贪污
发表于 2025-3-21 16:49:28
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机密
发表于 2025-3-22 00:10:08
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optional
发表于 2025-3-22 01:33:28
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Irrepressible
发表于 2025-3-22 07:36:53
Dark AdaptationThis test is no more frequently used as it is time-consuming and not always easy to realize. Also the diagnostic information it provides is more easily obtained with electroretinography. Dark adaptation however has a theoretical importance to assess the quality of night vision.
PAGAN
发表于 2025-3-22 11:14:54
Retinitis Pigmentosa and Allied DisordersThere are more than 250 entries with the term retinitis pigmentosa in OMIM. More than half of them describe a systemic disease associated with retinal dystrophy, whether central, peripheral or mixed.
密码
发表于 2025-3-22 14:57:53
Enhanced S-Cone SyndromeEnhanced S-cone syndrome (ESCS) is a rare autosomally recessively inherited disorder usually characterised by nummular pigmentary deposition in the region of the vascular arcades at the level of the RPE. The disorder was first so described in 1990.
拥挤前
发表于 2025-3-22 18:33:16
https://doi.org/10.1007/978-3-540-69466-3Fluorescein Angiography; Genetics; Ophthalmoscopy; Retinal dystrophies; Visual functions
放肆的你
发表于 2025-3-22 23:07:16
Late-Onset Retinal Dystrophy (LORD)e fundus. This progresses to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy. It was first recognised in the mid-1990s and is usually consequent upon mutation in ., but some patients have been reported who lack mutation in that gene.
出生
发表于 2025-3-23 02:46:01
Stargardt Diseasen OMIM other diseases are identified under the name Stargardt disease (60010, 603786, 612948). These have a phenotype that resembles Stargardt disease but differ genetically and clinically. They should be named Stargardt-like disorders and will be considered separately.
exquisite
发表于 2025-3-23 08:06:01
sents up-to-date information on their genetic basis.Written This lavishly illustrated atlas provides indispensable information to clinicians, geneticists and visual scientists working with inherited retinal diseases. It is filled with high-quality images, up-to-date genetic information and comprehen