These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
508 related articles for article (PubMed ID: 11854170)
1. 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]
2. 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]
3. 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]
4. 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]
6. Genetic basis of nephrotic syndrome--review. Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]]. Aucella F; Bisceglia L; Stallone C G Ital Nefrol; 2003; 20(4):356-67. PubMed ID: 14523896 [TBL] [Abstract][Full Text] [Related]
10. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect. Thomas MM; Ahmed HM; El-Dessouky SH; Ramadan A; Botrous OE; Abdel-Hamid MS Mol Genet Genomics; 2022 May; 297(3):689-698. PubMed ID: 35278126 [TBL] [Abstract][Full Text] [Related]
12. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Franceschini N; North KE; Kopp JB; McKenzie L; Winkler C Genet Med; 2006 Feb; 8(2):63-75. PubMed ID: 16481888 [TBL] [Abstract][Full Text] [Related]
13. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa. Nandlal L; Winkler CA; Bhimma R; Cho S; Nelson GW; Haripershad S; Naicker T Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919 [TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis. Aucella F; De Bonis P; Gatta G; Muscarella LA; Vigilante M; di Giorgio G; D'Errico M; Zelante L; Stallone C; Bisceglia L Nephron Clin Pract; 2005; 99(2):c31-6. PubMed ID: 15627790 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic forms of nephrotic syndrome. Niaudet P Pediatr Nephrol; 2004 Dec; 19(12):1313-8. PubMed ID: 15503167 [TBL] [Abstract][Full Text] [Related]
17. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis. Löwik M; Levtchenko E; Westra D; Groenen P; Steenbergen E; Weening J; Lilien M; Monnens L; van den Heuvel L Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern. Suvanto M; Patrakka J; Jahnukainen T; Sjöström PM; Nuutinen M; Arikoski P; Kataja J; Kestilä M; Jalanko H Clin Exp Nephrol; 2017 Aug; 21(4):677-684. PubMed ID: 27573339 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]