervous system that can be challenging to diagnose. Here, we describe a…”
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12
Metabolism-Mediated Thrombotic Microangiopathy in an Older Patient Without Malnutrition
Published in Curēus (Palo Alto, CA) (13-02-2023)“…Vitamin B12 deficiency can cause thrombotic microangiopathy (TMA)-like symptoms such as purpura caused by platelet reduction, general fatigue caused by anemia,…”
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13
Lumbar Subarachnoid-Peritoneal Shunting Deteriorates Superficial Siderosis Associated with a Dural Defect
Published in Curēus (Palo Alto, CA) (21-02-2024)“…Superficial siderosis is a disease in which hemosiderin is deposited under the leptomeninges and subpial layers of hindbrain structures, e.g., the cerebellum,…”
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14
A human T-lymphotropic virus-1 carrier who developed progressive multifocal leukoencephalopathy following immunotherapy for sarcoidosis: a case report
Published in BMC neurology (02-02-2023)“…Progressive multifocal leukoencephalopathy (PML) is a devastating demyelinating disorder of the central nervous system caused by opportunistic infection of the…”
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15
Blood transfusion‐induced posterior reversible encephalopathy syndrome with periodic sharp wave complexes, 14‐3‐3 protein elevation, and the pulvinar sign
Published in Neurology and clinical neuroscience (01-01-2021)“…A 52‐year‐old Japanese woman was admitted to our hospital with consciousness disturbance and convulsions at 10 days after transfusion with 10 U of blood due to…”
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16
Serum perampanel levels in patients with seizures are not affected by hemodialysis
Published in Epilepsia open (01-08-2024)“…Perampanel belongs to a novel class of antiseizure medications (ASMs). Studies examining the effect of hemodialysis on perampanel serum levels in clinical…”
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Downregulation of Neuronal and Dendritic Connexin36-Made Electrical Synapses Without Glutamatergic Axon Terminals in Spinal Anterior Horn Cells From the Early Stage of Amyotrophic Lateral Sclerosis
Published in Frontiers in neuroscience (28-11-2018)“…Connexin36 (Cx36) forms gap junctions between neurons, which are called electrical synapses, enabling adjacent neurons to communicate directly. The…”
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A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber’s hereditary optic neuropathy
Published in Multiple sclerosis (01-02-2014)“…We report the first case of definite neuromyelitis optica (NMO) with a pathogenic mitochondrial DNA (mtDNA) mutation for Leber’s hereditary optic neuropathy…”
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A case of multiple sclerosis with a tumefactive lesion during long-term treatment with fingolimod, leading to decompressive craniotomy
Published in Rinsho shinkeigaku = Clinical neurology (28-01-2023)“…We report a 57-year-old man with multiple sclerosis since his 30s who was treated with fingolimod for 9 years. He developed left hemiparesis and consciousness…”
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20
Oral phase dysphagia in facial onset sensory and motor neuronopathy
Published in Brain and behavior (01-06-2018)“…Introduction Facial onset motor and sensory neuronopathy (FOSMN) is a rare disease whose cardinal features are initial asymmetrical facial sensory deficits…”
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