Taniguchi-Ikeda M - Search Results

1

Comprehensive analysis of serum cytokines/chemokines in febrile children with primary human herpes virus-6B infection.

Nagasaka M, Morioka I, Kawabata A, Yamagishi Y, Iwatani S, Taniguchi-Ikeda M, Ishida A, Iijima K, Mori Y. Nagasaka M, et al. J Infect Chemother. 2016 Sep;22(9):593-8. doi: 10.1016/j.jiac.2016.05.010. Epub 2016 Jun 23. J Infect Chemother. 2016. PMID: 27346377

2

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.

Mishra D, Kato T, Inagaki H, Kosho T, Wakui K, Kido Y, Sakazume S, Taniguchi-Ikeda M, Morisada N, Iijima K, Fukushima Y, Emanuel BS, Kurahashi H. Mishra D, et al. Mol Cytogenet. 2014 Aug 13;7:55. doi: 10.1186/s13039-014-0055-x. eCollection 2014. Mol Cytogenet. 2014. PMID: 25478009 Free PMC article.

3

Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal period.

Katayama Y, Yokota T, Zhao H, Wong RJ, Stevenson DK, Taniguchi-Ikeda M, Nakamura H, Iijima K, Morioka I. Katayama Y, et al. Pediatr Int. 2015 Aug;57(4):645-9. doi: 10.1111/ped.12591. Epub 2015 Apr 28. Pediatr Int. 2015. PMID: 25625535

4

Demographics and outcomes of patients with pediatric febrile convulsive status epilepticus.

Nishiyama M, Nagase H, Tanaka T, Fujita K, Maruyama A, Toyoshima D, Nakagawa T, Taniguchi-Ikeda M, Morioka I, Morisada N, Takada S, Iijima K. Nishiyama M, et al. Pediatr Neurol. 2015 May;52(5):499-503. doi: 10.1016/j.pediatrneurol.2015.02.001. Epub 2015 Feb 11. Pediatr Neurol. 2015. PMID: 25769239

5

Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.

Fu XJ, Nozu K, Kaito H, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Ohtsubo H, Matsunoshita N, Kamiyoshi N, Matsumura C, Takagi N, Maekawa K, Taniguchi-Ikeda M, Iijima K. Fu XJ, et al. Eur J Hum Genet. 2016 Mar;24(3):387-91. doi: 10.1038/ejhg.2015.113. Epub 2015 May 27. Eur J Hum Genet. 2016. PMID: 26014433 Free PMC article.

6

Extremely preterm infants small for gestational age are at risk for motor impairment at 3 years corrected age.

Kato T, Mandai T, Iwatani S, Koda T, Nagasaka M, Fujita K, Kurokawa D, Yamana K, Nishida K, Taniguchi-Ikeda M, Tanimura K, Deguchi M, Yamada H, Iijima K, Morioka I. Kato T, et al. Brain Dev. 2016 Feb;38(2):188-95. doi: 10.1016/j.braindev.2015.07.008. Epub 2015 Aug 8. Brain Dev. 2016. PMID: 26265090

7

A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency.

Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K. Nakagawa T, et al. Am J Med Genet A. 2016 Jan;170A(1):183-8. doi: 10.1002/ajmg.a.37397. Epub 2015 Sep 30. Am J Med Genet A. 2016. PMID: 26419326

8

X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene.

Fu XJ, Nozu K, Eguchi A, Nozu Y, Morisada N, Shono A, Taniguchi-Ikeda M, Shima Y, Nakanishi K, Vorechovsky I, Iijima K. Fu XJ, et al. Clin Exp Nephrol. 2016 Oct;20(5):699-702. doi: 10.1007/s10157-015-1197-9. Epub 2015 Nov 18. Clin Exp Nephrol. 2016. PMID: 26581810

9

Prevalence of small for gestational age (SGA) and short stature in children born SGA who qualify for growth hormone treatment at 3 years of age: Population-based study.

Fujita K, Nagasaka M, Iwatani S, Koda T, Kurokawa D, Yamana K, Nishida K, Taniguchi-Ikeda M, Uchino E, Shirai C, Iijima K, Morioka I. Fujita K, et al. Pediatr Int. 2016 May;58(5):372-6. doi: 10.1111/ped.12859. Epub 2016 Feb 19. Pediatr Int. 2016. PMID: 26617415

10

Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.

Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K. Taniguchi-Ikeda M, et al. J Hum Genet. 2016 Apr;61(4):351-5. doi: 10.1038/jhg.2015.157. Epub 2016 Jan 7. J Hum Genet. 2016. PMID: 26740235

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