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Items: 1 to 20 of 785

1.

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
2.

[Thin glomerular basement membrane disease].

Frascà GM, Balestra E, Fanciulli E, Freddi P, Mazzucchelli R, Montironi R, D'Arezzo M, Sagripanti S.

G Ital Nefrol. 2008 Jan-Feb;25(1):49-56. Review. Italian.

PMID:
18264918
3.

Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.

Longo I, Scala E, Mari F, Caselli R, Pescucci C, Mencarelli MA, Speciale C, Giani M, Bresin E, Caringella DA, Borochowitz ZU, Siriwardena K, Winship I, Renieri A, Meloni I.

Nephrol Dial Transplant. 2006 Mar;21(3):665-71. Epub 2005 Dec 7.

PMID:
16338941
4.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
5.

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.

6.

Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease.

Ueda T, Nakajima M, Akazawa H, Maruhashi Y, Shimoyama H, Sakagami Y, Takagawa K, Kamitsuji H, Naito I, Sado Y, Yoshioka A.

Nephron. 2002 Oct;92(2):271-8.

PMID:
12218303
7.

Distribution of alpha-chains of type IV collagen in glomerular basement membranes with ultrastructural alterations suggestive of Alport syndrome.

Barsotti P, Muda AO, Mazzucco G, Massella L, Basolo B, De Marchi M, Rizzoni G, Monga G, Faraggiana T.

Nephrol Dial Transplant. 2001 May;16(5):945-52.

PMID:
11328899
8.

Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IV diseases.

Tazón Vega B, Badenas C, Ars E, Lens X, Milà M, Darnell A, Torra R.

Am J Kidney Dis. 2003 Nov;42(5):952-9.

PMID:
14582039
9.

Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlations.

Mazzucco G, Barsotti P, Muda AO, Fortunato M, Mihatsch M, Torri-Tarelli L, Renieri A, Faraggiana T, De Marchi M, Monga G.

J Am Soc Nephrol. 1998 Jun;9(6):1023-31.

10.

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
11.

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
12.

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
13.

Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants.

Liapis H, Gökden N, Hmiel P, Miner JH.

Hum Pathol. 2002 Aug;33(8):836-45.

PMID:
12203217
14.

Thin basement membrane disease in patients with familial IgA nephropathy.

Frascá GM, Soverini L, Gharavi AG, Lifton RP, Canova C, Preda P, Vangelista A, Stefoni S.

J Nephrol. 2004 Nov-Dec;17(6):778-85.

PMID:
15593051
15.

[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
16.

Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.

Vizjak A, Ferluga D.

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:323-6. Review.

17.

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Kashtan CE.

Medicine (Baltimore). 1999 Sep;78(5):338-60. Review.

18.

Quantitative analysis of type IV collagen subchains in the glomerular basement membrane of patients with Alport syndrome with confocal microscopy.

Su J, Liu ZH, Zeng CH, Wei-Gong, Chen HP, Li LS.

Nephrol Dial Transplant. 2006 Jul;21(7):1838-47. Epub 2006 Mar 30.

PMID:
16574687
19.

Autosomal dominant Alport's syndrome: study of a large Tunisian family.

Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J.

Saudi J Kidney Dis Transpl. 2006 Sep;17(3):320-5.

20.

A clinicopathological study of Alport syndrome and detection of type IV collagen chains in Alport patients.

Chen N, Pan X, Ren H, Dong D.

Chin Med J (Engl). 1998 Sep;111(9):797-802.

PMID:
11155669

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