Hayato Aoyagi
Obihiro, Japan
Last Updated: 09/26/2026
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Found 12 publications
A novel scoring system for the prediction of disease severity in STEC-HUS.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 13, 2023
M-type phospholipase A2 receptor-associated membranous nephropathy in a patient with Noonan-like syndrome with loose anagen hair.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 11, 2023
Changes in bone turnover markers after discontinuing long-term glucocorticoid administration in children with idiopathic nephrotic syndrome: a multicenter retrospective observational study.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 11, 2022
P1 gene of Mycoplasma pneumoniae isolated from 2016 to 2019 and relationship between genotyping and macrolide resistance in Hokkaido, Japan.
Journal: Journal of medical microbiology
Published: June 24, 2021
The effect of rituximab on the quality of life of children with refractory nephrotic syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 20, 2020
Left-sided inferior vena cava with nutcracker syndrome.
Journal: Clinical and experimental nephrology
Published: April 03, 2018
Periodically repeated rituximab administrations in children with refractory nephrotic syndrome: 2-year multicenter observational study.
Journal: Pediatric nephrology (Berlin, Germany)
Published: April 01, 2018
Clinical effectiveness of four neuraminidase inhibitors (oseltamivir, zanamivir, laninamivir, and peramivir) for children with influenza A and B in the 2014-2015 to 2016-2017 influenza seasons in Japan.
Journal: Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
Published: November 22, 2017
Streptococcus pulmonary empyema after varicella infection in a serologically immunocompetent boy.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: November 01, 2013
Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1.
Journal: Endocrine journal
Published: September 29, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026