333 related articles for article (PubMed ID: 19019929)
1. The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure.
Colville D; Wang YY; Tan R; Savige J
Br J Ophthalmol; 2009 Mar; 93(3):383-6. PubMed ID: 19019929
[TBL] [Abstract][Full Text] [Related]
2. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
Shaw EA; Colville D; Wang YY; Zhang KW; Dagher H; Fassett R; Guymer R; Savige J
Nephrol Dial Transplant; 2007 Jan; 22(1):104-8. PubMed ID: 17071739
[TBL] [Abstract][Full Text] [Related]
3. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
Liu J; Colville D; Wang YY; Baird PN; Guymer RH; Savige J
Br J Ophthalmol; 2009 Mar; 93(3):379-82. PubMed ID: 19019939
[TBL] [Abstract][Full Text] [Related]
4. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J
Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
[TBL] [Abstract][Full Text] [Related]
5. Opinion: Ocular features aid the diagnosis of Alport syndrome.
Savige J; Colville D
Nat Rev Nephrol; 2009 Jun; 5(6):356-60. PubMed ID: 19474829
[TBL] [Abstract][Full Text] [Related]
6. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
7. Retinal basement membrane abnormalities and the retinopathy of Alport syndrome.
Savige J; Liu J; DeBuc DC; Handa JT; Hageman GS; Wang YY; Parkin JD; Vote B; Fassett R; Sarks S; Colville D
Invest Ophthalmol Vis Sci; 2010 Mar; 51(3):1621-7. PubMed ID: 19850830
[TBL] [Abstract][Full Text] [Related]
8. Ocular features in Alport syndrome: pathogenesis and clinical significance.
Savige J; Sheth S; Leys A; Nicholson A; Mack HG; Colville D
Clin J Am Soc Nephrol; 2015 Apr; 10(4):703-9. PubMed ID: 25649157
[TBL] [Abstract][Full Text] [Related]
9. Alport syndrome. A review of the ocular manifestations.
Colville DJ; Savige J
Ophthalmic Genet; 1997 Dec; 18(4):161-73. PubMed ID: 9457747
[TBL] [Abstract][Full Text] [Related]
10. A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities.
Wilson JC; Yoon HS; Walker RJ; Eccles MR
Nephrol Dial Transplant; 2007 May; 22(5):1338-46. PubMed ID: 17277342
[TBL] [Abstract][Full Text] [Related]
11. Alport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure.
Tan R; Colville D; Wang YY; Rigby L; Savige J
Clin J Am Soc Nephrol; 2010 Jan; 5(1):34-8. PubMed ID: 19965530
[TBL] [Abstract][Full Text] [Related]
12. Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome.
Dagher H; Yan Wang Y; Fassett R; Savige J
Hum Mutat; 2002 Oct; 20(4):321-2. PubMed ID: 12325029
[TBL] [Abstract][Full Text] [Related]
13. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.
Marcocci E; Uliana V; Bruttini M; Artuso R; Silengo MC; Zerial M; Bergesio F; Amoroso A; Savoldi S; Pennesi M; Giachino D; Rombolà G; Fogazzi GB; Rosatelli C; Martinhago CD; Carmellini M; Mancini R; Di Costanzo G; Longo I; Renieri A; Mari F
Nephrol Dial Transplant; 2009 May; 24(5):1464-71. PubMed ID: 19129241
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.
Wang Y; Sivakumar V; Mohammad M; Colville D; Storey H; Flinter F; Dagher H; Savige J
Pediatr Nephrol; 2014 Mar; 29(3):391-6. PubMed ID: 24178893
[TBL] [Abstract][Full Text] [Related]
15. Bull's eye and pigment maculopathy are further retinal manifestations of an abnormal Bruch's membrane in Alport syndrome.
Savige J; Wang Y; Crawford A; Smith J; Symons A; Mack H; Nicholls K; Wilson D; Colville D
Ophthalmic Genet; 2017; 38(3):238-244. PubMed ID: 27485810
[TBL] [Abstract][Full Text] [Related]
16. [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; 146(52):2647-53. PubMed ID: 16468607
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 11155669
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 16338941
[TBL] [Abstract][Full Text] [Related]
19. [A new case of giant macular hole in a patient with Alport syndrome].
Mercé E; Korobelnik JF; Delyfer MN; Rougier MB
J Fr Ophtalmol; 2012 Oct; 35(8):573-9. PubMed ID: 22695059
[TBL] [Abstract][Full Text] [Related]
20. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
Chen Y; Colville D; Ierino F; Symons A; Savige J
Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
