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Items: 1 to 20 of 132

1.

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. doi: 10.1681/ASN.2010010029. Epub 2011 Feb 25.

2.

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; FSGS Spanish Study Group.

Clin J Am Soc Nephrol. 2011 Feb;6(2):344-54. doi: 10.2215/CJN.03770410. Epub 2010 Oct 14.

3.

Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.

Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T.

Pediatr Transplant. 2008 May;12(3):341-6. doi: 10.1111/j.1399-3046.2007.00752.x. Epub 2008 Jan 16.

PMID:
18208440
4.

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.

PMID:
12776285
5.

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. doi: 10.1093/ndt/gft532. Epub 2014 Feb 4.

PMID:
24500309
6.

Recurrence of focal-segmental glomerulosclerosis in children after renal transplantation: clinical and genetic aspects.

Weber S, Tönshoff B.

Transplantation. 2005 Sep 27;80(1 Suppl):S128-34. Review.

PMID:
16286890
7.

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. Epub 2006 May 24.

PMID:
16721582
8.

A retrospective study of focal segmental glomerulosclerosis: clinical criteria can identify patients at high risk for recurrent disease after first renal transplantation.

Maas RJ, Deegens JK, van den Brand JA, Cornelissen EA, Wetzels JF.

BMC Nephrol. 2013 Feb 22;14:47. doi: 10.1186/1471-2369-14-47.

9.

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. Epub 2006 Oct 25.

10.

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):2742-6.

11.

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.

PMID:
22732337
12.

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; Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group.

J Am Soc Nephrol. 2004 Mar;15(3):722-32.

13.

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. doi: 10.1093/ndt/gfn208. Epub 2008 Apr 28.

PMID:
18443213
14.

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.

15.

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. Epub 2004 Mar 10.

16.

NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.

Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.

J Nephrol. 2006 May-Jun;19(3):366-71.

PMID:
16874699
17.

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 29;9:13. doi: 10.1186/1471-2369-9-13.

18.

Primary focal segmental glomerulosclerosis--long-term outcome after pediatric renal transplantation.

Jungraithmayr TC, Bulla M, Dippell J, Greiner C, Griebel M, Leichter HE, Plank C, Tönshoff B, Weber LT, Zimmerhackl LB; German MMF Study Group.

Pediatr Transplant. 2005 Apr;9(2):226-31.

PMID:
15787798
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. doi: 10.1007/s10157-016-1237-0. Epub 2016 Jan 28. Erratum in: Clin Exp Nephrol. 2017 Feb;21(1):134-135.

PMID:
26820844
20.

Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children.

Dall'Amico R, Ghiggeri G, Carraro M, Artero M, Ghio L, Zamorani E, Zennaro C, Basile G, Montini G, Rivabella L, Cardillo M, Scalamogna M, Ginevri F.

Am J Kidney Dis. 1999 Dec;34(6):1048-55.

PMID:
10585314

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