KODAMA Hiroko Last updated: May 31, 2019 at 15:20
Name
KODAMA Hiroko E-mail
kodamah2018 Affiliation
Teikyo University Section
Faculty of Medicine, Department of Medicine, Department of Pediatrics Job title
Professor Degree
(BLANK) Research funding number
00093386
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]
MitsutoshiMunakata HirokoKodama NorihikoTani KazuhikoKimura HideyoTakahashi KazuoMaruyama YoshimasaSakamoto ShigeoKure
PediatricResearch 84(5) 770-777 Nov 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]
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
Gu YH, Kodama H, Shiga K, Nakata S, Yanagawa Y, Ozawa H.
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
Gu YH, Kodama H, Du SL.
Brain Dev. 27(8) 551-553 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
Eur J Pediatr 163(12): 745-746 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
J Pediatr 142(726-728) 2003
J Inherit Metab Dis 26(55-66) 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
Clin Genet 64: 479-484 2003
J Child Neurol 17(401-402) 2002
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
Am J Med Genet 99(217-222) 2001
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
Hum Pathol 32(887-889) 2001
Pediatr Int 43(437-440) 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
Am J Med Genet 92(195-199) 2000
Pediatr Int 42(440-447) 2000
Brain & Development 22(301-306) 2000
J Hum Genet 45(5) 275-279 2000
Am J Med Genet 92 195-199 2000
Endocr J 47(125-127) 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
Pediatr Int 41(430-435) 1999
Pediatr Int 41(423-429) 1999
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
Endocrine J 45(163-165) 1998
Osteogenesis imperfecta : Are fractures and growth hormone treatment linked?
J Pediatr 132(559-600) 1998
J Inher Metal Dis 21(199-202) 1998
J Inher Metal Dis 21(203-206) 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
Life Science 61(9) 899-907 1997
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
Tohoku J. Exp. Med 169,59-66 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
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
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
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
gmail.com