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

Year Number of Results
2002 1
2003 2
2004 2
2005 1
2006 1
2009 2
2010 1
2011 2
2012 3
2015 1
2016 2
2017 4
2018 2
2019 4
2020 4
2021 6
2022 3
2023 1
2024 2

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37 results

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Page 1
Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles.
Okamoto N, Ohto T, Enokizono T, Wada Y, Kohmoto T, Imoto I, Haga Y, Seino J, Suzuki T. Okamoto N, et al. Among authors: ohto t. Cells. 2021 Nov 10;10(11):3117. doi: 10.3390/cells10113117. Cells. 2021. PMID: 34831340 Free PMC article.
Novel ARX mutation identified in infantile spasm syndrome patient.
Takeshita Y, Ohto T, Enokizono T, Tanaka M, Suzuki H, Fukushima H, Uehara T, Takenouchi T, Kosaki K, Takada H. Takeshita Y, et al. Among authors: ohto t. Hum Genome Var. 2020 Mar 31;7:9. doi: 10.1038/s41439-020-0094-2. eCollection 2020. Hum Genome Var. 2020. PMID: 32257294 Free PMC article.
A Case of Anorexia Nervosa with Focal Cortical Dysplasia.
Nemoto H, Imagawa K, Enokizono T, Masuda Y, Ide M, Deguchi T, Hara M, Morita A, Kido T, Tanaka M, Ohto T, Takada H. Nemoto H, et al. Among authors: ohto t. Case Rep Psychiatry. 2024 Apr 12;2024:7478666. doi: 10.1155/2024/7478666. eCollection 2024. Case Rep Psychiatry. 2024. PMID: 38716398 Free PMC article.
A girl with 'six needles' in the heart.
Lin L, Yoneyama F, Takahashi-Igari M, Ohto T, Sakamoto H. Lin L, et al. Among authors: ohto t. Int J Cardiol. 2016 Apr 15;209:66-7. doi: 10.1016/j.ijcard.2016.02.045. Epub 2016 Feb 3. Int J Cardiol. 2016. PMID: 26882185 No abstract available.
Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency.
Morita A, Enokizono T, Ohto T, Tanaka M, Watanabe S, Takada Y, Iwama K, Mizuguchi T, Matsumoto N, Morita M, Takashima S, Shimozawa N, Takada H. Morita A, et al. Among authors: ohto t. Brain Dev. 2021 Mar;43(3):475-481. doi: 10.1016/j.braindev.2020.10.011. Epub 2020 Nov 21. Brain Dev. 2021. PMID: 33234382
37 results