Onigata K - Search Results

1

Onigata K. Onigata K. Nihon Rinsho. 2005 Oct;63 Suppl 10:105-10. Nihon Rinsho. 2005. PMID: 16279612 Review. Japanese. No abstract available.

2

[Resistance to thyrotropin (TSH) (TSH receptor gene mutations in human)].

Onigata K. Onigata K. Nihon Rinsho. 2006 May 28;Suppl 1:399-404. Nihon Rinsho. 2006. PMID: 16776175 Review. Japanese. No abstract available.

3

[POMC gene mutations in human].

Onigata K, Ogawa Y. Onigata K, et al. Nihon Rinsho. 2006 Sep 28;Suppl 3:255-9. Nihon Rinsho. 2006. PMID: 17022541 Review. Japanese. No abstract available.

4

Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese.

Kanda K, Mizuno H, Sugiyama Y, Imamine H, Togari H, Onigata K. Kanda K, et al. Among authors: onigata k. Endocrine. 2006 Dec;30(3):383-8. doi: 10.1007/s12020-006-0018-z. Endocrine. 2006. PMID: 17526952

5

Identification and functional analysis of novel inactivating thyrotropin receptor mutations in patients with thyrotropin resistance.

Tsunekawa K, Onigata K, Morimura T, Kasahara T, Nishiyama S, Kamoda T, Mori M, Morikawa A, Murakami M. Tsunekawa K, et al. Among authors: onigata k. Thyroid. 2006 May;16(5):471-9. doi: 10.1089/thy.2006.16.471. Thyroid. 2006. PMID: 16756469

6

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).

Mass Screening Committee; Japanese Society for Pediatric Endocrinology; Japanese Society for Mass Screening; Nagasaki K, Minamitani K, Anzo M, Adachi M, Ishii T, Onigata K, Kusuda S, Harada S, Horikawa R, Minagawa M, Mizuno H, Yamakami Y, Fukushi M, Tajima T. Mass Screening Committee, et al. Among authors: onigata k. Clin Pediatr Endocrinol. 2015 Jul;24(3):107-33. doi: 10.1297/cpe.24.107. Epub 2015 Jul 18. Clin Pediatr Endocrinol. 2015. PMID: 26594093 Free PMC article.

7

Longitudinal evaluation of patients with a homozygous R450H mutation of the TSH receptor gene.

Mizuno H, Kanda K, Sugiyama Y, Imamine H, Ito T, Kato I, Togari H, Kamoda T, Onigata K. Mizuno H, et al. Among authors: onigata k. Horm Res. 2009;71(6):318-23. doi: 10.1159/000223415. Epub 2009 Jun 6. Horm Res. 2009. PMID: 19506388

8

Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.

Zamproni I, Grasberger H, Cortinovis F, Vigone MC, Chiumello G, Mora S, Onigata K, Fugazzola L, Refetoff S, Persani L, Weber G. Zamproni I, et al. Among authors: onigata k. J Clin Endocrinol Metab. 2008 Feb;93(2):605-10. doi: 10.1210/jc.2007-2020. Epub 2007 Nov 27. J Clin Endocrinol Metab. 2008. PMID: 18042646 Free PMC article.

9

Resistance to thyroid hormone.

Onigata K, Szinnai G. Onigata K, et al. Endocr Dev. 2014;26:118-29. doi: 10.1159/000363159. Epub 2014 Aug 29. Endocr Dev. 2014. PMID: 25231448 Review.

10

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.

Takahashi A, Hasegawa M, Sumazaki R, Suzuki M, Toki F, Suehiro T, Onigata K, Tomomasa T, Suzuki T, Matsui A, Morikawa A, Kuwano H. Takahashi A, et al. Among authors: onigata k. Eur J Gastroenterol Hepatol. 2007 Nov;19(11):942-6. doi: 10.1097/MEG.0b013e3282ef4795. Eur J Gastroenterol Hepatol. 2007. PMID: 18049162

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