Disease: Maumenee syndrome
- 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
- 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: 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
- Ultrastructural ocular pathology of Hunter's syndrome. Systemic mucopolysaccharidosis type II
- 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