Ono H - Search Results

1

[A case suspected Sensory Guillain-Barré syndrome subsequent to Campylobacter jejuni enteritis].

Itamura S, Izumo H, Ono H. Itamura S, et al. Among authors: ono h. Rinsho Shinkeigaku. 2022 Apr 27;62(4):301-304. doi: 10.5692/clinicalneurol.cn-001702. Epub 2022 Mar 29. Rinsho Shinkeigaku. 2022. PMID: 35354727 Japanese.

2

An infant with rotavirus infection presenting as a severe acute duodenal ulcer.

Nejihashi N, Sakano T, Ono H, Furue T, Kinoshita Y, Ohta T. Nejihashi N, et al. Among authors: ono h. Pediatr Int. 2011 Feb;53(1):100-1. doi: 10.1111/j.1442-200X.2010.03143.x. Pediatr Int. 2011. PMID: 21342334 No abstract available.

3

Sodium valproate-induced Fanconi syndrome in two severely disabled patients receiving carnitine supplementation.

Ono H. Ono H. Clin Exp Nephrol. 2019 Jan;23(1):148-149. doi: 10.1007/s10157-018-1581-3. Epub 2018 Apr 20. Clin Exp Nephrol. 2019. PMID: 29679355 No abstract available.

4

Another Case of Glucose Transporter 1 Deficiency Syndrome with Periventricular Calcification, Cataracts, Hemolysis, and Pseudohyperkalemia.

Shibata T, Kobayashi K, Yoshinaga H, Ono H, Shinpo M, Kagitani-Shimono K. Shibata T, et al. Among authors: ono h. Neuropediatrics. 2017 Oct;48(5):390-393. doi: 10.1055/s-0037-1603520. Epub 2017 Jun 5. Neuropediatrics. 2017. PMID: 28582795 No abstract available.

5

A case of carbamoyl phosphate synthetase 1 deficiency presenting symptoms at one month of age.

Ono H, Suto T, Kinoshita Y, Sakano T, Furue T, Ohta T. Ono H, et al. Brain Dev. 2009 Nov;31(10):779-81. doi: 10.1016/j.braindev.2008.12.013. Epub 2009 Jan 23. Brain Dev. 2009. PMID: 19167850

6

Polyclonal proliferation of lymphocytes containing the epstein-barr virus genome in a patient dying of myocarditis in chronic active Epstein-Barr virus infection.

Fujiwara M, Shimozono H, Ono H, Fujita N, Nishimura S, Ueda K, Kaneko M. Fujiwara M, et al. Among authors: ono h. J Pediatr Hematol Oncol. 2003 Jan;25(1):85-8. doi: 10.1097/00043426-200301000-00018. J Pediatr Hematol Oncol. 2003. PMID: 12544781

7

Eculizumab in the treatment of atypical hemolytic uremic syndrome in an infant leads to cessation of peritoneal dialysis and improvement of severe hypertension.

Ohta T, Urayama K, Tada Y, Furue T, Imai S, Matsubara K, Ono H, Sakano T, Jinno K, Yoshida Y, Miyata T, Fujimura Y. Ohta T, et al. Among authors: ono h. Pediatr Nephrol. 2015 Apr;30(4):603-8. doi: 10.1007/s00467-014-2975-4. Epub 2014 Oct 16. Pediatr Nephrol. 2015. PMID: 25318620

8

Lactate/pyruvate in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Ono H, Tamada T, Shigematsu Y. Ono H, et al. Pediatr Int. 2018 Aug;60(8):762-764. doi: 10.1111/ped.13608. Epub 2018 Jul 30. Pediatr Int. 2018. PMID: 30058227 No abstract available.

9

Neonatal pertussis presenting as acute bronchiolitis: direct detection of the Bordetella pertussis genome using loop-mediated isothermal amplification.

Nakamura A, Sakano T, Nakayama T, Shimoda H, Okada Y, Hanayama R, Nomoto K, Suto T, Kinoshita Y, Furue T, Ono H, Ohta T. Nakamura A, et al. Among authors: ono h. Eur J Pediatr. 2009 Mar;168(3):347-9. doi: 10.1007/s00431-008-0744-8. Epub 2008 Jun 6. Eur J Pediatr. 2009. PMID: 18535840

10

Novel LAMA2 variants identified in a patient with white matter abnormalities.

Yamamoto-Shimojima K, Ono H, Imaizumi T, Yamamoto T. Yamamoto-Shimojima K, et al. Among authors: ono h. Hum Genome Var. 2020 May 26;7:16. doi: 10.1038/s41439-020-0103-5. eCollection 2020. Hum Genome Var. 2020. PMID: 32509318 Free PMC article.

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