Shinsuke Kato
Rumoi, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 28 publications
Rescue from Stx2-Producing E. coli-Associated Encephalopathy by Intravenous Injection of Muse Cells in NOD-SCID Mice.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: January 29, 2025
Molecular evolutionary analysis of novel NSP4 mono-reassortant G1P[8]-E2 rotavirus strains that caused a discontinuous epidemic in Japan in 2015 and 2018.
Journal: Frontiers in microbiology
Published: May 10, 2024
An integrated genetic analysis of epileptogenic brain malformed lesions.
Journal: Acta neuropathologica communications
Published: December 23, 2022
Transient personality changes with bilateral thalamic infarction in a 12-year-old girl.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 20, 2022
Stereotyped Upper Limb Movement in MECP2 Duplication Syndrome.
Journal: Neurology
Published: May 01, 2021
Molecular and clinical characterization of the equine-like G3 rotavirus that caused the first outbreak in Japan, 2016.
Journal: The Journal of general virology
Published: February 15, 2021
Ultrastructure of spinal anterior horn cells in human Niemann-Pick type C (NPC) patient and mouse model of NPC with retroposon insertion in NPC1 genes.
Journal: Pathology international
Published: November 08, 2019
Immunohistochemical and ultrastructural evidence for the pathogenesis of white matter degeneration in patients with panencephalopathic-type Creutzfeldt-Jakob disease: Inducible nitric oxide synthase overexpression in bizarre astrocytes.
Journal: Neuropathology : official journal of the Japanese Society of Neuropathology
Published: August 17, 2019
Rescue from Stx2-Producing E. coli-Associated Encephalopathy by Intravenous Injection of Muse Cells in NOD-SCID Mice.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: May 27, 2019
Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome.
Journal: Journal of the neurological sciences
Published: May 24, 2019
Ossified Metaplastic Spinal Meningioma Without Psammomatous Calcification: A Case Report.
Journal: Yonago acta medica
Published: February 15, 2019
Last Updated: 09/26/2026