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9.1.1 Congenital glaucoma, Buphthalmos (61)
Showing records 1 to 25
Display all abstracts in classification 9.1.1 Congenital glaucoma, Buphthalmos
Search within classification 9.1.1 Congenital glaucoma, Buphthalmos72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Yang Y
Genetic testing and molecular biomarkers 2017; 21: 252-258
72856 Long-term outcomes after cataract surgery in infants with congenital cataract
Qi JY
Chinese Journal of Ophthalmology 2017; 53: 266-273
72836 LADD syndrome with glaucoma is caused by a novel gene
Simpson A
Molecular Vision 2017; 23: 179-184
72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Firasat S
International Ophthalmology 2018; 38: 807-814
72951 Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma
García-Antón MT
PLoS ONE 2017; 12: e0176386
73161 Primary Congenital and Developmental Glaucomas
Lewis C
Human Molecular Genetics 2017; 26: R28-R36
72899 Long-term visual outcomes in children with primary congenital glaucoma
Yassin SA
European Journal of Ophthalmology 2017; 0: 0
72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Ferre-Fernández JJ
Scientific reports 2017; 7: 46175
72734 Epiblepharon in congenital glaucoma: case-control study
Kim N
British Journal of Ophthalmology 2017; 101: 1654-1657
72595 Two-year results of microcatheter-assisted trabeculotomy in paediatric glaucoma: a randomized controlled study
El Sayed Y
Acta Ophthalmologica 2017; 95: e713-e719
72717 Visual outcomes and complications of cataract surgery with primary implantation in infants
Vera L
Journal Français d'Ophtalmologie 2017; 40: 386-393
72836 LADD syndrome with glaucoma is caused by a novel gene
Avdic A
Molecular Vision 2017; 23: 179-184
73161 Primary Congenital and Developmental Glaucomas
Hedberg-Buenz A
Human Molecular Genetics 2017; 26: R28-R36
72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Aroca-Aguilar JD
Scientific reports 2017; 7: 46175
72951 Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma
Salazar JJ
PLoS ONE 2017; 12: e0176386
72734 Epiblepharon in congenital glaucoma: case-control study
Yoo YJ
British Journal of Ophthalmology 2017; 101: 1654-1657
72595 Two-year results of microcatheter-assisted trabeculotomy in paediatric glaucoma: a randomized controlled study
Gawdat G
Acta Ophthalmologica 2017; 95: e713-e719
72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Kaul H
International Ophthalmology 2018; 38: 807-814
72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Zhang L
Genetic testing and molecular biomarkers 2017; 21: 252-258
72856 Long-term outcomes after cataract surgery in infants with congenital cataract
Xiao W
Chinese Journal of Ophthalmology 2017; 53: 266-273
72717 Visual outcomes and complications of cataract surgery with primary implantation in infants
Lambert N
Journal Français d'Ophtalmologie 2017; 40: 386-393
72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Medina-Trillo C
Scientific reports 2017; 7: 46175
72856 Long-term outcomes after cataract surgery in infants with congenital cataract
Wang MY
Chinese Journal of Ophthalmology 2017; 53: 266-273
72734 Epiblepharon in congenital glaucoma: case-control study
Choung HK
British Journal of Ophthalmology 2017; 101: 1654-1657
72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Li S
Genetic testing and molecular biomarkers 2017; 21: 252-258
