Takeshima K, Li Y, Kakudo K, Hirokawa M, Nishihara E, Shimatsu A, Takahashi Y, Akamizu T.Proposal of diagnostic criteria for IgG4-related thyroid diseaseEndocr J. 2021 Jan 28;68(1):1-6. doi: 10.1507/endocrj.EJ20-0557. Epub 2020 Dec 12.dio: M2PubMed PMID: 33311000
Ueki K, Tanizawa Y, Nakamura J, Yamada Y, Inagaki N, Watada H, Shimomura I, Nishimura R, Miyoshi H, Abiko A, Katagiri H, Hayashi M, Shimada A, Naruse K, Fujimoto S, Fujiwara M, Shikata K, Okada Y, Araki E, Yamazaki T, Kadowaki T; J-BRAND Registry Group.Long-term safety and efficacy of alogliptin, a DPP-4 inhibitor, in patients with type 2 diabetes: a 3-year prospective, controlled, observational study (J-BRAND Registry)BMJ Open Diabetes Res Care. 2021 Jan;9(1):e001787. doi: 10.1136/bmjdrc-2020-001787.dio: M2PubMed PMID: 33441417
Morita S, Inai Y, Minakata S, Kishimoto S, Manabe S, Iwahashi N, Ino K, Ito Y, Akamizu T, Ihara Y.Quantification of serum C-mannosyl tryptophan by novel assay to evaluate renal function and vascular complications in patients with type 2 diabetesSci Rep. 2021 Jan 21;11(1):1946. doi: 10.1038/s41598-021-81479-y.dio: M2PubMed PMID: 33479412
2020年
Uraki S, Furuta H, Miyawaki M, Matsutani N, Shima Y, Iwamoto M, Matsuno S, Morita S, Furuta M, Doi A, Iwakura H, Ariyasu H, Nishi M, Suzuki H, Akamizu T.Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical courseJ Diabetes Investig. 2020 Mar;11(2):502-505. doi: 10.1111/jdi.13127. Epub 2019 Aug 27.dio: M2PubMed PMID: 31390154
Matsutani N, Furuta H, Matsuno S, Oku Y, Morita S, Uraki S, Doi A, Furuta M, Iwakura H, Ariyasu H, Nishi M, Akamizu T.Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencingJ Diabetes Investig. 2020 Mar;11(2):333-336. doi: 10.1111/jdi.13138. Epub 2019 Sep 19.dio: M2PubMed PMID: 31479591
Karatojima M, Furuta H, Matsutani N, Matsuno S, Tamai M, Komiya K, Morita S, Uraki S, Doi A, Furuta M, Iwakura H, Ariyasu H, Nishi M, Akamizu T.A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemiaJ Diabetes. 2020 Jan;12(1):21-24. doi: 10.1111/1753-0407.12990. Epub 2019 Oct 21.dio: M2PubMed PMID: 31578783
Takeuchi T, Ishigaki Y, Hirota Y, Hasegawa Y, Yorifuji T, Kadowaki H, Akamizu T, Ogawa W, Katagiri H.Clinical characteristics of insulin resistance syndromes: A nationwide survey in JapanJ Diabetes Investig. 2020 May;11(3):603-616. doi: 10.1111/jdi.13171. Epub 2019 Dec 5.dio: M2PubMed PMID: 31677333
Ishibashi T, Morita S, Kishimoto S, Uraki S, Takeshima K, Furukawa Y, Inaba H, Ariyasu H, Iwakura H, Furuta H, Nishi M, Papa FR, Akamizu T.Nicotinic acetylcholine receptor signaling regulates inositol-requiring enzyme 1α activation to protect β-cells against terminal unfolded protein response under irremediable endoplasmic reticulum stressJ Diabetes Investig. 2020 Jul;11(4):801-813. doi: 10.1111/jdi.13211. Epub 2020 Feb 17.dio: M2PubMed PMID: 31925927
Takeshima K, Ariyasu H, Uraki S, Kitahara C, Morita S, Inaba H, Iwakura H, Warigaya K, Murata SI, Yamazaki Y, Sasano H, Akamizu T.Head and Neck Paraganglioma Atypically Carrying a Succinate Dehydrogenase Subunit B Mutation (L157X)Intern Med. 2020 May 1;59(9):1167-1171. doi: 10.2169/internalmedicine.3607-19. Epub 2020 Feb 5.dio: M2PubMed PMID: 32023584
Takagi H, Iwama S, Sugimura Y, Takahashi Y, Oki Y, Akamizu T, Arima H.Diagnosis and treatment of autoimmune and IgG4-related hypophysitis: clinical guidelines of the Japan Endocrine SocietyEndocr J. 2020 Apr 28;67(4):373-378. doi: 10.1507/endocrj.EJ19-0569. Epub 2020 Mar 7.dio: M2PubMed PMID: 32037390
Kurimoto C, Inaba H, Ariyasu H, Iwakura H, Ueda Y, Uraki S, Takeshima K, Furukawa Y, Morita S, Yamamoto Y, Yamashita S, Katsuda M, Hayata A, Akamatsu H, Jinnin M, Hara I, Yamaue H, Akamizu T.Predictive and sensitive biomarkers for thyroid dysfunctions during treatment with immune-checkpoint inhibitorsCancer Sci. 2020 May;111(5):1468-1477. doi: 10.1111/cas.14363. Epub 2020 Mar 17.dio: M2PubMed PMID: 32086984
Inaba H, Ariyasu H, Iwakura H, Kurimoto C, Ueda Y, Uraki S, Takeshima K, Furukawa Y, Morita S, Nakayama Y, Ohashi T, Ito H, Nishimura Y, Akamizu T.Autoimmune polyglandular syndrome type 2 and autoimmune hepatitis with thymoma-associated myasthenia gravis: case reportBMC Endocr Disord. 2020 Apr 7;20(1):47. doi: 10.1186/s12902-020-0498-5.dio: M2PubMed PMID: 32264857
Uraki S, Ariyasu H, Doi A, Takeshima K, Morita S, Inaba H, Furuta H, Fukuhara N, Inoshita N, Nishioka H, Nakao N, Yamada S, Akamizu T.MSH6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma SubtypesInt J Mol Sci. 2020 Apr 18;21(8):2831. doi: 10.3390/ijms21082831.dio: M2PubMed PMID: 32325698
Inagaki Y, Takeshima K, Nishi M, Ariyasu H, Doi A, Kurimoto C, Uraki S, Morita S, Furukawa Y, Inaba H, Iwakura H, Shimokawa T, Utsunomiya T, Akamizu T.The influence of thyroid autoimmunity on pregnancy outcome in infertile women: a prospective studyEndocr J. 2020 Aug 28;67(8):859-868. doi: 10.1507/endocrj.EJ19-0604. Epub 2020 May 25.dio: M2PubMed PMID: 32336697
Takeshima K, Ariyasu H, Uraki S, Morita S, Furukawa Y, Inaba H, Iwakura H, Doi A, Warigaya K, Murata SI, Enomoto K, Hotomi M, Akamizu T.False-positive staining of thyroglobulin distinguished from mixed medullary and follicular thyroid carcinoma by duplex in situ hybridizationEndocr J. 2020 Oct 28;67(10):1007-1017. doi: 10.1507/endocrj.EJ20-0169. Epub 2020 Jun 10.dio: M2PubMed PMID: 32522910
Morita S, Takeshima K, Ariyasu H, Furukawa Y, Kishimoto S, Tsuji T, Uraki S, Mishima H, Kinoshita A, Takahashi Y, Inaba H, Iwakura H, Furuta H, Nishi M, Doi A, Murata SI, Yoshiura KI, Akamizu T.Expression of unfolded protein response markers in the pheochromocytoma with Waardenburg syndrome: a case reportBMC Endocr Disord. 2020 Jun 22;20(1):90. doi: 10.1186/s12902-020-00574-9.dio: M2PubMed PMID: 32571297
Kitahara C, Morita S, Kishimoto S, Matsuno S, Uraki S, Takeshima K, Furukawa Y, Inaba H, Iwakura H, Ariyasu H, Furuta H, Nishi M, Akamizu T.Early detection of euglycemic ketoacidosis during thoracic surgery associated with empagliflozin in a patient with type 2 diabetes: A case reportJ Diabetes Investig. 2020 Jul 19. doi: 10.1111/jdi.13365. Online ahead of print.dio: M2PubMed PMID: 32686282
Inaba H, Ariyasu H, Iwakura H, Kurimoto C, Takeshima K, Morita S, Furuta H, Hotomi M, Akamizu T.Distinct clinical features and prognosis between persistent and temporary thyroid dysfunctions by immune-checkpoint inhibitorsEndocr J. 2020 Oct 3. doi: 10.1507/endocrj.EJ20-0371. Online ahead of print.dio: M2PubMed PMID: 33012745
Mizuno S, Inaba H, Kobayashi KI, Kubo K, Ito S, Hirobata T, Inoue G, Akamizu T, Komiya N.A case of postpartum thyroiditis following SARS-CoV-2 infectionEndocr J. 2020 Nov 12. doi: 10.1507/endocrj.EJ20-0553. Online ahead of print.dio: M2PubMed PMID: 33177251
Umehara H, Okazaki K, Kawa S, Takahashi H, Goto H, Matsui S, Ishizaka N, Akamizu T, Sato Y, Kawano M; Research Program for Intractable Disease by the Ministry of Health, Labor and Welfare (MHLW) Japan.The 2020 Revised Comprehensive Diagnostic (RCD) Criteria for IgG4-RDMod Rheumatol. 2020 Dec 4:1-14. doi: 10.1080/14397595.2020.1859710. Online ahead of print.dio: M2PubMed PMID: 33274670
Nakao T, Takeshima K, Ariyasu H, Kurimoto C, Uraki S, Morita S, Furukawa Y, Iwakura H, Akamizu T.Thyroid storm with delayed hyperbilirubinemia and severe heart failure: indication and contraindication of plasma exchangeEndocrinol Diabetes Metab Case Rep. 2020 Sep 4;2020:20-0036. doi: 10.1530/EDM-20-0036. Online ahead of print.dio: M2PubMed PMID: 33434181
Kishimoto S, Sasaki H, Kurisu S, Ogawa K, Matsuno S, Furuta H, Arita M, Naka K, Nanjo K, Akamizu T.Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional “seiza” styleJ Diabetes Investig. 2020 Jul 20. doi: 10.1111/jdi.13367. Online ahead of print.dio: M2PubMed PMID: 33481342
Tsuji T, Hiroyuki A, Uraki S, Doi A, Morita S, Iwakura H, Nishi M, Furuta H, Akamizu T.Autosomal Dominant Hypocalcemia With Atypical Urine Findings Accompanied by Novel CaSR Gene Mutation and VitD DeficiencyJ Endocr Soc. 2020 Dec 4;5(3):bvaa190. doi: 10.1210/jendso/bvaa190. eCollection 2021 Mar 1.dio: M2PubMed PMID: 33506158
