Koyama N - Search Results

1

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.

Kawase K, Sugiura T, Nagaya Y, Yamada T, Sugimoto M, Ito K, Togawa T, Nagasaki R, Kato T, Kouwaki M, Koyama N, Saitoh S. Kawase K, et al. Among authors: koyama n. Pediatr Int. 2016 Jun;58(6):461-6. doi: 10.1111/ped.12861. Epub 2016 Feb 3. Pediatr Int. 2016. PMID: 26615960

2

Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis.

Sugiura T, Kouwaki M, Goto K, Endo T, Ito K, Koyama N, Togari H. Sugiura T, et al. Among authors: koyama n. Pediatr Int. 2012 Dec;54(6):931-3. doi: 10.1111/j.1442-200X.2012.03654.x. Pediatr Int. 2012. PMID: 23279025

3

Neurodevelopmental outcomes at 18 months' corrected age of infants born at 22 weeks of gestation.

Sugiura T, Kouwaki M, Togawa Y, Sugimoto M, Togawa T, Koyama N. Sugiura T, et al. Among authors: koyama n. Neonatology. 2011;100(3):228-32. doi: 10.1159/000324715. Epub 2011 Jun 22. Neonatology. 2011. PMID: 21701211

4

Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.

Nagara S, Kouwaki M, Togawa T, Sugiura T, Okada M, Koyama N. Nagara S, et al. Among authors: koyama n. Pediatr Neonatol. 2018 Jun;59(3):274-280. doi: 10.1016/j.pedneo.2017.09.005. Epub 2017 Sep 21. Pediatr Neonatol. 2018. PMID: 29030024 Free article.

5

Nusinersen helps restore walking ability in childhood spinal muscular atrophy.

Sugimoto M, Aiba K, Koyama N, Yokochi K, Nishio H. Sugimoto M, et al. Among authors: koyama n. Pediatr Int. 2019 Jul;61(7):728-729. doi: 10.1111/ped.13867. Epub 2019 Jul 9. Pediatr Int. 2019. PMID: 31290219 No abstract available.

6

Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report.

Watanabe Y, Sugiura T, Sugimoto M, Togawa Y, Kouwaki M, Koyama N, Saitoh S. Watanabe Y, et al. Among authors: koyama n. Front Pediatr. 2019 Nov 14;7:469. doi: 10.3389/fped.2019.00469. eCollection 2019. Front Pediatr. 2019. PMID: 31799224 Free PMC article.

7

Risk factors for early death in transient myeloproliferative disorder without phenotypic features of Down syndrome: a case report and literature review.

Kawase K, Azuma E, Ohshita H, Tanaka T, Hanada Y, Sasaki T, Sugimoto M, Togawa T, Kouwaki M, Ito T, Hirayama M, Koyama N. Kawase K, et al. Among authors: koyama n. J Pediatr Hematol Oncol. 2012 Aug;34(6):475-9. doi: 10.1097/MPH.0b013e318249597f. J Pediatr Hematol Oncol. 2012. PMID: 22510770 Review.

8

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.

Kawase K, Nishino I, Sugimoto M, Togawa T, Sugiura T, Kouwaki M, Kibe T, Koyama N, Yokochi K. Kawase K, et al. Among authors: koyama n. Brain Dev. 2015 Oct;37(9):887-90. doi: 10.1016/j.braindev.2015.02.002. Epub 2015 Feb 24. Brain Dev. 2015. PMID: 25721947

9

A case of systemic aplasia cutis congenita: a newly recognized syndrome?

Sugiura T, Kouwaki M, Kiyosawa S, Sasada Y, Maeda M, Goto K, Koyama N. Sugiura T, et al. Among authors: koyama n. Eur J Pediatr. 2008 Apr;167(4):409-13. doi: 10.1007/s00431-007-0512-1. Epub 2007 May 23. Eur J Pediatr. 2008. PMID: 17520283

10

Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.

Kawase K, Nishino I, Sugimoto M, Kouwaki M, Koyama N, Yokochi K. Kawase K, et al. Among authors: koyama n. Brain Dev. 2015 Feb;37(2):265-9. doi: 10.1016/j.braindev.2014.04.002. Epub 2014 Apr 29. Brain Dev. 2015. PMID: 24787270

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