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4. Delayed diagnosis of Alport syndrome without hematuria. Yin-Yin C; You-Ming P; Yu-Mei L Iran J Kidney Dis; 2014 May; 8(3):250-1. PubMed ID: 24878952 [TBL] [Abstract][Full Text] [Related]
5. [Alport syndrome in 23-year-old woman]. Finke D; Bilińska W; Kałuzyński A; Nowicki M Pol Merkur Lekarski; 2008; 24 Suppl 4():22-4. PubMed ID: 18924495 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Alport syndrome or progressive hereditary nephritis with hearing loss]. Gubler MC; Heidet L; Antignac C Nephrol Ther; 2007 Jun; 3(3):113-20. PubMed ID: 17540313 [TBL] [Abstract][Full Text] [Related]
8. [Hereditary nephritis (Alport)]. Popović-Rolović M; Smiljanić S Srp Arh Celok Lek; 1978 Apr; 106(4):353-68. PubMed ID: 751225 [No Abstract] [Full Text] [Related]
9. Alport syndrome: A puzzling case of thrombocytopenia and giant unusual platelets in blood smear. Ocal J; Sola-Visner M; Rimsza L Am J Hematol; 2024 Jun; 99(6):1168-1169. PubMed ID: 38174980 [TBL] [Abstract][Full Text] [Related]
10. [Hereditary nephritis (Alport). II. Clinical and morphological correlations]. Popović-Rolović M; Sindjić M; Smiljanić S; Calić-Perisić N; Stefanović Z Srp Arh Celok Lek; 1978 Oct; 106(10):883-96. PubMed ID: 752943 [No 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]