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1
Hiperornitinemia con atrofia gyrata de coroides y retina
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2
Gyrate atrophy-like phenotype with normal plasma ornithine and low plasma taurine
Published 2020-02-01Subjects: “…gyrate atrophy…”
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3
Ornithine Aminotransferase, an Important Glutamate-Metabolizing Enzyme at the Crossroads of Multiple Metabolic Pathways
Published 2017-03-01Subjects: Get full text
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4
Staging and optical coherence tomography characteristics of gyrate atrophy of choroid and retina
Published 2021-01-01Subjects: “…gyrate atrophy…”
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5
A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy
Published 2024-03-01Subjects: “…gyrate atrophy mutation ornithine aminotransferase vitamin b6…”
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6
Multimodal imaging of foveoschisis and macular pseudohole associated with gyrate atrophy: a family report
Published 2018-04-01Subjects: “…Gyrate atrophy…”
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7
CRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophy
Published 2022-06-01Subjects: Get full text
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8
Partial regression of foveoschisis following vitamin B6 supplementary therapy for gyrate atrophy in a Chinese girl
Published 2021-02-01Subjects: “…Gyrate atrophy…”
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9
Double macular hole with gyrate atrophy: A long-term postoperative follow-up
Published 2022-01-01Subjects: Get full text
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10
Optical coherence tomography angiography of astrocytic hamartoma demonstrates intrinsic vascularity
Published 2020-12-01Subjects: Get full text
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11
Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina
Published 2021-07-01Subjects: “…gyrate atrophy…”
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12
Obscured interdigitation zone at the early stage of gyrate atrophy: A case report
Published 2022-03-01Subjects: “…Gyrate atrophy of retina and choroid…”
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13
Goldmann-Favre/Enhanced S Cone Syndrome, 30 years mysdiagnosed as gyrate atrophy
Published 2021-03-01Subjects: Get full text
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14
A neonate with ornithine aminotransferase deficiency; insights on the hyperammonemia-associated biochemical phenotype of gyrate atrophy
Published 2022-06-01Subjects: Get full text
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15
Clinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy
Published 2023-09-01Subjects: “…Gyrate atrophy…”
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16
The retarded hair growth (rhg) mutation in mice is an allele of ornithine aminotransferase (Oat)
Published 2014-01-01Subjects: Get full text
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17
Liver‐directed gene therapy for ornithine aminotransferase deficiency
Published 2023-01-01Subjects: Get full text
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18
Unilateral conjunctival ulcer due to Stenotrophomonas maltophilia infection
Published 2012-01-01Subjects: Get full text
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19
Floppy iris syndrome with oral imipramine: A case series
Published 2012-01-01Subjects: Get full text
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20
Fulminant toxoplasmic retinochoroiditis following intravitreal triamcinolone administration
Published 2012-01-01Subjects: Get full text
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