Fukata S - Search Results

1

Tajiri J, Goshi K, Fukata S. Tajiri J, et al. Among authors: fukata s. Lancet. 2007 Sep 15;370(9591):934. doi: 10.1016/S0140-6736(07)61440-8. Lancet. 2007. PMID: 17869630 No abstract available.

2

Prediction of post-treatment hypothyroidism using changes in thyroid volume after radioactive iodine therapy in adolescent patients with Graves' disease.

Nakatake N, Fukata S, Tajiri J. Nakatake N, et al. Among authors: fukata s. Int J Pediatr Endocrinol. 2011 Nov 7;2011(1):14. doi: 10.1186/1687-9856-2011-14. Int J Pediatr Endocrinol. 2011. PMID: 22060749 Free PMC article.

3

Acute transient thyroid swelling after fine-needle aspiration biopsy: three cases during only 6 weeks - a rare complication?

Nakatake N, Fukata S, Tajiri J. Nakatake N, et al. Among authors: fukata s. Clin Endocrinol (Oxf). 2012 Jul;77(1):152-4. doi: 10.1111/j.1365-2265.2011.04294.x. Clin Endocrinol (Oxf). 2012. PMID: 22098596 No abstract available.

4

Diagnosis of iodide transport defect: do we need to measure the saliva/serum radioactive iodide ratio to diagnose iodide transport defect?

Fukata S, Hishinuma A, Nakatake N, Tajiri J. Fukata S, et al. Thyroid. 2010 Dec;20(12):1419-21. doi: 10.1089/thy.2010.0069. Epub 2010 Nov 7. Thyroid. 2010. PMID: 21054210

5

A Japanese family with familial nonautoimmune hyperthyroidism with a novel mutation (Asn406Ser) in extracellular domain of thyrotrophin receptor.

Fukata S, Hishinuma A, Nakatake N, Tajiri J. Fukata S, et al. Clin Endocrinol (Oxf). 2012 Aug;77(2):329-30. doi: 10.1111/j.1365-2265.2011.04324.x. Clin Endocrinol (Oxf). 2012. PMID: 22175420 No abstract available.

6

Iodide Transport Defect and Breast Milk Iodine.

Mizokami T, Fukata S, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: fukata s. Eur Thyroid J. 2016 Jul;5(2):145-8. doi: 10.1159/000446496. Epub 2016 May 27. Eur Thyroid J. 2016. PMID: 27493890 Free PMC article.

7

Congenital Primary Hypothyroidism with the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-sized Thyroid Gland on Levothyroxine Replacement.

Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: fukata s. Intern Med. 2019 Sep 15;58(18):2669-2673. doi: 10.2169/internalmedicine.1163-18. Epub 2019 Jun 7. Intern Med. 2019. PMID: 31178475 Free PMC article.

8

High incidence of thyroid cancer in long-standing goiters with thyroglobulin mutations.

Hishinuma A, Fukata S, Kakudo K, Murata Y, Ieiri T. Hishinuma A, et al. Among authors: fukata s. Thyroid. 2005 Sep;15(9):1079-84. doi: 10.1089/thy.2005.15.1079. Thyroid. 2005. PMID: 16187918

9

A novel homozygous missense mutation of the dual oxidase 2 (DUOX2) gene in an adult patient with large goiter.

Ohye H, Fukata S, Hishinuma A, Kudo T, Nishihara E, Ito M, Kubota S, Amino N, Ieiri T, Kuma K, Miyauchi A. Ohye H, et al. Among authors: fukata s. Thyroid. 2008 May;18(5):561-6. doi: 10.1089/thy.2007.0258. Thyroid. 2008. PMID: 18426362

10

Prevalence of thyrotropin receptor germline mutations and clinical courses in 89 hyperthyroid patients with diffuse goiter and negative anti-thyrotropin receptor antibodies.

Nishihara E, Fukata S, Hishinuma A, Amino N, Miyauchi A. Nishihara E, et al. Among authors: fukata s. Thyroid. 2014 May;24(5):789-95. doi: 10.1089/thy.2013.0431. Epub 2014 Jan 24. Thyroid. 2014. PMID: 24279482

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