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Items: 1 to 20 of 312

1.

X-linked Alport syndrome in females.

Meleg-Smith S, Magliato S, Cheles M, Garola RE, Kashtan CE.

Hum Pathol. 1998 Apr;29(4):404-8.

PMID:
9563792
2.

Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.

Nakanishi K, Iijima K, Kuroda N, Inoue Y, Sado Y, Nakamura H, Yoshikawa N.

J Am Soc Nephrol. 1998 Aug;9(8):1433-40.

3.

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.

5.

[Molecular genetics of Alport syndrome].

Yamazaki H, Saito A, Nakagawa Y, Arakawa M.

Nihon Rinsho. 1992 Dec;50(12):3021-6. Review. Japanese.

PMID:
1491454
6.

Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.

Yoshioka K, Hino S, Takemura T, Maki S, Wieslander J, Takekoshi Y, Makino H, Kagawa M, Sado Y, Kashtan CE.

Am J Pathol. 1994 May;144(5):986-96.

7.

Identification of alpha3, alpha4, and alpha5 chains of type IV collagen as alloantigens for Alport posttransplant anti-glomerular basement membrane antibodies.

Kalluri R, Torre A, Shield CF 3rd, Zamborsky ED, Werner MC, Suchin E, Wolf G, Helmchen UM, van den Heuvel LP, Grossman R, Aradhye S, Neilson EG.

Transplantation. 2000 Feb 27;69(4):679-83.

PMID:
10708133
8.

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
9.

Alpha 5 COLIV chain distribution in glomerular basement membrane in a male with X-linked Alport syndrome and thin basement membrane.

Rizzoni G, Massella L, Muda AO.

Pediatr Nephrol. 2000 Dec;15(3-4):325. No abstract available.

PMID:
11149132
10.

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
11.

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

Kashtan CE.

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

12.

Absence of alpha 6(IV) collagen in kidney and skin of X-linked Alport syndrome patients.

Hino S, Takemura T, Sado Y, Kagawa M, Oohashi T, Ninomiya Y, Yoshioka K.

Pediatr Nephrol. 1996 Dec;10(6):742-4.

PMID:
8971895
13.

Alport syndrome. A review of the ocular manifestations.

Colville DJ, Savige J.

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

PMID:
9457747
14.

Alport disease: a review of the diagnostic difficulties.

Meleg-Smith S.

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

PMID:
11465475
16.

A novel model of autosomal dominant Alport syndrome in Dalmatian dogs.

Hood JC, Huxtable C, Naito I, Smith C, Sinclair R, Savige J.

Nephrol Dial Transplant. 2002 Dec;17(12):2094-8.

17.

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.

Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys.

Heidet L, Cai Y, Guicharnaud L, Antignac C, Gubler MC.

Am J Pathol. 2000 Jun;156(6):1901-10.

20.

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.

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