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

Year Number of Results
2002 4
2003 5
2004 2
2005 6
2006 9
2007 3
2008 9
2009 9
2010 7
2011 6
2012 10
2013 13
2014 8
2015 9
2016 10
2017 10
2018 5
2019 1
2020 6
2021 3
2022 10
2023 4
2024 5

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138 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.
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.
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.
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
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.
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision).
Nagasaki K, Minamitani K, Nakamura A, Kobayashi H, Numakura C, Itoh M, Mushimoto Y, Fujikura K, Fukushi M, Tajima T. Nagasaki K, et al. Among authors: tajima t. Clin Pediatr Endocrinol. 2023;32(1):26-51. doi: 10.1297/cpe.2022-0063. Epub 2022 Dec 4. Clin Pediatr Endocrinol. 2023. PMID: 36761493 Free PMC article.
138 results