Results 151 to 160 of about 1,176,555 (172)
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1972
We now proceed to a systematic study of cones — sets of a special type which will play an important role in the sequel.
Igor Vladimirovich Girsanov +1 more
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We now proceed to a systematic study of cones — sets of a special type which will play an important role in the sequel.
Igor Vladimirovich Girsanov +1 more
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2019
Retinal imaging has advanced to enable noninvasive in vivo visualization of macular photoreceptors with cellular resolution. Images of retinal structure are best interpreted in the context of visual function, but clinical measures of visual function lack resolution on the scale of individual cells.
Jacque L, Duncan, Austin, Roorda
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Retinal imaging has advanced to enable noninvasive in vivo visualization of macular photoreceptors with cellular resolution. Images of retinal structure are best interpreted in the context of visual function, but clinical measures of visual function lack resolution on the scale of individual cells.
Jacque L, Duncan, Austin, Roorda
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Are ‘Partial Cones’ Aberrated Cones?
AIP Conference Proceedings, 2008‘Partial cones’ are classified as pulsars where the steepest gradient (SG) of the polarization‐position angle (PPA) traverse lies towards one edge of the pulse profile. Here we present single pulse polarimetric observations of various ‘partial cones’ observed with the Giant Meterwave Radio Telescope (GMRT) and the Arecibo Observatory(AO).
Dipanjan Mitra +6 more
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Geological Magazine, 1885
In the June Number of the Geological Magazine an abstract is given of a paper on Cone-in-cone, read by Mr. John Young before the Geological Society of Glasgow, in which he advances the theory that this peculiar structure is caused by the escape of gases.
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In the June Number of the Geological Magazine an abstract is given of a paper on Cone-in-cone, read by Mr. John Young before the Geological Society of Glasgow, in which he advances the theory that this peculiar structure is caused by the escape of gases.
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Maintaining Cone Function in Rod-Cone Dystrophies
2018Retinal degenerative diseases are a major cause of untreatable blindness due to a loss of photoreceptors. Recent advances in genetics and gene therapy for inherited retinal dystrophies (IRDs) showed that therapeutic gene transfer holds a great promise for vision restoration in people with currently incurable blinding diseases.
José-Alain, Sahel, Thierry, Léveillard
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Standing cones and lying cones
Rheologica Acta, 1971It can be demonstrated in reconstructive surgery when using a fusiform excision that as the ratio of its lengthL to widthW is increased, the probability of a satisfactory closure is also increased. It is found that there is a minimum value ofL/W for a given area of skin beyond which small “standing cones” appear at the ends of the excision on closure ...
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Cone Dysfunction Syndromes, Cone Dystrophies, and Cone-Rod Degenerations
Abstract Predominant abnormalities of cone photoreceptor function are present in retinal disorders previously classified under several headings such as cone dystrophies (COD), cone-rod dystrophies (CORD), complete and incomplete achromatopsia, Stargardt disease, and a number of inherited systemic diseases with retinal degeneration.Sarah Hull, Elias I. Traboulsi
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Cone Dysfunction Syndromes, Cone Dystrophies, and Cone-Rod Degenerations
2012Abstract Predominant abnormalities of cone photoreceptor function are present in retinal disorders previously classified under a number of headings, such as cone dystrophies, cone-rod degenerations, color blindness, complete and incomplete achromatopsia, some types of retinitis pigmentosa, Stargardt disease, and many inherited systemic ...
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2014
The cone and cone–rod dystrophies are a heterogeneous group of disorders, both in terms of clinical features and underlying genetic basis, that are a major cause of childhood blindness and arguably the most devastating of inherited retinal conditions due to the loss of central vision at an early stage.
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The cone and cone–rod dystrophies are a heterogeneous group of disorders, both in terms of clinical features and underlying genetic basis, that are a major cause of childhood blindness and arguably the most devastating of inherited retinal conditions due to the loss of central vision at an early stage.
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