159 related articles for article (PubMed ID: 30171708)
1. Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndrome.
Mohanapriya CD; Vettriselvi V; Nammalwar BR; Gowrishankar K; Ekambaram S; Sengutavan P; Venkatachalam P
J Cell Biochem; 2018 Dec; 119(12):10143-10150. PubMed ID: 30171708
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Dhandapani MC; Venkatesan V; Rengaswamy NB; Gowrishankar K; Ekambaram S; Sengutavan P; Perumal V
Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
[TBL] [Abstract][Full Text] [Related]
7. Mutation spectrum of genes associated with steroid-resistant nephrotic syndrome in Chinese children.
Wang Y; Dang X; He Q; Zhen Y; He X; Yi Z; Zhu K
Gene; 2017 Aug; 625():15-20. PubMed ID: 28476686
[TBL] [Abstract][Full Text] [Related]
8. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
Li Y; He Q; Wang Y; Dang X; Wu X; Li X; Shuai L; Yi Z
Ann Clin Lab Sci; 2019 May; 49(3):330-337. PubMed ID: 31308032
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
Büscher AK; Beck BB; Melk A; Hoefele J; Kranz B; Bamborschke D; Baig S; Lange-Sperandio B; Jungraithmayr T; Weber LT; Kemper MJ; Tönshoff B; Hoyer PF; Konrad M; Weber S;
Clin J Am Soc Nephrol; 2016 Feb; 11(2):245-53. PubMed ID: 26668027
[TBL] [Abstract][Full Text] [Related]
11. Association between NPHS1 and NPHS2 gene variants and nephrotic syndrome in children.
Hashemi M; Sadeghi-Bojd S; Rahmania K; Eskandari-Nasab E
Iran J Kidney Dis; 2015 Jan; 9(1):25-30. PubMed ID: 25599733
[TBL] [Abstract][Full Text] [Related]
12. NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.
Mao J; Zhang Y; Du L; Dai Y; Gu W; Liu A; Shang S; Liang L
Pediatr Res; 2007 Jan; 61(1):117-22. PubMed ID: 17211152
[TBL] [Abstract][Full Text] [Related]
13. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
Ramanathan AS; Vijayan M; Rajagopal S; Rajendiran P; Senguttuvan P
Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
[TBL] [Abstract][Full Text] [Related]
14. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
Ruf RG; Lichtenberger A; Karle SM; Haas JP; Anacleto FE; Schultheiss M; Zalewski I; Imm A; Ruf EM; Mucha B; Bagga A; Neuhaus T; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
J Am Soc Nephrol; 2004 Mar; 15(3):722-32. PubMed ID: 14978175
[TBL] [Abstract][Full Text] [Related]
15. Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change.
Kuusniemi AM; Lapatto R; Holmberg C; Karikoski R; Rapola J; Jalanko H
Kidney Int; 2005 Jul; 68(1):121-32. PubMed ID: 15954901
[TBL] [Abstract][Full Text] [Related]
16. Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
Al Riyami MS; Al Alawi I; Al Gaithi B; Al Maskari A; Al Kalbani N; Al Hashmi N; Al Balushi A; Al Shahi M; Al Saidi S; Al Bimani M; Al Hatali F; Mabillard H; Sayer JA
Mol Genet Genomic Med; 2023 Sep; 11(9):e2201. PubMed ID: 37204080
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
Berdeli A; Mir S; Yavascan O; Serdaroglu E; Bak M; Aksu N; Oner A; Anarat A; Donmez O; Yildiz N; Sever L; Tabel Y; Dusunsel R; Sonmez F; Cakar N
Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
[TBL] [Abstract][Full Text] [Related]
20. Polymorphic variants of MIF gene and prognosis in steroid therapy in children with idiopathic nephrotic syndrome.
Świerczewska M; Ostalska-Nowicka D; Kempisty B; Szczepankiewicz A; Nowicki M
Acta Biochim Pol; 2014; 61(1):67-75. PubMed ID: 24644543
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
