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Year Number of Results
2002 4
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2006 9
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2009 9
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2011 6
2012 10
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2014 8
2015 9
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148 results

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Page 1
Newborn Screening in Japan-2021.
Tajima T. Tajima T. Int J Neonatal Screen. 2022 Jan 4;8(1):3. doi: 10.3390/ijns8010003. Int J Neonatal Screen. 2022. PMID: 35076455 Free PMC article.
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.
Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G, Polak M, Butler G; ESPE-PES-SLEP-JSPE-APEG-APPES-ISPAE; Congenital Hypothyroidism Consensus Conference Group. Léger J, et al. J Clin Endocrinol Metab. 2014 Feb;99(2):363-84. doi: 10.1210/jc.2013-1891. Epub 2014 Jan 21. J Clin Endocrinol Metab. 2014. PMID: 24446653 Free PMC article.
Genetic causes of central precocious puberty.
Tajima T. Tajima T. Clin Pediatr Endocrinol. 2022;31(3):101-109. doi: 10.1297/cpe.2022-0021. Epub 2022 May 29. Clin Pediatr Endocrinol. 2022. PMID: 35928377 Free PMC article. Review.
A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency.
Adachi E, Nakagawa R, Tsuji-Hosokawa A, Gau M, Kirino S, Yogi A, Nakatani H, Takasawa K, Yamaguchi T, Kosho T, Murakami M, Tajima T, Hasegawa T, Yamada T, Morio T, Ohara O, Kashimada K. Adachi E, et al. Among authors: tajima t. J Clin Endocrinol Metab. 2024 Feb 20;109(3):750-760. doi: 10.1210/clinem/dgad577. J Clin Endocrinol Metab. 2024. PMID: 37804107
Molecular basis of adrenal insufficiency.
Fujieda K, Tajima T. Fujieda K, et al. Among authors: tajima t. Pediatr Res. 2005 May;57(5 Pt 2):62R-69R. doi: 10.1203/01.PDR.0000159568.31749.4D. Epub 2005 Apr 6. Pediatr Res. 2005. PMID: 15817507 Review.
Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision).
Ishii T, Kashimada K, Amano N, Takasawa K, Nakamura-Utsunomiya A, Yatsuga S, Mukai T, Ida S, Isobe M, Fukushi M, Satoh H, Yoshino K, Otsuki M, Katabami T, Tajima T. Ishii T, et al. Among authors: tajima t. Clin Pediatr Endocrinol. 2022;31(3):116-143. doi: 10.1297/cpe.2022-0009. Epub 2022 Apr 10. Clin Pediatr Endocrinol. 2022. PMID: 35928387 Free PMC article.
Successful living-donor liver transplantation for neonatal hemochromatosis due to transient abnormal myelopoiesis with Down syndrome: Case report and review of the literature.
Nagai K, Mitani T, Kato M, Kojima K, Fukushima N, Omaeuda T, Sanada Y, Terui K, Tajima T, Osaka H, Shimada A. Nagai K, et al. Among authors: tajima t. Pediatr Blood Cancer. 2024 Oct;71(10):e31228. doi: 10.1002/pbc.31228. Epub 2024 Aug 1. Pediatr Blood Cancer. 2024. PMID: 39090683 Review. No abstract available.
Neonatal mass screening for 21-hydroxylase deficiency.
Tajima T, Fukushi M. Tajima T, et al. Clin Pediatr Endocrinol. 2016 Jan;25(1):1-8. doi: 10.1297/cpe.25.1. Epub 2016 Jan 30. Clin Pediatr Endocrinol. 2016. PMID: 26865749 Free PMC article.
Temporal Trend of the SARS-CoV-2 Omicron Variant and RSV in the Nasal Cavity and Accuracy of the Newly Developed Antigen-Detecting Rapid Diagnostic Test.
Tamura D, Morisawa Y, Mato T, Nunomiya S, Yoshihiro M, Maehara Y, Ito S, Ochiai Y, Yamagishi H, Tajima T, Yamagata T, Osaka H. Tamura D, et al. Among authors: tajima t. Diagnostics (Basel). 2024 Jan 4;14(1):119. doi: 10.3390/diagnostics14010119. Diagnostics (Basel). 2024. PMID: 38201428 Free PMC article.
148 results