ONIGATA Kazumichi

J-GLOBAL         Last updated: Dec 4, 2019 at 02:41
 
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Name
ONIGATA Kazumichi
Affiliation
Shimane University
Section
Hospital
Degree
(BLANK)(Gunma University)

Research Areas

 
 

Misc

 
Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin.
MURAKAMI MASAMI / ONIGATA KAZUMICHI / MORIMURA TADASHI / MORI MASATOMO / MORIKAWA AKIHIRO / Nagashima T / Nagashima K
Thyroid   11(6):551-559    2001
MURAKAMI MASAMI / ONIGATA KAZUMICHI / MORIMURA TADASHI / KASAHARA TAKAYUKI / MORI MASATOMO / MORIKAWA AKIHIRO / Nishiyama S / Kamoda S
Thyroid   16(5):471-479    2006
ONIGATA KAZUMICHI
Proceeding National Academy of Science   98/2,575    2001
Lipoprotein(a) levels in Japanese children with IDDM.
Nagashima K, Yutani S, Miyake H, Onigata K, Yagi H, Kuroume T.
Diabetes Care   16(5) 846   1993

Conference Activities & Talks

 
TSH receptor gene mutations in hyperthyrotropinema and congenital hypothyroidism.
New York Academy of Science: Skeletal Development and Remodeling in Health, Disease and Aging   2005   
Bone mineral density in human cases with TSH receptor gene mutations.
1st Congress of Asian Society for Pediatric Research   2005   
Clinical Management Sessions “Management of congenital hypothyroidism”
2nd meeting of APPES; Asia Pan-pacific Pediatric Endocrinology   2004   
Phenotype of the PAX8 gene mutations in human: predominance of PAX8 gene mutations in females
The 6th Meeting of the International Society for Neonatal Screening (ISNS)   2006   
High prevalence of R450H TSH receptor gene mutation in Japanese patients with congenital hypothyroidism who have hypoplastic or normally sized gland in the proper position.
The 6th Meeting of the International Society for Neonatal Screening (ISNS)   2006   

Works

 
Committee of screening for congenital metabolic error in Gunma.
1995
Clinical Genetics Conference
1998
Educational camping for children with type 1 diabetes mellitus in Gunma.
1995
Longitudinal evaluation of high-risk group of life style disease screening in Hokkistu area.
2000

Research Grants & Projects

 
Molecular genetics of congenital hypothyroidism
Cooperative Research
Project Year: 2002