Yoshiro Amano
Nagano, Japan
Last Updated: 09/26/2026
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Found 10 publications
A Japanese Case of Infantile Liver Failure Syndrome Type 2 With Novel NBAS Variants.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: January 27, 2026
Estimated basal metabolic rate and maintenance fluid volume in children: A proposal for a new equation.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 28, 2018
An infant case of diffuse cerebrospinal lesions and cardiomyopathy caused by a BOLA3 mutation.
Journal: Brain & development
Published: October 22, 2017
Three pentraxins C-reactive protein, serum amyloid p component and pentraxin 3 mediate complement activation using Collectin CL-P1.
Journal: Biochimica et biophysica acta. General subjects
Published: July 14, 2016
Cytomegalovirus Encephalitis in a Patient with Severe Combined Immunodeficiency.
Journal: Journal of clinical immunology
Published: June 05, 2015
Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan.
Journal: Clinical and experimental nephrology
Published: February 19, 2015
Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).
Journal: American journal of medical genetics. Part A
Published: May 03, 2014
Successful treatment of fulminant Wilson's disease without liver transplantation.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: September 10, 2013
Demonstration of novel gain-of-function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia-like phenotype.
Journal: Molecular genetics & genomic medicine
Published: January 28, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026