157 related articles for article (PubMed ID: 17274342)
21. Ectopia lentis, chorioretinal dystrophy and myopia. A new autosomal recessive syndrome.
Noble KG; Bass S; Sherman J
Doc Ophthalmol; 1993; 83(2):97-102. PubMed ID: 8334934
[TBL] [Abstract][Full Text] [Related]
22. Congenital heart defects in two siblings in an Axenfeld-Rieger syndrome family.
Akkus MN; Argin A
Clin Dysmorphol; 2010 Apr; 19(2):56-61. PubMed ID: 20179581
[TBL] [Abstract][Full Text] [Related]
23. [Glaucoma with Axenfeld-Rieger syndrome in three generations. Aqueous humor dynamics].
Hayashi M; Inoda S
Nippon Ganka Gakkai Zasshi; 1994 Jun; 98(6):584-9. PubMed ID: 8030574
[TBL] [Abstract][Full Text] [Related]
24. A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
Honkanen RA; Nishimura DY; Swiderski RE; Bennett SR; Hong S; Kwon YH; Stone EM; Sheffield VC; Alward WL
Am J Ophthalmol; 2003 Mar; 135(3):368-75. PubMed ID: 12614756
[TBL] [Abstract][Full Text] [Related]
25. Ectopia lentis et pupillae.
Cross HE
Am J Ophthalmol; 1979 Sep; 88(3 Pt 1):381-4. PubMed ID: 314755
[TBL] [Abstract][Full Text] [Related]
26. Bilateral prominent schwalbe ring in the anterior chamber in a patient with axenfeld-rieger syndrome and megalocornea.
Espana EM; Mora R; Liebmann J; Ritch R
Cornea; 2007 Apr; 26(3):379-81. PubMed ID: 17413972
[TBL] [Abstract][Full Text] [Related]
27. Traboulsi Syndrome in Pakistan.
Awais T; Ali M; Khan SA
J Coll Physicians Surg Pak; 2019 Jun; 29(6):S37-S40. PubMed ID: 31142416
[TBL] [Abstract][Full Text] [Related]
28. [Glaucoma attacks in Weill-Marchesani syndrome].
Czechowicz-Janicka K; Staszkiewicz J
Klin Oczna; 1992; 94(2-3):76-7. PubMed ID: 1640689
[TBL] [Abstract][Full Text] [Related]
29. [Hereditary ectopia lentis].
Neuhann TM
Klin Monbl Augenheilkd; 2015 Mar; 232(3):259-65. PubMed ID: 25654236
[TBL] [Abstract][Full Text] [Related]
30. Clinical manifestations of ectopia lentis et pupillae in 16 patients.
Goldberg MF
Trans Am Ophthalmol Soc; 1988; 86():158-77. PubMed ID: 2979048
[TBL] [Abstract][Full Text] [Related]
31. Isolated congenital ectopia lentis with autosomal dominant inheritance.
Jaureguy BM; Hall JG
Clin Genet; 1979 Jan; 15(1):97-109. PubMed ID: 310371
[TBL] [Abstract][Full Text] [Related]
32. Ectopia lentis in a family.
Sinha A; Rahman A
Indian J Ophthalmol; 1980 Apr; 28(1):33-5. PubMed ID: 6970725
[No 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. Cardiac valvular disease and Axenfeld-Rieger syndrome.
Tsai JC; Grajewski AL
Am J Ophthalmol; 1994 Aug; 118(2):255-6. PubMed ID: 8053476
[No Abstract] [Full Text] [Related]
35. Ectopia Lentis et Pupillae Caused by ADAMTSL4 Pathogenic Variants and an Algorithm for Work-up.
Safi M; Nejad SK; O'Hara M; Shankar SP
J Pediatr Ophthalmol Strabismus; 2019 Jul; 56():e45-e48. PubMed ID: 31282960
[TBL] [Abstract][Full Text] [Related]
36. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
37. Ectopia lentis et pupillae syndrome in three generations.
Cruysberg JR; Pinckers A
Br J Ophthalmol; 1995 Feb; 79(2):135-8. PubMed ID: 7696232
[TBL] [Abstract][Full Text] [Related]
38. Dental and craniofacial anomalies of Axenfeld-Rieger syndrome.
Childers NK; Wright JT
J Oral Pathol; 1986 Nov; 15(10):534-9. PubMed ID: 3104560
[TBL] [Abstract][Full Text] [Related]
39. Cleft lip and palate with ectopia lentis et pupillae.
Sha'ban RI; Asfour WM
Saudi Med J; 2003 Aug; 24(8):901-3. PubMed ID: 12939682
[TBL] [Abstract][Full Text] [Related]
40. Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance.
Haddad R; Uwaydat S; Dakroub R; Traboulsi EI
Am J Med Genet; 2001 Mar; 99(3):185-9. PubMed ID: 11241487
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
