158 related articles for article (PubMed ID: 28392951)
1. Three Novel Mutations in the
Nguyen TK; Pham VD; Nguyen TH; Pham TK; Nguyen TQ; Nguyen HH
Case Rep Genet; 2017; 2017():2357282. PubMed ID: 28392951
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
Lenkkeri U; Männikkö M; McCready P; Lamerdin J; Gribouval O; Niaudet PM; Antignac C K; Kashtan CE; Homberg C; Olsen A; Kestilä M; Tryggvason K
Am J Hum Genet; 1999 Jan; 64(1):51-61. PubMed ID: 9915943
[TBL] [Abstract][Full Text] [Related]
10. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
Beltcheva O; Martin P; Lenkkeri U; Tryggvason K
Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
Patrakka J; Kestilä M; Wartiovaara J; Ruotsalainen V; Tissari P; Lenkkeri U; Männikkö M; Visapää I; Holmberg C; Rapola J; Tryggvason K; Jalanko H
Kidney Int; 2000 Sep; 58(3):972-80. PubMed ID: 10972661
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. 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]
17. Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community.
Frishberg Y; Ben-Neriah Z; Suvanto M; Rinat C; Männikkö M; Feinstein S; Becker-Cohen R; Jalanko H; Zlotogora J; Kestilä M
Genet Med; 2007 Mar; 9(3):180-4. PubMed ID: 17413422
[TBL] [Abstract][Full Text] [Related]
18. Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome.
Liu L; Doné SC; Khoshnoodi J; Bertorello A; Wartiovaara J; Berggren PO; Tryggvason K
Hum Mol Genet; 2001 Nov; 10(23):2637-44. PubMed ID: 11726550
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
Gigante M; Monno F; Roberto R; Laforgia N; Assael MB; Livolti S; Caringella A; La Manna A; Masella L; Iolascon A
J Nephrol; 2002; 15(6):696-702. PubMed ID: 12495287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
