Naomi Kuranobu
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Explore the profile of Naomi Kuranobu including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
47
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Recent Articles
1.
Miyaishi M, Fukushima K, Kuranobu N, Murakami J, Namba N
Cureus
. 2025 Mar;
17(2):e78396.
PMID: 40046366
A previously healthy 18-month-old boy presented with hepatomegaly, accompanied by liver injury. Imaging and liver biopsy findings suggested a hepatic glycogen storage disease (GSD) but not GSD type I. Genetic...
2.
Fukushima K, Itaba N, Kono Y, Okazaki S, Enokida S, Kuranobu N, et al.
Regen Ther
. 2021 Sep;
18:292-301.
PMID: 34504910
Introduction: Transplantation of IC-2-engineered bone marrow-derived mesenchymal stem cell (BM-MSC) sheets (IC-2 sheets) was previously reported to potentially reduce liver fibrosis. Methods: This study prepared IC-2-engineered cell sheets from multiple...
3.
Shimura M, Kuranobu N, Ogawa-Tominaga M, Akiyama N, Sugiyama Y, Ebihara T, et al.
Orphanet J Rare Dis
. 2020 Jul;
15(1):169.
PMID: 32703289
Background: Hepatocerebral mitochondrial DNA depletion syndrome (MTDPS) is a disease caused by defects in mitochondrial DNA maintenance and leads to liver failure and neurological complications during infancy. Liver transplantation (LT)...
4.
Suyama T, Shimura M, Fushimi T, Kuranobu N, Ichimoto K, Matsunaga A, et al.
Mol Genet Metab Rep
. 2020 Jun;
24:100610.
PMID: 32509533
Mitochondrial trifunctional protein (TFP) deficiency is a rare inherited metabolic disorder caused by defects in fatty acid β-oxidation (FAO) of long-chain fatty acids, leading to impaired energy production. Fasting avoidance,...
5.
Yao Y, Nishimura M, Murayama K, Kuranobu N, Tojo S, Beppu M, et al.
Sci Rep
. 2019 Nov;
9(1):17411.
PMID: 31757988
Next-generation sequencing (NGS) is a revolutionary sequencing technology for analyzing genomes. However, preprocessing methods for mitochondrial DNA (mtDNA) sequencing remain complex, and it is required to develop an authenticated preprocessing...
6.
Kuranobu H, Murakami J, Kuranobu N, Okamoto K, Murayama K, Kanzaki S
Pediatr Int
. 2016 Dec;
58(12):1337-1340.
PMID: 28008731
We report the case of a 13-month-old girl with frequent vomiting, intractable diarrhea, hyperlactatemia, and liver dysfunction. Although the symptoms were treatment resistant, enteral nutrition formula containing medium-chain triglycerides reduced...
7.
Kuranobu N, Murakami J, Okamoto K, Nishimura R, Murayama K, Takamura A, et al.
Hepatol Res
. 2015 Sep;
46(5):477-82.
PMID: 26385844
Cholesterol ester storage disease (CESD) is an autosomal recessive disorder caused by deficient lysosomal acid lipase (LAL) activity, resulting in cholesteryl ester (CE) accumulation. CESD patients have liver disease associated...