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Year Number of Results
2018 1
2019 3
2020 3
2021 7
2022 3
2023 1
2024 0

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Page 1
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan.
Noguchi Y, Bo R, Nishio H, Matsumoto H, Matsui K, Yano Y, Sugawara M, Ueda G, Wijaya YOS, Niba ETE, Shinohara M, Bouike Y, Takeuchi A, Okamoto K, Saito T, Shimomura H, Lee T, Takeshima Y, Iijima K, Nozu K, Awano H. Noguchi Y, et al. Among authors: wijaya yos. Genes (Basel). 2022 Nov 14;13(11):2110. doi: 10.3390/genes13112110. Genes (Basel). 2022. PMID: 36421785 Free PMC article.
Phenotypes of SMA patients retaining SMN1 with intragenic mutation.
Wijaya YOS, Ar Rohmah M, Niba ETE, Morisada N, Noguchi Y, Hidaka Y, Ozasa S, Inoue T, Shimazu T, Takahashi Y, Tozawa T, Chiyonobu T, Inoue T, Shiroshita T, Yokoyama A, Okamoto K, Awano H, Takeshima Y, Saito T, Saito K, Nishio H, Shinohara M. Wijaya YOS, et al. Brain Dev. 2021 Aug;43(7):745-758. doi: 10.1016/j.braindev.2021.03.006. Epub 2021 Apr 20. Brain Dev. 2021. PMID: 33892995
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan.
Kimizu T, Ida S, Okamoto K, Awano H, Niba ETE, Wijaya YOS, Okazaki S, Shimomura H, Lee T, Tominaga K, Nabatame S, Saito T, Hamazaki T, Sakai N, Saito K, Shintaku H, Nozu K, Takeshima Y, Iijima K, Nishio H, Shinohara M. Kimizu T, et al. Among authors: wijaya yos. Int J Neonatal Screen. 2021 Jul 20;7(3):45. doi: 10.3390/ijns7030045. Int J Neonatal Screen. 2021. PMID: 34287247 Free PMC article.
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene.
Niba ETE, Nishio H, Wijaya YOS, Lai PS, Tozawa T, Chiyonobu T, Yamadera M, Okamoto K, Awano H, Takeshima Y, Saito T, Shinohara M. Niba ETE, et al. Among authors: wijaya yos. Brain Dev. 2021 Feb;43(2):294-302. doi: 10.1016/j.braindev.2020.09.005. Epub 2020 Oct 6. Brain Dev. 2021. PMID: 33036822
Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 Patients.
Rochmah MA, Wijaya YOS, Harahap NIF, Tode C, Takeuchi A, Ohuchi K, Shimazawa M, Hara H, Funato M, Saito T, Saito K, Lai PS, Awano H, Shinohara M, Nishio H, Niba ETE. Rochmah MA, et al. Among authors: wijaya yos. Kobe J Med Sci. 2020 Apr 1;66(1):E1-E11. Kobe J Med Sci. 2020. PMID: 32814752 Free PMC article.
Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.
Harahap NIF, Niba ETE, Ar Rochmah M, Wijaya YOS, Saito T, Saito K, Awano H, Morioka I, Iijima K, Lai PS, Matsuo M, Nishio H, Shinohara M. Harahap NIF, et al. Among authors: wijaya yos. Brain Dev. 2018 Sep;40(8):670-677. doi: 10.1016/j.braindev.2018.03.001. Epub 2018 Mar 23. Brain Dev. 2018. PMID: 29580671
Correction: Noguchi et al. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. Genes 2022, 13, 2110.
Noguchi Y, Bo R, Nishio H, Matsumoto H, Matsui K, Yano Y, Sugawara M, Ueda G, Wijaya YOS, Niba ETE, Shinohara M, Bouike Y, Takeuchi A, Okamoto K, Saito T, Shimomura H, Lee T, Takeshima Y, Iijima K, Nozu K, Awano H. Noguchi Y, et al. Among authors: wijaya yos. Genes (Basel). 2023 Mar 21;14(3):759. doi: 10.3390/genes14030759. Genes (Basel). 2023. PMID: 36981045 Free PMC article.
17 results