日本の女性研究者

健康・スポーツ科学

Researcher List >> KODAMA Hiroko
 

KODAMA Hiroko

 
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NameKODAMA Hiroko
e-mailkodamah2018gmail.com
AffiliationTeikyo University
SectionFaculty of Medicine, Department of Medicine, Department of Pediatrics
Job titleProfessor
Degree(BLANK)
Research funding number00093386

Research Interests

 
Zinc , Pediatrics , Endocrinology , Metabolism , Nutrition

Research Areas

 
  • Health/Sports science / Applied health science / 
  • Clinical internal medicine / Metabolomics / 
  • Clinical internal medicine / Endocrinology / 
  • Clinical internal medicine / Pediatrics / 

Education

 
 
 - 
1970
Faculty of Medicine, Osaka University
 

Published Papers

 
Sexual precocity in a girl with early-oneset Graves' disease
Ogawa E, Isojima T, Sato Y, Motoyama K, Kodama H
Clin Pediatr Endocrinol   27(3) 165-169   Sep 2018   [Refereed]
Hoshina T, Nozaki S, Hamazaki T, Kudo S, Nakatani Y, Kodama H, Shintaku H, Watanabe Y.
J Inherit Metab Dis.      Aug 2018   [Refereed]
Eda K, Mizuochi T, Iwama I, Inui A, Etani Y, Araki M, Hara S, Kumagai H, Hagiwara S, Murayama K, Murakami J, Shimizu N, Kodama H, Yasuda R, Takaki Y, Yamashita Y
J.Gastroenterology and Hepatology   33(1) 264-269   Jan 2018   [Refereed]
Itsumura N, Kibihara Y, Fukue K, Miyata A, Fukushima K, Tamagawa-Mineoka R, Katoh N, Nishito Y, Ishida R, Narita H, Kodama H, Kambe T.
Pediatr Res.   80(4) 586-594   Oct 2016   [Refereed]
Wakabayashi K, Kodama H, Ogawa E, Sato Y, Motoyama K, Suzuki M.
Pediatr Int.   58(9) 872-876   Sep 2016   [Refereed]
Low serum biotin in Japanese children fed with hydrolystate formula
Sato Y, Wakabayashi K, Ogawa E, Kodama H, Mimaki M.
Pediatr Int   58(9) 867-871   Sep 2016   [Refereed]
Ogawa E, Ishige M, Takahashi Y, Kodama H, Fuchigami T, Takahashi S.
Pediatr Int.   58(8) 778-781   Aug 2016   [Refereed]
Matsuki T, Yahagi K, Mori H, Matsumoto H, Hara T, Tajima S, Ogawa E, Kodama H, Yamamoto K, Yamada T, Matsumoto S, Kurokawa K.
Nat Commun   DOI:10.1038 1-12   Jun 2016   [Refereed]
Matsuki T, Tajima S, Hara T, Yahagi K, Ogawa E, Kodama H.
Benef Microbes.   7(4) 453-461   Apr 2016   [Refereed]
Hikita T, Kodama H, Ogita K, Kaneko S, Nakamoto N, Mimaki M
pediatric Neurology   57 29-33   Jan 2016   [Refereed]

Misc

 
Nakagawa T, Inoue Y, Kodama H, Yamazaki H, Kawai K, Suemizu H, Masuda R, Iwazaki M, Ymamada S, Ueyama Y, Inoue H, Nakamura M
Oncol Rep.   20(2) 265-270   2008
Gu YH, Kodama H, Watanabe S, Kikuchi N, Ishitsuka I, Ozawa H, Fujisawa C, Shiga K
Brain Dev.   29(2) 105-108   2007
Kobayashi K, Katsuya Y, Abdulah R, Fujisawa C, Nagamine T, Morikawa A, Murakami M, Koda Koyama H
Biomed Res Trace Elements   18(1) 91-95   2007
Kodama H, Fujisawa C, Gu YH, Shiga K
Biomed Res Trace Elements   18(3) 249-254   2007
J.Inherit Metab Dis   28(1):89-93    2005
Kobayashi S, Kodama H, Inuzuka R, Mori Y, Yanagawa Y.
Pediatr Int.   47(5) 589-591   2005
Kodama H, Sato E, Gu YH, Shiga K, Fujisawa C, Kozuma T.
J Inherit Metab Dis.   28 971-978   2005
Biomed Res Trace Elements   15(1): 33-36    2004
Kako K, Takehara A, Arai H, Onodera T, Takahashi Y, Hanagata H, Ogra Y, Takagi H, Kodama H, Suzuki KT, Munekata E, Fukamizu A.
Biochem Biophys Res Commun.   324(4) 1379-1385   2004
Trace Element Deficiency in Infants and Children -Clinical practice-
Kodama H,
JMAJ   47(8) 376-382   2004
Eur J Pediatr   162(51-52)    2003
POSSIBILITY OF GENE THERAPY FOR MENKES DISEASE
J Inherit Metab Dis   26(2) 184   2003
MUTATIONS SCREENING、AND GENOTYPE AND PHENOTYPE RELATIONSHIP IN 40 CHINESE PATIENTS WITH WILSON DISEASE
J Inherit Metab Dis   26(2) 184   2003
EFFECT OF COMBINATION THERAPY WITH COPPER AND A CHELATOR IN THE MACULAR MOUSE, AN ANIMAL MODEL OF MENKES DISEASE
J Inherit Metab Dis   26(2) 186   2003
GENE MUTATIONS IN 11 JAPANESE PATIENTS WITH WILSON'S DISEASE
J Inherit Metab Dis   26(2) 186   2003
Delayed closure of physiological porto-systemic shunt can be caused by citrin deficiency
New Developments in Urea Cycle Disorders ICIEM 2003 Satellite meeting      2003
Genotype and phenotype in patients with Menkes disease and occipital horn syndrome
J Inherit Metab Dis   25(166)    2002
Genotype and phenotype in patients with Menkes disease and occipital horn syndrome
The 40th annual symposium of the society for the study of inherited errors of metabolism (SSIEM)      2002
Comparative study on gene mutation and treatment of Wilson disease, a congenital metabolic disease in China and Japan
China-Japan Medical conference 2002      2002
Drug targets in Menkes disease-prospective developments "jointly worked"
Expert Opin Ther Targets   5(5) 625-635   2001
Mutation analysis of type II Gaucher disease in five Taiwanese children:identification of two novel mutations
Acta Paediatr Taiwan   42(231-235)    2001
Clinical markers for connective tissue abnormalities in patients with Menkesdisease
8th International Conference on Wilson Disease and Menkes Disease      2001
Combination therapy for Wilson disease with severe liver dysfunction - a case report
8th International Conference on Wilson Disease and Menkes Disease      2001
Genotype and Phenotype in Patients with Menkes Disease and Occipital Horn Syndrome
23rd International Congress of Pediatrics      2001
Carrier and Prenatal Diagnosis of Menkes Disease
23rd International Congress of Pediatrics      2001
Pediatr Int   42(440-447)    2000
Brain & Development   22(301-306)    2000
Successful eary copper histidine therapy in a patient with Menkes
Society for the Study of Inborn Errors of Metabolism      2000
Possible markers for connective tissue abnormalities in patients with Menkes disease
8th International Congress of Inborn Errors Metabolism      2000
Gene analysis and copper metabolism of patients with Menkes disease and occipital horn syndrome
8th International Congress of Inborn Errors Metabolism      2000
A patient with short stature displaying normal GH secretion, but a low serum IGF-1
GH and Growth Factors in Endocrinology and Metabolism      1999
A Patient with short stature displaying normal GH Seretion, but a low serum IGF-1 level
11th Symposium on Growth Hormone and Related Factors      1999
Copper metabolism and mutation analysis in patients with Menkes disease and occipital horn syndrome
2nd Copper Homeostasis and Its Disorders: Molecular and Cellular Aspects      1999
Successful early copper histidine therapy in a patient with Menkes disease
2nd Copper Homeostasis and Its Disorders: Molecular and Cellular Aspects      1999
Connective tissue abnormalities in patients with Menkes disease
37th Annual Symposium Society for the Study of Inborn Errors of Metabolism      1999
Calcium lactate, Allopurinol, Arginine hydrochloride, Diazoxide
小児科診療   61(Suppl) 374-377   1998
Osteogenesis imperfecta : Are fractures and growth hormone treatment linked?
J Pediatr   132(559-600)    1998
Copper metabolism and mutation analysis of Patients with Menkes disease
J Trace Elements Exp Med   11(407)    1998
Mottled gene expressin in normal and macular mouse model of Menkes disease
J Trace Elements Exp Med   11(434)    1998
Familial hypercholestronemia
30(1) 46-50   1998
Menkes disease
30(3) 378-381   1998
Copper metabolism and mutation of patients with Menkes disease
5th conference of the International Society for Trace Element Research in Humans      1998
Mottled gene expression in normal and macular mouse, Model of Menkes disease
5th conference of the International Society for Trace Element Research in Humans      1998
Mutation analysis and expression of the mottled gene in the macular mouse of Menkes diseas
Pediatric Res   42(436-442)    1997
Prognosis of hepercholestronemia in children
(3840) 109-110   1997
Menkes disease
41,13/,1802-1806    1997
Metabolism and efficacy of administertic drug of Wilson's disease
7th International Congress of Inborn Errors of Metabolism      1997
Intravenous arginine dramatically improves hyperammonemia in a patient with late-onset ornithine transcarbamylase deficiency
7th International Congress of Inborn Errors of Metabolism      1997
Hiroko Kodama, Yosuke Mori, Kazuoki Kubota, Toshiaki Iitsuka, Yutaka Nakazato, Toshiaki Abe
Tohoku J Exp. Med.   180(1) 83-86   1996
Late-night snacking decrease nocturnal secretion of growth hormone
Clin Pediatr Endocrinol   5(2) 79-81   1996
Pamidronate treatment vs combined treatment of pamidronate and growth hormone in a patient with osteogenesis inperfeta
The International Conference in Hormone and Cytokine in Bone      1995
Histochemical localization of copper in the liver of LEC rats
VI th International Congress of Inborn Errors of Metabolism      1994
The metabolism of the administered triethylenetetramine dihydrochloride, a therapeutic drug of Wilson's disease
VIth International Congress of Inborn Errors of Metabolism      1994
Sibling cases of a degenerative neurological disease associated with hypocupraemia and hypobetalipoproteinemia
Eur J Pediat   152(368-371)    1993
Recent developments in Menkces disease
J Inher Metab Dis   16(791-799)    1993
Histochemical localization of copper in the mtetive and kidney of macular mice
J Histochem Cytochem   41(10) 1529-1535   1993
A therapeutic trial with(3-amino-1-hydroxypropylidene)-1,1-bisphosphonate(APD) in a patient with osteogenesis imperfecta
The 7th Meeting of The Research Society for Growth Disturbance in Children      1993
Renal tubular function of patients with classical Menkes disease
J Inher Metab Dis   15    1992
HIROKO KODAMA, TOSHIHIRO KURAMATSU, MASAYOSHI YANAGISAWA, TETSU UCHIYA, ATSUSHI TAKAHASHI
Endocrinol Japan   39(4) 397-400   1992
Diet treatment of ulcerative colitis and Crohn disease
55(8)    1992
Menkes disease and copper metabolism
25(2)    1992
Copper metabolism of LEC rats
30th Annual Symposium of the Society for the Study of Inborn Errors of Metabolism      1992
Urinary exceretion of the orally administered triethylenetetramine dihydrochloride
30th Annual Symposium of the Society for the Study of Inborn Errors of Metabolism      1992
Histochemical localization of copper in the intestine and kidney of macular mouse
The 3rd International Meeting on Metallothionein      1992
Changes of copper level and cytochrome coxidase activity in the macular mouse with age.
Brain & Dev   13    1991
Abnormality of Skin, mail and hair
54    1991
Endoscopic threatment of duodenal ulcer
44    1991
Study of urinary organic acids in five patients with glutaric aciduria type II
95    1991
Chronic thyroiditis
23    1991
Clinicopathological observation during and after fatty change of the liver occuring in a patient with Dublin-Johnson syndrome
Asian Congress of Pediatrics      1991
Therapeutic Benefit of Growth Hormone in Achondroplastic Dwarfism.
Acta. Pediater. Jpn.   33    1990
A 2 year-old girl with premature thelarche and tall a stature
35(2)    1990
Carrier detection by the hair and duodenal biopsy samples.
53    1990
Change of copper concentration and cytochrome C oxidase activity with age in some organs of macular mice treated with copper
Vth International Congress of Inborn Errors of Metabolism      1990
The localization of copper in the kidney, intestine and brain of macular mouse
Vth International Congress of Inborn Errors of Metabolism      1990
Copper deficiency in the mitochondria of cultured skin fibroblasts from patients with Menkes syndrome.
J Inher Metab Dis   12    1989
The long term effects of a Cu injection in the macular mouse.
J trace Elements in Experimental Medicine   2(2-3)    1989
Propriety of combined regiment of chelating agent and zinc as therapy for Wilson's disease.
J Trace Elements in Experimental Medicine   2(2-3)    1989

Books etc

 
Gene defects and clinical aspects in Menkes disease and occipital horn
syndrome. Massaro E ed. Handfbook of Copper Pharmacoligy, Human Press. Totowa(USA)   2002   
Rickets
1998   
Viral encephlitis : new concept and treatment "jointly worked"
New Developments in Child Neurology, Monduzzl Rditore. Bologna(Italy)   1998   
Genetic Disorders of Copper Metabolism "jointly worked"
Toxicology of Metals, Boca Raton. CRC Press   1996   
Wilson's disease
1989   

Conference Activities & Talks

 
Nutritional biotin deficiency in Japan:biotin contents in infant formulas and serum biotin levels in children
Ogawa E, Sato Y, Wakabayashi K, Motoyama K, Kodama H
ACN2015 12th Asian Congress of Nutrition   14 May 2015   

Association Memberships

 
THE JAPANESE SOCIETY FOR PEDIATRIC GASTROENTEROLOGY, HEPATOLOGY AND NUTRITION , JAPANESE SOCIETY FOR INHERITED METABOLIC DISEASES

Works

 
Gene analysis of Menkes disease
2001 - 2002
Study on genetic disorders of copper metabolism
2001 - 2002

Research Grants & Projects

 
Gene analysis and metabolic studies in patients with Menkes disease or Wilson's disease
Gene Science Research
Gene Analysis of patients with inborn errors of copper metabolism
Gene Science Research
Structure and Function of coppertransporting ATPases
Gene Science Research