Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

1,661 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
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. Genes (Basel). 2022 Nov 14;13(11):2110. doi: 10.3390/genes13112110. Genes (Basel). 2022. PMID: 36421785 Free PMC article.
Telomeric Region of the Spinal Muscular Atrophy Locus Is Susceptible to Structural Variations.
Noguchi Y, Onishi A, Nakamachi Y, Hayashi N, Harahap NI, Rochmah MA, Shima A, Yanagisawa S, Morisada N, Nakagawa T, Iijima K, Kasagi S, Saegusa J, Kawano S, Shinohara M, Tairaku S, Saito T, Kubo Y, Saito K, Nishio H. Noguchi Y, et al. Pediatr Neurol. 2016 May;58:83-9. doi: 10.1016/j.pediatrneurol.2016.01.019. Epub 2016 Jan 30. Pediatr Neurol. 2016. PMID: 27268759
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. Among authors: noguchi y. 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
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. Genes (Basel). 2023 Mar 21;14(3):759. doi: 10.3390/genes14030759. Genes (Basel). 2023. PMID: 36981045 Free PMC article.
Prenatal genetic testing for familial severe congenital protein C deficiency.
Tairaku S, Taniguchi-Ikeda M, Okazaki Y, Noguchi Y, Nakamachi Y, Mori T, Kubokawa I, Hayakawa A, Shibata A, Emoto T, Kurahashi H, Toda T, Kawano S, Yamada H, Morioka I, Iijima K. Tairaku S, et al. Among authors: noguchi y. Hum Genome Var. 2015 Jun 25;2:15017. doi: 10.1038/hgv.2015.17. eCollection 2015. Hum Genome Var. 2015. PMID: 27081530 Free PMC article.
Low total IgM values and high cytomegalovirus loads in the blood of newborns with symptomatic congenital cytomegalovirus infection.
Kobayashi Y, Morioka I, Koda T, Nakamachi Y, Okazaki Y, Noguchi Y, Ogi M, Chikahira M, Tanimura K, Ebina Y, Funakoshi T, Ohashi M, Iijima K, Inoue N, Kawano S, Yamada H. Kobayashi Y, et al. Among authors: noguchi y. J Perinat Med. 2015 Mar;43(2):239-43. doi: 10.1515/jpm-2014-0071. J Perinat Med. 2015. PMID: 24968403 Free article.
[Acute myeloid leukemia with t(16;21)(q24;q22) in a child].
Noguchi Y, Nakamachi Y, Oyabu C, Kikuma T, Hasegawa D, Yamashita T, Nishiyama M, Kosaka Y, Kawano S. Noguchi Y, et al. Rinsho Ketsueki. 2011 Dec;52(12):1893-5. Rinsho Ketsueki. 2011. PMID: 22241158 Japanese.
1,661 results