Matsuura N - Search Results

1

Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan.

Hishinuma A, Fukata S, Nishiyama S, Nishi Y, Oh-Ishi M, Murata Y, Ohyama Y, Matsuura N, Kasai K, Harada S, Kitanaka S, Takamatsu J, Kiwaki K, Ohye H, Uruno T, Tomoda C, Tajima T, Kuma K, Miyauchi A, Ieiri T. Hishinuma A, et al. Among authors: matsuura n. J Clin Endocrinol Metab. 2006 Aug;91(8):3100-4. doi: 10.1210/jc.2005-2702. Epub 2006 May 23. J Clin Endocrinol Metab. 2006. PMID: 16720658

2

Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene.

Shibayama K, Ohyama Y, Hishinuma A, Yokota Y, Kazahari K, Kazahari M, Ieiri T, Matsuura N. Shibayama K, et al. Among authors: matsuura n. Pediatr Int. 2005 Feb;47(1):105-8. doi: 10.1111/j.1442-200x.2005.02020.x. Pediatr Int. 2005. PMID: 15693879 No abstract available.

3

Assays for thyroid-stimulating antibodies and thyrotropin-binding inhibitory immunoglobulins in children with Graves' disease.

Shibayama K, Ohyama Y, Yokota Y, Ohtsu S, Takubo N, Matsuura N. Shibayama K, et al. Among authors: matsuura n. Endocr J. 2005 Oct;52(5):505-10. doi: 10.1507/endocrj.52.505. Endocr J. 2005. PMID: 16284425 Free article.

4

Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature Review.

Sugisawa C, Takamizawa T, Abe K, Hasegawa T, Shiga K, Sugawara H, Ohsugi K, Muroya K, Asakura Y, Adachi M, Daitsu T, Numakura C, Koike A, Tsubaki J, Kitsuda K, Matsuura N, Taniyama M, Ishii S, Satoh T, Yamada M, Narumi S. Sugisawa C, et al. Among authors: matsuura n. J Clin Endocrinol Metab. 2019 Dec 1;104(12):6229-6237. doi: 10.1210/jc.2019-00657. J Clin Endocrinol Metab. 2019. PMID: 31504637

5

Screening and treatment of childhood type 1 and type 2 diabetes mellitus in Japan.

Urakami T, Suzuki J, Mugishima H, Amemiya S, Sugihara S, Kawamura T, Kikuchi T, Sasaki N, Matsuura N, Kitagawa T. Urakami T, et al. Among authors: matsuura n. Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:51-61. Pediatr Endocrinol Rev. 2012. PMID: 23330246 Review.

6

Association study between interleukin-12 receptor beta1/beta2 genes and type 1 diabetes or asthma in the Japanese population.

Bassuny WM, Ihara K, Kimura J, Ichikawa S, Kuromaru R, Miyako K, Kusuhara K, Sasaki Y, Kohno H, Matsuura N, Nishima S, Hara T. Bassuny WM, et al. Among authors: matsuura n. Immunogenetics. 2003 Jun;55(3):189-192. doi: 10.1007/s00251-003-0568-7. Epub 2003 Apr 26. Immunogenetics. 2003. PMID: 12719941

7

Zinc transporter 8 autoantibodies in fulminant, acute-onset, and slow-onset patients with type 1 diabetes.

Kawasaki E, Nakamura K, Kuriya G, Satoh T, Kobayashi M, Kuwahara H, Abiru N, Yamasaki H, Matsuura N, Miura J, Uchigata Y, Eguchi K. Kawasaki E, et al. Among authors: matsuura n. Diabetes Metab Res Rev. 2011 Nov;27(8):895-8. doi: 10.1002/dmrr.1269. Diabetes Metab Res Rev. 2011. PMID: 22069281

8

Identification of a novel type 1 diabetes susceptibility gene, T-bet.

Sasaki Y, Ihara K, Matsuura N, Kohno H, Nagafuchi S, Kuromaru R, Kusuhara K, Takeya R, Hoey T, Sumimoto H, Hara T. Sasaki Y, et al. Among authors: matsuura n. Hum Genet. 2004 Aug;115(3):177-84. doi: 10.1007/s00439-004-1146-2. Epub 2004 Jul 6. Hum Genet. 2004. PMID: 15241679

9

Analysis of weight at birth and at diagnosis of childhood-onset type 2 diabetes mellitus in Japan.

Sugihara S, Sasaki N, Amemiya S, Kohno H, Tanaka T, Matsuura N. Sugihara S, et al. Among authors: matsuura n. Pediatr Diabetes. 2008 Jul 28;9(4 Pt 1):285-90. doi: 10.1111/j.1399-5448.2008.00402.x. Epub 2008 May 7. Pediatr Diabetes. 2008. PMID: 18466207

10

Screening for diabetes by urine glucose testing at school in Japan.

Yokota Y, Kikuchi N, Matsuura N. Yokota Y, et al. Among authors: matsuura n. Pediatr Diabetes. 2004 Dec;5(4):212-8. doi: 10.1111/j.1399-543X.2004.00086.x. Pediatr Diabetes. 2004. PMID: 15601365 No abstract available.

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