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Items: 1 to 20 of 61

1.

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.

Haas M.

Arch Pathol Lab Med. 2009 Feb;133(2):224-32. doi: 10.1043/1543-2165-133.2.224. Review.

PMID:
19195966
2.

Alport syndrome and thin basement membrane nephropathy.

Thorner PS.

Nephron Clin Pract. 2007;106(2):c82-8. Review.

PMID:
17570934
3.

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.

4.

The genetics of thin basement membrane nephropathy.

Rana K, Wang YY, Buzza M, Tonna S, Zhang KW, Lin T, Sin L, Padavarat S, Savige J.

Semin Nephrol. 2005 May;25(3):163-70. Review.

PMID:
15880327
5.

[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
6.
7.

Thin basement membrane nephropathy.

Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY.

Kidney Int. 2003 Oct;64(4):1169-78. Review.

8.

Clinical and molecular diagnosis of Alport syndrome.

Kashtan CE.

Proc Assoc Am Physicians. 1995 Oct;107(3):306-13. Review.

PMID:
8608415
9.

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

Kashtan CE.

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

10.

[From Alport syndrome to benign familial hematuria: clinical and genetic aspect].

Maziers N, Dahan K, Pirson Y.

Nephrol Ther. 2005 May;1(2):90-100. Review. French.

PMID:
16895672
11.

The clinical features of thin basement membrane nephropathy.

Gregory MC.

Semin Nephrol. 2005 May;25(3):140-5. Review.

PMID:
15880323
12.

Alport syndrome. A review of the ocular manifestations.

Colville DJ, Savige J.

Ophthalmic Genet. 1997 Dec;18(4):161-73. Review.

PMID:
9457747
13.

Alport Syndrome and Thin Basement Membrane Nephropathy.

Kashtan CE.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2001 Aug 28 [updated 2015 Nov 25].

14.

Alport syndrome: from bedside to genome to bedside.

Kashtan CE, Michael AF.

Am J Kidney Dis. 1993 Nov;22(5):627-40. Review.

PMID:
8238007
15.

Inherited diseases of the glomerular basement membrane.

Gubler MC.

Nat Clin Pract Nephrol. 2008 Jan;4(1):24-37. Review.

PMID:
18094725
16.

[Clinical and genetic features of the Alport 'syndromes'].

Pescucci C, Longo I, Mari F, Scala E, Bruttini M, Caselli R, Renieri A.

G Ital Nefrol. 2005 Sep-Oct;22(5):466-76. Review. Italian.

PMID:
16267804
17.

The clinical spectrum of type IV collagen mutations.

Lemmink HH, Schröder CH, Monnens LA, Smeets HJ.

Hum Mutat. 1997;9(6):477-99. Review.

PMID:
9195222
18.

Renal biopsy interpretation in Alport Syndrome.

Mazzucco G, De Marchi M, Monga G.

Semin Diagn Pathol. 2002 Aug;19(3):133-45. Review.

PMID:
12180634
19.

Alport disease: a review of the diagnostic difficulties.

Meleg-Smith S.

Ultrastruct Pathol. 2001 May-Jun;25(3):193-200. Review.

PMID:
11465475
20.

Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life.

Deltas C, Savva I, Voskarides K, Papazachariou L, Pierides A.

Nephron. 2015;130(4):271-80. doi: 10.1159/000435789. Review.

PMID:
26201269
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