157 related articles for article (PubMed ID: 17274342)
41. Familial Ectopia Lentis: Looking Beyond Marfan's Syndrome.
Hussain SJ; Amalnath D; Kasthuri N; Subramaniyan VK
J Assoc Physicians India; 2023 Nov; 71(11):94-95. PubMed ID: 38720505
[TBL] [Abstract][Full Text] [Related]
42. Craniosynostosis associated with ectopia lentis in monozygotic twin sisters.
Cruysberg JR; van Ravenswaaij-Arts CM; Pinckers A; Roddi R; Brunner HG
Am J Med Genet; 1999 Jan; 82(3):201-5. PubMed ID: 10215540
[TBL] [Abstract][Full Text] [Related]
43. Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family.
Mortemousque B; Amati-Bonneau P; Couture F; Graffan R; Dubois S; Colin J; Bonneau D; Morissette J; Lacombe D; Raymond V
Arch Ophthalmol; 2004 Oct; 122(10):1527-33. PubMed ID: 15477465
[TBL] [Abstract][Full Text] [Related]
44. Anterior axial lens subluxation, progressive myopia, and angle-closure glaucoma: recognition and treatment of atypical presentation of ectopia lentis.
Dagi LR; Walton DS
J AAPOS; 2006 Aug; 10(4):345-50. PubMed ID: 16935236
[TBL] [Abstract][Full Text] [Related]
45. Genetics of ectopia lentis.
Sadiq MA; Vanderveen D
Semin Ophthalmol; 2013; 28(5-6):313-20. PubMed ID: 24138040
[TBL] [Abstract][Full Text] [Related]
46. Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentis.
David D; Anand D; Araújo C; Gloss B; Fino J; Dinger M; Lindahl P; Pöyhönen M; Hannele L; Lavinha J
Exp Eye Res; 2018 Mar; 168():161-170. PubMed ID: 29305299
[TBL] [Abstract][Full Text] [Related]
47. Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae.
Zhao J; Zhou Y; Zhang J; Zhang K; Shang L; Li J
Exp Eye Res; 2022 Nov; 224():109243. PubMed ID: 36089008
[TBL] [Abstract][Full Text] [Related]
48. Axenfeld-Rieger syndrome in the age of molecular genetics.
Alward WL
Am J Ophthalmol; 2000 Jul; 130(1):107-15. PubMed ID: 11004268
[TBL] [Abstract][Full Text] [Related]
49. Oxycephaly, bilateral ectopia lentis, and retinal detachment.
Reichel E; Wiggs JL; Mukai S; D'Amico DJ
Ann Ophthalmol; 1992 Mar; 24(3):97-8. PubMed ID: 1570930
[TBL] [Abstract][Full Text] [Related]
50. Familial simple ectopia lentis: a case study.
Casper DS; Simon JW; Nelson LB; Porter IH; Lichtenstein SB
J Pediatr Ophthalmol Strabismus; 1985; 22(6):227-30. PubMed ID: 3878400
[TBL] [Abstract][Full Text] [Related]
51. A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
Vanita V; Singh JR; Singh D; Varon R; Robinson PN; Sperling K
Mol Vis; 2007 Oct; 13():2035-40. PubMed ID: 18079676
[TBL] [Abstract][Full Text] [Related]
52. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
[TBL] [Abstract][Full Text] [Related]
53. Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow up.
Lowry RB; Gould DB; Walter MA; Savage PR
Am J Med Genet A; 2007 Jun; 143A(11):1227-30. PubMed ID: 17486624
[TBL] [Abstract][Full Text] [Related]
54. The Axenfeld syndrome and the Rieger syndrome.
Fitch N; Kaback M
J Med Genet; 1978 Feb; 15(1):30-4. PubMed ID: 416212
[TBL] [Abstract][Full Text] [Related]
55. Traboulsi syndrome due to ASPH mutation: an under-recognised cause of ectopia lentis.
Kulkarni N; Lloyd IC; Ashworth J; Biswas S; Black GCM; Clayton-Smith J;
Clin Dysmorphol; 2019 Oct; 28(4):184-189. PubMed ID: 31274573
[TBL] [Abstract][Full Text] [Related]
56. Bilateral ametropic functional amblyopia in genetic ectopia lentis: its relation to the amount of subluxation, an indicator for early surgical management.
Romano PE; Kerr NC; Hope GM
Binocul Vis Strabismus Q; 2002; 17(3):235-41. PubMed ID: 12171598
[TBL] [Abstract][Full Text] [Related]
57. Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4.
Chandra A; Aragon-Martin JA; Sharif S; Parulekar M; Child A; Arno G
Ophthalmic Genet; 2013; 34(1-2):78-82. PubMed ID: 22871183
[TBL] [Abstract][Full Text] [Related]
58. Congenital ectopia lentis and secondary buphthalmos likely occurring as an autosomal recessive trait.
Bjerrum K; Kessing SV
Acta Ophthalmol (Copenh); 1991 Oct; 69(5):630-4. PubMed ID: 1776417
[TBL] [Abstract][Full Text] [Related]
59. The Rieger syndrome.
Jorgenson RJ; Levin LS; Cross HE; Yoder F; Kelly TE
Am J Med Genet; 1978; 2(3):307-18. PubMed ID: 263445
[TBL] [Abstract][Full Text] [Related]
60. Achondroplasia With Congenital Onset Glaucoma, and Presumed Axenfeld-Rieger Anomaly.
Nastasi S; Gonzalez A; Blake CR; Beck A; Agarwal-Sinha S
J Glaucoma; 2018 Oct; 27(10):e165-e167. PubMed ID: 30095606
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]