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4. Non-syndromic posterior lenticonus a cause of childhood cataract: evidence for X-linked inheritance. Russell-Eggitt IM Eye (Lond); 2000 Dec; 14(Pt 6):861-3. PubMed ID: 11584843 [TBL] [Abstract][Full Text] [Related]
5. Anterior lentiplane and posterior lenticonus in two cases. Deng C Ophthalmologica; 1991; 202(4):187-90. PubMed ID: 1945297 [TBL] [Abstract][Full Text] [Related]
6. Diagnosis and management of bilateral posterior lenticonus in 7 members of the same family. Schipper I; Senn P; Schmid M J Cataract Refract Surg; 2006 Feb; 32(2):261-3. PubMed ID: 16565002 [TBL] [Abstract][Full Text] [Related]
7. Anterior lentiplane associated with posterior lenticonus and microcornea. Lingao MD; Liu GT; Gunton K; Levin AV J AAPOS; 2014 Apr; 18(2):191-2. PubMed ID: 24698622 [TBL] [Abstract][Full Text] [Related]
8. [Associated anterior lenticonus, deafness and familial nephropathy(Alport's syndrome)]. Ardouin M; Coutel Y; Bourguet J; Urvoy M; Thomet G J Genet Hum; 1966; 15():Suppl:44-8. PubMed ID: 4968158 [No Abstract] [Full Text] [Related]
10. Immunohistochemical and molecular genetic evidence for type IV collagen alpha5 chain abnormality in the anterior lenticonus associated with Alport syndrome. Ohkubo S; Takeda H; Higashide T; Ito M; Sakurai M; Shirao Y; Yanagida T; Oda Y; Sado Y Arch Ophthalmol; 2003 Jun; 121(6):846-50. PubMed ID: 12796257 [TBL] [Abstract][Full Text] [Related]
11. A new form of X-linked, high-frequency, sensorineural deafness. Wellesley D; Goldblatt J Clin Genet; 1992 Feb; 41(2):79-81. PubMed ID: 1544216 [TBL] [Abstract][Full Text] [Related]
12. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
13. Sex linked deafness: Wilde revisited. Reardon W J Med Genet; 1990 Jun; 27(6):376-9. PubMed ID: 2359100 [TBL] [Abstract][Full Text] [Related]
14. Anterior lens capsule abnormalities in Alport syndrome. Choi Jh; Na Ks; Bae Sh; Roh Gh Korean J Ophthalmol; 2005 Mar; 19(1):84-9. PubMed ID: 15929494 [TBL] [Abstract][Full Text] [Related]
15. Infantile leukocoria caused by posterior lenticonus. Fett D; Paez JH; Isenberg S Ann Ophthalmol; 1984 Jul; 16(7):679-80, 684. PubMed ID: 6476701 [TBL] [Abstract][Full Text] [Related]
16. [Usher syndrome and possible heredity linked to X chromosome]. Baldellou Vázquez A; Navarro Zapata C; Albalad Cebrian E; Mateo Blanco A An Esp Pediatr; 1993 Nov; 39(5):462-4. PubMed ID: 8285470 [No Abstract] [Full Text] [Related]
18. 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]
19. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness. Reardon W; Roberts S; Phelps PD; Thomas NS; Beck L; Issac R; Hughes HE Am J Med Genet; 1992 Nov; 44(4):513-7. PubMed ID: 1442898 [TBL] [Abstract][Full Text] [Related]
20. Clear lens phacoemulsification with continuous curvilinear capsulorhexis and foldable intraocular lens implantation for the treatment of a patient with bilateral anterior lenticonus due to Alport syndrome. Liu YB; Tan SJ; Sun ZY; Li X; Huang BY; Hu QM J Int Med Res; 2008; 36(6):1440-4. PubMed ID: 19094456 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]