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Kazumichi Onigata

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Kazumichi Onigata
[Monogenic obesity in human].
Rie Anzai; Yumi Asakura; Koji Muroya; Masanori Adachi; Noriko Sho; Kazumichi Onigata
Long-term 3,5,3'-triiodothyroacetic acid therapy in a child with hyperthyroidism caused by thyroid hormone resistance: pharmacological study and therapeutic recommendations.
Alfonso Massimiliano Ferrara; Kazumichi Onigata; Roy E Weiss; Helen Woodhead; Oya Ercan; Samuel Refetoff
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.

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All Publications

2013: Kazumichi Onigata
[Monogenic obesity in human].
Nihon rinsho. Japanese journal of clinical medicine 2013;71(2):297-302.
2012: Rie Anzai; Yumi Asakura; Koji Muroya; Masanori Adachi; Noriko Sho; Kazumichi Onigata
Long-term 3,5,3'-triiodothyroacetic acid therapy in a child with hyperthyroidism caused by thyroid hormone resistance: pharmacological study and therapeutic recommendations.
Thyroid : official journal of the American Thyroid Association 2012;22(10):1069-75.
2012: Alfonso Massimiliano Ferrara; Kazumichi Onigata; Roy E Weiss; Helen Woodhead; Oya Ercan; Samuel Refetoff
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
The Journal of clinical endocrinology and metabolism 2012;97(4):1328-36.
2012: Takashi Hamajima; Hironori Kobayashi; Yuichi Mushimoto; Yoshiro Saito; Kazumichi Onigata
Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation.
European journal of endocrinology / European Federation of Endocrine Societies 2012;166(4):757-64.
2010: Yasuyo Nakajima; Masanobu Yamada; Kazuhiko Horiguchi; Tetsurou Satoh; Koshi Hashimoto; Etsuro Tokuhiro; Kazumichi Onigata; Masatomo Mori
Resistance to thyroid hormone due to a novel thyroid hormone receptor mutant in a patient with hypothyroidism secondary to lingual thyroid and functional characterization of the mutant receptor.
Thyroid : official journal of the American Thyroid Association 2010;20(8):917-26.
2009: Haruo Mizuno; Keisuke Kanda; Yukari Sugiyama; Hiroki Imamine; Tetsuya Ito; Ineko Kato; Hajime Togari; Tomohiro Kamoda; Kazumichi Onigata
Longitudinal evaluation of patients with a homozygous R450H mutation of the TSH receptor gene.
Hormone research 2009;71(6):318-23.
2008: Kazuki Yamazawa; Masayo Kagami; Toshiro Nagai; Tatsuro Kondoh; Kazumichi Onigata; Katsuhiro Maeyama; Tomonobu Hasegawa; Yukihiro Hasegawa; Toshio Yamazaki; Seiji Mizuno; Yoko Miyoshi; Shinichiro Miyagawa; Reiko Horikawa; Kentaro Matsuoka; Tsutomu Ogata
Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.
Journal of molecular medicine (Berlin, Germany) 2008;86(10):1171-81.
2008: Ilaria Zamproni; Helmut Grasberger; Francesca Cortinovis; Maria Cristina Vigone; Giuseppe Chiumello; Stefano Mora; Kazumichi Onigata; Laura Fugazzola; Samuel Refetoff; Luca Persani; Giovanna Weber
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.
The Journal of clinical endocrinology and metabolism 2008;93(2):605-10.
2007: Atsushi Takahashi; Makoto Hasegawa; Ryo Sumazaki; Makoto Suzuki; Fumiaki Toki; Taketoshi Suehiro; Kazumichi Onigata; Takeshi Tomomasa; Tomoko Suzuki; Akira Matsui; Akihiro Morikawa; Hiroyuki Kuwano
Gradual improvement of liver function after administration of ursodeoxycholic acid in an infant with a novel ABCB11 gene mutation with phenotypic continuum between BRIC2 and PFIC2.
European journal of gastroenterology & hepatology 2007;19(11):942-6.
2006: Keisuke Kanda; Haruo Mizuno; Yukari Sugiyama; Hiroki Imamine; Hajime Togari; Kazumichi Onigata
Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese.
Endocrine 2006;30(3):383-8.
2006: Kazumichi Onigata; Yoshihiro Ogawa
[POMC gene mutations in human].
Nihon rinsho. Japanese journal of clinical medicine 2006;Suppl 3():255-9.
2006: Kazumichi Onigata
[Resistance to thyrotropin (TSH) (TSH receptor gene mutations in human)].
Nihon rinsho. Japanese journal of clinical medicine 2006;Suppl 1():399-404.
2006: Katsuhiko Tsunekawa; Kazumichi Onigata; Tadashi Morimura; Takayuki Kasahara; Soroku Nishiyama; Tomohito Kamoda; Masatomo Mori; Akihiro Morikawa; Masami Murakami
Identification and functional analysis of novel inactivating thyrotropin receptor mutations in patients with thyrotropin resistance.
Thyroid : official journal of the American Thyroid Association 2006;16(5):471-9.
2006: Hayato Yamauchi; Atsushi Takahashi; Tomoko Hirakata; Kazumichi Onigata; Takashi Kanazawa; Chitose Ogawa; Minoru Kuroiwa; Akihiro Morikawa; Hiroyuki Kuwano
Bilateral ovarian teratomas successfully treated by ovary-conserving technique.
Pediatrics international : official journal of the Japan Pediatric Society 2006;48(2):181-4.
2005: Kazumichi Onigata
[Congenital hypothyroidism].
Nihon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 10():105-10.
2004: Sumiyasu Ishii; Masanobu Yamada; Teturou Satoh; Tsuyoshi Monden; Koshi Hashimoto; Nobuyuki Shibusawa; Kazumichi Onigata; Akihiro Morikawa; Masatomo Mori
Aberrant dynamics of histone deacetylation at the thyrotropin-releasing hormone gene in resistance to thyroid hormone.
Molecular endocrinology (Baltimore, Md.) 2004;18(7):1708-20.
2003: Mie Mochizuki; Shin Amemiya; Kisho Kobayashi; Koji Kobayashi; Yoshie Shimura; Toshihide Ishihara; Yoshiko Nakagomi; Kazumichi Onigata; Shinya Tamai; Akira Kasuga; Shinpei Nanazawa
Association of the CTLA-4 gene 49 A/G polymorphism with type 1 diabetes and autoimmune thyroid disease in Japanese children.
Diabetes care 2003;26(3):843-7.
2002: Naoko Tonooka; Hideaki Tomura; Y Takahashi; Kazumichi Onigata; N Kikuchi; Y Horikawa; Masatomo Mori; Jun Takeda
High frequency of mutations in the HNF-1alpha gene in non-obese patients with diabetes of youth in Japanese and identification of a case of digenic inheritance.
Diabetologia 2002;45(12):1709-12.
2002: Kenichi Maruyama; Hiroyuki Watanabe; Kazumichi Onigata
Reversible secondary pseudohypoaldosteronism due to pyelonephritis.
Pediatric nephrology (Berlin, Germany) 2002;17(12):1069-70.
2002: Kenichi Maruyama; Makoto Shinohara; Shinitsu Hatakeyama; Kazumichi Onigata
Distal renal tubular acidosis associated with hypercalcemia and nephrocalcinosis in an infant.
Pediatric nephrology (Berlin, Germany) 2002;17(11):977-8.
2002: Gudrun A Rappold; Maki Fukami; Beate Niesler; Simone Schiller; Walter Zumkeller; Markus Bettendorf; Udo Heinrich; Elpis Vlachopapadoupoulou; Thomas Reinehr; Kazumichi Onigata; Tsutomu Ogata
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.
The Journal of clinical endocrinology and metabolism 2002;87(3):1402-6.
2001: Hiroto Koike; Masahiko Motooka; Tsugiyasu Kanda; Kazumichi Onigata; Masami Murakami; Takahiro Suzuki; Isao Kobayashi
Detection of point mutation for human growth hormone in patients with anti-pituitary antibody positive type 1 diabetes mellitus.
The Journal of international medical research 2001;29(5):397-408.
2001: T Nagashima; Masami Murakami; Kazumichi Onigata; Tadashi Morimura; K Nagashima; Masatomo Mori; Akihiro Morikawa
Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin.
Thyroid : official journal of the American Thyroid Association 2001;11(6):551-9.
2001: Hidekazu Nishigori; Hideaki Tomura; Naoko Tonooka; M Kanamori; Satoko Yamada; K Sho; I Inoue; N Kikuchi; Kazumichi Onigata; Itaru Kojima; T Kohama; Kazuya Yamagata; Q Yang; Yuji Matsuzawa; T Miki; Susumu Seino; M Y Kim; H S Choi; Y K Lee; D D Moore; Jun Takeda
Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(2):575-80.
1999: Satoko Yamada; Hideaki Tomura; Hidekazu Nishigori; K Sho; Hiroyo Mabe; Noritaka Iwatani; T Takumi; Y Kito; N Moriya; K Muroya; Takeki Ogata; Kazumichi Onigata; A Morikawa; I Inoue; Jun Takeda
Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins.
Diabetes 1999;48(3):645-8.
1999: Akira Harigaya; Kazumichi Onigata; Yasushi Nako; K Nagashima; Akihiro Morikawa
Role of serum leptin in the regulation of weight gain in early infancy.
Biology of the neonate 1999;75(4):234-8.
1999: H Miyake; K Nagashima; Kazumichi Onigata; T Nagashima; Y Takano; A Morikawa
Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature.
Journal of human genetics 1999;44(1):26-9.
1998: Y Suzuki; T Nagashima; Y Nomura; Kazumichi Onigata; K Nagashima; Akihiro Morikawa
A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency.
The Journal of clinical endocrinology and metabolism 1998;83(1):199-202.
1997: T Nagashima; H Yagi; K Nagashima; A Sakurai; Kazumichi Onigata; Y Nomura; Akihiro Morikawa; G Matazow; R M Couch; R E Weiss; S Refetoff
A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormone.
Thyroid : official journal of the American Thyroid Association 1997;7(5):771-3.
1997: Y Nomura; Kazumichi Onigata; T Nagashima; S Yutani; H Mochizuki; K Nagashima; Akihiro Morikawa
Detection of skewed X-inactivation in two female carriers of vasopressin type 2 receptor gene mutation.
The Journal of clinical endocrinology and metabolism 1997;82(10):3434-7.
1997: Satoko Yamada; Hidekazu Nishigori; H Onda; T Utsugi; T Yanagawa; T Maruyama; Kazumichi Onigata; K Nagashima; Ryozo Nagai; A Morikawa; Toshiyuki Takeuchi; Jun Takeda
Identification of mutations in the hepatocyte nuclear factor (HNF)-1 alpha gene in Japanese subjects with IDDM.
Diabetes 1997;46(10):1643-7.
1995: Y Nomura; H Yagi; Kazumichi Onigata; S Yutani; T Nagashima; R Ogawa; K Nagashima; A Morikawa
A sex reversal infant with XX karyotype and complete male external genitalia.
Acta paediatrica Japonica; Overseas edition 1995;37(6):706-9.
1995: Kazumichi Onigata; H Yagi; A Sakurai; T Nagashima; Y Nomura; K Nagashima; K Hashizume; A Morikawa
A novel point mutation (R243Q) in exon 7 of the c-erbA beta thyroid hormone receptor gene in a family with resistance to thyroid hormone.
Thyroid : official journal of the American Thyroid Association 1995;5(5):355-8.
1994: H Yagi; K Nagashima; H Miyake; S Tamai; Kazumichi Onigata; S Yutani; T Kuroume
Familial congenital hypopituitarism with central diabetes insipidus.
The Journal of clinical endocrinology and metabolism 1994;78(4):884-9.
1993: K Nagashima; H Yagi; S Yutani; H Miyake; Kazumichi Onigata; T Kuroume
Relationship between serum levels of methylguanidine and glycemic control in IDDM children.
Diabetes care 1993;16(8):1196-8.
1993: K Nagashima; S Yutani; H Miyake; Kazumichi Onigata; H Yagi; T Kuroume
Lipoprotein(a) levels in Japanese children with IDDM.
Diabetes care 1993;16(5):846.
1993: K Nagashima; Kazumichi Onigata; H Yagi; T Kuroume
Transport of triiodothyronine by erythrocytes from premature and term infants.
Biology of the neonate 1993;64(6):354.
1993: H Miyake; K Nagashima; H Yagi; Kazumichi Onigata
Urinary laminin P1 as an index of glycemic control in children with insulin-dependent diabetes mellitus.
Diabetes research (Edinburgh, Scotland) 1993;23(3):131-8.