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Items: 1 to 20 of 225

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Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Slotterbeck BD, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM.

Genomics. 1999 Jun 1;58(2):113-20.

PMID:
10368108
4.

[A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].

Aucella F, Bisceglia L, Stallone C.

G Ital Nefrol. 2003 Jul-Aug;20(4):356-67. Review. Italian. Erratum in: G Ital Nefrol. 2003 Sep-Oct;20(5):533.

PMID:
14523896
5.

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. Review.

PMID:
16752799
6.

Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis.

Rana K, Isbel N, Buzza M, Dagher H, Henning P, Kainer G, Savige J.

Am J Kidney Dis. 2003 Jun;41(6):1170-8.

PMID:
12776268
7.

Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.

Zhang Q, Ma J, Xie J, Wang Z, Zhu B, Hao X, Yang L, Ren H, Chen N.

Contrib Nephrol. 2013;181:91-100. doi: 10.1159/000348471. Epub 2013 May 8.

PMID:
23689571
8.

Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.

Komatsuda A, Wakui H, Maki N, Kigawa A, Goto H, Ohtani H, Hamai K, Oyama Y, Makoto H, Sawada K, Imai H.

Ren Fail. 2003 Jan;25(1):87-93.

PMID:
12617336
9.

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
10.

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
11.

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
12.

Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.

Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI.

Am J Kidney Dis. 2008 May;51(5):834-8. doi: 10.1053/j.ajkd.2008.01.018.

PMID:
18436095
13.

Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States.

Kitiyakara C, Eggers P, Kopp JB.

Am J Kidney Dis. 2004 Nov;44(5):815-25.

PMID:
15492947
14.

Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis.

Mistry K, Ireland JH, Ng RC, Henderson JM, Pollak MR.

Am J Kidney Dis. 2007 Nov;50(5):855-64.

PMID:
17954299
15.

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. Epub 2004 Dec 21.

PMID:
15627790
16.

Focal segmental glomerulosclerosis and renal transplantation.

Crosson JT.

Transplant Proc. 2007 Apr;39(3):737-43. Review.

PMID:
17445586
17.

Increasing incidence of focal segmental glomerulosclerosis and an examination of demographic patterns.

Dragovic D, Rosenstock JL, Wahl SJ, Panagopoulos G, DeVita MV, Michelis MF.

Clin Nephrol. 2005 Jan;63(1):1-7.

PMID:
15678691
18.

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31.

Tsukaguchi H, Yager H, Dawborn J, Jost L, Cohlmia J, Abreu PF, Pereira AB, Pollak MR.

J Am Soc Nephrol. 2000 Sep;11(9):1674-80.

19.

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
20.

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.

Pierides A, Voskarides K, Athanasiou Y, Ioannou K, Damianou L, Arsali M, Zavros M, Pierides M, Vargemezis V, Patsias C, Zouvani I, Elia A, Kyriacou K, Deltas C.

Nephrol Dial Transplant. 2009 Sep;24(9):2721-9. doi: 10.1093/ndt/gfp158. Epub 2009 Apr 8.

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