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

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

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69 results

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Page 1
Guide for diagnosis and treatment of hyperphenylalaninemia.
Shintaku H, Ohura T, Takayanagi M, Kure S, Owada M, Matsubara Y, Yoshino M, Okano Y, Ito T, Okuyama T, Nakamura K, Matuo M, Endo F, Ida H. Shintaku H, et al. Among authors: ohura t. Pediatr Int. 2021 Jan;63(1):8-12. doi: 10.1111/ped.14399. Epub 2021 Jan 10. Pediatr Int. 2021. PMID: 33423362
Food Preferences of Patients with Citrin Deficiency.
Okamoto M, Okano Y, Okano M, Yazaki M, Inui A, Ohura T, Murayama K, Watanabe Y, Tokuhara D, Takeshima Y. Okamoto M, et al. Among authors: ohura t. Nutrients. 2021 Sep 6;13(9):3123. doi: 10.3390/nu13093123. Nutrients. 2021. PMID: 34579000 Free PMC article.
Citrulline for urea cycle disorders in Japan.
Tanaka K, Nakamura K, Matsumoto S, Kido J, Mitsubuchi H, Ohura T, Endo F. Tanaka K, et al. Among authors: ohura t. Pediatr Int. 2017 Apr;59(4):422-426. doi: 10.1111/ped.13163. Epub 2016 Dec 22. Pediatr Int. 2017. PMID: 27613354
Maternal feeding controls fetal biological clock.
Ohta H, Xu S, Moriya T, Iigo M, Watanabe T, Nakahata N, Chisaka H, Hanita T, Matsuda T, Ohura T, Kimura Y, Yaegashi N, Tsuchiya S, Tei H, Okamura K. Ohta H, et al. Among authors: ohura t. PLoS One. 2008 Jul 2;3(7):e2601. doi: 10.1371/journal.pone.0002601. PLoS One. 2008. PMID: 18596966 Free PMC article.
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14).
Minatogawa M, Unzaki A, Morisaki H, Syx D, Sonoda T, Janecke AR, Slavotinek A, Voermans NC, Lacassie Y, Mendoza-Londono R, Wierenga KJ, Jayakar P, Gahl WA, Tifft CJ, Figuera LE, Hilhorst-Hofstee Y, Maugeri A, Ishikawa K, Kobayashi T, Aoki Y, Ohura T, Kawame H, Kono M, Mochida K, Tokorodani C, Kikkawa K, Morisaki T, Kobayashi T, Nakane T, Kubo A, Ranells JD, Migita O, Sobey G, Kaur A, Ishikawa M, Yamaguchi T, Matsumoto N, Malfait F, Miyake N, Kosho T. Minatogawa M, et al. Among authors: ohura t. J Med Genet. 2022 Sep;59(9):865-877. doi: 10.1136/jmedgenet-2020-107623. Epub 2021 Nov 23. J Med Genet. 2022. PMID: 34815299 Free PMC article.
69 results