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Genotype-Phenotype Correlations in Thirty 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: shimura k. J Clin Endocrinol Metab. 2024 Feb 19:dgae098. doi: 10.1210/clinem/dgae098. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38373250
A Pitfall of Adrenal Hypoplasia Congenita.
Abe J, Tsubaki J, Shimura K, Hasegawa T. Abe J, et al. Among authors: shimura k. Clin Pediatr (Phila). 2024 Jan 27:99228231222714. doi: 10.1177/00099228231222714. Online ahead of print. Clin Pediatr (Phila). 2024. PMID: 38279818 Free article. No abstract available.
Negative impact of immunoparesis in response to anti-SARS-CoV-2 mRNA vaccination of patients with multiple myeloma.
Onishi A, Matsumura-Kimoto Y, Mizutani S, Isa R, Fujino T, Tsukamoto T, Miyashita A, Okumura K, Nishiyama D, Hirakawa K, Shimura K, Kaneko H, Kiyota M, Kawata E, Takahashi R, Kobayashi T, Uchiyama H, Uoshima N, Nukui Y, Shimura Y, Inaba T, Kuroda J; Kyoto Clinical Hematology Study Group investigators. Onishi A, et al. Among authors: shimura k. Int J Hematol. 2024 Jan;119(1):50-61. doi: 10.1007/s12185-023-03680-1. Epub 2023 Dec 12. Int J Hematol. 2024. PMID: 38082201
A case of 46,XY complete gonadal dysgenesis with a novel missense variant in SRY.
Narita C, Takubo N, Sammori M, Matsumura Y, Shimura K, Ozaki R, Haruna H, Narumi S, Ishii T, Hasegawa T, Shimizu T. Narita C, et al. Among authors: shimura k. Clin Pediatr Endocrinol. 2023;32(4):235-238. doi: 10.1297/cpe.2023-0032. Epub 2023 Sep 8. Clin Pediatr Endocrinol. 2023. PMID: 37842143 Free PMC article.
474 results