Michiyo Urata
Fukuoka, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Toxic myopathy with multiple deletions in mitochondrial DNA associated with long-term use of oral anti-viral drugs for hepatitis B: A case study.
Journal: Neuropathology : official journal of the Japanese Society of Neuropathology
Published: January 11, 2019
Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection.
Journal: Annals of clinical microbiology and antimicrobials
Published: April 12, 2018
The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.
Journal: Pediatric blood & cancer
Published: June 24, 2016
Coping strategies and risk of cardiovascular disease incidence and mortality: the Japan Public Health Center-based prospective Study.
Journal: European heart journal
Published: May 12, 2015
Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan
Journal: Fukuoka igaku zasshi = Hukuoka acta medica
Published: May 07, 2015
Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency.
Journal: Brain & development
Published: April 12, 2015
A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.
Journal: Pediatric blood & cancer
Published: July 07, 2013
Paediatric presentation and outcome of congenital protein C deficiency in Japan.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: December 20, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026