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Hypopituitarism and cranial nerve involvement mimicking Tolosa-Hunt syndrome as the initially presenting feature of diffuse large B-cell lymphoma: a case report.
Kishimoto S, Morita S, Kurimoto C, Kitahara C, Tsuji T, Uraki S, Takeshima K, Furukawa Y, Iwakura H, Furuta H, Nishi M, Matsuoka TA. Kishimoto S, et al. Among authors: morita s. BMC Endocr Disord. 2022 Mar 14;22(1):65. doi: 10.1186/s12902-022-00973-0. BMC Endocr Disord. 2022. PMID: 35287660 Free PMC article.
Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course.
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. Uraki S, et al. Among authors: morita s. J Diabetes Investig. 2020 Mar;11(2):502-505. doi: 10.1111/jdi.13127. Epub 2019 Aug 27. J Diabetes Investig. 2020. PMID: 31390154 Free PMC article.
Comparative analysis of human leucocyte antigen between idiopathic and anti-PD-1 antibody induced isolated adrenocorticotropic hormone deficiency: A pilot study.
Inaba H, Ariyasu H, Iwakura H, Ueda Y, Kurimoto C, Uraki S, Takeshima K, Yamaoka H, Furukawa Y, Morita S, Nishi M, Akamizu T. Inaba H, et al. Among authors: morita s. Clin Endocrinol (Oxf). 2019 Dec;91(6):786-792. doi: 10.1111/cen.14082. Epub 2019 Sep 12. Clin Endocrinol (Oxf). 2019. PMID: 31468541
A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia.
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. Karatojima M, et al. Among authors: morita s. J Diabetes. 2020 Jan;12(1):21-24. doi: 10.1111/1753-0407.12990. Epub 2019 Oct 21. J Diabetes. 2020. PMID: 31578783 No abstract available.
3,491 results