Akira Hishinuma - Publications

Affiliations: 
Dokkyo University School of Medicine, Mibu-machi, Tochigi-ken, Japan 

33 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Nagamine T, Noh JY, Emoto N, Kogai T, Hishinuma A, Okajima F, Sugihara H. Painless destructive thyroiditis in a patient with resistance to thyroid hormone: a case report. Thyroid Research. 12: 8. PMID 31673293 DOI: 10.1186/s13044-019-0072-2  0.36
2019 Mizokami T, Fukata S, Kogai T, Hishinuma A, Hamada K, Maruta T, Higashi K, Tajiri J. Congenital Primary Hypothyroidism with the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-sized Thyroid Gland on Levothyroxine Replacement. Internal Medicine (Tokyo, Japan). PMID 31178475 DOI: 10.2169/internalmedicine.1163-18  0.407
2017 Nyuzuki H, Kogai T, Hishinuma A, Ogawa Y, Saitoh A, Nagasaki K. PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule. Pediatrics International : Official Journal of the Japan Pediatric Society. 59: 1223-1224. PMID 29359449 DOI: 10.1111/ped.13427  0.37
2017 Thienpont LM, Van Uytfanghe K, De Grande LAC, Reynders D, Das B, Faix JD, MacKenzie F, Decallonne B, Hishinuma A, Lapauw B, Taelman P, Van Crombrugge P, Van den Bruel A, Velkeniers B, Williams P, et al. Harmonization of Serum Thyroid-Stimulating Hormone Measurements Paves the Way for the Adoption of a More Uniform Reference Interval. Clinical Chemistry. PMID 28522444 DOI: 10.1373/clinchem.2016.269456  0.32
2017 Mizokami T, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Radioiodine Treatment For Hyperthyroidism In A Patient With Pendred Syndrome Aace Clinical Case Reports. 3. DOI: 10.4158/Ep161405.Cr  0.321
2016 Nishihara E, Hishinuma A, Kogai T, Takada N, Hirokawa M, Fukata S, Ito M, Yabuta T, Nishikawa M, Nakamura H, Amino N, Miyauchi A. A Novel Germline Mutation of KEAP1 (R483H) Associated with a Non-Toxic Multinodular Goiter. Frontiers in Endocrinology. 7: 131. PMID 27703446 DOI: 10.3389/fendo.2016.00131  0.326
2016 Mizokami T, Fukata S, Hishinuma A, Kogai T, Hamada K, Maruta T, Higashi K, Tajiri J. Iodide Transport Defect and Breast Milk Iodine. European Thyroid Journal. 5: 145-8. PMID 27493890 DOI: 10.1159/000446496  0.313
2015 Taki K, Kogai T, Sakumoto J, Namatame T, Hishinuma A. Familial hypocalciuric hypercalcemia with a de novo heterozygous mutation of calcium-sensing receptor. Endocrinology, Diabetes & Metabolism Case Reports. 2015: 150016. PMID 26019872 DOI: 10.1530/EDM-15-0016  0.332
2013 Sakurai K, Hata M, Hishinuma A, Ushijima R, Okada A, Taeda Y, Arihara Z, Fukazawa H, Takahashi K. Papillary thyroid carcinoma in one of identical twin patients with Pendred syndrome. Endocrine Journal. 60: 805-11. PMID 23459462 DOI: DN/JST.JSTAGE/endocrj/EJ12-0396  0.362
2012 Kahara T, Igarashi N, Hishinuma A, Nakanishi Y, Uchiyama A, Miwa A, Ishizawa S, Yamamoto Y, Noto H, Sumiya H, Ishikura K, Usuda R, Iida H. Thyroglobulin gene mutation with cold nodule on thyroid scintigraphy. Case Reports in Endocrinology. 2012: 280319. PMID 22934199 DOI: 10.1155/2012/280319  0.42
2010 Fukata S, Hishinuma A, Nakatake N, Tajiri J. Diagnosis of iodide transport defect: do we need to measure the saliva/serum radioactive iodide ratio to diagnose iodide transport defect? Thyroid : Official Journal of the American Thyroid Association. 20: 1419-21. PMID 21054210 DOI: 10.1089/thy.2010.0069  0.381
2008 Ohye H, Fukata S, Hishinuma A, Kudo T, Nishihara E, Ito M, Kubota S, Amino N, Ieiri T, Kuma K, Miyauchi A. A novel homozygous missense mutation of the dual oxidase 2 (DUOX2) gene in an adult patient with large goiter. Thyroid : Official Journal of the American Thyroid Association. 18: 561-6. PMID 18426362 DOI: 10.1089/thy.2007.0258  0.396
2007 Nishihara E, Nagayama Y, Amino N, Hishinuma A, Takano T, Yoshida H, Kubota S, Fukata S, Kuma K, Miyauchi A. A novel thyrotropin receptor germline mutation (Asp617Tyr) causing hereditary hyperthyroidism. Endocrine Journal. 54: 927-34. PMID 18025759 DOI: JST.JSTAGE/endocrj/K07-088  0.359
2007 Kanou Y, Hishinuma A, Tsunekawa K, Seki K, Mizuno Y, Fujisawa H, Imai T, Miura Y, Nagasaka T, Yamada C, Ieiri T, Murakami M, Murata Y. Thyroglobulin gene mutations producing defective intracellular transport of thyroglobulin are associated with increased thyroidal type 2 iodothyronine deiodinase activity. The Journal of Clinical Endocrinology and Metabolism. 92: 1451-7. PMID 17244789 DOI: 10.1210/jc.2006-1242  0.368
2006 Nishihara E, Fukata S, Hishinuma A, Kudo T, Ohye H, Ito M, Kubota S, Amino N, Kuma K, Miyauchi A. Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patient. Endocrine Journal. 53: 735-40. PMID 16960398 DOI: JST.JSTAGE/endocrj/K06-090  0.374
2006 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, et al. Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan. The Journal of Clinical Endocrinology and Metabolism. 91: 3100-4. PMID 16720658 DOI: 10.1210/jc.2005-2702  0.321
2006 Kitanaka S, Takeda A, Sato U, Miki Y, Hishinuma A, Ieiri T, Igarashi T. A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels. Journal of Human Genetics. 51: 379-82. PMID 16477365 DOI: 10.1007/s10038-006-0360-2  0.377
2005 Hishinuma A, Fukata S, Kakudo K, Murata Y, Ieiri T. High incidence of thyroid cancer in long-standing goiters with thyroglobulin mutations. Thyroid : Official Journal of the American Thyroid Association. 15: 1079-84. PMID 16187918 DOI: 10.1089/thy.2005.15.1079  0.402
2005 Shibayama K, Ohyama Y, Hishinuma A, Yokota Y, Kazahari K, Kazahari M, Ieiri T, Matsuura N. Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene. Pediatrics International : Official Journal of the Japan Pediatric Society. 47: 105-8. PMID 15693879 DOI: 10.1111/j.1442-200x.2005.02020.x  0.337
2004 Hishinuma A, Ohmika N, Namatame T, Ieiri T. TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development. Molecular and Cellular Endocrinology. 221: 33-46. PMID 15223130 DOI: 10.1016/j.mce.2004.04.003  0.364
2004 Baryshev M, Sargsyan E, Wallin G, Lejnieks A, Furudate S, Hishinuma A, Mkrtchian S. Unfolded protein response is involved in the pathology of human congenital hypothyroid goiter and rat non-goitrous congenital hypothyroidism. Journal of Molecular Endocrinology. 32: 903-20. PMID 15171721 DOI: 10.1677/jme.0.0320903  0.301
2003 Kotani T, Umeki K, Kawano J, Suganuma T, Hishinuma A, Ieiri T, Harada S. Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings. Clinical Endocrinology. 59: 198-206. PMID 12864797 DOI: 10.1046/j.1365-2265.2003.01823.x  0.357
2001 Hishinuma A, Ohyama Y, Kuribayashi T, Nagakubo N, Namatame T, Shibayama K, Arisaka O, Matsuura N, Ieiri T. Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis. European Journal of Endocrinology / European Federation of Endocrine Societies. 145: 385-9. PMID 11580993 DOI: 10.1530/Eje.0.1450385  0.377
2000 Hishinuma A, Furudate S, Oh-Ishi M, Nagakubo N, Namatame T, Ieiri T. A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats. Endocrinology. 141: 4050-5. PMID 11089535 DOI: 10.1210/endo.141.11.7794  0.343
2000 Kuribayashi T, Hishinuma A, Kanazawa S, Nihei Y, Hoshi M, Oyama M, Nitta A, Ieiri T, Arisaka O. Sequence analysis of thyroid transcription factor-2 (TTF-2) gene in ten patients with congenital hypothyroidism due to thyroid dysgenesis Clinical Pediatric Endocrinology. 9: 37-40. DOI: 10.1297/cpe.9.37  0.359
1999 Hishinuma A, Takamatsu J, Ohyama Y, Yokozawa T, Kanno Y, Kuma K, Yoshida S, Matsuura N, Ieiri T. Two novel cysteine substitutions (C1263R and C1995S) of thyroglobulin cause a defect in intracellular transport of thyroglobulin in patients with congenital goiter and the variant type of adenomatous goiter. The Journal of Clinical Endocrinology and Metabolism. 84: 1438-44. PMID 10199792 DOI: 10.1210/jcem.84.4.5633  0.358
1998 Hishinuma A, Kuribayashi T, Kanno Y, Onigata K, Nagashima K, Ieiri T. Sequence analysis of thyroid transcription factor-1 gene reveals absence of mutations in patients with thyroid dysgenesis but presence of polymorphisms in the 5' flanking region and intron. Endocrine Journal. 45: 563-7. PMID 9881907 DOI: 10.1507/Endocrj.45.563  0.348
1998 Hishinuma A, Kasai K, Masawa N, Kanno Y, Arimura M, Shimoda SI, Ieiri T. Missense mutation (C1263R) in the thyroglobulin gene causes congenital goiter with mild hypothyroidism by impaired intracellular transport. Endocrine Journal. 45: 315-27. PMID 9790265 DOI: 10.1507/Endocrj.45.315  0.401
1998 Hishinuma A, Takamatsu J, Kanno Y, Yoshida S, Ieiri T. Analysis of the promoter of the thyrotropin receptor gene and the entire genomic sequence of thyroid transcription factor-1 in familial congenital hypothyroidism due to thyrotropin unresponsiveness. Thyroid : Official Journal of the American Thyroid Association. 8: 305-9. PMID 9588495 DOI: 10.1089/Thy.1998.8.305  0.36
1995 Hishinuma A, Yamanaka T, Kasai K, So S, Tseng CC, Bamba N, Ohtake H, Shimoda S. Different growth control of the two human thyroid cell lines of adenomatous goiter and papillary carcinoma. Thyroid : Official Journal of the American Thyroid Association. 5: 41-6. PMID 7787432 DOI: 10.1089/Thy.1995.5.41  0.308
1992 Kasai K, Yamaguchi F, Hosoya T, Ichimura K, Banba N, Emoto T, Hiraiwa M, Hishinuma A, Hattori Y, Shimoda S. Effects of inorganic iodide, epidermal growth factor and phorbol ester on hormone synthesis by porcine thyroid follicles cultured in suspension. Life Sciences. 51: 1095-103. PMID 1518372 DOI: 10.1016/0024-3205(92)90510-V  0.322
1988 Hishinuma A, Hockfield S, McKay R, Hildebrand JG. Monoclonal antibodies reveal cell-type-specific antigens in the sexually dimorphic olfactory system of Manduca sexta. II. Expression of antigens during postembryonic development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 8: 308-15. PMID 3339412 DOI: 10.1523/Jneurosci.08-01-00308.1988  0.435
1988 Hishinuma A, Hockfield S, McKay R, Hildebrand JG. Monoclonal antibodies reveal cell-type-specific antigens in the sexually dimorphic olfactory system of Manduca sexta. I. Generation of monoclonal antibodies and partial characterization of the antigens. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 8: 296-307. PMID 2448431 DOI: 10.1523/Jneurosci.08-01-00296.1988  0.43
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