Koya Kawase
Nagoya, 4678601, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 14 publications
Significance of birth in the maintenance of quiescent neural stem cells.
Journal: Science advances
Published: January 22, 2025
Transformation of radial glia into postnatal neural stem cells depends on birth.
Journal: Cell reports
Published: May 13, 2024
Influence of Intrauterine Inflammation, Delivery, and Postnatal Feeding on the Temporal Changes of Serum Alpha 1 Acid Glycoprotein Levels in Extremely-Low-Birth-Weight Infants.
Journal: Nutrients
Published: October 27, 2022
Foetal growth, birth transition, enteral nutrition and brain light scattering.
Journal: Scientific reports
Published: March 20, 2021
Utility of breakpoint-specific nested polymerase chain reaction for the diagnosis of Emanuel syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 03, 2020
Promoting sound development of preterm infants in the name of developmental neuroscience: Beyond advanced life support and neuroprotection.
Journal: Pediatrics and neonatology
Published: October 03, 2020
Case Report: Management of Cholestasis Associated With Congenital Syphilis.
Journal: Frontiers in pediatrics
Published: September 17, 2020
Regional Differences in Clinical Features of Kaposiform Hemangioendothelioma of the Intestinal Tract.
Journal: Journal of pediatric hematology/oncology
Published: March 20, 2018
Radial Glial Fibers Promote Neuronal Migration and Functional Recovery after Neonatal Brain Injury.
Journal: Cell stem cell
Published: May 02, 2017
Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 25, 2015
A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.
Journal: American journal of medical genetics. Part A
Published: December 05, 2014
Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.
Journal: Brain & development
Published: November 17, 2014
Last Updated: 09/26/2026