From Transverse Myelitis to Optic Atrophy: An Unfavorable Clinical Course of AQP4-Positive Neuromyelitis Optica With Onset During Pregnancy and Multiple Relapses. [PDF]
Zuluaga Gómez LV, Messu Llano CD.
europepmc +1 more source
From Lab to Landscape: Environmental Biohybrid Robotics for Ecological Futures
This Perspective explores environmental biohybrid robotics, integrating living tissues, microorganisms, and insects for operation in real‐world ecosystems. It traces the leap from laboratory experiments to forests, wetlands, and urban environments and discusses key challenges, development pathways, and opportunities for ecological monitoring and ...
Miriam Filippi
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Correlation between quality of vision and clinical and structural parameters in patients with Autosomal Dominant Optic Atrophy. [PDF]
Camós-Carreras A +5 more
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OPA1 mutations in dominant optic atrophy: domain-specific defects in mitochondrial fusion and apoptotic regulation. [PDF]
Zhang K +7 more
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Predictive factors for visual prognosis in neurosyphilis presenting with optic atrophy: a Chinese case series study. [PDF]
Zhu M, Gu X, Zhou P, Yan Y.
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Novel in vivo models of autosomal optic atrophy reveal conserved pathological changes in neuronal mitochondrial structure and function. [PDF]
Strachan EL +9 more
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A bibliometric analysis of optic atrophy from 2003 to 2023: research trends and hot spots. [PDF]
Wang L +7 more
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Case Report: A <i>de novo</i> NR2F1 mutation and clinical characteristics of Bosch-Boonstra-Schaaf optic atrophy syndrome in a Chinese patient. [PDF]
Tang S +5 more
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Optic atrophy is a clinical term used to describe an optic disc thought to be paler than normal. Optic atrophy is not a diagnosis but an ophthalmoscopic sign. Evidence of visual loss (acuity, color vision, peripheral vision) should be present.
Karl Golnik
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An attempt has been made to determine the significance and outcome of optic atrophy as an apparently isolated entity in the pediatric age group. A follow-up study was made of 48 children who presented in early childhood with optic atrophy with no known cause and no obvious systemic or neurological disease. It was found that the prognosis
J F, SCHWARTZ +3 more
exaly +3 more sources

