Uchida S - Search Results

1

HPRT-related hyperuricemia with a novel p.V35M mutation in HPRT1 presenting familial juvenile gout.

Mishima E, Mori T, Nakajima Y, Toyohara T, Kikuchi K, Oikawa Y, Matsuhashi T, Maeda Y, Suzuki T, Kudo M, Ito S, Sohara E, Uchida S, Abe T. Mishima E, et al. Among authors: uchida s. CEN Case Rep. 2020 Aug;9(3):210-214. doi: 10.1007/s13730-020-00459-9. Epub 2020 Mar 3. CEN Case Rep. 2020. PMID: 32128695 Free PMC article.

2

Inherited, not acquired, Gitelman syndrome in a patient with Sjögren's syndrome: importance of genetic testing to distinguish the two forms.

Mishima E, Mori T, Sohara E, Uchida S, Abe T, Ito S. Mishima E, et al. Among authors: uchida s. CEN Case Rep. 2017 Nov;6(2):180-184. doi: 10.1007/s13730-017-0271-4. Epub 2017 Aug 17. CEN Case Rep. 2017. PMID: 28819721 Free PMC article.

3

Acute kidney injury caused by sarcoid granulomatous interstitial nephritis without extrarenal manifestations.

Kikuchi H, Mori T, Rai T, Uchida S. Kikuchi H, et al. Among authors: uchida s. CEN Case Rep. 2015 Nov;4(2):212-217. doi: 10.1007/s13730-015-0171-4. Epub 2015 Mar 5. CEN Case Rep. 2015. PMID: 28509105 Free PMC article.

4

Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiency.

Umene R, Kitamura M, Arai H, Matsumura K, Ishimaru Y, Maeda K, Uramatsu T, Obata Y, Mori T, Sohara E, Uchida S, Nishino T. Umene R, et al. Among authors: uchida s. CEN Case Rep. 2020 Nov;9(4):375-379. doi: 10.1007/s13730-020-00489-3. Epub 2020 Jun 6. CEN Case Rep. 2020. PMID: 32506365 Free PMC article.

5

A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype.

Oe Y, Mishima E, Mori T, Okamoto K, Honkura Y, Nagasawa T, Yoshida M, Sato H, Suzuki J, Ikeda R, Sohara E, Uchida S, Katori Y, Miyazaki M. Oe Y, et al. Among authors: uchida s. Intern Med. 2021 Sep 15;60(18):2991-2996. doi: 10.2169/internalmedicine.6987-20. Epub 2021 Apr 5. Intern Med. 2021. PMID: 33814499 Free PMC article.

6

LMX1B-associated nephropathy that showed myelin figures on electron microscopy.

Shimohata H, Miyake Y, Yoshida Y, Usui J, Mori T, Sohara E, Uchida S, Hirayama K, Kobayashi M. Shimohata H, et al. Among authors: uchida s. CEN Case Rep. 2021 Nov;10(4):588-591. doi: 10.1007/s13730-021-00612-y. Epub 2021 Jun 2. CEN Case Rep. 2021. PMID: 34076843 Free PMC article.

7

Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus.

Iio K, Mori T, Bessho S, Imai Y, Hatanaka M, Omori H, Kouhara H, Chiga M, Sohara E, Uchida S, Kaimori JY. Iio K, et al. Among authors: uchida s. CEN Case Rep. 2022 May;11(2):191-195. doi: 10.1007/s13730-021-00652-4. Epub 2021 Oct 6. CEN Case Rep. 2022. PMID: 34617250 Free PMC article.

8

Kelch-like 3/Cullin 3 ubiquitin ligase complex and WNK signaling in salt-sensitive hypertension and electrolyte disorder.

Sohara E, Uchida S. Sohara E, et al. Among authors: uchida s. Nephrol Dial Transplant. 2016 Sep;31(9):1417-24. doi: 10.1093/ndt/gfv259. Epub 2015 Jul 6. Nephrol Dial Transplant. 2016. PMID: 26152401 Review.

9

Development of minimal-change glomerular disease and Hashimoto's thyroiditis during the treatment of sarcoidosis.

Ando F, Okado T, Sohara E, Rai T, Uchida S, Sasaki S. Ando F, et al. Among authors: uchida s. CEN Case Rep. 2013 Nov;2(2):248-251. doi: 10.1007/s13730-013-0072-3. Epub 2013 Mar 17. CEN Case Rep. 2013. PMID: 28509299 Free PMC article.

10

Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation.

Tanaka T, Oki E, Mori T, Tsuruga K, Sohara E, Uchida S, Tanaka H. Tanaka T, et al. Among authors: uchida s. Nephrology (Carlton). 2019 Apr;24(4):489-490. doi: 10.1111/nep.13391. Nephrology (Carlton). 2019. PMID: 30919533 No abstract available.

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