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

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Page 1
[Treatment and Pathomechanism of Citrin Deficiency].
Hayasaka K, Numakura C, Watanabe H. Hayasaka K, et al. Among authors: numakura c. Brain Nerve. 2015 Jun;67(6):739-47. doi: 10.11477/mf.1416200211. Brain Nerve. 2015. PMID: 26062589 Review. Japanese.
Growth impairment in individuals with citrin deficiency.
Numakura C, Tamiya G, Ueki M, Okada T, Maisawa SI, Kojima-Ishii K, Murakami J, Horikawa R, Tokuhara D, Ito K, Adachi M, Abiko T, Mitsui T, Hayasaka K. Numakura C, et al. J Inherit Metab Dis. 2019 May;42(3):501-508. doi: 10.1002/jimd.12051. Epub 2019 Feb 4. J Inherit Metab Dis. 2019. PMID: 30715743
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: numakura c. 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.
Diabetes mellitus exacerbates citrin deficiency via glucose toxicity.
Watanabe Y, Numakura C, Tahara T, Fukui K, Torimura T, Hiromatsu Y, Tomotsune K, Yamakawa M, Hayasaka K. Watanabe Y, et al. Among authors: numakura c. Diabetes Res Clin Pract. 2020 Jun;164:108159. doi: 10.1016/j.diabres.2020.108159. Epub 2020 Apr 23. Diabetes Res Clin Pract. 2020. PMID: 32335094
Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study.
Hosokawa M, Ichihashi Y, Sato Y, Shibata N, Nagasaki K, Ikegawa K, Hasegawa Y, Hamajima T, Nagamatsu F, Suzuki S, Numakura C, Amano N, Sasaki G, Nagahara K, Soneda S, Ariyasu D, Maeda M, Kamasaki H, Aso K, Hasegawa T, Ishii T. Hosokawa M, et al. Among authors: numakura c. J Clin Endocrinol Metab. 2023 Dec 21:dgad753. doi: 10.1210/clinem/dgad753. Online ahead of print. J Clin Endocrinol Metab. 2023. PMID: 38128002
Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct.
Kanno M, Suzuki M, Tanikawa K, Numakura C, Matsuzawa SI, Niihori T, Aoki Y, Matsubara Y, Makino S, Tamiya G, Nakano S, Funayama R, Shirota M, Nakayama K, Mitsui T, Hayasaka K. Kanno M, et al. Among authors: numakura c. J Hum Genet. 2022 Jul;67(7):393-397. doi: 10.1038/s10038-022-01017-0. Epub 2022 Jan 28. J Hum Genet. 2022. PMID: 35087201
56 results