Gyrate Atrophy

Known as: HOGA, Gyrate Atrophy [Disease/Finding], GACR 
A rare autosomal recessive inherited disorder caused by mutations in the OAT gene. It is characterized by progressive atrophy of the retina and… (More)
National Institutes of Health

Papers overview

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2012
2012
PURPOSE To describe phenotypic variability and to report novel mutational data in patients with gyrate atrophy. DESIGN… (More)
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Review
2012
Review
2012
Astroglia possess excitability based on movements of Ca(2+) ions between intracellular compartments and plasmalemmal Ca(2… (More)
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Highly Cited
2006
Highly Cited
2006
Aim: Concentration of species occurrences in groups of classified sites can be quantified with statistical measures of fidelity… (More)
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Review
1998
Review
1998
Gyrate atrophy of the choroid and retina, which is often shortened to gyrate atrophy, is an inherited disorder characterized by… (More)
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Highly Cited
1981
Highly Cited
1981
Gyrate atrophy of the choroid and retina is a disease characterized by progressive constriction of visual fields, a 10-fold to 20… (More)
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1981
1981
Twenty-nine Finnish patients (8-80 years old during follow-up) with hyperornithinemia and gyrate atrophy (HOGA) were followed 2… (More)
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1978
1978
To establish the enzyme defect in gyrate atrophy, we measured the activity of ornithine aminotransferase in phytohemagglutinin… (More)
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1977
1977
Gyrate atrophy of the choroid and retina is an inherited form of chorioretinal degeneration associated with hyperornithinemia. We… (More)
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1975
1975
A case of gyrate atrophy of the choroid and retina and hyperornithinemia in a 28-year-old man was subjected to extensive clinical… (More)
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1974
1974
The inheritance of the autosomal recessive type of gyrate atrophy of the choroid and retina seems well documented (Botermans, I… (More)
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