Ohtsuka Y - Search Results

1

Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.

Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M. Nozu K, et al. Among authors: ohtsuka y. Pediatr Nephrol. 2008 Nov;23(11):2085-90. doi: 10.1007/s00467-008-0878-y. Epub 2008 Jun 27. Pediatr Nephrol. 2008. PMID: 18584212

2

Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.

Ohtsuka Y, Zaitsu M, Ichida K, Isomura N, Tsuji K, Sato T, Hamasaki Y. Ohtsuka Y, et al. Pediatr Int. 2007 Apr;49(2):235-7. doi: 10.1111/j.1442-200X.2007.02337.x. Pediatr Int. 2007. PMID: 17445045 No abstract available.

3

Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome.

Nozu K, Krol RP, Nakanishi K, Yoshikawa N, Nozu Y, Ohtsuka Y, Iijima K, Matsuo M. Nozu K, et al. Among authors: ohtsuka y. Pediatr Nephrol. 2009 Sep;24(9):1773-4. doi: 10.1007/s00467-009-1122-0. Epub 2009 Jan 24. Pediatr Nephrol. 2009. PMID: 19169714 No abstract available.

4

A notable case report of May-Hegglin anomaly with immune complex-related nephropathy: a genetic and histological analysis.

Ohtsuka Y, Kanaji T, Nishi M, Sakai N, Sato T, Aoki S, Wakayama K, Nakazato S, Hisano S, Sado Y, Kawachi H, Izuhara K, Hamasaki Y. Ohtsuka Y, et al. Clin Nephrol. 2011 Mar;75(3):255-62. doi: 10.5414/cnp75255. Clin Nephrol. 2011. PMID: 21329637

5

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY.

Nozu K, Iijima K, Ohtsuka Y, Fu XJ, Kaito H, Nakanishi K, Vorechovsky I. Nozu K, et al. Among authors: ohtsuka y. Mol Genet Genomic Med. 2014 Sep;2(5):451-3. doi: 10.1002/mgg3.89. Epub 2014 May 28. Mol Genet Genomic Med. 2014. PMID: 25333070 Free PMC article.

6

Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: medical therapy.

Ishikura K, Matsumoto S, Sako M, Tsuruga K, Nakanishi K, Kamei K, Saito H, Fujinaga S, Hamasaki Y, Chikamoto H, Ohtsuka Y, Komatsu Y, Ohta T, Nagai T, Kaito H, Kondo S, Ikezumi Y, Tanaka S, Kaku Y, Iijima K; Japanese Society for Pediatric Nephrology; Japanese Society for Pediatric Nephrology. Ishikura K, et al. Among authors: ohtsuka y. Clin Exp Nephrol. 2015 Feb;19(1):6-33. doi: 10.1007/s10157-014-1030-x. Clin Exp Nephrol. 2015. PMID: 25653046 No abstract available.

7

Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: general therapy.

Kaku Y, Ohtsuka Y, Komatsu Y, Ohta T, Nagai T, Kaito H, Kondo S, Ikezumi Y, Tanaka S, Matsumoto S, Sako M, Tsuruga K, Nakanishi K, Kamei K, Saito H, Fujinaga S, Hamasaki Y, Chikamoto H, Ishikura K, Iijima K; Japanese Society for Pediatric Nephrology. Kaku Y, et al. Among authors: ohtsuka y. Clin Exp Nephrol. 2015 Feb;19(1):34-53. doi: 10.1007/s10157-014-1031-9. Clin Exp Nephrol. 2015. PMID: 25653047 No abstract available.

8

Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.

Ohtsuka Y, Higashimoto K, Oka T, Yatsuki H, Jozaki K, Maeda T, Kawahara K, Hamasaki Y, Matsuo M, Nishioka K, Joh K, Mukai T, Soejima H. Ohtsuka Y, et al. Hum Mol Genet. 2016 Apr 1;25(7):1406-19. doi: 10.1093/hmg/ddw023. Epub 2016 Jan 28. Hum Mol Genet. 2016. PMID: 26908620

9

Successful Treatment of Transplantation-associated Atypical Hemolytic Uremic Syndrome With Eculizumab.

Hasegawa D, Saito A, Nino N, Uemura S, Takafuji S, Yokoi T, Kozaki A, Ishida T, Kawasaki K, Yasumi T, Sakata N, Ohtsuka Y, Hirase S, Mori T, Nishimura N, Kusumoto M, Ogawa Y, Tominaga K, Nakagawa T, Kanda K, Tanaka R, Kosaka Y. Hasegawa D, et al. Among authors: ohtsuka y. J Pediatr Hematol Oncol. 2018 Jan;40(1):e41-e44. doi: 10.1097/MPH.0000000000000862. J Pediatr Hematol Oncol. 2018. PMID: 28538511

10

Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.

Unzaki A, Morisada N, Nozu K, Ye MJ, Ito S, Matsunaga T, Ishikura K, Ina S, Nagatani K, Okamoto T, Inaba Y, Ito N, Igarashi T, Kanda S, Ito K, Omune K, Iwaki T, Ueno K, Yahata M, Ohtsuka Y, Nishi E, Takahashi N, Ishikawa T, Goto S, Okamoto N, Iijima K. Unzaki A, et al. Among authors: ohtsuka y. J Hum Genet. 2018 May;63(5):647-656. doi: 10.1038/s10038-018-0429-8. Epub 2018 Mar 2. J Hum Genet. 2018. PMID: 29500469

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