Saida K - Search Results

1

Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants.

Saida K, Kawasaki K, Hirabayashi K, Akazawa Y, Kubota S, Kasuga E, Kusakari M, Ishida T, Kitamura M, Baba A, Koike K. Saida K, et al. Eur J Pediatr. 2015 Apr;174(4):551-5. doi: 10.1007/s00431-014-2414-3. Epub 2014 Sep 7. Eur J Pediatr. 2015. PMID: 25194957

2

Ampicillin- and ampicillin/sulbactam-resistant Escherichia coli infection in a neonatal intensive care unit in Japan.

Saida K, Ito Y, Shima Y, Kasuga E, Kusakari M, Miyosawa Y, Baba A. Saida K, et al. Pediatr Int. 2016 Jun;58(6):537-9. doi: 10.1111/ped.12984. Pediatr Int. 2016. PMID: 27322865

3

Right-to-left shunting in the ductus arteriosus is induced readily by intense crying and rapid postural change in neonates with meconium-stained amniotic fluid.

Baba A, Ishida T, Okada M, Akazawa Y, Hirabayashi K, Saida K, Sakaguchi K, Koike K. Baba A, et al. Among authors: saida k. Pediatr Crit Care Med. 2012 Jan;13(1):60-5. doi: 10.1097/PCC.0b013e3182191a35. Pediatr Crit Care Med. 2012. PMID: 21460760

4

Nakazawa Y, Sakashita K, Kinoshita M, Saida K, Shigemura T, Yanagisawa R, Shikama N, Kamijo T, Koike K. Nakazawa Y, et al. Among authors: saida k. Int J Hematol. 2004 Oct;80(3):287-90. doi: 10.1532/ijh97.04079. Int J Hematol. 2004. PMID: 15540906

5

A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.

Saida K, Inaba Y, Hirano M, Satake W, Toda T, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K. Saida K, et al. Brain Dev. 2014 Sep;36(8):721-4. doi: 10.1016/j.braindev.2013.10.013. Epub 2013 Nov 26. Brain Dev. 2014. PMID: 24290075

6

A case of adult Dent disease in Japan with advanced chronic kidney disease.

Saida K, Kamijo Y, Matsuoka D, Noda S, Hidaka Y, Mori T, Shimojo H, Ehara T, Miura K, Takita J, Sekine T, Igarashi T, Koike K. Saida K, et al. CEN Case Rep. 2014 Nov;3(2):132-138. doi: 10.1007/s13730-013-0102-1. Epub 2013 Nov 2. CEN Case Rep. 2014. PMID: 28509186 Free PMC article.

7

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.

Hirano M, Satake W, Ihara K, Tsuge I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: saida k. PLoS One. 2015 Sep 1;10(9):e0136317. doi: 10.1371/journal.pone.0136317. eCollection 2015. PLoS One. 2015. PMID: 26325687 Free PMC article.

8

Bardet-Biedl syndrome and related disorders in Japan.

Hirano M, Satake W, Moriyama N, Saida K, Okamoto N, Cha PC, Suzuki Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: saida k. J Hum Genet. 2020 Oct;65(10):847-853. doi: 10.1038/s10038-020-0778-y. Epub 2020 May 25. J Hum Genet. 2020. PMID: 32451492

9

Preoperative left ventricular internal dimension in end-diastole as earlier identification of early patent ductus arteriosus operation and postoperative intensive care in very low birth weight infants.

Saida K, Nakamura T, Hiroma T, Takigiku K, Yasukochi S. Saida K, et al. Early Hum Dev. 2013 Oct;89(10):821-3. doi: 10.1016/j.earlhumdev.2013.07.011. Epub 2013 Jul 31. Early Hum Dev. 2013. PMID: 23916057

10

Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene.

Miyata Y, Saida K, Kumada S, Miyake N, Mashimo H, Nishida Y, Shirai I, Kurihara E, Nakata Y, Matsumoto N. Miyata Y, et al. Among authors: saida k. Brain Dev. 2018 Aug;40(7):566-569. doi: 10.1016/j.braindev.2018.03.012. Epub 2018 Apr 17. Brain Dev. 2018. PMID: 29678278

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