Saitoh S - Search Results

1

Novel SPEG variants in a neonate with severe dilated cardiomyopathy and relatively mild hypotonia.

Fujimoto HM, Fujimoto M, Sugiura T, Nakane S, Wakano Y, Sato E, Oshita H, Togawa Y, Sugimoto M, Kato T, Yasuda K, Muramatsu K, Saitoh S. Fujimoto HM, et al. Among authors: saitoh s. Hum Genome Var. 2023 Sep 6;10(1):24. doi: 10.1038/s41439-023-00253-w. Hum Genome Var. 2023. PMID: 37673875 Free PMC article.

2

Effects of tolvaptan on congestive heart failure complicated with chylothorax in a neonate.

Sato N, Sugiura T, Nagasaki R, Suzuki K, Ito K, Kato T, Inukai S, Saitoh S. Sato N, et al. Among authors: saitoh s. Pediatr Int. 2015 Oct;57(5):1020-2. doi: 10.1111/ped.12697. Epub 2015 Sep 10. Pediatr Int. 2015. PMID: 26508187

3

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.

Kawase K, Sugiura T, Nagaya Y, Yamada T, Sugimoto M, Ito K, Togawa T, Nagasaki R, Kato T, Kouwaki M, Koyama N, Saitoh S. Kawase K, et al. Among authors: saitoh s. Pediatr Int. 2016 Jun;58(6):461-6. doi: 10.1111/ped.12861. Epub 2016 Feb 3. Pediatr Int. 2016. PMID: 26615960

4

Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum.

Nakamura Y, Togawa Y, Okuno Y, Muramatsu H, Nakabayashi K, Kuroki Y, Ieda D, Hori I, Negishi Y, Togawa T, Hattori A, Kojima S, Saitoh S. Nakamura Y, et al. Among authors: saitoh s. Brain Dev. 2018 Feb;40(2):134-139. doi: 10.1016/j.braindev.2017.08.003. Epub 2017 Oct 12. Brain Dev. 2018. PMID: 28893434

5

Antiviral therapy for hepatitis B virus during second pregnancies.

Wakano Y, Sugiura T, Endo T, Ito K, Suzuki M, Tajiri H, Tanaka Y, Saitoh S. Wakano Y, et al. Among authors: saitoh s. J Obstet Gynaecol Res. 2018 Mar;44(3):566-569. doi: 10.1111/jog.13540. Epub 2017 Dec 11. J Obstet Gynaecol Res. 2018. PMID: 29227001

6

A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia.

Ieda D, Hori I, Nakamura Y, Ohshita H, Negishi Y, Shinohara T, Hattori A, Kato T, Inukai S, Kitamura K, Kawai T, Ohara O, Kunishima S, Saitoh S. Ieda D, et al. Among authors: saitoh s. Brain Dev. 2018 Jun;40(6):489-492. doi: 10.1016/j.braindev.2018.01.010. Epub 2018 Feb 12. Brain Dev. 2018. PMID: 29449050

7

Estimation of elevated intracranial pressure in infants with hydroce-phalus by using transcranial Doppler velocimetry with fontanel compression.

Yoshizuka T, Kinoshita M, Iwata S, Tsuda K, Kato T, Saikusa M, Shindou R, Hara N, Harada E, Takashima S, Takeshige N, Saitoh S, Yamashita Y, Iwata O. Yoshizuka T, et al. Among authors: saitoh s. Sci Rep. 2018 Aug 7;8(1):11824. doi: 10.1038/s41598-018-30274-3. Sci Rep. 2018. PMID: 30087390 Free PMC article.

8

A novel splicing mutation in SLC9A6 in a boy with Christianson syndrome.

Ieda D, Hori I, Nakamura Y, Ohashi K, Negishi Y, Hattori A, Arisaka A, Hasegawa S, Saitoh S. Ieda D, et al. Among authors: saitoh s. Hum Genome Var. 2019 Mar 25;6:15. doi: 10.1038/s41439-019-0046-x. eCollection 2019. Hum Genome Var. 2019. PMID: 30937176 Free PMC article.

9

A novel CUL4B splice site variant in a young male exhibiting less pronounced features.

Nakamura Y, Okuno Y, Muramatsu H, Kawai T, Satou K, Ieda D, Hori I, Ohashi K, Negishi Y, Hattori A, Takahashi Y, Kojima S, Saitoh S. Nakamura Y, et al. Among authors: saitoh s. Hum Genome Var. 2019 Sep 4;6:43. doi: 10.1038/s41439-019-0074-6. eCollection 2019. Hum Genome Var. 2019. PMID: 31645981 Free PMC article.

10

Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report.

Watanabe Y, Sugiura T, Sugimoto M, Togawa Y, Kouwaki M, Koyama N, Saitoh S. Watanabe Y, et al. Among authors: saitoh s. Front Pediatr. 2019 Nov 14;7:469. doi: 10.3389/fped.2019.00469. eCollection 2019. Front Pediatr. 2019. PMID: 31799224 Free PMC article.

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