Satoru Morikawa
Kobe, Japan
Last Updated: 09/26/2026
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Found 15 publications
Development of an Oral Immunotherapy-Related Parental Burden Scale.
Journal: International archives of allergy and immunology
Published: May 19, 2023
A Rapid, Accurate and Simple Screening Method for Spinal Muscular Atrophy: High-Resolution Melting Analysis Using Dried Blood Spots on Filter Paper.
Journal: Clinical laboratory
Published: June 30, 2015
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.
Journal: Brain & development
Published: September 03, 2013
Acetaminophen administration in a patient with Gilbert's syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: January 03, 2013
Minimal residual disease monitoring in neuroblastoma patients based on the expression of a set of real-time RT-PCR markers in tumor-initiating cells.
Journal: Oncology reports
Published: December 03, 2012
Quantitative evaluation of ventricular dilatation using computed tomography in infants with congenital cytomegalovirus infection.
Journal: Brain & development
Published: October 01, 2012
Spinal muscular atrophy: from gene discovery to clinical trials.
Journal: Annals of human genetics
Published: August 30, 2012
Correlation and precision of serum free bilirubin concentrations determined by single and two peroxidase concentration methods in term or late-preterm newborn infants using a FDA-approved analyzer.
Journal: Clinical laboratory
Published: July 13, 2012
Severely high serum unbound bilirubin level after abdominal surgery in a newborn.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 14, 2012
Novel treatment strategy for Japanese newborns with high serum unbound bilirubin.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 05, 2012
Paramyotonia congenita: from clinical diagnosis to in silico protein modeling analysis.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 18, 2012
A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
Journal: The Kobe journal of medical sciences
Published: December 16, 2011
Last Updated: 09/26/2026