201 related articles for article (PubMed ID: 15015071)
1. NPHS2 mutation associated with recurrence of proteinuria after transplantation.
Billing H; Müller D; Ruf R; Lichtenberger A; Hildebrandt F; August C; Querfeld U; Haffner D
Pediatr Nephrol; 2004 May; 19(5):561-4. PubMed ID: 15015071
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus.
Höcker B; Knüppel T; Waldherr R; Schaefer F; Weber S; Tönshoff B
Pediatr Nephrol; 2006 Oct; 21(10):1476-9. PubMed ID: 16721582
[TBL] [Abstract][Full Text] [Related]
4. Recurrence of focal-segmental glomerulosclerosis in children after renal transplantation: clinical and genetic aspects.
Weber S; Tönshoff B
Transplantation; 2005 Sep; 80(1 Suppl):S128-34. PubMed ID: 16286890
[TBL] [Abstract][Full Text] [Related]
5. Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.
Bertelli R; Ginevri F; Caridi G; Dagnino M; Sandrini S; Di Duca M; Emma F; Sanna-Cherchi S; Scolari F; Neri TM; Murer L; Massella L; Basile G; Rizzoni G; Perfumo F; Ghiggeri GM
Am J Kidney Dis; 2003 Jun; 41(6):1314-21. PubMed ID: 12776285
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.
Carraro M; Caridi G; Bruschi M; Artero M; Bertelli R; Zennaro C; Musante L; Candiano G; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2002 Jul; 13(7):1946-52. PubMed ID: 12089392
[TBL] [Abstract][Full Text] [Related]
9. The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation.
Mohey H; Thibaudin L; Laurent B; Berthoux F
Ann Transplant; 2013 Aug; 18():436-42. PubMed ID: 23982418
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [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]
12. First Report of Recurrent Nephrotic Syndrome After Kidney Transplantation in a Patient With NUP93 Gene Mutations: A Case Report.
Seeman T; Vondrak K
Transplant Proc; 2018 Dec; 50(10):3954-3956. PubMed ID: 30577294
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.
Frishberg Y; Rinat C; Megged O; Shapira E; Feinstein S; Raas-Rothschild A
J Am Soc Nephrol; 2002 Feb; 13(2):400-405. PubMed ID: 11805168
[TBL] [Abstract][Full Text] [Related]
17. Genetic forms of nephrotic syndrome.
Niaudet P
Pediatr Nephrol; 2004 Dec; 19(12):1313-8. PubMed ID: 15503167
[TBL] [Abstract][Full Text] [Related]
18. Successful Preemptive Kidney Transplantation With Rituximab Induction in a Patient With Focal Segmental Glomerulosclerosis and Massive Nephrotic Syndrome: A Case Report.
Kolonko A; Piecha G; Więcek A
Transplant Proc; 2016 Nov; 48(9):3092-3094. PubMed ID: 27932154
[TBL] [Abstract][Full Text] [Related]
19. Post-Transplant Recurrence of Focal Segmental Glomerulosclerosis in a Child With Heterozygous Mutations in NPHS1 and NPHS2.
Battelino N; Arnol M; Kandus A; Ponikvar R; Novljan G
Ther Apher Dial; 2016 Jun; 20(3):312-7. PubMed ID: 27312921
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]