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3,019 results

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Long-Term Evaluation of Low-Dose Betamethasone for Ataxia Telangiectasia.
Hasegawa S, Kumada S, Tanuma N, Tsuji-Hosokawa A, Kashimada A, Mizuno T, Moriyama K, Sugawara Y, Shirai I, Miyata Y, Nishida H, Mashimo H, Hasegawa T, Hosokawa T, Hisakawa H, Uematsu M, Fujine A, Miyata R, Sakuma H, Kashimada K, Imai K, Morio T, Hayashi M, Mizutani S, Takagi M. Hasegawa S, et al. Among authors: hasegawa t. Pediatr Neurol. 2019 Nov;100:60-66. doi: 10.1016/j.pediatrneurol.2019.05.006. Epub 2019 May 13. Pediatr Neurol. 2019. PMID: 31272782 Clinical Trial.
Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders.
Kashimada A, Hasegawa S, Nomura T, Shiraku H, Moriyama K, Suzuki T, Nakajima K, Mizuno T, Imai K, Sugawara Y, Morio T, Kumada S, Takagi M. Kashimada A, et al. Among authors: hasegawa s. Brain Dev. 2019 Feb;41(2):150-157. doi: 10.1016/j.braindev.2018.09.007. Epub 2018 Oct 6. Brain Dev. 2019. PMID: 30301590
Whole-exome sequence analysis of ataxia telangiectasia-like phenotype.
Hasegawa S, Imai K, Yoshida K, Okuno Y, Muramatsu H, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Kojima S, Ogawa S, Morio T, Mizutani S, Takagi M. Hasegawa S, et al. J Neurol Sci. 2014 May 15;340(1-2):86-90. doi: 10.1016/j.jns.2014.02.033. Epub 2014 Mar 4. J Neurol Sci. 2014. PMID: 24631270
Targeting the enhanced ER stress response in Marinesco-Sjögren syndrome.
Kashimada A, Hasegawa S, Isagai T, Uchiyama T, Matsuo M, Kawai M, Goto M, Morio T, Hayashi YK, Takagi M. Kashimada A, et al. Among authors: hasegawa s. J Neurol Sci. 2018 Feb 15;385:49-56. doi: 10.1016/j.jns.2017.12.010. Epub 2017 Dec 9. J Neurol Sci. 2018. PMID: 29406913
ATM Regulates Adipocyte Differentiation and Contributes to Glucose Homeostasis.
Takagi M, Uno H, Nishi R, Sugimoto M, Hasegawa S, Piao J, Ihara N, Kanai S, Kakei S, Tamura Y, Suganami T, Kamei Y, Shimizu T, Yasuda A, Ogawa Y, Mizutani S. Takagi M, et al. Among authors: hasegawa s. Cell Rep. 2015 Feb 17;10(6):957-967. doi: 10.1016/j.celrep.2015.01.027. Epub 2015 Feb 12. Cell Rep. 2015. PMID: 25683718 Free article.
A novel splicing mutation in SLC9A6 in a boy with Christianson syndrome.
Ieda D, Hori I, Nakamura Y, Ohashi K, Negishi Y, Hattori A, Arisaka A, Hasegawa S, Saitoh S. Ieda D, et al. Among authors: hasegawa s. Hum Genome Var. 2019 Mar 25;6:15. doi: 10.1038/s41439-019-0046-x. eCollection 2019. Hum Genome Var. 2019. PMID: 30937176 Free PMC article.
3,019 results