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9.1.1 Congenital glaucoma, Buphthalmos (102)
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68966 Diagnosis of pupillary block glaucoma after removal of congenital cataracts with intraoperative ultrasound biomicroscopy: a case reportZhu XJ
BMC Ophthalmology 2016; 16: 58
69250 Fiberoptic Microcatheter-assisted 360-Degree Trabeculotomy Ab Externo After Unsuccessful Trabeculotome Trabeculotomy in Primary Congenital Glaucoma: A Case ReportD'Amelio S
Journal of Glaucoma 2016; 25: e753-e755
69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucomaChen X
Molecular Vision 2016; 22: 528-535
68862 Pediatric Glaucoma: Pharmacotherapeutic OptionsSamant M
Pediatric Drugs 2016; 18: 209-219
68905 An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)Dimitri P
American Journal of Medical Genetics, Part A 2016; 170: 1918-1923
68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)Kuehn MH
PLoS ONE 2016; 11: e0154412
68573 Mitochondrial transfer RNA variants and primary congenital glaucomaYi QY
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407
69069 Central Corneal Thickness in Aphakic Children With Microcornea-MicrophthalmiaBayoumi NH
Journal of Glaucoma 2016; 25: 497-500
69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomaliesReis LM
Clinical Genetics 2016; 90: 378-382
69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromesArunrut T
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718
69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These DiseasesBanerjee A
PLoS ONE 2016; 11: e0156252
69097 Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivitySouma T
Journal of Clinical Investigation 2016; 126: 2575-2587
69065 Acute Corneal Hydrops in Children with Primary Infantile Glaucoma: A Report of 31 Cases over 23 Years at the LVPEIMandal AK
PLoS ONE 2016; 11: e0156108
69012 The p.(Glu809Lys) mutation in the WFS1 gene is associated with the occurrence of the Wolfram-like syndrome-WFSL: a case reportProchazkova D
Journal of clinical research in pediatric endocrinology 2016; 8: 482-483
69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital GlaucomaMicheal S
PLoS ONE 2016; 11: e0159259
69083 Neurofibromatosis: an update of ophthalmic characteristics and applications of optical coherence tomographyAbdolrahimzadeh B
Clinical Ophthalmology 2016; 10: 851-860
69084 Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and managementMantelli F
Clinical Ophthalmology 2016; 10: 871-878
69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromesSabbadini M
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718
68573 Mitochondrial transfer RNA variants and primary congenital glaucomaDeng G
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407
69069 Central Corneal Thickness in Aphakic Children With Microcornea-MicrophthalmiaEl Shakankiri NM
Journal of Glaucoma 2016; 25: 497-500
69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomaliesTyler RC
Clinical Genetics 2016; 90: 378-382
68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)Lipsett KA
PLoS ONE 2016; 11: e0154412
69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucomaChen Y
Molecular Vision 2016; 22: 528-535
68905 An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)De Franco E
American Journal of Medical Genetics, Part A 2016; 170: 1918-1923
69084 Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and managementBruscolini A
Clinical Ophthalmology 2016; 10: 871-878
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