Naomi Kuranobu
Yonago, Japan
Last Updated: 09/26/2026
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Found 8 publications
The status of adult patients with citrin deficiency in Japan: A report from the nation-wide study.
Journal: Molecular genetics and metabolism
Published: July 02, 2025
Secreted matrix metalloproteinase-14 is a predictor for antifibrotic effect of IC-2-engineered mesenchymal stem cell sheets on liver fibrosis in mice.
Journal: Regenerative therapy
Published: June 07, 2021
Efficacy of bezafibrate in two patients with mitochondrial trifunctional protein deficiency.
Journal: Molecular genetics and metabolism reports
Published: May 20, 2020
Clinical and molecular basis of hepatocerebral mitochondrial DNA depletion syndrome in Japan: evaluation of outcomes after liver transplantation.
Journal: Orphanet journal of rare diseases
Published: March 15, 2020
A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing.
Journal: Scientific reports
Published: January 18, 2019
Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report.
Journal: Hepatology research : the official journal of the Japan Society of Hepatology
Published: March 02, 2015
Mitochondrial respiratory chain complex I deficiency causes intractable gastrointestinal symptoms.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: February 24, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026