280 related articles for article (PubMed ID: 24138040)
21. Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.
Tsipouras P; Del Mastro R; Sarfarazi M; Lee B; Vitale E; Child AH; Godfrey M; Devereux RB; Hewett D; Steinmann B
N Engl J Med; 1992 Apr; 326(14):905-9. PubMed ID: 1542340
[TBL] [Abstract][Full Text] [Related]
22. Ectopia lentis et pupillae.
Gupta NK; Ayra AV; Azad R
Indian J Ophthalmol; 1989; 37(1):32-4. PubMed ID: 2807501
[TBL] [Abstract][Full Text] [Related]
23. Marfan syndrome and other systemic disorders with congenital ectopia lentis. A Danish national survey.
Fuchs J
Acta Paediatr; 1997 Sep; 86(9):947-52. PubMed ID: 9343273
[TBL] [Abstract][Full Text] [Related]
24. A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis.
Ahram D; Sato TS; Kohilan A; Tayeh M; Chen S; Leal S; Al-Salem M; El-Shanti H
Am J Hum Genet; 2009 Feb; 84(2):274-8. PubMed ID: 19200529
[TBL] [Abstract][Full Text] [Related]
25. The eye as a window to a rare disease: ectopia lentis and homocystinuria, a Pakistani perspective.
Shafique M; Muzaffar W; Ishaq M
Int Ophthalmol; 2016 Feb; 36(1):79-83. PubMed ID: 25982157
[TBL] [Abstract][Full Text] [Related]
26. Targeted deletion of fibrillin-1 in the mouse eye results in ectopia lentis and other ocular phenotypes associated with Marfan syndrome.
Jones W; Rodriguez J; Bassnett S
Dis Model Mech; 2019 Jan; 12(1):. PubMed ID: 30642872
[TBL] [Abstract][Full Text] [Related]
27. Ectopia lentis et pupillae: the genetic aspects and differential diagnosis.
Colley A; Lloyd IC; Ridgway A; Donnai D
J Med Genet; 1991 Nov; 28(11):791-4. PubMed ID: 1770538
[TBL] [Abstract][Full Text] [Related]
28. ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent.
Scanga HL; Nischal KK
Am J Med Genet A; 2022 Jun; 188(6):1853-1857. PubMed ID: 35218299
[TBL] [Abstract][Full Text] [Related]
29. Incidence and de novo mutation rate of Marfan syndrome and risk of ectopia lentis.
Cui RZ; Hodge DO; Mohney BG
J AAPOS; 2023 Oct; 27(5):273.e1-273.e4. PubMed ID: 37716433
[TBL] [Abstract][Full Text] [Related]
30. Classical familial homocystinuria in an adult presenting as an isolated lens subluxation.
Martínez-Gutiérrez JD; Mencía-Gutiérrez E; Gracia-García-Miguel T; Gutiérrez-Díaz E; López-Tizón E
Int Ophthalmol; 2011 Jun; 31(3):227-32. PubMed ID: 21626167
[TBL] [Abstract][Full Text] [Related]
31. Familial unilateral ectopia lentis.
Simon JW; Cotliar JM; Burke LW
J AAPOS; 2007 Dec; 11(6):620-1. PubMed ID: 17720572
[TBL] [Abstract][Full Text] [Related]
32. Weill-Marchesani syndrome in mother and son.
Young ID; Fielder AR; Casey TA
Clin Genet; 1986 Dec; 30(6):475-80. PubMed ID: 3493095
[TBL] [Abstract][Full Text] [Related]
33. Evaluation of surgical intervention in familial isolated simple ectopia lentis: younger v. older generations.
Galvin JA; Baker JD; Bawle EV
Binocul Vis Strabismus Q; 2002; 17(3):229-34. PubMed ID: 12171597
[TBL] [Abstract][Full Text] [Related]
34. Novel
Guo D; Yang F; Zhou Y; Zhang X; Cao Q; Jin G; Zheng D
Br J Ophthalmol; 2023 Jun; 107(6):774-779. PubMed ID: 35042684
[TBL] [Abstract][Full Text] [Related]
35. [Hereditary ectopia lentis: diagnosis and surgical treatment].
Chizhonkova EA; Avetisov KS; Avetisov SE
Vestn Oftalmol; 2023; 139(1):129-136. PubMed ID: 36924525
[TBL] [Abstract][Full Text] [Related]
36. Ectopia lentis et pupillae in four generations caused by novel mutations in the ADAMTSL4 gene.
Sharifi Y; Tjon-Fo-Sang MJ; Cruysberg JR; Maat-Kievit AJ
Br J Ophthalmol; 2013 May; 97(5):583-7. PubMed ID: 23426735
[TBL] [Abstract][Full Text] [Related]
37. The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis.
Musleh M; Bull A; Linton E; Liu J; Waller S; Hardcastle C; Clayton-Smith J; Sharma V; Black GC; Biswas S; Ashworth JL; Sergouniotis PI
Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107549
[TBL] [Abstract][Full Text] [Related]
38. Retinal degeneration associated with ectopia lentis.
Simonelli F; De Crecchio G; Testa F; Nunziata G; Mazzeo S; Romano N; Cavaliere L; Rinaldi MM; Rinaldi E
Ophthalmic Genet; 1999 Jun; 20(2):121-6. PubMed ID: 10420198
[TBL] [Abstract][Full Text] [Related]
39. The eye in the Marfan syndrome.
Maumenee IH
Birth Defects Orig Artic Ser; 1982; 18(6):515-24. PubMed ID: 6983370
[No Abstract] [Full Text] [Related]
40. The phenotypic spectrum of
Knight LSW; Mullany S; Taranath DA; Ruddle JB; Barnett CP; Sallevelt SCEH; Berry EC; Marshall HN; Hollitt GL; Souzeau E; Craig JE; Siggs OM
Mol Vis; 2022; 28():257-268. PubMed ID: 36284667
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
