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A Novel Germline Mutation of KEAP1 (R483H) Associated with a Non-Toxic Multinodular Goiter.
Nishihara E, Hishinuma A, Kogai T, Takada N, Hirokawa M, Fukata S, Ito M, Yabuta T, Nishikawa M, Nakamura H, Amino N, Miyauchi A. Nishihara E, et al. Among authors: kogai t. Front Endocrinol (Lausanne). 2016 Sep 20;7:131. doi: 10.3389/fendo.2016.00131. eCollection 2016. Front Endocrinol (Lausanne). 2016. PMID: 27703446 Free PMC article.
Graves' disease and Gitelman syndrome.
Mizokami T, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Mizokami T, et al. Among authors: kogai t. Clin Endocrinol (Oxf). 2016 Jan;84(1):149-50. doi: 10.1111/cen.12829. Epub 2015 Jul 3. Clin Endocrinol (Oxf). 2016. PMID: 26041598 No abstract available.
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: kogai t. 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.
A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation.
Kishi H, Jojima T, Kogai T, Iijima T, Ohira E, Tanuma D, Konno S, Kato K, Kezuka A, Akimoto K, Sakumoto J, Hishinuma A, Tomaru T, Makita N, Usui I, Aso Y. Kishi H, et al. Among authors: kogai t. Clin Case Rep. 2020 Aug 14;8(12):2619-2624. doi: 10.1002/ccr3.3186. eCollection 2020 Dec. Clin Case Rep. 2020. PMID: 33363791 Free PMC article.
A CASE OF FAMILIAL NONAUTOIMMUNE HYPERTHYROIDISM DURING PREGNANCY.
Okazaki Y, Arata N, Umehara N, Yamauchi T, Tajiri J, Hishinuma A, Kogai T, Idegami T, Murashima A, Sago H. Okazaki Y, et al. Among authors: kogai t. AACE Clin Case Rep. 2020 Jan 22;6(2):e94-e97. doi: 10.4158/ACCR-2019-0361. eCollection 2020 Mar-Apr. AACE Clin Case Rep. 2020. PMID: 32524019 Free PMC article.
53 results