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Death review of children receiving medical care at home.
Natsume J, Numaguchi A, Ohno A, Mizuno M, Takahashi Y, Okumura A, Yoshikawa T, Saitoh S, Miura K, Noda M. Natsume J, et al. Among authors: saitoh s. Pediatr Res. 2022 Apr;91(5):1286-1289. doi: 10.1038/s41390-021-01606-3. Epub 2021 Jul 8. Pediatr Res. 2022. PMID: 34239067 Free PMC article.
Acute encephalopathy in children with Dravet syndrome.
Okumura A, Uematsu M, Imataka G, Tanaka M, Okanishi T, Kubota T, Sudo A, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T. Okumura A, et al. Among authors: saitoh s. Epilepsia. 2012 Jan;53(1):79-86. doi: 10.1111/j.1528-1167.2011.03311.x. Epub 2011 Nov 16. Epilepsia. 2012. PMID: 22092154 Free article.
Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome.
Hosoki K, Ohta T, Natsume J, Imai S, Okumura A, Matsui T, Harada N, Bacino CA, Scaglia F, Jones JY, Niikawa N, Saitoh S. Hosoki K, et al. Among authors: saitoh s. Am J Med Genet A. 2012 Aug;158A(8):1891-6. doi: 10.1002/ajmg.a.35439. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711443
Probability curves for predicting symptom severity during oral food challenge with milk.
Yoneyama M, Nomura T, Kato T, Sobajima T, Tanida H, Morishita T, Sugiura S, Suda Y, Hirabayashi Y, Misawa C, Kamioka N, Tanaka H, Mizuno M, Terada A, Kanda Y, Saitoh S. Yoneyama M, et al. Among authors: saitoh s. Ann Allergy Asthma Immunol. 2015 Sep;115(3):251-3. doi: 10.1016/j.anai.2015.06.019. Epub 2015 Jul 21. Ann Allergy Asthma Immunol. 2015. PMID: 26208760 No abstract available.
Clinical and neuroimaging findings in children with posterior reversible encephalopathy syndrome.
Yamamoto H, Natsume J, Kidokoro H, Ishihara N, Suzuki M, Tsuji T, Kubota T, Yamada A, Ozeki M, Kato Z, Kawamura Y, Yoshikawa T, Okumura A, Ando N, Saitoh S, Takahashi Y, Watanabe K, Kojima S. Yamamoto H, et al. Among authors: saitoh s. Eur J Paediatr Neurol. 2015 Nov;19(6):672-8. doi: 10.1016/j.ejpn.2015.07.005. Epub 2015 Jul 22. Eur J Paediatr Neurol. 2015. PMID: 26232050
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
Yokoi S, Ishihara N, Miya F, Tsutsumi M, Yanagihara I, Fujita N, Yamamoto H, Kato M, Okamoto N, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Kojima S, Saitoh S, Kurahashi H, Natsume J. Yokoi S, et al. Among authors: saitoh s. Sci Rep. 2015 Oct 23;5:15165. doi: 10.1038/srep15165. Sci Rep. 2015. PMID: 26493046 Free PMC article.
Probability curves for predicting symptom severity during an oral food challenge with wheat.
Kamioka N, Nomura T, Kato T, Yoneyama M, Sobajima T, Tanida H, Morishita T, Sugiura S, Suda Y, Hirabayashi Y, Misawa C, Tanaka H, Mizuno M, Terada A, Kanda Y, Saitoh S. Kamioka N, et al. Among authors: saitoh s. Allergol Int. 2017 Oct;66(4):627-628. doi: 10.1016/j.alit.2017.02.011. Epub 2017 Mar 8. Allergol Int. 2017. PMID: 28284490 Free article. No abstract available.
1,588 results