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9.1.1 Congenital glaucoma, Buphthalmos (9)
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54850 Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe GlaucomaMartí,nez-Jacobo L; Có,rdova-Fletes C; Ortiz-Ló,pez R; Rivas F; Saucedo-Carrasco C; Rojas-Martí,nez A
Molecular syndromology 2013; 4: 285-291
54630 Ocular Manifestations of 22q11.2 MicroduplicationCordovez JA; Capasso J; Lingao MD; Sadagopan KA; Spaeth GL; Wasserman BN; Levin AV
Ophthalmology 2014; 121: 392-398
54748 Markedly asymmetric buphthalmos but without anisometropia in a girl with primary congenital glaucomaAlharkan DH; Khan AO
Journal of AAPOS 2013; 17: 533-534
54540 Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish populationMillá E; Mañ,é B; Duch S; Hernan I; Borrà,s E; Planas E; Dias Mde S; Carballo M; Gamundi MJ,
Molecular Vision 2013; 19: 1707-1722
54666 A Novel CYP1B1 Mutation with Congenital Glaucoma and Total AniridiaAlzuhairy S; Abu-Amero KK; Al-Shahwan S; Edward DP
Ophthalmic Genetics 2015; 36: 89-91
54676 Comparative evaluation of RetCam vs. gonioscopy images in congenital glaucomaAzad RV; Chandra P; Chandra A; Gupta A; Gupta V; Sihota R
Indian Journal of Ophthalmology 2014; 62: 163-166
54721 Small eyes big problems: is cataract surgery the best option for the nanophthalmic eyes?Utman SA
Journal of the College of Physicians and Surgeons Pakistan 2013; 23: 653-656
54705 A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1Reis LM; Tyler RC; Zori R; Burgess J; Mueller J; Semina EV
Ophthalmic Genetics 2015; 36: 92-94
54699 Surgical management of malignant glaucoma with white cataract in nanophthalmosFeng YF; Wang DD; Zhao YE; Li JH; Savini G; Huang JH
Journal of Cataract and Refractive Surgery 2013; 39: 1774-1777