Kouwaki M - Search Results

1

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: kouwaki m. Front Pediatr. 2019 Nov 14;7:469. doi: 10.3389/fped.2019.00469. eCollection 2019. Front Pediatr. 2019. PMID: 31799224 Free PMC article.

2

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: kouwaki m. Pediatr Int. 2016 Jun;58(6):461-6. doi: 10.1111/ped.12861. Epub 2016 Feb 3. Pediatr Int. 2016. PMID: 26615960

3

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: kouwaki m. 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

4

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: kouwaki m. Neonatology. 2011;100(3):228-32. doi: 10.1159/000324715. Epub 2011 Jun 22. Neonatology. 2011. PMID: 21701211

5

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: kouwaki m. J Pediatr Hematol Oncol. 2012 Aug;34(6):475-9. doi: 10.1097/MPH.0b013e318249597f. J Pediatr Hematol Oncol. 2012. PMID: 22510770 Review.

6

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: kouwaki m. 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.

7

A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.

Suzuki T, Togawa T, Kanno H, Ogura H, Yamamoto T, Sugiura T, Kouwaki M, Saitoh S. Suzuki T, et al. Among authors: kouwaki m. J Pediatr Hematol Oncol. 2021 Mar 1;43(2):e250-e254. doi: 10.1097/MPH.0000000000001796. J Pediatr Hematol Oncol. 2021. PMID: 32287101

8

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: kouwaki m. Pediatr Int. 2012 Dec;54(6):931-3. doi: 10.1111/j.1442-200X.2012.03654.x. Pediatr Int. 2012. PMID: 23279025

9

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: kouwaki m. 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

10

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: kouwaki m. 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

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