128 related articles for article (PubMed ID: 37560858)
1. Three Novel Heterozygous Mutations of NPHS1 Gene Causing Infants with Congenital Nephrotic Syndrome: Two Chinese (Han) Cases.
Lv H; Liu F; Wang Q; Dong Z; Ren P; Zhang H; Yan X; Li L
Clin Lab; 2023 Aug; 69(8):. PubMed ID: 37560858
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome.
Wu LQ; Hu JJ; Xue JJ; Liang DS
Genet Mol Res; 2011 Oct; 10(4):2517-22. PubMed ID: 22009864
[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. 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]
7. 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]
8. Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type.
Lee BH; Ahn YH; Choi HJ; Kang HK; Kim SD; Cho BS; Moon KC; Ha IS; Cheong HI; Choi Y
J Korean Med Sci; 2009 Jan; 24 Suppl(Suppl 1):S210-4. PubMed ID: 19194555
[TBL] [Abstract][Full Text] [Related]
9. Congenital nephrotic syndrome with a novel NPHS1 mutation.
Yoshizawa C; Kobayashi Y; Ikeuchi Y; Tashiro M; Kakegawa S; Watanabe T; Goto Y; Nakanishi K; Yoshikawa N; Arakawa H
Pediatr Int; 2016 Nov; 58(11):1211-1215. PubMed ID: 27882743
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.
Xie D; Wu J; Zhang W; Jin T; Wu P; An B; Huang S
Medicine (Baltimore); 2023 Feb; 102(7):e32970. PubMed ID: 36800604
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. A case report of congenital nephrotic syndrome caused by new mutations of NPHS1.
Li Z; Zhuang L; Han M; Li F
J Int Med Res; 2021 Aug; 49(8):3000605211038133. PubMed ID: 34396835
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
