Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey. - Wikidata - awgldk - TriplyDB

Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

http://www.wikidata.org/entity/Q31061094

about

Paediatric Fabry disease Pediatric cataract: challenges and future directions Cornea verticillata caused by Fabry disease Effects of enzyme replacement therapy in adult patients with Fabry disease on cardiac structure and function: a retrospective cohort study of the Fabry Munster Study (FaMuS) data Fabry disease and the skin: data from FOS, the Fabry outcome survey.Update on role of agalsidase alfa in management of Fabry disease.Ocular signs correlate well with disease severity and genotype in Fabry disease.Defects in the retina of Niemann-pick type C 1 mutant mice.Paediatric Fabry disease: prognostic significance of ocular changes for disease severity.Fabry disease-often seen, rarely diagnosed.Vision loss in juvenile neuronal ceroid lipofuscinosis (CLN3 disease)Vascular tortuosities of the upper eyelid: a new clinical finding in fabry patient screening.Beyond the cherry-red spot: Ocular manifestations of sphingolipid-mediated neurodegenerative and inflammatory disorders.A novel mutation and in vivo confocal microscopic findings in Fabry disease.Fabry disease: a review of current management strategies.Cornea verticillata supports a diagnosis of Fabry disease in non-classical phenotypes: results from the Dutch cohort and a systematic review.Lysosomal delivery of therapeutic enzymes in cell models of Fabry disease.Computer assisted evaluation of retinal vessels tortuosity in Fabry disease.Ophthalmic experience over 10 years in an observational nationwide Danish cohort of Fabry patients with access to enzyme replacement.Eye features in three Danish patients with multisystemic smooth muscle dysfunction syndrome.Subclinical optic neuropathy in Fabry disease.Multidimensional analysis of clinical symptoms in patients with Fabry's disease.Diagnostic dilemma and delay in Fabry disease: insights from a case series of young female patients.Cilioretinal artery occlusion and anterior ischemic optic neuropathy as the initial presentation in a child female carrier of Fabry disease.Vascular tortuosity: a mathematical modeling perspective.In Vivo Confocal Microscopic Observations of Vortex Keratopathy in Patients with Amiodarone-Induced Keratopathy and Fabry Disease.Fabry disease Corneal confocal microscopy detects corneal nerve damage and increased dendritic cells in Fabry disease

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P2860

Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

http://www.wikidata.org/entity/Q31061094

description

2006 nî lūn-bûn

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2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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BJO.2006.100602

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British Journal of Ophthalmology

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Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

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P2093

Alexander S Ioannidis

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Andrea Sodi

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Atul Mehta

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Clare Davey

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Michael Beck

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Suzanne Pitz

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P2860

Vascular complications of Fabry disease: enzyme replacement and other therapies

Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey

Genotype and phenotype in Fabry disease: analysis of the Fabry Outcome Survey

Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey.

Corneal ultrastructural changes in Fabry's disease.

Prevalence of lysosomal storage disorders.

Advances in the management of Anderson-Fabry disease: enzyme replacement therapy.

The expanding clinical spectrum of Anderson-Fabry disease: a challenge to diagnosis in the novel era of enzyme replacement therapy.

[Fabry's disease (alpha-galactosidase-A deficiency): recent therapeutic innovations].

The ocular manifestations in Fabry's disease.

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210-214

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