Hiroko Kodama
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Explore the profile of Hiroko Kodama including associated specialties, affiliations and a list of published articles.
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85
Citations
771
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Recent Articles
1.
Bhakta S, Kodama H, Mimaki M, Tsukahara T
Biomolecules
. 2025 Jan;
15(1.
PMID: 39858530
RNA editing is a significant mechanism underlying genetic variation and protein molecule alteration; C-to-U RNA editing, specifically, is important in the regulation of mammalian genetic diversity. The ability to define...
2.
Asaoka D, Ishihara T, Ezoe S, Hamada I, Kitamura M, Uchino K, et al.
J Trace Elem Med Biol
. 2024 Dec;
87:127558.
PMID: 39705879
Objective: This study evaluated the efficacy and safety of NPC-25, zinc histidine hydrate, in patients with hypozincemia. This randomized multicenter active-controlled open-label trial aimed to verify the non-inferiority of NPC-25...
3.
Kodama M, Okano S, Nojri S, Abe K, Fukata M, Nagase Y, et al.
PLoS One
. 2024 May;
19(5):e0300580.
PMID: 38776273
Although a Western diet has been identified as a risk factor for Crohn's disease (CD), there is still controversy surrounding the specific foods that may contribute to the development of...
4.
Yasukawa M, Arai S, Nagura M, Kido R, Asakawa S, Hirohama D, et al.
Kidney Int Rep
. 2022 Jul;
7(7):1565-1574.
PMID: 35812286
Introduction: Impaired response to erythropoiesis-stimulating agents (ESAs) is associated with increased mortality in patients with end-stage kidney disease. However, the underlying mechanisms are not fully elucidated. Accumulating data reveal that...
5.
Fujisawa C, Kodama H, Sato Y, Mimaki M, Yagi M, Awano H, et al.
Mol Genet Metab Rep
. 2022 Mar;
31:100849.
PMID: 35242581
Menkes disease (MD) is an X-linked recessive disorder caused by mutations in . Patients with MD exhibit severe neurological and connective tissue disorders due to copper deficiency and typically die...
6.
Ohmori H, Kodama H, Takemoto M, Yamasaki M, Matsumoto T, Kumode M, et al.
World J Clin Cases
. 2021 Nov;
9(29):8825-8830.
PMID: 34734062
Background: Percutaneous endoscopic gastrostomy with jejunal extension (PEG-J) is often used to treat patients with neurological impairment and difficulty in swallowing. However, these patients often develop copper deficiency. This report...
7.
Nomura K, Itakura Y, Minamizono S, Okayama K, Suzuki Y, Takemi Y, et al.
Front Psychol
. 2021 Oct;
12:576089.
PMID: 34675829
Body image self-discrepancy reflects a preference for weight loss regardless of normal body size and is a distorted cognition that may be a precursor to eating disorders. The aim of...
8.
Yamagishi Y, Kudo T, Oyumi M, Sakamoto Y, Takahashi K, Akashi T, et al.
Pharm Res
. 2021 Aug;
38(8):1335-1344.
PMID: 34403032
Purpose: Menkes disease is a rare hereditary disease in which systemic deficiency of copper due to mutation of the ATP7A gene causes severe neurodegenerative disorders. The present parenteral drugs have...
9.
Sato Y, Isojima T, Takamiya K, Motoyama K, Enkai S, Ogawa E, et al.
Horm Res Paediatr
. 2021 Aug;
94(5-6):229-234.
PMID: 34348302
Introduction: Transient neonatal diabetes mellitus (TNDM) is a rare condition that is characterized by the presence of diabetes mellitus during the first 6 months of life and remission by 18...
10.
Kodama H, Anan Y, Izumi Y, Sato Y, Ogra Y
BMJ Paediatr Open
. 2021 Jul;
5(1):e000948.
PMID: 34222678
Objective: To evaluate the concentrations of copper and zinc in the breast milk of mothers undergoing treatment for Wilson's disease (WD) and clarify whether they can safely breast feed their...