Morisada N - Search Results

1

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.

Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K. Kamiyoshi N, et al. Among authors: morisada n. Clin J Am Soc Nephrol. 2016 Aug 8;11(8):1441-1449. doi: 10.2215/CJN.01000116. Epub 2016 Jun 8. Clin J Am Soc Nephrol. 2016. PMID: 27281700 Free PMC article.

2

Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion.

Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K. Morisada N, et al. Pediatr Nephrol. 2010 Jul;25(7):1343-8. doi: 10.1007/s00467-010-1445-x. Epub 2010 Feb 4. Pediatr Nephrol. 2010. PMID: 20130917

3

Alport-like glomerular basement membrane changes with renal-coloboma syndrome.

Ohtsubo H, Morisada N, Kaito H, Nagatani K, Nakanishi K, Iijima K. Ohtsubo H, et al. Among authors: morisada n. Pediatr Nephrol. 2012 Jul;27(7):1189-92. doi: 10.1007/s00467-012-2125-9. Epub 2012 Feb 21. Pediatr Nephrol. 2012. PMID: 22350371

4

Right hypoplastic kidney.

Ogawa A, Kitamura S, Nakayama K, Sugiyama H, Morisada N, Iijima K, Makino H. Ogawa A, et al. Among authors: morisada n. Kidney Int. 2012 Nov;82(9):1037. doi: 10.1038/ki.2012.201. Kidney Int. 2012. PMID: 23064196 Free article. No abstract available.

5

Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.

Hashimoto F, Nishiumi S, Miyake O, Takeichi H, Chitose M, Ohtsubo H, Ishimori S, Ninchoji T, Hashimura Y, Kaito H, Morisada N, Morioka I, Fukuoka H, Yoshida M, Iijima K. Hashimoto F, et al. Among authors: morisada n. Early Hum Dev. 2013 May;89(5):315-20. doi: 10.1016/j.earlhumdev.2012.10.010. Epub 2012 Nov 22. Early Hum Dev. 2013. PMID: 23178109

6

SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations.

Ishimori S, Kaito H, Matsunoshita N, Otsubo H, Hashimoto F, Ninchoji T, Nozu K, Morisada N, Iijima K. Ishimori S, et al. Among authors: morisada n. Kobe J Med Sci. 2013 Apr 18;59(2):E36-43. Kobe J Med Sci. 2013. PMID: 23756661 Free article.

7

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.

Hashimura Y, Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K. Hashimura Y, et al. Among authors: morisada n. Kidney Int. 2014 May;85(5):1208-13. doi: 10.1038/ki.2013.479. Epub 2013 Dec 4. Kidney Int. 2014. PMID: 24304881 Free article.

8

Natural history of genetically proven autosomal recessive Alport syndrome.

Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K. Oka M, et al. Among authors: morisada n. Pediatr Nephrol. 2014 Sep;29(9):1535-44. doi: 10.1007/s00467-014-2797-4. Epub 2014 Mar 15. Pediatr Nephrol. 2014. PMID: 24633401

9

Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.

Morisada N, Nozu K, Iijima K. Morisada N, et al. Pediatr Int. 2014 Jun;56(3):309-14. doi: 10.1111/ped.12357. Pediatr Int. 2014. PMID: 24730701 Review.

10

16q12 microdeletion syndrome in two Japanese boys.

Morisada N, Sekine T, Ishimori S, Tsuda M, Adachi M, Nozu K, Nakanishi K, Tanaka R, Iijima K. Morisada N, et al. Pediatr Int. 2014 Oct;56(5):e75-8. doi: 10.1111/ped.12426. Pediatr Int. 2014. PMID: 25336016

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

123 results

Search Page