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2. MACULAR HOLES, VITELLIFORM LESIONS, AND MIDPERIPHERAL RETINOSCHISIS IN ALPORT SYNDROME. Thomas AS; Baynham JT; Flaxel CJ Retin Cases Brief Rep; 2016; 10(2):109-11. PubMed ID: 26200386 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
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. 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]
7. 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]
8. Cho IH; Kim HD; Jung SJ; Park TK Indian J Ophthalmol; 2017 Sep; 65(9):877-879. PubMed ID: 28905837 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
13. 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]
14. Alport syndrome: a rare cause of uraemia. Ghosh S; Singh M; Sahoo R; Rao S BMJ Case Rep; 2014 Feb; 2014():. PubMed ID: 24526194 [TBL] [Abstract][Full Text] [Related]
15. Increased microvascular disease in X-linked and autosomal recessive Alport syndrome: a case control cross sectional observational study. Smith JD; Colville D; Lyttle N; Lamoureux E; Savige J Ophthalmic Genet; 2019 Apr; 40(2):129-134. PubMed ID: 30985254 [TBL] [Abstract][Full Text] [Related]
18. It is an Alport syndrome, not a simple hypertensive retinopathy. Gadde AK; Srirampur A; Manwani S; Agraharam S Indian J Ophthalmol; 2018 Sep; 66(9):1319-1321. PubMed ID: 30127153 [No Abstract] [Full Text] [Related]
19. Tapetal-like sheen associated with fleck retinopathy in Alport syndrome. Cervantes-Coste G; Fuentes-Paez G; Yeshurun I; Jimenez-Sierra JM Retina; 2003 Apr; 23(2):245-7. PubMed ID: 12707609 [No Abstract] [Full Text] [Related]
20. Unusual macular thickness in Alport syndrome: case report. Igami TZ; Lavezzo MM; Ferraz DA; Takahashi WY; Nakashima Y Arq Bras Oftalmol; 2012; 75(4):283-5. PubMed ID: 23258663 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]