426 related articles for article (PubMed ID: 20947785)
21. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
Maruyama K; Iijima K; Ikeda M; Kitamura A; Tsukaguchi H; Yoshiya K; Hoshii S; Wada N; Uemura O; Satomura K; Honda M; Yoshikawa N
Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
[TBL] [Abstract][Full Text] [Related]
22. mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.
Benetti E; Caridi G; Centi S; Vella MD; Ghiggeri GM; Artifoni L; Murer L
Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):854-7. PubMed ID: 24969201
[TBL] [Abstract][Full Text] [Related]
23. Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
Megremis S; Mitsioni A; Mitsioni AG; Fylaktou I; Kitsiou-Tzelli S; Stefanidis CJ; Kanavakis E; Traeger-Synodinos J
Genet Test Mol Biomarkers; 2009 Apr; 13(2):249-56. PubMed ID: 19371226
[TBL] [Abstract][Full Text] [Related]
24. NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
Dai Y; Yang H; Gao P; Liu WD
Ren Fail; 2014 Oct; 36(9):1395-8. PubMed ID: 25112471
[TBL] [Abstract][Full Text] [Related]
25. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
Drozdz D; Pietrzyk JA; Wierzchowska-Słowiaczek E; Sancewicz-Pach K; Antignac C; Miezyński W
Przegl Lek; 2006; 63 Suppl 3():85-6. PubMed ID: 16898497
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.
He N; Zahirieh A; Mei Y; Lee B; Senthilnathan S; Wong B; Mucha B; Hildebrandt F; Cole DE; Cattran D; Pei Y
Clin J Am Soc Nephrol; 2007 Jan; 2(1):31-7. PubMed ID: 17699384
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
Santín S; Bullich G; Tazón-Vega B; García-Maset R; Giménez I; Silva I; Ruíz P; Ballarín J; Torra R; Ars E
Clin J Am Soc Nephrol; 2011 May; 6(5):1139-48. PubMed ID: 21415313
[TBL] [Abstract][Full Text] [Related]
30. Prevalence of the
de Almeida R; da Silva WC; Garbin HI; Itaquy TP; Dos Santos Pereira F; Garcia CD; Keitel E; Sales Luiz Vianna F; Veronese FV
Clin Nephrol; 2020 Oct; 94(4):187-196. PubMed ID: 32691731
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Chernin G; Heeringa SF; Gbadegesin R; Liu J; Hinkes BG; Vlangos CN; Vega-Warner V; Hildebrandt F
Pediatr Nephrol; 2008 Sep; 23(9):1455-60. PubMed ID: 18543005
[TBL] [Abstract][Full Text] [Related]
33. Broadening the spectrum of diseases related to podocin mutations.
Caridi G; Bertelli R; Di Duca M; Dagnino M; Emma F; Onetti Muda A; Scolari F; Miglietti N; Mazzucco G; Murer L; Carrea A; Massella L; Rizzoni G; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2003 May; 14(5):1278-86. PubMed ID: 12707396
[TBL] [Abstract][Full Text] [Related]
34. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
Büscher AK; Konrad M; Nagel M; Witzke O; Kribben A; Hoyer PF; Weber S
Clin Nephrol; 2012 Jul; 78(1):47-53. PubMed ID: 22732337
[TBL] [Abstract][Full Text] [Related]
35. Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
Rood IM; Deegens JKJ; Lugtenberg D; Bongers EMHF; Wetzels JFM
Am J Kidney Dis; 2019 Mar; 73(3):400-403. PubMed ID: 30241959
[TBL] [Abstract][Full Text] [Related]
36. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
Zununi Vahed S; Moghaddas Sani H; Haghi M; Mohajel Shoja M; Ardalan M
Mol Biol Rep; 2019 Dec; 46(6):6339-6344. PubMed ID: 31529341
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. The mutation-dependent pathogenicity of NPHS2 p.R229Q: A guide for clinical assessment.
Mikó Á; K Menyhárd D; Kaposi A; Antignac C; Tory K
Hum Mutat; 2018 Dec; 39(12):1854-1860. PubMed ID: 30260545
[TBL] [Abstract][Full Text] [Related]
39. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE; Lovric S; Ashraf S; Pabst WL; Gee HY; Kohl S; Engelmann S; Vega-Warner V; Fang H; Halbritter J; Somers MJ; Tan W; Shril S; Fessi I; Lifton RP; Bockenhauer D; El-Desoky S; Kari JA; Zenker M; Kemper MJ; Mueller D; Fathy HM; Soliman NA; ; Hildebrandt F
J Am Soc Nephrol; 2015 Jun; 26(6):1279-89. PubMed ID: 25349199
[TBL] [Abstract][Full Text] [Related]
40. Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
Jungraithmayr TC; Hofer K; Cochat P; Chernin G; Cortina G; Fargue S; Grimm P; Knueppel T; Kowarsch A; Neuhaus T; Pagel P; Pfeiffer KP; Schäfer F; Schönermarck U; Seeman T; Toenshoff B; Weber S; Winn MP; Zschocke J; Zimmerhackl LB
J Am Soc Nephrol; 2011 Mar; 22(3):579-85. PubMed ID: 21355056
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
