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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: hishinuma a. 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.
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. 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
[Thyroglobulin gene abnormalities].
Fukata S, Hishinuma A. Fukata S, et al. Among authors: hishinuma a. Nihon Rinsho. 2006 May 28;Suppl 1:363-6. Nihon Rinsho. 2006. PMID: 16776166 Review. Japanese. No abstract available.
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: hishinuma a. 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.
[Thyroglobulin gene abnormalities].
Hishinuma A, Ieiri T, Fukata S, Miyauchi A. Hishinuma A, et al. Nihon Rinsho. 2005 Oct;63 Suppl 10:31-5. Nihon Rinsho. 2005. PMID: 16279599 Review. Japanese. No abstract available.
95 results