148 related articles for article (PubMed ID: 19321760)
1. NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.
Aya K; Shimizu J; Ohtomo Y; Satomura K; Suzuki H; Yan K; Sado Y; Morishima T; Tanaka H
Nephrol Dial Transplant; 2009 Aug; 24(8):2411-4. PubMed ID: 19321760
[TBL] [Abstract][Full Text] [Related]
2. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
Sako M; Nakanishi K; Obana M; Yata N; Hoshii S; Takahashi S; Wada N; Takahashi Y; Kaku Y; Satomura K; Ikeda M; Honda M; Iijima K; Yoshikawa N
Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
[TBL] [Abstract][Full Text] [Related]
3. [NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].
Shi Y; Ding J; Liu JC; Wang H; Bu DF
Zhonghua Er Ke Za Zhi; 2005 Nov; 43(11):805-9. PubMed ID: 16316524
[TBL] [Abstract][Full Text] [Related]
4. Novel NPHS1 splice site mutations in a Chinese child with congenital nephrotic syndrome.
Fu R; Gou MF; Ma WH; He JJ; Luan Y; Liu J
Genet Mol Res; 2015 Jan; 14(1):433-9. PubMed ID: 25729976
[TBL] [Abstract][Full Text] [Related]
5. Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome.
Li GM; Cao Q; Shen Q; Sun L; Zhai YH; Liu HM; An Y; Xu H
BMC Nephrol; 2018 Dec; 19(1):382. PubMed ID: 30594156
[TBL] [Abstract][Full Text] [Related]
6. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Hinkes BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F;
Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
[TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.
Ovunc B; Ashraf S; Vega-Warner V; Bockenhauer D; Elshakhs NA; Joseph M; Hildebrandt F;
Nephron Clin Pract; 2012; 120(3):c139-46. PubMed ID: 22584503
[TBL] [Abstract][Full Text] [Related]
8. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
[TBL] [Abstract][Full Text] [Related]
9. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P
Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170
[TBL] [Abstract][Full Text] [Related]
10. The Role of p.Ser1105Ser (in
Thi Kim Lien N; Van Dem P; Thu Huong N; Minh Dien T; Thi Thu Thuy T; Van Tung N; Huy Hoang N; Thi Quynh Huong N
Medicina (Kaunas); 2019 Apr; 55(4):. PubMed ID: 31013750
[No Abstract] [Full Text] [Related]
11. Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children.
Mbarek IB; Abroug S; Omezzine A; Pawtowski A; Gubler MC; Bouslama A; Harbi A; Antignac C
Pediatr Nephrol; 2011 Feb; 26(2):241-9. PubMed ID: 21125408
[TBL] [Abstract][Full Text] [Related]
12. Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
Schoeb DS; Chernin G; Heeringa SF; Matejas V; Held S; Vega-Warner V; Bockenhauer D; Vlangos CN; Moorani KN; Neuhaus TJ; Kari JA; MacDonald J; Saisawat P; Ashraf S; Ovunc B; Zenker M; Hildebrandt F;
Nephrol Dial Transplant; 2010 Sep; 25(9):2970-6. PubMed ID: 20172850
[TBL] [Abstract][Full Text] [Related]
13. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
Abid A; Khaliq S; Shahid S; Lanewala A; Mubarak M; Hashmi S; Kazi J; Masood T; Hafeez F; Naqvi SA; Rizvi SA; Mehdi SQ
Gene; 2012 Jul; 502(2):133-7. PubMed ID: 22565185
[TBL] [Abstract][Full Text] [Related]
14. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
Heeringa SF; Vlangos CN; Chernin G; Hinkes B; Gbadegesin R; Liu J; Hoskins BE; Ozaltin F; Hildebrandt F;
Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012
[TBL] [Abstract][Full Text] [Related]
15. Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome.
Yu ZH; Wang DJ; Meng DC; Huang J; Nie XJ
Genet Mol Res; 2012 May; 11(2):1460-4. PubMed ID: 22653594
[TBL] [Abstract][Full Text] [Related]
16. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
[TBL] [Abstract][Full Text] [Related]
17. NPHS2 mutations account for only 15% of nephrotic syndrome cases.
Guaragna MS; Lutaif AC; Piveta CS; Souza ML; de Souza SR; Henriques TB; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
BMC Med Genet; 2015 Sep; 16():88. PubMed ID: 26420286
[TBL] [Abstract][Full Text] [Related]
18. NPHS1 gene mutations in children with Nephrotic Syndrome in northwest Iran.
Behbahan AG; Poorshiri B; Mortazavi F; Khaniani MS; Derakhshan SM
Pak J Biol Sci; 2013 Sep; 16(17):882-6. PubMed ID: 24498843
[TBL] [Abstract][Full Text] [Related]
19. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
Bińczak-Kuleta A; Rubik J; Litwin M; Ryder M; Lewandowska K; Taryma-Leśniak O; Clark JS; Grenda R; Ciechanowicz A
Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380
[TBL] [Abstract][Full Text] [Related]
20. No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.
Schultheiss M; Ruf RG; Mucha BE; Wiggins R; Fuchshuber A; Lichtenberger A; Hildebrandt F
Pediatr Nephrol; 2004 Dec; 19(12):1340-8. PubMed ID: 15338398
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
