Akira Hishinuma
Affiliations: | Dokkyo University School of Medicine, Mibu-machi, Tochigi-ken, Japan |
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Publications
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| Nagamine T, Noh JY, Emoto N, et al. (2019) Painless destructive thyroiditis in a patient with resistance to thyroid hormone: a case report. Thyroid Research. 12: 8 |
| Mizokami T, Fukata S, Kogai T, et al. (2019) 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) |
| Nyuzuki H, Kogai T, Hishinuma A, et al. (2017) PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule. Pediatrics International : Official Journal of the Japan Pediatric Society. 59: 1223-1224 |
| Thienpont LM, Van Uytfanghe K, De Grande LAC, et al. (2017) Harmonization of Serum Thyroid-Stimulating Hormone Measurements Paves the Way for the Adoption of a More Uniform Reference Interval. Clinical Chemistry |
| Mizokami T, Hishinuma A, Kogai T, et al. (2017) Radioiodine Treatment For Hyperthyroidism In A Patient With Pendred Syndrome Aace Clinical Case Reports. 3 |
| Nishihara E, Hishinuma A, Kogai T, et al. (2016) A Novel Germline Mutation of KEAP1 (R483H) Associated with a Non-Toxic Multinodular Goiter. Frontiers in Endocrinology. 7: 131 |
| Mizokami T, Fukata S, Hishinuma A, et al. (2016) Iodide Transport Defect and Breast Milk Iodine. European Thyroid Journal. 5: 145-8 |
| Taki K, Kogai T, Sakumoto J, et al. (2015) Familial hypocalciuric hypercalcemia with a de novo heterozygous mutation of calcium-sensing receptor. Endocrinology, Diabetes & Metabolism Case Reports. 2015: 150016 |
| Sakurai K, Hata M, Hishinuma A, et al. (2013) Papillary thyroid carcinoma in one of identical twin patients with Pendred syndrome. Endocrine Journal. 60: 805-11 |
| Kahara T, Igarashi N, Hishinuma A, et al. (2012) Thyroglobulin gene mutation with cold nodule on thyroid scintigraphy. Case Reports in Endocrinology. 2012: 280319 |