Nakamura E - Search Results

1

Increased expression of matrix metalloproteinase-9 and hepatocyte growth factor in the cerebrospinal fluid of infants with posthemorrhagic hydrocephalus.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K. Okamoto T, et al. Among authors: nakamura e. Early Hum Dev. 2010 Apr;86(4):251-4. doi: 10.1016/j.earlhumdev.2010.03.007. Epub 2010 May 10. Early Hum Dev. 2010. PMID: 20457496

2

Matrix metalloproteinases in infants with posthemorrhagic hydrocephalus.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K. Okamoto T, et al. Among authors: nakamura e. Early Hum Dev. 2008 Feb;84(2):137-9. doi: 10.1016/j.earlhumdev.2007.08.006. Epub 2007 Oct 4. Early Hum Dev. 2008. PMID: 17919852

3

Airway humidification with a heated wire humidifier during high-frequency ventilation using Babylog 8000 plus in neonates.

Nagaya K, Okamoto T, Nakamura E, Hayashi T, Fujieda K. Nagaya K, et al. Among authors: nakamura e. Pediatr Pulmonol. 2009 Mar;44(3):260-6. doi: 10.1002/ppul.20990. Pediatr Pulmonol. 2009. PMID: 19208373

4

Transforming growth factor-beta1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K. Okamoto T, et al. Among authors: nakamura e. Biochem Biophys Res Commun. 2009 Jun 12;383(4):475-9. doi: 10.1016/j.bbrc.2009.04.038. Epub 2009 Apr 14. Biochem Biophys Res Commun. 2009. PMID: 19371720

5

Paternal allele of IGF2 gene haplotype CTG is associated with fetal and placental growth in Japanese.

Nagaya K, Makita Y, Taketazu G, Okamoto T, Nakamura E, Hayashi T, Fujieda K. Nagaya K, et al. Among authors: nakamura e. Pediatr Res. 2009 Aug;66(2):135-9. doi: 10.1203/PDR.0b013e3181a9e818. Pediatr Res. 2009. PMID: 19390492

6

5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.

Nakamura E, Makita Y, Okamoto T, Nagaya K, Hayashi T, Sugimoto M, Manabe H, Taketazu G, Kajino H, Fujieda K. Nakamura E, et al. Eur J Med Genet. 2011 May-Jun;54(3):354-6. doi: 10.1016/j.ejmg.2010.12.004. Epub 2010 Dec 21. Eur J Med Genet. 2011. PMID: 21172461

7

Patient reports: Two novel frameshift mutations in the SOX9 gene in two patients with campomelic dysplasia who showed long-term survival.

Okamoto T, Nakamura E, Nagaya K, Hayashi T, Mukai T, Fujieda K. Okamoto T, et al. Among authors: nakamura e. J Pediatr Endocrinol Metab. 2010 Nov;23(11):1189-93. doi: 10.1515/jpem.2010.187. J Pediatr Endocrinol Metab. 2010. PMID: 21284335 Review.

8

Maternal deletion allele of Angiotensin-converting enzyme gene is associated with fetal growth restriction.

Nakamura E, Okamoto T, Nagaya K, Hayashi T. Nakamura E, et al. Pediatr Dev Pathol. 2012 Mar-Apr;15(2):114-7. doi: 10.2350/11-09-1092-OA.1. Epub 2011 Dec 9. Pediatr Dev Pathol. 2012. PMID: 22150532

9

Developmental alterations of physical properties and components of neonatal-infantile stratum corneum of upper thighs and diaper-covered buttocks during the 1st year of life.

Minami-Hori M, Honma M, Fujii M, Nomura W, Kanno K, Hayashi T, Nakamura E, Nagaya K, Miyauchi Y, Fujimura T, Hotta M, Takagi Y, Kitahara T, Takema Y, Iizuka H. Minami-Hori M, et al. Among authors: nakamura e. J Dermatol Sci. 2014 Jan;73(1):67-73. doi: 10.1016/j.jdermsci.2013.08.015. Epub 2013 Sep 7. J Dermatol Sci. 2014. PMID: 24074652

10

Asian Neonatal Network Collaboration (AsianNeo): a study protocol for international collaborative comparisons of health services and outcomes to improve quality of care for sick newborn infants in Asia - survey, cohort and quality improvement studies.

Isayama T, Miyake F, Rohsiswatmo R, Dewi R, Ozawa Y, Tomotaki S, Morisaki N, Chee SC, Neoh SH, Imperial MLS, Velasco BAE, Chang YS, Cho SJ, Youn Y, Quek BH, Poon WB, Amin Z, Jayaratne K, Kumara S, Lin YJ, Chang JH, Lin HY, Lin MC, Nuntnarumit P, Ngerncham S, Prempunpong C, Prempraphan P, Supapannachart S, Kusuda S; Asian Neonatal Network Collaboration (AsianNeo). Isayama T, et al. BMJ Open. 2024 Jul 13;14(7):e082712. doi: 10.1136/bmjopen-2023-082712. BMJ Open. 2024. PMID: 39388526 Free PMC article.

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