 | Eiji KuriharaDepartment of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan | Tokyo Metropolitan Neurological Hospital Department of Neuropediatrics Tokyo Japan | ... |
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Eiji Kurihara:Expert Impact
Concepts for whichEiji Kuriharahas direct influence:Severe motor,Static encephalopathy,Video report,Reversion error,Acute stage,Murinederived antigens,Receptor encephalitis,Aspartate receptor.
Eiji Kurihara:KOL impact
Concepts related to the work of other authors for whichfor which Eiji Kurihara has influence:Nmdar encephalitis,Aspartate receptor,Streptococcal infections,Tic disorders,Severe motor,Teratoma removal,Juvenile myasthenia gravis.
KOL Resume for Eiji Kurihara
| Year | |
|---|---|
| 2018 | Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan |
| 2016 | Tokyo Metropolitan Neurological Hospital Department of Neuropediatrics Tokyo Japan |
| 2013 | Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, 2-6-1 Musashidai, Fuchu, Tokyo 183-0042, Japan |
| 2008 | 1Department of Pediatrics, Tokyo Metropolitan Fuchu Medical Center for Disabled, 2Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, 3Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neuroscience, 4Department of Pediatrics, National Rehabilitation Center for Disabled Children and 5Department of Pediatrics, Tokyo Children’s Rehabilitation Hospital, Tokyo, Japan |
| Concept | World rank |
|---|---|
| reversion error | #18 |
| myoclonus neuroprotective | #22 |
| disability smid | #23 |
| static encephalopathy childhood | #51 |
| video report | #60 |
| neurodegeneration adulthood | #67 |
| gabhs infection | #70 |
| childhood neurodegeneration | #81 |
| shortlived plasmablasts | #83 |
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Prominent publications by Eiji Kurihara
Rituximab ameliorates anti-N-methyl-d-aspartate receptor encephalitis by removal of short-lived plasmablasts
[ PUBLICATION ]
We measured anti-N-methyl-D-aspartate receptor (NMDAR) autoantibody levels and assessed B cell subsets using multicolor flow cytometry of peripheral blood mononuclear cells (PBMCs) from a recurrent anti-NMDAR encephalitis case to evaluate the effectiveness of rituximab treatment. Rituximab depleted CD20(+) fractions of naïve and memory B cell subsets and reduced the number of CD20(-) plasmablasts. This study suggests that short-lived plasmablasts are removed by rituximab-induced ...
| Known for Receptor Encephalitis | Murinederived Antigens | Shortlived Plasmablasts | Methyl Aspartate | Rituximab Treatment |
Hemorrhage due to tracheoarterial fistula with severe motor and intellectual disability
[ PUBLICATION ]
BACKGROUND: Tracheoarterial fistula (TAF) is an unusual but highly lethal complication of tracheostomy, and successful surgical intervention for TAF has been reported. Few investigations are available for TAF in severe motor and intellectual disability (SMID). The aim of the present paper was to analyzed TAF in SMID to clarify which clinical variables might predict the occurrence of TAF, and adequate management for lifesaving.
METHODS: Medical records at Metropolitan Fuchu Medical Center ...
| Known for Severe Motor | Intellectual Disability | Artery Fistula | Clinical Status | Successful Surgical Intervention |
Different X‐linked KDM5C mutations in affected male siblings: is maternal reversion error involved?
[ PUBLICATION ]
Genetic reversion is the phenomenon of spontaneous gene correction by which gene function is partially or completely rescued. However, it is unknown whether this mechanism always correctly repairs mutations, or is prone to error. We investigated a family of three boys with intellectual disability, and among them we identified two different mutations in KDM5C, located at Xp11.22, using whole-exome sequencing. Two affected boys have c.633delG and the other has c.631delC. We also confirmed ...
| Known for Reversion Error | Intellectual Disability | Wholeexome Sequencing | Somatic Mutation | Female Genes |
Autoimmune neurological disorders associated with group-A beta-hemolytic streptococcal infection
[ PUBLICATION ]
Although central nervous system (CNS) disorders associated with group-A beta-hemolytic streptococcal (GABHS) infection occur only rarely, Sydenham's chorea is a well-recognized disease that can arise following infection. Children may develop a tic, obsessive compulsive disorder (OCD), and extrapyramidal movement subsequent to GABHS infection. These disorders have been termed pediatric autoimmune neuropsychiatric disorders associated with streptococci (PANDAS). Herein we report one case ...
| Known for Gabhs Infection | Autoimmune Diseases | Streptococcus Pyogenes | Nervous Cns | Beta Hemolytic |
First video report of static encephalopathy of childhood with neurodegeneration in adulthood
[ PUBLICATION ]
| Known for Static Encephalopathy | Video Report | Childhood Neurodegeneration | Neurodegenerative Diseases |
Choreo–ballistic movements in a case carrying a missense mutation in syntaxin binding protein 1 gene
[ PUBLICATION ]
| Known for Missense Mutation | Protein 1 | Brain Child | Humans Magnetic | Syntaxin Binding |
