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The incidences of and risk factors for severe retinopathy requiring photocoagulation and albuminuria in Japanese patients with childhood-onset type 1 diabetes.
Takaike H, Uchigata Y, Matsuura N, Sasaki N, Amemiya S, Urakami T, Kawamura T, Kikuchi N, Sugihara S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT). Takaike H, et al. Diabetol Int. 2017 Sep 22;9(2):121-128. doi: 10.1007/s13340-017-0336-9. eCollection 2018 May. Diabetol Int. 2017. PMID: 30603359 Free PMC article.
Mortality rate and standardized mortality ratio of childhood-onset type 1 diabetes according to incidentally detected non-acute-onset or acute-onset subtype, sex, and onset age: A cohort study.
Yokomichi H, Mochizuki M, Suzuki S, Ito Y, Hotsubo T, Matsuura N. Yokomichi H, et al. Among authors: hotsubo t. Clin Pediatr Endocrinol. 2025 Jan;34(1):83-88. doi: 10.1297/cpe.2024-0050. Epub 2024 Sep 16. Clin Pediatr Endocrinol. 2025. PMID: 39777131 Free PMC article. No abstract available.
Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version.
Urakami T, Hotsubo T, Ogawa Y, Kikuchi T, Usuda R, Matsui K, Hirose M, Hirai H, Abiru N, Fujiwara I, Mizuno H, Miyako K, Takahashi K, Shimada A; Committee of Pediatric Diabetes in the Japan Diabetes Society. Urakami T, et al. Among authors: hotsubo t. Diabetol Int. 2024 Aug 15;15(4):666-672. doi: 10.1007/s13340-024-00742-5. eCollection 2024 Oct. Diabetol Int. 2024. PMID: 39469563
Genotype-Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects.
Tanase-Nakao K, Iwahashi-Odano M, Sugisawa C, Abe K, Muroya K, Yamamoto Y, Kawada Y, Mushimoto Y, Ohkubo K, Kinjo S, Shimura K, Aoyama K, Mizuno H, Hotsubo T, Takahashi C, Isojima T, Kina Y, Takakuwa S, Hamada J, Sawaki M, Shigehara K, Sugimoto S, Etani Y, Narumi-Wakayama H, Mine Y, Hasegawa T, Hishinuma A, Narumi S. Tanase-Nakao K, et al. Among authors: hotsubo t. J Clin Endocrinol Metab. 2024 Aug 13;109(9):2358-2365. doi: 10.1210/clinem/dgae098. J Clin Endocrinol Metab. 2024. PMID: 38373250
Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.
Kawashima Y, Hakuno F, Okada S, Hotsubo T, Kinoshita T, Fujimoto M, Nishimura R, Fukushima T, Hanaki K, Takahashi S, Kanzaki S. Kawashima Y, et al. Among authors: hotsubo t. Clin Endocrinol (Oxf). 2014 Aug;81(2):312-4. doi: 10.1111/cen.12317. Epub 2013 Sep 30. Clin Endocrinol (Oxf). 2014. PMID: 24033502 No abstract available.
32 results