Recent Publications on Ectopia Lentis: |  |
Intraoperative performance and postoperative outcomes of endocapsular ring implantation in pediatric eyes.
PURPOSE: To study the intraoperative performance and postoperative...
Direct Link | 30th August, 2008
| From the John A. Moran Eye Center, University of Utah School of Medicine,
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The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.
Mutations in the fibrillin-1 (FBN1) gene have been identified in patients...
Direct Link | 12th August, 2008
| Department of Genetics, National Research Institute for Family Planning,
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Ehlers-Danlos syndromes and Marfan syndrome.
Ehlers-Danlos syndromes (EDS) and Marfan syndrome (MFS) are multisystemic...
Direct Link | 8th August, 2008
| Ghent University Hospital, Centre for Medical Genetics, De Pintelaan 185,
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| [Contact lens in children: epidemiological aspects]
| 22nd July, 2008
| Universidade Federal de Sao Paulo, Sao Paulo, SP, Brasil.
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| Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1.
| 11th July, 2008
| Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital
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The value of keratometry and central corneal thickness measurements in the clinical diagnosis of Marfan syndrome.
PURPOSE: To explore the utility of keratometry and central corneal...
Direct Link | 25th June, 2008
| Cole Eye Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH
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| Long-term results of lensectomy in children with ectopia lentis.
| 2nd May, 2008
| Department of Ophthalmology, Soonchunhyang University Cheonan Hospital,
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| Ectopia lentis in childhood.
| 2nd May, 2008
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Iris-sutured intraocular lenses for ectopia lentis in children.
PURPOSE: To compare outcomes and complications of pars plana...
Direct Link | 30th April, 2008
| Cullen Eye Institute, Baylor College of Medicine, 6565 Fannin, Houston, TX
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FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.
Fibrillin-1 gene (FBN1) mutations cause Marfan syndrome (MFS), an...
Direct Link | 26th April, 2008
| Department of Medical and Surgical Critical Care, Center of the Study at
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| [Transsclerally fixated intraocular artificial lenses in children--analysis of long-term postoperative complications]
| 2nd April, 2008
| Kliniki Okulistyki Instytutu Pomnik, Centrum Zdrowia Dziecka w Warszawie.
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Pathophysiology of zonular diseases.
PURPOSE OF REVIEW: The mechanisms implicated in the clinical...
Direct Link | 5th March, 2008
| Fondation Ophtalmologique Adolphe de Rothschild, Pediatric Ophthalmology
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Vascular and connective tissue features in 5 Italian patients with homocystinuria.
Homocystinuria is a metabolic disorder associated with defects in genes...
Direct Link | 19th February, 2008
| Department of Medical and Surgical Critical Care, University of Florence;
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| A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
| 30th January, 2008
| Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India.
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| Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? Need for a long-term follow-up.
| 19th January, 2008
| Department of Medical and Surgical Critical Care, University of Florence,
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