• A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome)
• A cutaneous marker in the Hunter syndrome a report of four cases
• Acute glaucoma in systemic mucopolysaccharidosis I-S
• Anterior segment malformations in 18q- (de Grouchy) syndrome
• Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome
• Autologous serum eye drops for dry eye
• Autologous serum eye drops for dry eye
• Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation
• Bardet-Biedl syndrome and related disorders
• Biometry Characteristics in Adults and Children With Marfan Syndrome: From the Marfan Eye Consortium of Chicago
• Birdshot retinochoroidopathy
• Birdshot Retinopathy
• Birdshot Retinopathy
• Bitemporal hemianopia caused by an intracranial vascular loop
• Cataract extraction and intraocular lens implantation in patients with retinitis pigmentosa or Usher's syndrome
• Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes
• Colobomatous macrophthalmia with microcornea
• Comparative data on SD-OCT for the retinal nerve fiber layer and retinal macular thickness in a large cohort with Marfan syndrome
• Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
• Confirmation of the colobomatous macrophthalmia with microcornea syndrome: report of another family
• Congenital cavitary optic disc anomaly and Axenfeld's anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature
• Congenital hypertrophy of the retinal pigment epithelium predicts colorectal polyposis in Gardner's syndrome
• CRIM1 haploinsufficiency causes defects in eye development in human and mouse
• Demonstration of exclusive cilioretinal vascular system supplying the retina in man: vacant discs
• Ectopia lentis
• Ehlers-Danlos syndrome
• Elevated episcleral venous pressure and its implications: A case of Radius-Maumenee syndrome
• Extraocular muscle aplasia in Moebius syndrome
• Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome
• Fibroglial proliferation in pars planitis
• Genetic and clinical heterogeneity of Stickler syndrome
• Glaucoma associated with Radius-Maumenee syndrome: A case report
• Glaucoma due to elevated episcleral venous pressure
• Glaucoma in the Marfan syndrome
• Hepatoblastoma, pigmented ocular fundus lesions and jaw lesions in Gardner syndrome
• Hereditary connective tissue diseases involving the eye
• Heterogeneity of retinal degeneration and hearing impairment syndromes
• Histopathology of Sanfilippo's syndrome
• Idiopathic dilated episcleral vessels (Radius-Maumenee syndrome): case report
• Idiopathic elevated episcleral venous pressure in a teenager
• Idiopathic episcleral venous stasis with secondary open-angle glaucoma (Radius-Maumenee syndrome)
• Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome
• Importance of proper diagnosis for management: multifocal choroiditis mimicking ocular histoplasmosis syndrome
• IQCB1 mutations in patients with leber congenital amaurosis
• Iris transillumination and variable expression in ectopia lentis et pupillae
• Keratinization of the conjunctiva
• Leber's congenital amaurosis. Retrospective review of 43 cases and a new fundus finding in two cases
• Management of Radius-Maumenee syndrome : Treatment with deep sclerectomy, viscocanalostomy and collagen matrix implantation
• Managing a rare case of familial Radius Maumenee syndrome
• Marfan syndrome
• Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis
• Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutation
• Ocular findings in Cockayne syndrome
• Ocular histopathology and ultrastructure of Morquio syndrome (systemic mucopolysaccharidosis IV A)
• Ocular histopathology of systemic mucopolysaccharidosis, type II-A (Hunter syndrome, severe)
• Ocular histoplasmosis: clinicopathologic correlation of 3 cases
• Ocular pathology of the Maroteaux-Lamy syndrome (systemic mucopolysaccharidosis type VI). Histologic and ultrastructural report of two cases
• Omega-3 and omega-6 polyunsaturated fatty acids for dry eye disease
• Optic atrophy and glaucomatous cupping
• Orthostatic intolerance and chronic fatigue syndrome associated with Ehlers-Danlos syndrome
• Periocular pigmentation in the Peutz-Jeghers syndrome
• Peters' anomaly and associated congenital malformations
• Photocoagulation of disciform macular lesions in the ocular histoplasmosis syndrome
• Pigmented ocular fundus lesions in the inherited gastrointestinal polyposis syndromes and in hereditary nonpolyposis colorectal cancer
• Possible origins of the gene of Hermansky-Pudlak in Puerto Rico
• Postoperative choroidal detachment despite normal intraocular pressure? A case of Radius-Maumenee syndrome
• Pressure-Lowering Effect of Interventional Fistula Occlusion in Secondary Glaucoma due to Orbital Draining Intracerebral Fistulae
• Publisher Correction: Marfan syndrome
• Radius-Maumenee syndrome-associated glaucoma, a therapeutic challenge: A case report
• Radius-Maumenee Syndrome, A Rare Entity: A Case Report
• Radius-Maumenee syndrome: A case series with a long-term follow-up
• Radius-Maumenee syndrome: a rare cause of glaucoma
• Radius-Maumenee syndrome: A rare cause of glaucoma
• Radius-Maumenee syndrome: Beyond a diagnostic and therapeutic challenge
• Re: Seckel's syndrome with pseudopolycoria
• Retinal Detachment in Down Syndrome: Characteristics and Surgical Outcomes
• Retinal detachment in Marfan syndrome
• Retinal Disease in Marfan Syndrome: From the Marfan Eye Consortium of Chicago
• Retrobulbar blood flow in idiopathic dilated episcleral veins and glaucoma
• Secondary open angle glaucoma with idiopathic episcleral venous pressure (Radius-Maumenee syndrome). Sinus-otomy as operative procedure of choice
• Sterile corneal melt after descemet stripping endothelial keratoplasty in patients with previously undiagnosed Sjogren syndrome
• Strabismus in the Marfan syndrome
• Study design and baseline findings from the progression of ocular findings (PROOF) natural history study of dry eye
• Surgical management of glaucoma secondary to idiopathic elevated episcleral venous pressure
• The cornea in connective tissue diseases
• The eye and the chromosome
• The eye in connective tissue diseases
• The eye in the Marfan syndrome
• The eye in the Marfan syndrome
• The Lenz microphthalmia syndrome
• The Marfan syndrome is caused by a point mutation in the fibrillin gene
• The ocular findings in Kniest dysplasia
• The Stickler syndrome is closely linked to COL2A1, the structural gene for type II collagen
• The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen
• The Wagner syndrome versus hereditary arthroophthalmopathy
• Topical retinoid treatment for various dry-eye disorders
• Uveitis in relation to connective tissue disease
• Venous Tortuosity in <em>COL4A2</em>-Associated Gould Syndrome
• Venous Tortuosity in COL4A2-Associated Gould Syndrome
• Vitreoretinal degeneration as a sign of generalized connective tissue diseases