Kenji Fujieda - My portal

Profile Information

Affiliation: School of Medicine, Medical Course, Asahikawa Medical College

Degree: Doctor of Medical Science(Hokkaido University)

J-GLOBAL ID: 200901068975654941
researchmap Member ID: 1000000198

External link: http://asahikawa-med.ac.jp

Research Interests

Research Areas

Research History

1994 - 2000

School of Medicine, Hokkaido University
1994 - 2000

Dept. of Pediatrics, Hokkaido University School of Medical
1984 - 1994

School of Medicine, Hokkaido University
1984 - 1994

Dept. of Pediatrics, Hokkaido University School of Medical
1980 - 1981

アメリカ国立衛生研究所
1980 - 1981

National Institute of Health, U.S.A
1977 - 1980

ウィニペッグ小児病院研究員
1977 - 1980

Children's Hospital of Winnipeg, Research Fellow

Education

- 1976

Hokkaido University
- 1976

Graduate School, Division of Medicine, Hokkaido University
- 1971

School of Medicine, Hokkaido University
- 1971

Faculty of Medicine, Hokkaido University

Committee Memberships

Awards

Misc.

Mutations in NADPH-cytochrome P450 oxidoreductase in patients with multiple steroidogenic defects with and without associated Antley-Bixler Syndrome

Nature Genet, 36 2228-2291, 2004
Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenita

K Fujieda, K Okuhara, S Abe, T Tajima, T Mukai, J Nakae

JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 85(2-5) 483-489, Jun, 2003
Monozygotic twins with diocordant sexcial phenotypes due to different ratios of mosaiusm of 47, X, idic(Y), idc(Y)/ 46, x, idic(Y) 45, x

Endocrine J, 49: 497-501, 2002
Induction chemotherapy followed by low-dose involved-field rodiotherapy for intracranial germ cell tumors

J. Clin Oncology, 20: 857-865, 2002
Sexually dimorphic expression of Dax-1 in the adrenal cortex

Genes to Cells, 7: 717-729, 2002
Two novel mutations of thiazide-sensitive Na-Cl cotransporter (TSC) gen in two sporadic Japanese patients with Gitelman syndrome

Endocrine J., 49: 91-96, 2002
Monozygotic twins with diocordant sexcial phenotypes due to different ratios of mosaiusm of 47, X, idic(Y), idc(Y)/ 46, x, idic(Y) 45, x

Endocrine J, 49: 497-501, 2002
Induction chemotherapy followed by low-dose involved-field rodiotherapy for intracranial germ cell tumors

J. Clin Oncology, 20: 857-865, 2002
Sexually dimorphic expression of Dax-1 in the adrenal cortex

Genes to Cells, 7: 717-729, 2002
Two novel mutations of thiazide-sensitive Na-Cl cotransporter (TSC) gen in two sporadic Japanese patients with Gitelman syndrome

Endocrine J., 49: 91-96, 2002
Compound heterozygous mutations in the γ subunit gene of ENaC(1627del G and 1570-1G→A)in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type (]G0001[)

J Clin Endocrinol Metab, 86 9-12, 2001
A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type (]G0001[)

J Clin Endocrinol Metab, 85 4690-4694, 2001
Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets

K Sato, T Tajima, J Nakae, M Adachi, Y Asakura, K Tachibana, S Suwa, N Katsumata, T Tanaka, Y Hayashi …

PEDIATRIC RESEARCH, 48(4) 536-540, Oct, 2000
先天性副腎過形成症

難病の最新情報-疫学から臨床ケアまで, 南山堂, 125, 2000
A novel mrssmse mutation in the NMG fow regior of the SRY gene in a Japanese patient with a XY sex reversal

J Hum. Genet, 45(2) 112-114, 2000
Gonadotropin releasing hormone analoge therpy failure to improve predicted final height in two children with central precocious puberty and microcephalus

Endouinl J, 47(80pyls) 8121-8132, 2000
Recent status in the occurrence of leukemia in growth hormone-treated patients in Japan

Y Nishi, T Tanaka, K Takano, K Fujieda, Y Igarashi, K Hanew, T Hirano, S Yokoya

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 84(6) 1961-1965, Jun, 1999
Height responses in complete idiopathic growth hormone deficient children less than three years of age during growth hormone therapy.

Endocrine J, 46(Suppl) S1-S4, 1999
Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-I.

Horm Res, 51(4) 184-188, 1999
A 8 yera-old girl with severe growth failure due to hypertrophic pyloric stenosis(HPS) : Report of a case

Clin Pediatr Endocrinol, 8(Supple12) 131-133, 1999

Books and Other Publications

DAX-1 mutations in adronal hypoplassa congnita

Molecular Steroidogenesis, 2000
Molecular genetics of congenital adrenal Hyperplasia

New Trends in Neonatal Screening Hokkaido University Press, 1994
尿崩症

今日の小児治療指針第10版.医学書院, 1993
Treatment of Turrn syndrome with transdermal estradial(Estradern^R)

Basic and Clinical Approach to Turner Syndrome, 1993
思春期遅発症

外来診療のすべて.メディカルレビュー社, 1992
思春期早発症

外来診療のすべて.メディカルレビュー社, 1992
Pulsatile secretion of gonadotropin in pre- and pubertal children

Hokkaido University Press, 1992
Five years experience of newborn screening program for congenital adrenal hyperplasia in Sapporo

Elsevier Science Publishes, 1987

Professional Memberships

Works

低出圧体重児の成長障害機構に関する臨床的研究

1992

Research Projects

IGF及びIGFBPの生理的意義に関する検討

厚生労働科学研究費補助金, 1990
成長と成長障害

厚生労働科学研究費補助金, 1990
先天性副腎過形成の分子遺伝

厚生労働科学研究費補助金, 1990
Physiological role of IGF and IGFBP

Health and Labour Sciences Research Grants, 1990
Growth and Growth Disorder

Health and Labour Sciences Research Grants, 1990
Molecular Genetics of Congenital Adrenal Hyperplasia

Health and Labour Sciences Research Grants, 1990