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9.1.1 Congenital glaucoma, Buphthalmos (9)
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Display all abstracts in classification 9.1.1 Congenital glaucoma, Buphthalmos
Search within classification 9.1.1 Congenital glaucoma, Buphthalmos49128 Magnitude and Causes of Low Vision Disability (Moderate and Severe Visual Impairment) among Students of Al-Noor Institute for the Blind in Al-Hassa, Saudi Arabia: A case series
Al-Wadani F; Khandekar R; Al-Hussain MA; Alkhawaja AA; Khan MS; Alsulaiman RA
Sultan Qaboos University Medical Journal 2012; 12: 62-68
49165 Retinal intrinsic optical signals in a cat model of primary congenital glaucoma
Schallek JB; McLellan GJ; Viswanathan S; Ts',o DY
Investigative Ophthalmology and Visual Science 2012; 53: 1971-1981
48522 Renal lymphangiomatosis, interrupted IVC with persistent primitive hepatic venous plexus and multiple anomalous venous channels: parts of an overlap syndrome?
Watson T; Martinez E; Crabbe D; Chetcuti P; Kraft JK
Pediatric Radiology 2012; 42: 253-256
48821 Peripheral retinal vascular abnormalities in primary infantile glaucoma
Shane TS; Berrocal AM; Hodapp EA; Grajewski AL; Hess DJ
Ophthalmic Surgery Lasers and Imaging 2011; 42: e144-146
48750 Uveal melanoma in a 19-month-old child
Grabowska A; Abelarias J; Peralta J; Asencio M; Garcí,a-Cabezas MÁ,; Escabias-Del Pozo C; Nevado J; Vallespin E; Solera J; Pilar PM; Sastre-Urgellé,s A
Journal of AAPOS 2011; 15: 606-608
49319 Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma
Mao M; Solivan-Timpe F; Roos BR; Mullins RF; Oetting TA; Kwon YH; Brzeskiewicz PM; Stone EM; Alward WL; Anderson MG; Fingert JH
Molecular Vision 2012; 18: 705-713
48866 Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucoma
Lee JH; Ki CS; Kim HJ; Suh W; Lee ST; Kim JW; Kee C
Molecular Vision 2011; 17: 3583-3590
48681 Glaucoma-related adverse events in the Infant Aphakia Treatment Study: 1-year results
Beck AD; Freedman SF; Lynn MJ; Bothun E; Neely DE; Lambert SR;
Archives of Ophthalmology 2012; 130: 300-305
49266 Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient
Burglen L; Chantot-Bastaraud S; Garel C; Milh M; Touraine R; Zanni G; Petit F; Afenjar A; Goizet C; Barresi S; Coussement A; Ioos C; Lazaro L; Joriot S; Desguerre I; Lacombe D; des Portes V; Bertini E; Siffroi JP; Billette de Villemeur T; Rodriguez D
Orphanet Journal of Rare Diseases 2012; 7: 18
