Ida H - Search Results

1

Adverse drug events and medication errors in Japanese paediatric inpatients: a retrospective cohort study.

Sakuma M, Ida H, Nakamura T, Ohta Y, Yamamoto K, Seki S, Hiroi K, Kikuchi K, Nakayama K, Bates DW, Morimoto T. Sakuma M, et al. Among authors: ida h. BMJ Qual Saf. 2014 Oct;23(10):830-7. doi: 10.1136/bmjqs-2013-002658. Epub 2014 Apr 17. BMJ Qual Saf. 2014. PMID: 24742779

2

The Burden of Preventable Adverse Drug Events on Hospital Stay and Healthcare Costs in Japanese Pediatric Inpatients: The JADE Study.

Iwasaki H, Sakuma M, Ida H, Morimoto T. Iwasaki H, et al. Among authors: ida h. Clin Med Insights Pediatr. 2021 Feb 22;15:1179556521995833. doi: 10.1177/1179556521995833. eCollection 2021. Clin Med Insights Pediatr. 2021. PMID: 33746523 Free PMC article.

3

Prenatal vitamin A supplementation associated with adverse child behavior at 3 years in a prospective birth cohort in Japan.

Ishikawa Y, Tanaka H, Akutsu T, Koide K, Sakuma M, Okazaki M, Ida H, Urashima M. Ishikawa Y, et al. Among authors: ida h. Pediatr Int. 2016 Sep;58(9):855-61. doi: 10.1111/ped.12925. Epub 2016 Jun 21. Pediatr Int. 2016. PMID: 26769572

4

Clinical manifestations and natural history of Japanese heterozygous females with Fabry disease.

Kobayashi M, Ohashi T, Sakuma M, Ida H, Eto Y. Kobayashi M, et al. Among authors: ida h. J Inherit Metab Dis. 2008 Dec;31 Suppl 3:483-7. doi: 10.1007/s10545-007-0740-6. Epub 2008 Jan 21. J Inherit Metab Dis. 2008. PMID: 18202903

5

Independent Risk Factors and 2-Year Outcomes of Acute Kidney Injury after Surgery for Congenital Heart Disease.

Hirano D, Ito A, Yamada A, Kakegawa D, Miwa S, Umeda C, Chiba K, Takemasa Y, Tokunaga A, Ida H. Hirano D, et al. Among authors: ida h. Am J Nephrol. 2017;46(3):204-209. doi: 10.1159/000480358. Epub 2017 Sep 1. Am J Nephrol. 2017. PMID: 28858859

6

Clinical and genetic study of Japanese patients with type 3 Gaucher disease.

Tajima A, Yokoi T, Ariga M, Ito T, Kaneshiro E, Eto Y, Ida H. Tajima A, et al. Among authors: ida h. Mol Genet Metab. 2009 Aug;97(4):272-7. doi: 10.1016/j.ymgme.2009.05.001. Epub 2009 May 10. Mol Genet Metab. 2009. PMID: 19481486

7

Severe skeletal complications in Japanese patients with type 1 Gaucher disease.

Ida H, Rennert OM, Kato S, Ueda T, Oishi K, Maekawa K, Eto Y. Ida H, et al. J Inherit Metab Dis. 1999 Feb;22(1):63-73. doi: 10.1023/a:1005451300167. J Inherit Metab Dis. 1999. PMID: 10070619

8

[Efficacy and safety of intravenous phenobarbital for status epilepticus and frequent seizures in children].

Kikuchi K, Hamano S, Koichihara R, Oritsu T, Tanaka M, Minamitani M, Ida H. Kikuchi K, et al. Among authors: ida h. No To Hattatsu. 2010 Jul;42(4):304-6. No To Hattatsu. 2010. PMID: 20666139 Japanese. No abstract available.

9

Prevalence of arylsulphatase A mutations in 11 Japanese patients with metachromatic leukodystrophy: identification of two novel mutations.

Kurosawa K, Ida H, Eto Y. Kurosawa K, et al. Among authors: ida h. J Inherit Metab Dis. 1998 Oct;21(7):781-2. doi: 10.1023/a:1005405418215. J Inherit Metab Dis. 1998. PMID: 9819708 No abstract available.

10

Clinical and molecular analysis of Japanese patients with neuronal ceroid lipofuscinosis.

Oishi K, Ida H, Kurosawa K, Eto Y. Oishi K, et al. Among authors: ida h. Mol Genet Metab. 1999 Apr;66(4):344-8. doi: 10.1006/mgme.1999.2835. Mol Genet Metab. 1999. PMID: 10191127

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