Sugimoto M - Search Results

1

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: sugimoto m. Front Pediatr. 2019 Nov 14;7:469. doi: 10.3389/fped.2019.00469. eCollection 2019. Front Pediatr. 2019. PMID: 31799224 Free PMC article.

2

Neurodevelopmental outcomes at 18 months' corrected age of infants born at 22 weeks of gestation.

Sugiura T, Kouwaki M, Togawa Y, Sugimoto M, Togawa T, Koyama N. Sugiura T, et al. Among authors: sugimoto m. Neonatology. 2011;100(3):228-32. doi: 10.1159/000324715. Epub 2011 Jun 22. Neonatology. 2011. PMID: 21701211

3

Risk factors for early death in transient myeloproliferative disorder without phenotypic features of Down syndrome: a case report and literature review.

Kawase K, Azuma E, Ohshita H, Tanaka T, Hanada Y, Sasaki T, Sugimoto M, Togawa T, Kouwaki M, Ito T, Hirayama M, Koyama N. Kawase K, et al. Among authors: sugimoto m. J Pediatr Hematol Oncol. 2012 Aug;34(6):475-9. doi: 10.1097/MPH.0b013e318249597f. J Pediatr Hematol Oncol. 2012. PMID: 22510770 Review.

4

Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.

Kawase K, Nishino I, Sugimoto M, Kouwaki M, Koyama N, Yokochi K. Kawase K, et al. Among authors: sugimoto m. Brain Dev. 2015 Feb;37(2):265-9. doi: 10.1016/j.braindev.2014.04.002. Epub 2014 Apr 29. Brain Dev. 2015. PMID: 24787270

5

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.

Kawase K, Nishino I, Sugimoto M, Togawa T, Sugiura T, Kouwaki M, Kibe T, Koyama N, Yokochi K. Kawase K, et al. Among authors: sugimoto m. Brain Dev. 2015 Oct;37(9):887-90. doi: 10.1016/j.braindev.2015.02.002. Epub 2015 Feb 24. Brain Dev. 2015. PMID: 25721947

6

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: sugimoto m. Pediatr Int. 2016 Jun;58(6):461-6. doi: 10.1111/ped.12861. Epub 2016 Feb 3. Pediatr Int. 2016. PMID: 26615960

7

[A case report of mitochondrial respiratory chain disorder in the neonatal period for which home mechanical ventilation was introduced].

Sugimoto M, Togawa T, Aiba K, Koyama N, Yokochi K, Murayama K, Ohtake A. Sugimoto M, et al. No To Hattatsu. 2017 Jan;49(1):37-41. No To Hattatsu. 2017. PMID: 30011153 Japanese.

8

Nusinersen helps restore walking ability in childhood spinal muscular atrophy.

Sugimoto M, Aiba K, Koyama N, Yokochi K, Nishio H. Sugimoto M, et al. Pediatr Int. 2019 Jul;61(7):728-729. doi: 10.1111/ped.13867. Epub 2019 Jul 9. Pediatr Int. 2019. PMID: 31290219 No abstract available.

9

A case of ATR-X syndrome with mitochondrial respiratory chain dysfunction.

Aiba K, Nakamura Y, Sugimoto M, Yatsuka Y, Okazaki Y, Murayama K, Ohtake A, Yokochi K, Saitoh S. Aiba K, et al. Among authors: sugimoto m. Eur J Med Genet. 2021 Aug;64(8):104251. doi: 10.1016/j.ejmg.2021.104251. Epub 2021 May 27. Eur J Med Genet. 2021. PMID: 34051360

10

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: sugimoto m. 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.

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