Konomoto T - Search Results

1

Clinical and histological findings of autosomal dominant renal-limited disease with LMX1B mutation.

Konomoto T, Imamura H, Orita M, Tanaka E, Moritake H, Sato Y, Fujimoto S, Harita Y, Hisano S, Yoshiura K, Nunoi H. Konomoto T, et al. Nephrology (Carlton). 2016 Sep;21(9):765-73. doi: 10.1111/nep.12666. Nephrology (Carlton). 2016. PMID: 26560070

2

Nephrotic syndrome complicated by idiopathic central diabetes insipidus.

Konomoto T, Tanaka E, Imamura H, Orita M, Sawada H, Nunoi H. Konomoto T, et al. Pediatr Nephrol. 2014 May;29(5):927-30. doi: 10.1007/s00467-013-2728-9. Epub 2014 Jan 10. Pediatr Nephrol. 2014. PMID: 24408226

3

Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B.

Imamura H, Konomoto T, Tanaka E, Hisano S, Yoshida Y, Fujimura Y, Miyata T, Nunoi H. Imamura H, et al. Among authors: konomoto t. Nephrol Dial Transplant. 2015 May;30(5):862-4. doi: 10.1093/ndt/gfv054. Epub 2015 Mar 10. Nephrol Dial Transplant. 2015. PMID: 25758434

4

Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.

Imamura H, Muroya K, Tanaka E, Konomoto T, Moritake H, Sato T, Kimura N, Takekoshi K, Nunoi H. Imamura H, et al. Among authors: konomoto t. Eur J Pediatr. 2016 Jan;175(1):137-41. doi: 10.1007/s00431-015-2614-5. Epub 2015 Aug 19. Eur J Pediatr. 2016. PMID: 26283294

5

Osteogenesis imperfecta complicated with renal hypoplasia leads to chronic kidney disease.

Konomoto T, Kurogi J, Sawada H, Hisano S, Nunoi H. Konomoto T, et al. Pediatr Int. 2017 Mar;59(3):369-370. doi: 10.1111/ped.13221. Pediatr Int. 2017. PMID: 28317307 No abstract available.

6

Novel PRKAR1A mutation in Carney complex with cardiac myxoma.

Kondo K, Harada M, Konomoto T, Hatanaka M, Nunoi H. Kondo K, et al. Among authors: konomoto t. Pediatr Int. 2017 Jul;59(7):840-841. doi: 10.1111/ped.13302. Pediatr Int. 2017. PMID: 28745458 No abstract available.

7

Essential points from Evidence-based Clinical Practice Guidelines for Chronic Kidney Disease 2018.

Japanese Society of Nephrology. Japanese Society of Nephrology. Clin Exp Nephrol. 2019 Jan;23(1):1-15. doi: 10.1007/s10157-018-1648-1. Clin Exp Nephrol. 2019. PMID: 30506489 Free PMC article. No abstract available.

8

TAE226, a dual inhibitor of focal adhesion kinase and insulin-like growth factor-I receptor, is effective for Ewing sarcoma.

Moritake H, Saito Y, Sawa D, Sameshima N, Yamada A, Kinoshita M, Kamimura S, Konomoto T, Nunoi H. Moritake H, et al. Among authors: konomoto t. Cancer Med. 2019 Dec;8(18):7809-7821. doi: 10.1002/cam4.2647. Epub 2019 Nov 6. Cancer Med. 2019. PMID: 31692287 Free PMC article.

9

Clinical and histological features in pediatric and adolescent/young adult patients with renal disease: a cross-sectional analysis of the Japan Renal Biopsy Registry (J-RBR).

Urushihara M, Sato H, Shimizu A, Sugiyama H, Yokoyama H, Hataya H, Matsuoka K, Okamoto T, Ogino D, Miura K, Hamada R, Hibino S, Shima Y, Yamamura T, Kitamoto K, Ishihara M, Konomoto T, Hattori M; the Committee for Renal Biopsy and Disease Registry of the Japanese Society of Nephrology. Urushihara M, et al. Among authors: konomoto t. Clin Exp Nephrol. 2021 Sep;25(9):1018-1026. doi: 10.1007/s10157-021-02077-w. Epub 2021 May 28. Clin Exp Nephrol. 2021. PMID: 34047871

10

X-linked Alport syndrome caused by splicing mutations in COL4A5.

Nozu K, Vorechovsky I, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Hashimoto F, Kamei K, Ito S, Kaku Y, Imasawa T, Ushijima K, Shimizu J, Makita Y, Konomoto T, Yoshikawa N, Iijima K. Nozu K, et al. Among authors: konomoto t. Clin J Am Soc Nephrol. 2014 Nov 7;9(11):1958-64. doi: 10.2215/CJN.04140414. Epub 2014 Sep 2. Clin J Am Soc Nephrol. 2014. PMID: 25183659 Free PMC article.

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