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27. [Cone dystrophy associated with Alport syndrome]. Spraul CW; Lang GE Klin Monbl Augenheilkd; 2000 Sep; 217(3):194-7. PubMed ID: 11076352 [TBL] [Abstract][Full Text] [Related]
28. Giant macular hole in Alport syndrome. Rahman W; Banerjee S Can J Ophthalmol; 2007 Apr; 42(2):314-5. PubMed ID: 17392861 [TBL] [Abstract][Full Text] [Related]
29. [Esophageal leiomyomatosis revealing an Alport syndrome]. Abbes K; Ayadi L; Makni S; Kharrat M; Affes N; Kallel R; Gouiaa N; Ben Hmida M; Hachicha J; Beyrouti MI; Sellami Boudawara T Rev Med Interne; 2009 Jan; 30(1):88-90. PubMed ID: 18433941 [TBL] [Abstract][Full Text] [Related]
30. Ocular manifestations of Alport's syndrome: a case report. Acke I; Priem H Bull Soc Belge Ophtalmol; 1992; 243():123-8. PubMed ID: 1302141 [TBL] [Abstract][Full Text] [Related]
31. A triad of retinal signs in Alport syndrome: The 'stair-case' fovea, choroidal thinning and peripheral schisis. Ghadiri NJ; Stanojcic N; Raja M; Burton BJ Eur J Ophthalmol; 2019 Jul; 29(1_suppl):10-14. PubMed ID: 30957516 [TBL] [Abstract][Full Text] [Related]
32. [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]
33. Role of multimodal ocular imaging in Alport syndrome. Kapoor A; Kapoor S; Chawla R Can J Ophthalmol; 2022 Jun; 57(3):e77-e78. PubMed ID: 34324875 [No Abstract] [Full Text] [Related]
34. Ocular manifestations of autosomal recessive Alport syndrome. Colville D; Savige J; Morfis M; Ellis J; Kerr P; Agar J; Fasset R Ophthalmic Genet; 1997 Sep; 18(3):119-28. PubMed ID: 9361309 [TBL] [Abstract][Full Text] [Related]
35. Outcome of females with Alport syndrome. Koyun M; Aksoy GK; Çomak E; Akman S Pediatr Nephrol; 2022 Aug; 37(8):1937. PubMed ID: 35478268 [No Abstract] [Full Text] [Related]
36. Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome. Kamiyoshi N; Nozu K; Fu XJ; Morisada N; Nozu Y; Ye MJ; Imafuku A; Miura K; Yamamura T; Minamikawa S; Shono A; Ninchoji T; Morioka I; Nakanishi K; Yoshikawa N; Kaito H; Iijima K Clin J Am Soc Nephrol; 2016 Aug; 11(8):1441-1449. PubMed ID: 27281700 [TBL] [Abstract][Full Text] [Related]
37. Autosomal recessive Alport syndrome: mutation in the COL4A3 gene in a woman with Alport syndrome and posttransplant antiglomerular basement membrane nephritis. Ding J; Stitzel J; Berry P; Hawkins E; Kashtan CE J Am Soc Nephrol; 1995 Mar; 5(9):1714-7. PubMed ID: 7780062 [TBL] [Abstract][Full Text] [Related]
38. Alport Syndrome in Women and Girls. Savige J; Colville D; Rheault M; Gear S; Lennon R; Lagas S; Finlay M; Flinter F Clin J Am Soc Nephrol; 2016 Sep; 11(9):1713-1720. PubMed ID: 27287265 [TBL] [Abstract][Full Text] [Related]
39. Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis. Antignac C; Heidet L Contrib Nephrol; 1996; 117():172-82. PubMed ID: 8801045 [No Abstract] [Full Text] [Related]
40. [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; 22(5):466-76. PubMed ID: 16267804 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]