轻推
发表于 2025-3-23 10:58:38
Retinitis Pigmentosa,uch as a high-resolution spectral domain optical coherence tomography (OCT) revealed new aspects of RP . In RP patients, the vision-specific quality of life cannot be explained only by visual acuity or field, and both are related to the visual function .
cardiac-arrest
发表于 2025-3-23 16:45:00
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invert
发表于 2025-3-23 19:42:39
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焦虑
发表于 2025-3-23 23:34:22
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抛媚眼
发表于 2025-3-24 03:22:25
Molecular Genetics of Inherited Retinal Diseases, but also the development of new therapeutic alternatives. In this chapter, we review the molecular genetic characteristics and techniques of genetic analysis associated with IRDs. We also discuss the molecular biology of the common mutations causing IRDs.
outskirts
发表于 2025-3-24 08:03:46
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他去就结束
发表于 2025-3-24 13:43:03
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bioavailability
发表于 2025-3-24 15:02:19
Other Macular Dystrophies 2,na macular dystrophy, Doyne honeycomb retinal dystrophy, and Bietti’s crystalline dystrophy, in which gene variants have been identified as a cause of the disease. The purpose of this chapter is to provide an overview of these disorders.
sclera
发表于 2025-3-24 20:41:06
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granite
发表于 2025-3-25 00:46:36
Syndromic Retinitis Pigmentosa,thy. A multidisciplinary approach is needed because systemic manifestations are quite heterogenous. In this chapter, inherited syndromic disorders showing typical pigmentary retinopathy will be described. Syndromic RP in this chapter includes Usher syndrome, ciliopathy, inborn errors of metabolism, and mitochondrial disorders (Table 5.2).