Yoshida A - Search Results

1

Intervention with a humanoid robot avatar for individuals with social anxiety disorders comorbid with autism spectrum disorders.

Yoshida A, Kumazaki H, Muramatsu T, Yoshikawa Y, Ishiguro H, Mimura M. Yoshida A, et al. Asian J Psychiatr. 2022 Dec;78:103315. doi: 10.1016/j.ajp.2022.103315. Epub 2022 Nov 4. Asian J Psychiatr. 2022. PMID: 36343574 Free article.

2

Predominantly placenta-expressed mRNAs in maternal plasma as predictive markers for twin-twin transfusion syndrome.

Miura K, Higashijima A, Miura S, Mishima H, Yamasaki K, Abe S, Hasegawa Y, Kaneuchi M, Yoshida A, Kinoshita A, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: yoshida a. Prenat Diagn. 2014 Apr;34(4):345-9. doi: 10.1002/pd.4307. Epub 2014 Jan 17. Prenat Diagn. 2014. PMID: 24375464

3

Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy.

Higashijima A, Miura K, Mishima H, Kinoshita A, Jo O, Abe S, Hasegawa Y, Miura S, Yamasaki K, Yoshida A, Yoshiura K, Masuzaki H. Higashijima A, et al. Among authors: yoshida a. Prenat Diagn. 2013 Mar;33(3):214-22. doi: 10.1002/pd.4045. Epub 2013 Jan 27. Prenat Diagn. 2013. PMID: 23354729

4

Effect of labor on plasma concentrations and postpartum clearance of cell-free, pregnancy-associated, placenta-specific microRNAs.

Morisaki S, Miura K, Higashijima A, Abe S, Miura S, Hasegawa Y, Yoshida A, Kaneuchi M, Yoshiura K, Masuzaki H. Morisaki S, et al. Among authors: yoshida a. Prenat Diagn. 2015 Jan;35(1):44-50. doi: 10.1002/pd.4479. Epub 2014 Sep 17. Prenat Diagn. 2015. PMID: 25125329

5

Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancer.

Abe S, Miura K, Kinoshita A, Mishima H, Miura S, Yamasaki K, Hasegawa Y, Higashijima A, Jo O, Sasaki K, Yoshida A, Yoshiura K, Masuzaki H. Abe S, et al. Among authors: yoshida a. J Hum Genet. 2013 May;58(5):250-3. doi: 10.1038/jhg.2013.7. Epub 2013 Mar 7. J Hum Genet. 2013. PMID: 23466823

6

Evaluation of obstetrical factors related to Sheehan syndrome.

Matsuwaki T, Khan KN, Inoue T, Yoshida A, Masuzaki H. Matsuwaki T, et al. Among authors: yoshida a. J Obstet Gynaecol Res. 2014 Jan;40(1):46-52. doi: 10.1111/jog.12119. Epub 2013 Aug 15. J Obstet Gynaecol Res. 2014. PMID: 23945005

7

Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders.

Miura K, Higashijima A, Shimada T, Miura S, Yamasaki K, Abe S, Jo O, Kinoshita A, Yoshida A, Yoshimura S, Niikawa N, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: yoshida a. J Hum Genet. 2011 Apr;56(4):296-9. doi: 10.1038/jhg.2011.7. Epub 2011 Feb 10. J Hum Genet. 2011. PMID: 21307866

8

Annual report of Perinatology Committee, Japan Society of Obstetrics and Gynecology, 2013: development of perinatal emergency care systems and suggestions.

Masuzaki H, Unno N, Matsuda Y, Nakabayashi M, Takeda S, Mitsuda N, Sugawara J, Yoshizato T, Yoshida A. Masuzaki H, et al. Among authors: yoshida a. J Obstet Gynaecol Res. 2014 Feb;40(2):335. doi: 10.1111/jog.12350. J Obstet Gynaecol Res. 2014. PMID: 24472050 No abstract available.

9

Annual report of Subcommittee for Examination of Causes of Maternal Death and their Prevention in Perinatology Committee, Japan Society of Obstetrics and Gynecology, 2013.

Masuzaki H, Unno N, Kanayama N, Ikeda T, Minakami H, Murakoshi T, Nakata M, Ishiwata I, Itoh H, Yoshida A. Masuzaki H, et al. Among authors: yoshida a. J Obstet Gynaecol Res. 2014 Feb;40(2):336-7. doi: 10.1111/jog.12349. J Obstet Gynaecol Res. 2014. PMID: 24472051 No abstract available.

10

Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause.

Miura K, Yoshiura K, Miura S, Kondoh T, Harada N, Yamasaki K, Fujimoto Y, Yamasaki Y, Tanigawa T, Kitajima Y, Shimada T, Yoshida A, Nakayama D, Tagawa M, Yoshimura S, Wagstaff J, Jinno Y, Ishimaru T, Niikawa N, Masuzaki H. Miura K, et al. Among authors: yoshida a. Am J Med Genet A. 2006 Sep 1;140A(17):1827-33. doi: 10.1002/ajmg.a.31389. Am J Med Genet A. 2006. PMID: 16892301

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