Sawai H - Search Results

1

Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT.

Suzumori N, Sekizawa A, Takeda E, Samura O, Sasaki A, Akaishi R, Wada S, Hamanoue H, Hirahara F, Kuriki H, Sawai H, Nakamura H, Yamada T, Miura K, Masuzaki H, Yamashita T, Kamei Y, Namba A, Murotsuki J, Tanemoto T, Fukushima A, Haino K, Tairaku S, Matsubara K, Maeda K, Kaji T, Ogawa M, Osada H, Nishizawa H, Okamoto Y, Kanagawa T, Kakigano A, Endo M, Kitagawa M, Ogawa M, Izumi S, Katagiri Y, Takeshita N, Kasai Y, Naruse K, Neki R, Masuyama H, Hyodo M, Kawano Y, Ohba T, Ichizuka K, Nagamatsu T, Watanabe A, Nishikawa N, Hamajima N, Shirato N, Yotsumoto J, Nishiyama M, Koide K, Hirose T, Sago H. Suzumori N, et al. Among authors: sawai h. Prenat Diagn. 2019 Jan;39(2):100-106. doi: 10.1002/pd.5408. Epub 2019 Jan 10. Prenat Diagn. 2019. PMID: 30586157

2

Prenatal diagnosis of thanatophoric dysplasia by mutational analysis of the fibroblast growth factor receptor 3 gene and a proposed correction of previously published PCR results.

Sawai H, Komori S, Ida A, Henmi T, Bessho T, Koyama K. Sawai H, et al. Prenat Diagn. 1999 Jan;19(1):21-4. doi: 10.1002/(sici)1097-0223(199901)19:1<21::aid-pd457>3.0.co;2-5. Prenat Diagn. 1999. PMID: 10073901

3

Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal period.

Kataoka S, Sawai H, Yamada H, Kanazawa N, Koyama K, Nishimura G, Morikawa M, Sakuragi N, Minakami H. Kataoka S, et al. Among authors: sawai h. Prenat Diagn. 2004 Jan;24(1):45-9. doi: 10.1002/pd.746. Prenat Diagn. 2004. PMID: 14755409

4

Platyspondylic lethal skeletal dysplasia San Diego type (thanatophoric dysplasia type 1) associated with trisomy 21 presenting with nuchal translucency: a case report.

Yamada T, Sawai H, Nishimura G, Numabe H, Cho K, Minakami H. Yamada T, et al. Among authors: sawai h. Prenat Diagn. 2009 Jul;29(7):715-7. doi: 10.1002/pd.2268. Prenat Diagn. 2009. PMID: 19340824 No abstract available.

5

Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers.

Watanabe A, Karasugi T, Sawai H, Naing BT, Ikegawa S, Orimo H, Shimada T. Watanabe A, et al. Among authors: sawai h. J Hum Genet. 2011 Feb;56(2):166-8. doi: 10.1038/jhg.2010.161. Epub 2010 Dec 23. J Hum Genet. 2011. PMID: 21179104

6

Low prevalence of genetic prenatal diagnosis in Japan.

Sasaki A, Sawai H, Masuzaki H, Hirahara F, Sago H. Sasaki A, et al. Among authors: sawai h. Prenat Diagn. 2011 Oct;31(10):1007-9. doi: 10.1002/pd.2816. Epub 2011 Jul 5. Prenat Diagn. 2011. PMID: 21732393 No abstract available.

7

Recurrence of osteogenesis imperfecta due to maternal mosaicism of a novel COL1A1 mutation.

Yamada T, Takagi M, Nishimura G, Akaishi R, Furuta I, Morikawa M, Yamada T, Cho K, Sawai H, Ikegawa S, Hasegawa T, Minakami H. Yamada T, et al. Among authors: sawai h. Am J Med Genet A. 2012 Nov;158A(11):2969-71. doi: 10.1002/ajmg.a.35602. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987783 No abstract available.

8

The current state of genetic counseling before and after amniocentesis for fetal karyotyping in Japan: a survey of obstetric hospital clients of a prenatal testing laboratory.

Nishiyama M, Sawai H, Kosugi S. Nishiyama M, et al. Among authors: sawai h. J Genet Couns. 2013 Dec;22(6):795-804. doi: 10.1007/s10897-013-9632-0. Epub 2013 Aug 24. J Genet Couns. 2013. PMID: 23974868

9

Nationwide radiation dose survey of computed tomography for fetal skeletal dysplasias.

Miyazaki O, Sawai H, Murotsuki J, Nishimura G, Horiuchi T. Miyazaki O, et al. Among authors: sawai h. Pediatr Radiol. 2014 Aug;44(8):971-9. doi: 10.1007/s00247-014-2916-1. Epub 2014 Apr 16. Pediatr Radiol. 2014. PMID: 24737001

10

Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations.

Nishiyama M, Yan J, Yotsumoto J, Sawai H, Sekizawa A, Kamei Y, Sago H. Nishiyama M, et al. Among authors: sawai h. J Hum Genet. 2015 Mar;60(3):133-7. doi: 10.1038/jhg.2014.116. Epub 2015 Jan 8. J Hum Genet. 2015. PMID: 25566756

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