【参考文献】
1 Alport AC. Hereditary familial congenital haemorrhagic nephritis. Br Med J 1927;1:504506
2 Srinivasan M, Uzel SG, Gautieri A, Keten S, Buehler MJ. Alport Syndrome mutations in type IV tropocollagen alter molecular structure and nanomechanical properties. J Structural Biology 2009;168(3):503510
3 Pescucci C, Mari F, Longo I, Vogiatzi P, Caselli R, Scala E, Abaterusso C, Gusmano R, Seri M, Miglietti N, Bresin E, Renieri A. Autosomaldominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene. Kidney Int 2004;65(5):1598 1603
4 Kashtan CE. Alport syndrome and thin glomerular basement membrane disease. J Am Soc Nephrol 1998;9(9):17361750
5 Flinter F, Chantler C. Alports syndrome: inheritance and clinical features. In: Spitzer A, Auner E, eds. Inheritance of Kidney and Renal Tract Disease. Boston: Kluwer Academic 1990:107
6 Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL. Alport syndromeclinical phenotypes, incidence, and pathology. Contrib
Nephrol 1996;117:128
7 Colville DJ, Savige J. Alport syndrome: a review of the ocular manifestation. Ophthalmic Genet 1997;18:161173
8 Kashtam CE, Michael AF. Alport syndrome: from bedside to genome to bedside. Am J Kidney Dis 1993;22:627640
9 Jacobs M,Jeffrey B,Kriss A,Taylor D,Sa G,Barratt TM. Ophthalmologic assessment of young patients with Alport syndrome. Ophthalmology 1992;99:10391044
10 Hentati N, Sellami D, Makni K, Kharrat M, Hachicha J, Hammadi A, Feki J. Ocular findings in Alport syndrome: 32 case studies. J Fr
Ophthalmol 2008;31:597604
11 Govan JA. Ocular manifestation of Alports syndrome: a hereditary disorder of basement membranes? Br J Ophthalmol 1983;67:493503
12 Sargon MF, Celik HH, Sener C. Ultrastructure of the lens epithelium in Alports syndrome. Ophthalmogica 1999; 213:3033
13 Junk AK, Stefani FH, Ludwig K. Bilateral anterior lenticonus. Arch
Ophthalmol 2000;118:895897
14 Gehrs KM, Pollock SC, Zilkha G. Clinical features and pathogenesis of Alport retinopathy. Retina 1995;15:305311 上一页 [1] [2] |