298 related articles for article (PubMed ID: 12464671)
1. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.
Tsukaguchi H; Sudhakar A; Le TC; Nguyen T; Yao J; Schwimmer JA; Schachter AD; Poch E; Abreu PF; Appel GB; Pereira AB; Kalluri R; Pollak MR
J Clin Invest; 2002 Dec; 110(11):1659-66. PubMed ID: 12464671
[TBL] [Abstract][Full Text] [Related]
2. NPHS2 variation in focal and segmental glomerulosclerosis.
Tonna SJ; Needham A; Polu K; Uscinski A; Appel GB; Falk RJ; Katz A; Al-Waheeb S; Kaplan BS; Jerums G; Savige J; Harmon J; Zhang K; Curhan GC; Pollak MR
BMC Nephrol; 2008 Sep; 9():13. PubMed ID: 18823551
[TBL] [Abstract][Full Text] [Related]
3. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
Santín S; Tazón-Vega B; Silva I; Cobo MÁ; Giménez I; Ruíz P; García-Maset R; Ballarín J; Torra R; Ars E;
Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
Machuca E; Hummel A; Nevo F; Dantal J; Martinez F; Al-Sabban E; Baudouin V; Abel L; Grünfeld JP; Antignac C
Kidney Int; 2009 Apr; 75(7):727-35. PubMed ID: 19145239
[TBL] [Abstract][Full Text] [Related]
7. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
Lu L; Wan H; Yin Y; Feng WJ; Wang M; Zou YC; Huang B; Wang DT; Shi Y; Zhao Y; Wei LB
Int Urol Nephrol; 2014 Jul; 46(7):1383-93. PubMed ID: 24715228
[TBL] [Abstract][Full Text] [Related]
8. Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure.
Stefanou C; Pieri M; Savva I; Georgiou G; Pierides A; Voskarides K; Deltas C
Nephron; 2015; 130(3):200-12. PubMed ID: 26138234
[TBL] [Abstract][Full Text] [Related]
9. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
Kerti A; Csohány R; Wagner L; Jávorszky E; Maka E; Tory K
Pediatr Nephrol; 2013 Oct; 28(10):2061-4. PubMed ID: 23800802
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
Fotouhi N; Ardalan M; Jabbarpour Bonyadi M; Abdolmohammadi R; Kamalifar A; Nasri H; Einollahi B
Iran J Kidney Dis; 2013 Sep; 7(5):399-403. PubMed ID: 24072153
[TBL] [Abstract][Full Text] [Related]
13. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
Laurin LP; Lu M; Mottl AK; Blyth ER; Poulton CJ; Weck KE
Nephrol Dial Transplant; 2014 Nov; 29(11):2062-9. PubMed ID: 24500309
[TBL] [Abstract][Full Text] [Related]
14. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
Monteiro EJ; Pereira AC; Pereira AB; Krieger JE; Mastroianni-Kirsztajn G
J Nephrol; 2006; 19(3):366-71. PubMed ID: 16874699
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
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. 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]
19. 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]
20. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
Caridi G; Bertelli R; Carrea A; Di Duca M; Catarsi P; Artero M; Carraro M; Zennaro C; Candiano G; Musante L; Seri M; Ginevri F; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2001 Dec; 12(12):2742-2746. PubMed ID: 11729243
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
