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Items: 1 to 20 of 113

1.

Diffuse thin glomerular basement membrane in association with Fabry disease in a Chinese female patient.

Cai ZY, Zhang YK, Wang SX, Fang QY, Chen YQ.

Nephrol Dial Transplant. 2011 Nov;26(11):3813-6. doi: 10.1093/ndt/gfr455. Epub 2011 Aug 22.

PMID:
21862460
2.

COL4A3/COL4A4 mutations link familial hematuria and focal segmental glomerulosclerosis. glomerular epithelium destruction via basement membrane thinning?

Voskarides K, Pierides A, Deltas C.

Connect Tissue Res. 2008;49(3):283-8. doi: 10.1080/03008200802148280.

PMID:
18661361
3.

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.

Voskarides K, Damianou L, Neocleous V, Zouvani I, Christodoulidou S, Hadjiconstantinou V, Ioannou K, Athanasiou Y, Patsias C, Alexopoulos E, Pierides A, Kyriacou K, Deltas C.

J Am Soc Nephrol. 2007 Nov;18(11):3004-16. Epub 2007 Oct 17.

4.

A novel mutation of COL4A3 presents a different contribution to Alport syndrome and thin basement membrane nephropathy.

Hou P, Chen Y, Ding J, Li G, Zhang H.

Am J Nephrol. 2007;27(5):538-44. Epub 2007 Aug 24.

PMID:
17726307
5.

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.

PMID:
19357112
6.

Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.

Frascà GM, Onetti-Muda A, Mari F, Longo I, Scala E, Pescucci C, Roccatello D, Alpa M, Coppo R, Li Volti G, Feriozzi S, Bergesio F, Schena FP, Renieri A; Italian Renal Immunopathology Group.

Nephrol Dial Transplant. 2005 Mar;20(3):545-51. Epub 2004 Dec 23.

PMID:
15618242
7.

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.

Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA.

Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17.

8.

Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy.

Beirowski B, Weber M, Gross O.

J Am Soc Nephrol. 2006 Jul;17(7):1986-94. Epub 2006 Jun 14.

9.

Intramembranous microspherical structures in focal segmental glomerulosclerosis.

Inoue Y, Kanda Y, Kinoshita C, Kanda C, Joh K.

Clin Exp Nephrol. 2008 Dec;12(6):504-8. doi: 10.1007/s10157-008-0101-2. Epub 2008 Nov 13.

PMID:
19002748
10.

Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing.

Papazachariou L, Demosthenous P, Pieri M, Papagregoriou G, Savva I, Stavrou C, Zavros M, Athanasiou Y, Ioannou K, Patsias C, Panagides A, Potamitis C, Demetriou K, Prikis M, Hadjigavriel M, Kkolou M, Loukaidou P, Pastelli A, Michael A, Lazarou A, Arsali M, Damianou L, Goutziamani I, Soloukides A, Yioukas L, Elia A, Zouvani I, Polycarpou P, Pierides A, Voskarides K, Deltas C.

PLoS One. 2014 Dec 16;9(12):e115015. doi: 10.1371/journal.pone.0115015. eCollection 2014.

11.

COL4A3 founder mutations in Greek-Cypriot families with thin basement membrane nephropathy and focal segmental glomerulosclerosis dating from around 18th century.

Voskarides K, Patsias C, Pierides A, Deltas C.

Genet Test. 2008 Jun;12(2):273-8. doi: 10.1089/gte.2007.0110.

PMID:
18439107
12.

Focal segmental glomerulosclerosis with intramembranous vesicle-like microstructures and podocytic infolding lesion.

Yamada S, Masutani K, Katafuchi R, Fujigaki Y, Muranaka Y, Tsuruya K, Iida M.

Clin Exp Nephrol. 2008 Dec;12(6):509-12. doi: 10.1007/s10157-008-0088-8. Epub 2008 Nov 1.

PMID:
18979062
13.

A case of lupus nephritis with diffuse podocytic infolding into the glomerular basement membrane.

Mii A, Shimizu A, Masuda Y, Ishizaki M, Sato S, Hara K, Kaneko T, Utsumi K, Iino Y, Katayama Y, Fukuda Y.

Clin Exp Nephrol. 2008 Dec;12(6):479-84. doi: 10.1007/s10157-008-0097-7. Epub 2008 Oct 29.

PMID:
18958394
14.

The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy.

Tonna S, Wang YY, Wilson D, Rigby L, Tabone T, Cotton R, Savige J.

Pediatr Nephrol. 2008 Dec;23(12):2201-7. doi: 10.1007/s00467-008-0934-7. Epub 2008 Aug 26.

PMID:
18726620
15.

Glomerular basement membrane thickness in an Asian population using a novel image analysis software.

Teng YH, Ang HS, Mao KZ, Lui JY, Lin JY, Yue LL, Loh HL, Chiang G, Yip GW, Tan PH.

Pathology. 2009;41(4):342-7. doi: 10.1080/00313020902884485.

PMID:
19404846
16.

Fabry disease: a morphologic study of 11 cases.

Fischer EG, Moore MJ, Lager DJ.

Mod Pathol. 2006 Oct;19(10):1295-301. Epub 2006 Jun 23.

17.

Quantitative immunoelectron-microscopic analysis of the type IV collagen alpha1-6 chains in the glomerular basement membrane in childhood thin basement membrane disease.

Akazawa H, Nakajima M, Nishiguchi M, Yamoto Y, Sado Y, Naito I, Yoshioka A.

Clin Nephrol. 2005 Nov;64(5):329-36.

PMID:
16312259
18.

[Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].

Endreffy E, Ondrik Z, Kemény E, Vas Z, Maróti Z, Lencse G, Bereczki C, Haszon I, Túri S, Iványi B.

Orv Hetil. 2005 Dec 25;146(52):2647-53. Hungarian.

PMID:
16468607
19.

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. doi: 10.1159/000432406. Epub 2015 Jun 26.

PMID:
26138234
20.

Thin basement membrane disease with heavy proteinuria or nephrotic syndrome at presentation.

Nogueira M, Cartwright J Jr, Horn K, Doe N, Shappell S, Barrios R, Coroneos E, Truong LD.

Am J Kidney Dis. 2000 Apr;35(4):E15.

PMID:
10739808

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