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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
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2009 2
2010 1
2011 1
2012 3
2013 1
2014 3
2015 10
2016 6
2017 15
2018 5
2019 4
2020 6
2021 6
2022 6
2023 2
2024 2

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Page 1
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: isojima t. J Clin Endocrinol Metab. 2024 Feb 19:dgae098. doi: 10.1210/clinem/dgae098. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38373250
Growth in girls with Turner syndrome.
Isojima T, Yokoya S. Isojima T, et al. Front Endocrinol (Lausanne). 2023 Jan 12;13:1068128. doi: 10.3389/fendo.2022.1068128. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36714599 Free PMC article. Review.
66 results