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Hiroko Kodama

Explore the profile of Hiroko Kodama including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 85
Citations 771
Followers 0
Related Specialties
Pediatrics
Neurology
Endocrinology
Top 10 Co-Authors
Chie Fujisawa
Eishin Ogawa
Yasuhiro Sato
Masakazu Mimaki
Yan-Hong Gu
Kahoko Motoyama
Mariko Yagi
Natsue Nakamoto
Hiroshi Ozawa
Tomoko Hiroki
Published In
Brain Dev
Pediatr Int
No To Hattatsu
J Trace Elem Med Biol
Pediatr Res
Affiliations
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Recent Articles
11.
Trace element levels in mature breast milk of recently lactating Japanese women
Motoyama K, Isojima T, Sato Y, Aihara A, Asakura H, Hiraike H, et al.
Pediatr Int . 2020 Nov; 63(8):910-917. PMID: 33190386
Background: Many trace elements are essential for infant growth and development during early life. Their concentrations in breast milk vary depending on social and economic factors. Nonetheless, the present available...
12.
[The impact of support from medical professionals on families' decision-making during end-of-life care]
Nakazato K, Wakui T, Kodama H, Shimada C
Nihon Ronen Igakkai Zasshi . 2020 Jun; 57(2):163-172. PMID: 32475944
Families are involved in decision-making regarding end-of-life (EOL) care in Japan. However, how support from medical professionals toward families' decision-making affects families' satisfaction with EOL care has not been adequately...
13.
Japan's Practical Guidelines for Zinc Deficiency with a Particular Focus on Taste Disorders, Inflammatory Bowel Disease, and Liver Cirrhosis
Kodama H, Tanaka M, Naito Y, Katayama K, Moriyama M
Int J Mol Sci . 2020 Apr; 21(8). PMID: 32331308
Zinc deficiency is common in Japan, yet awareness on this disorder is lacking. The Japanese Society of Clinical Nutrition recently issued the Japan's Practical Guideline for Zinc Deficiency 2018 setting...
14.
Policy statement of enteral nutrition for preterm and very low birthweight infants
Mizuno K, Shimizu T, Ida S, Ito S, Inokuchi M, Ohura T, et al.
Pediatr Int . 2020 Feb; 62(2):124-127. PMID: 32026585
For preterm and very low birthweight infants, the mother's own milk is the best nutrition. Based on the latest information for mothers who give birth to preterm and very low...
15.
Maternal Undernutrition and Breast Milk Macronutrient Content Are Not Associated with Weight in Breastfed Infants at 1 and 3 Months after Delivery
Minato T, Nomura K, Asakura H, Aihara A, Hiraike H, Hino Y, et al.
Int J Environ Res Public Health . 2019 Sep; 16(18). PMID: 31505822
This study examined whether maternal nutritional intake and breast milk macronutrient content influence the weight of breastfed infants. We investigated 129 healthy mothers with singleton babies born from July 2016...
16.
Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial
Katayama K, Hosui A, Sakai Y, Itou M, Matsuzaki Y, Takamori Y, et al.
Biol Trace Elem Res . 2019 Aug; 195(1):71-81. PMID: 31392541
The essential trace element zinc maintains liver functions. Liver diseases can alter overall zinc concentrations, and hypozincemia is associated with various hepatic pathologies. Modulating systemic zinc through dietary supplementation is...
17.
A severe case of Menkes disease with repeated bone fracture during the neonatal period, followed by multiple arterial occlusion
Kobayashi S, Yokoi K, Kamioka N, Hamajima N, Ban K, Kodama H, et al.
Brain Dev . 2019 Jul; 41(10):878-882. PMID: 31279518
Menkes disease (MD) is a lethal infantile neurodegenerative disorder with X-linked inheritance, characterized by progressive neurodegenerative symptoms caused by pathogenic variants in the ATP7A. Early diagnosis and treatment are important,...
18.
ATP7A mutations in 66 Japanese patients with Menkes disease and carrier detection: A gene analysis
Fujisawa C, Kodama H, Hiroki T, Akasaka Y, Hamanoue M
Pediatr Int . 2019 Feb; 61(4):345-350. PMID: 30809870
Background: Menkes disease (MNK; MIN 309400) is an X-linked recessive lethal disorder of copper metabolism caused by mutations in ATP7A (MIM 300011), which encodes a transmembrane copper-transporting P-type ATPase. This...
19.
Disulfiram enhanced delivery of orally administered copper into the central nervous system in Menkes disease mouse model
Hoshina T, Nozaki S, Hamazaki T, Kudo S, Nakatani Y, Kodama H, et al.
J Inherit Metab Dis . 2018 Aug; 41(6):1285-1291. PMID: 30132231
Introduction: Menkes disease (MD) is an X-linked recessive disorder caused by dysfunction of a copper-transporting protein, leading to severe neurodegeneration in early childhood. We investigated whether a lipophilic copper chelator,...
20.
Menkes disease: Oral administration of glyoxal-bis(N(4)-methylthiosemicarbazonato)-copper(II) rescues the macular mouse
Munakata M, Kodama H, Tani N, Kimura K, Takahashi H, Maruyama K, et al.
Pediatr Res . 2018 Aug; 84(5):770-777. PMID: 30127521
Background: Menkes disease is a copper metabolism disorder caused by mutations in ATP7A, a copper-transporting P-type ATPase. In this study, oral copper supplementation via glyoxal-bis(N(4)-methylthiosemicarbazonato)-copper(II) (CuGTSM), a lipophilic copper complex,...