Morioka I - Search Results

1

Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.

Harahap NIF, Niba ETE, Ar Rochmah M, Wijaya YOS, Saito T, Saito K, Awano H, Morioka I, Iijima K, Lai PS, Matsuo M, Nishio H, Shinohara M. Harahap NIF, et al. Among authors: morioka i. Brain Dev. 2018 Sep;40(8):670-677. doi: 10.1016/j.braindev.2018.03.001. Epub 2018 Mar 23. Brain Dev. 2018. PMID: 29580671

2

PDGF-alpha receptor expression following hypoxic-ischemic injury in the neonatal rat brain.

Morioka I, Tsuneishi S, Takada S, Matsuo M. Morioka I, et al. Kobe J Med Sci. 2004 Jan;50(1-2):21-30. Kobe J Med Sci. 2004. PMID: 15342968 Free article.

3

Blood lysophosphatidylcholine (LPC) levels and characteristic molecular species in neonates: prolonged low blood LPC levels in very low birth weight infants.

Takatera A, Takeuchi A, Saiki K, Morioka I, Yokoyama N, Matsuo M. Takatera A, et al. Among authors: morioka i. Pediatr Res. 2007 Oct;62(4):477-82. doi: 10.1203/PDR.0b013e31814625ca. Pediatr Res. 2007. PMID: 17667851

4

Ureaplasma urealyticum and Mycoplasma hominis presence in umbilical cord is associated with pathogenesis of funisitis.

Egawa T, Morioka I, Morisawa T, Yokoyama N, Nakao H, Ohashi M, Matsuo M. Egawa T, et al. Among authors: morioka i. Kobe J Med Sci. 2007;53(5):241-9. Kobe J Med Sci. 2007. PMID: 18204300 Free article.

5

Identification of N-acetyl Proline-Glycine-Proline (acPGP) in human serum of adults and newborns by liquid chromatography-tandem mass spectrometry.

Shibata A, Morioka I, Ashi C, Nagasaki S, Tode C, Morikawa S, Miwa A, Enomoto M, Saiki K, Yokoyama N, Takeuchi A, Matsuo M. Shibata A, et al. Among authors: morioka i. Clin Chim Acta. 2009 Apr;402(1-2):124-8. doi: 10.1016/j.cca.2008.12.031. Epub 2009 Jan 5. Clin Chim Acta. 2009. PMID: 19166824

6

A novel diagnostic tool for detecting neonatal infections using multiplex polymerase chain reaction.

Enomoto M, Morioka I, Morisawa T, Yokoyama N, Matsuo M. Enomoto M, et al. Among authors: morioka i. Neonatology. 2009;96(2):102-8. doi: 10.1159/000208791. Epub 2009 Mar 12. Neonatology. 2009. PMID: 19279393

7

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.

Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M. Kanda K, et al. Among authors: morioka i. BMC Nephrol. 2009 Nov 14;10:37. doi: 10.1186/1471-2369-10-37. BMC Nephrol. 2009. PMID: 19912655 Free PMC article.

8

A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.

Yusoff S, Takeuchi A, Ashi C, Tsukada M, Ma'amor NH, Zilfalil BA, Yusoff NM, Nakamura T, Hirai M, Harahap IS, Gunadi, Lee MJ, Nishimura N, Takaoka Y, Morikawa S, Morioka I, Yokoyama N, Matsuo M, Nishio H, van Rostenberghe H. Yusoff S, et al. Among authors: morioka i. Pediatr Res. 2010 Apr;67(4):401-6. doi: 10.1203/PDR.0b013e3181d22f78. Pediatr Res. 2010. PMID: 20057336

9

Congenital pneumonia with sepsis caused by intrauterine infection of Ureaplasma parvum in a term newborn: a first case report.

Morioka I, Fujibayashi H, Enoki E, Yokoyama N, Yokozaki H, Matsuo M. Morioka I, et al. J Perinatol. 2010 May;30(5):359-62. doi: 10.1038/jp.2009.145. J Perinatol. 2010. PMID: 20428179

10

The lowest surviving birth weight infant delivered from a systemic lupus erythematosus mother with antiphospholipid syndrome.

Fujioka K, Morioka I, Urade T, Suzuki K, Morizane M, Yokoyama N, Matsuo M. Fujioka K, et al. Among authors: morioka i. J Matern Fetal Neonatal Med. 2010 Sep;23(9):1050-2. doi: 10.3109/14767050903414492. J Matern Fetal Neonatal Med. 2010. PMID: 20476875 Free article. Review.

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