Fu XJ - Search Results

1

OCRL1 mutations in patients with Dent disease phenotype in Japan.

Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui E, Harita Y, Inatomi J, Igarashi T. Sekine T, et al. Among authors: fu xj. Pediatr Nephrol. 2007 Jul;22(7):975-80. doi: 10.1007/s00467-007-0454-x. Epub 2007 Mar 24. Pediatr Nephrol. 2007. PMID: 17384968

2

A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.

Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M. Nozu K, et al. Among authors: fu xj. Pediatr Nephrol. 2007 Aug;22(8):1219-23. doi: 10.1007/s00467-007-0468-4. Epub 2007 Mar 31. Pediatr Nephrol. 2007. PMID: 17401586 Free article.

3

Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.

Fu XJ, Iijima K, Nozu K, Hamahira K, Tanaka R, Oda T, Yoshikawa N, Matsuo M. Fu XJ, et al. Pediatr Nephrol. 2004 Aug;19(8):844-52. doi: 10.1007/s00467-004-1502-4. Epub 2004 Jun 17. Pediatr Nephrol. 2004. PMID: 15206036

4

Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR.

Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M. Nozu K, et al. Among authors: fu xj. Pediatr Res. 2007 Sep;62(3):364-9. doi: 10.1203/PDR.0b013e318123fb90. Pediatr Res. 2007. PMID: 17622951

5

Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.

Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N. Krol RP, et al. Among authors: fu xj. Nephrol Dial Transplant. 2008 Aug;23(8):2525-30. doi: 10.1093/ndt/gfn005. Epub 2008 Mar 10. Nephrol Dial Transplant. 2008. PMID: 18332068

6

Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y, Fu XJ, Matsuo M, Iijima K, Gejyo F. Yamazaki H, et al. Among authors: fu xj. Pediatr Nephrol. 2009 Feb;24(2):415-8. doi: 10.1007/s00467-008-0999-3. Epub 2008 Oct 2. Pediatr Nephrol. 2009. PMID: 18830715

7

A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome.

Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M. Nozu K, et al. Among authors: fu xj. Pediatr Res. 2009 Nov;66(5):590-3. doi: 10.1203/PDR.0b013e3181b9b4d3. Pediatr Res. 2009. PMID: 19668106

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: fu xj. 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

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: fu xj. 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.

10

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M. Nozu K, et al. Among authors: fu xj. J Med Genet. 2008 Mar;45(3):182-6. doi: 10.1136/jmg.2007.052944. J Med Genet. 2008. PMID: 18310267

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