 | Emi Kasai‐YoshidaDepartments of Neuropediatrics and | Departments of Pediatrics and | Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, 2-6-1 Musashidai, Fuchu, Tokyo ... |
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Emi Kasai‐Yoshida:Expert Impact
Concepts for whichEmi Kasai‐Yoshidahas direct influence:Static encephalopathy,Novo mutations,Autophagy gene,Video report,Childhood neurodegeneration,Neurodegeneration adulthood,Static encephalopathy childhood,Murinederived antigens.
Emi Kasai‐Yoshida:KOL impact
Concepts related to the work of other authors for whichfor which Emi Kasai‐Yoshida has influence:Brain iron accumulation,Intellectual disability,Developmental delay,Epileptic encephalopathy,Novo mutations,Nmdar encephalitis,Rett syndrome.
KOL Resume for Emi Kasai‐Yoshida
| Year | |
|---|---|
| 2013 | Departments of Neuropediatrics and Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, 2-6-1 Musashidai, Fuchu, Tokyo 183-0042, Japan |
| Concept | World rank |
|---|---|
| wdr45 static | #13 |
| wdr45 static encephalopathy | #13 |
| adulthood hirotomo saitsu | #17 |
| wdr45 encodes homolog | #17 |
| iron lennox | #17 |
| infantile hirotomo saitsu | #17 |
| hirotomo saitsu | #17 |
| mizushima naomichi matsumoto | #17 |
| hirotomo saitsu noboru | #17 |
| naomichi matsumoto wdr45 | #17 |
| adulthood wdr45 encodes | #17 |
| adulthood wdr45 | #17 |
| naomichi matsumoto colleagues | #21 |
| naomichi matsumoto | #21 |
| autophagy protein humans | #23 |
| noboru mizushima | #24 |
| wdr45 encodes | #25 |
| yeast autophagy protein | #26 |
| static encephalopathy childhood | #26 |
| identification novo mutations | #30 |
| neurodegeneration adulthood | #30 |
| humans infantile | #33 |
| video report | #49 |
| childhood neurodegeneration | #49 |
| gene wdr45 | #65 |
| shortlived plasmablasts | #77 |
| novo mutations wdr45 | #79 |
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Prominent publications by Emi Kasai‐Yoshida
De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood
[ PUBLICATION ]
Hirotomo Saitsu, Noboru Mizushima, Naomichi Matsumoto and colleagues report the identification of de novo mutations in WDR45 that cause static encephalopathy of childhood with neurodegeneration in adulthood. WDR45 encodes a homolog of the yeast autophagy protein Atg18.
| Known for Novo Mutations | Static Encephalopathy | Autophagy Gene | Wdr45 Encodes | Intellectual Disability |
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 |
Of 71 acute lymphoblastic leukemia survivors at our hospital over the past 10 years, 2 children developed mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS). This is the first report to describe the clinical course of MTLE-HS observed longitudinally by EEG and MRI. Patient 1 experienced a seizure during chemotherapy involving intrathecal methotrexate. Postseizure MRI suggested methotrexate encephalopathy or leukemic invasion. Anticonvulsant therapy was initiated; ...
| Known for Hippocampal Sclerosis | Acute Lymphoblastic | Temporal Lobe | Precursor Cell | Leukemia Lymphoma |
First video report of static encephalopathy of childhood with neurodegeneration in adulthood
[ PUBLICATION ]
| Known for Static Encephalopathy | Video Report | Childhood Neurodegeneration | Neurodegenerative Diseases |
