高田五郎 (Goro Takada) - マイポータル - researchmap

基本情報

所属: 旧所属秋田大学医学部医学科教授

学位: 医学博士(大阪市立大学)

J-GLOBAL ID: 200901039643830240
researchmap会員ID: 1000006446

研究キーワード

4

研究分野

1

ライフサイエンス / 胎児医学、小児成育学 /

委員歴

6

受賞

3

MISC

53

A new locus for a dominant form of multinodular goiter on 3q126.1-q26.3

T Takahashi, J Nozaki, M Komatsu, Y Wada, M Utsunomiya, K Inoue, G Takada, A Koizumi

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 284(3) 648-654 2001年6月
SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families.

2000年
A cluster of lysinuric protein intolerance(LPI) patients in a northern part of Iwate, Japan due to a founder effect.

Hum Mutat 16(3) 270-271 2000年
Immunohistochemical study on transforming growth factor-beta1 expression in liver fibrosis of Down's syndrome with transient abnormal myelopoiesis

H Arai, A Ishida, W Nakajima, F Nishinomiya, A Yamazoe, G Takada

HUMAN PATHOLOGY 30(4) 474-476 1999年4月
Genetic epidemidogy of carnitine transporter OCTN2 gene in a Japanese poputation and phenotypic characteriation in Japanese pedigrees with primary carnitine deficiency.

Hum Mol Genet 8(12) 2247-2254 1999年
Serum Z┣D5N┫D5²⁺- stimutated sphingomyelinase deficiency in type B Niemann-Pick disease.

Europ J Pediatr. 158 953 1999年
Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1

H Hirono, Y Shoji, T Takahashi, W Sato, E Takeda, T Nishijo, Y Kuroda, T Nishigaki, K Inui, G Takada

JOURNAL OF INHERITED METABOLIC DISEASE 21(8) 846-852 1998年12月
Enzyme therapy in Gaucher disease type 2: An autopsy case

T Takahashi, Y Yoshida, W Sato, T Yano, Y Shoji, Y Sawaishi, Sakuma, I, T Sashi, K Enomoto, H Ida …

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE 186(2) 143-149 1998年10月
Evidence for linkage of human primary systemic carnitine deficiency with D5S436: A novel gene locus on chromosome 5q

Y Shoji, A Koizumi, T Kayo, T Ohata, T Takahashi, K Harada, G Takada

AMERICAN JOURNAL OF HUMAN GENETICS 63(1) 101-108 1998年7月
Acute life-threatening event with rhabdomyolysis after starting on high-dose pyridoxine therapy in an infant with homocystinuria

Y Shoji, T Takahashi, W Sato, Y Shoji, G Takada

JOURNAL OF INHERITED METABOLIC DISEASE 21(4) 439-440 1998年6月
Effect of carnitine on valproic acid concentrations in serum, brain, and liver

K Sakemi, G Takada

PEDIATRIC NEUROLOGY 18(4) 331-333 1998年4月
Transient neurotoxicity associated with FK 506 : MR findings

J Comp Assist Tomography 22(3) 505-507 1998年
Probability estimation of final height

Endocr J 45(Supple1) S145-149 1998年
Mutational analyses of AVPR2 gene in three Japanese families with X-linked nephrogenic diabetes insipidus : Two recurrent mutations, R137H and △ V278, caused by the Hypermutability of CpG dinucleotides

Hum Mut Sup 1 S278-S283 1998年
Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family

Hum Genet 103(4) 470-474 1998年
Short-term fasting alters neonatal rat striatal dopamine levels and serotonin metabolism: an in vivo microdialysis study

A Ishida, W Nakajima, G Takada

DEVELOPMENTAL BRAIN RESEARCH 104(1-2) 131-136 1997年12月
Methaemoglobinaemia after inhalation of nitric oxide in infant with pulmonary hypertension

W Nakajima, A Ishida, H Arai, G Takada

LANCET 350(9083) 1002-1003 1997年10月
Loss of EDB+ fibronectin isoform is associated with differentiation of alveolar epithelial cells in human fetal lung

H Arai, H Hirano, S Mushiake, M Nakayama, G Takada, K Sekiguchi

AMERICAN JOURNAL OF PATHOLOGY 151(2) 403-412 1997年8月
Childhood multiple sclerosis treated with plasmapheresis

Takahashi, I, Y Sawaishi, O Takeda, M Enoki, G Takada

PEDIATRIC NEUROLOGY 17(1) 83-87 1997年7月
Excessive playing of home computer games by children presenting unexplained symptoms

Y Tazawa, AV Soukalo, K Okada, G Takada

JOURNAL OF PEDIATRICS 130(6) 1010-1011 1997年6月

もっとみる

書籍等出版物

1

Effect of tetrahydrobiopterin and 5-hydroxytryptophan on hereditary pragressive dystonia with marked diurnal fluctuation : a sulgextion of serotonergyic system involvement.

Hereditary Pryressive Dystonia with Marked Diurnal Tructuation 1993年

所属学協会

15

Works(作品等)

4

共同研究・競争的資金等の研究課題

3