標(biāo)題: Titlebook: Atlas of Inherited Retinal Diseases; Stephen H. Tsang,Tarun Sharma Book 2018 Springer International Publishing AG, part of Springer Nature [打印本頁] 作者: 烈酒 時(shí)間: 2025-3-21 17:52
書目名稱Atlas of Inherited Retinal Diseases影響因子(影響力)
書目名稱Atlas of Inherited Retinal Diseases影響因子(影響力)學(xué)科排名
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書目名稱Atlas of Inherited Retinal Diseases網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Atlas of Inherited Retinal Diseases被引頻次
書目名稱Atlas of Inherited Retinal Diseases被引頻次學(xué)科排名
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書目名稱Atlas of Inherited Retinal Diseases年度引用學(xué)科排名
書目名稱Atlas of Inherited Retinal Diseases讀者反饋
書目名稱Atlas of Inherited Retinal Diseases讀者反饋學(xué)科排名
作者: 無瑕疵 時(shí)間: 2025-3-21 20:31 作者: 火車車輪 時(shí)間: 2025-3-22 03:16
https://doi.org/10.1007/978-3-658-07382-4en accompanied by day blindness (hemeralopia) and light intolerance (photophobia). Over time, affected individuals develop night blindness and loss of peripheral field. Visual acuity deteriorates to 20/200 or even counting fingers. There is some association between X-linked cone-rod dystrophy (CORD) and high myopia.作者: 積習(xí)已深 時(shí)間: 2025-3-22 05:14 作者: opportune 時(shí)間: 2025-3-22 10:28 作者: ordain 時(shí)間: 2025-3-22 15:12 作者: Apogee 時(shí)間: 2025-3-22 19:10 作者: Estrogen 時(shí)間: 2025-3-23 00:04 作者: 惰性氣體 時(shí)間: 2025-3-23 01:46 作者: TOXIC 時(shí)間: 2025-3-23 06:09
Optical Coherence Tomography the early 2000s. The introduction of spectral-domain OCT in the mid-2000s and the later introduction of swept-source OCT provided faster scanning strategies and high-resolution images of the retina and choroid.作者: 征稅 時(shí)間: 2025-3-23 11:56
Electroretinographyctrode (a contact lens in contact with bulbar conjunctiva) and a reference electrode (at the outer canthus); the active electrode can also be a gold foil electrode or HK-loop electrode. There are three types of ERG: the full-field (Ganzfeld) ERG, the multifocal ERG, and the pattern ERG.作者: 生命層 時(shí)間: 2025-3-23 16:37 作者: Terrace 時(shí)間: 2025-3-23 21:34
X-linked Juvenile Retinoschisisually school-age and are experiencing visual disturbances, especially in reading. The prevalence is estimated to be 1 in 5000–25,000 men, worldwide. XLRS has complete penetrance but variable expressivity. Carrier females generally remain asymptomatic.作者: MURKY 時(shí)間: 2025-3-24 01:30 作者: 說明 時(shí)間: 2025-3-24 05:25 作者: arousal 時(shí)間: 2025-3-24 10:27 作者: 缺乏 時(shí)間: 2025-3-24 11:57 作者: 情節(jié)劇 時(shí)間: 2025-3-24 18:53
Optical Coherence Tomography the early 2000s. The introduction of spectral-domain OCT in the mid-2000s and the later introduction of swept-source OCT provided faster scanning strategies and high-resolution images of the retina and choroid.作者: 現(xiàn)存 時(shí)間: 2025-3-24 22:25
Electroretinographyctrode (a contact lens in contact with bulbar conjunctiva) and a reference electrode (at the outer canthus); the active electrode can also be a gold foil electrode or HK-loop electrode. There are three types of ERG: the full-field (Ganzfeld) ERG, the multifocal ERG, and the pattern ERG.作者: 不感興趣 時(shí)間: 2025-3-24 23:34 作者: archenemy 時(shí)間: 2025-3-25 03:25 作者: 煩憂 時(shí)間: 2025-3-25 11:01 作者: conscribe 時(shí)間: 2025-3-25 14:20 作者: Immunoglobulin 時(shí)間: 2025-3-25 17:16
Bedarf an Frühen Hilfen: Epidemiologie the early 2000s. The introduction of spectral-domain OCT in the mid-2000s and the later introduction of swept-source OCT provided faster scanning strategies and high-resolution images of the retina and choroid.作者: Accord 時(shí)間: 2025-3-25 22:45 作者: 減至最低 時(shí)間: 2025-3-26 02:51 作者: 奴才 時(shí)間: 2025-3-26 06:40
Kerstin Scholtes,Marisa Benz,Hortense Demantually school-age and are experiencing visual disturbances, especially in reading. The prevalence is estimated to be 1 in 5000–25,000 men, worldwide. XLRS has complete penetrance but variable expressivity. Carrier females generally remain asymptomatic.作者: 傻瓜 時(shí)間: 2025-3-26 11:10 作者: Bumptious 時(shí)間: 2025-3-26 15:45
https://doi.org/10.1007/978-3-658-07382-4n 30,000–40,000 individuals. Patients usually present with decreased central vision and a color vision deficit; the visual loss is progressive and often accompanied by day blindness (hemeralopia) and light intolerance (photophobia). Over time, affected individuals develop night blindness and loss of作者: Cosmopolitan 時(shí)間: 2025-3-26 17:31
https://doi.org/10.1007/978-3-662-49262-8The wall of the eye consists of three layers: the sclera (the outermost layer), the choroid (the middle layer), and the retina (the innermost layer).作者: inflame 時(shí)間: 2025-3-27 00:30
https://doi.org/10.1007/978-3-662-49262-8Fundus autofluorescence (FAF) imaging is a rapid and noninvasive technique to evaluate retinal pigment epithelial (RPE) function. The predominant source of FAF in the macula is lipofuscin granules.作者: 減少 時(shí)間: 2025-3-27 03:02
Konzept der Frühen Hilfen im WandelThe electrooculogram (EOG) assesses the function of the retinal pigment epithelium (RPE), and also the interaction between the RPE and photoreceptors. This is done by noting the changes in the corneoretinal standing potential (the difference between the retina and electropositive cornea) during the dark-adapted and light-adapted states.作者: 新星 時(shí)間: 2025-3-27 06:58
Fütterst?rungen in der frühen KindheitX-linked retinitis pigmentosa (XLRP) is considered to be one of the most severe forms of retinitis pigmentosa (RP). It accounts for about 6–20% of all RP cases, including about 10% in the United States and 25% in England.作者: Compassionate 時(shí)間: 2025-3-27 12:15
Zur Diagnostik der Regulationsst?rungenChoroideremia (CHM) is the most common X-linked hereditary choroidal dystrophy, characterized by progressive degeneration of the choriocapillaris, retinal pigment epithelium (RPE), and retina. Its prevalence is about 1 in 50,000–100,000 people.作者: Classify 時(shí)間: 2025-3-27 16:13
https://doi.org/10.1007/978-3-658-44386-3Unlike rod monochromatism, which is an autosomal recessive disease that affects all three types of cones, blue cone monochromatism (BCM) is an X-linked disease that affects only L-cones and M-cones. The rods and S-cones are normal. The estimated prevalence is 1 in 100,00 individuals.作者: Flatus 時(shí)間: 2025-3-27 19:00 作者: amplitude 時(shí)間: 2025-3-27 23:54
https://doi.org/10.1007/978-3-662-65238-1Best vitelliform macular dystrophy (VMD or BVMD) is one of the most common macular dystrophies, affecting 1 in 10,000 individuals. The clinical presentation varies, depending on the stage of the disease at which the patient presents, usually one of these five stages:作者: Alopecia-Areata 時(shí)間: 2025-3-28 02:30 作者: Indict 時(shí)間: 2025-3-28 08:53 作者: Subdue 時(shí)間: 2025-3-28 11:26 作者: Monotonous 時(shí)間: 2025-3-28 18:13 作者: 高度贊揚(yáng) 時(shí)間: 2025-3-28 18:47
X-linked ChoroideremiaChoroideremia (CHM) is the most common X-linked hereditary choroidal dystrophy, characterized by progressive degeneration of the choriocapillaris, retinal pigment epithelium (RPE), and retina. Its prevalence is about 1 in 50,000–100,000 people.作者: FLASK 時(shí)間: 2025-3-29 00:23
Blue Cone MonochromatismUnlike rod monochromatism, which is an autosomal recessive disease that affects all three types of cones, blue cone monochromatism (BCM) is an X-linked disease that affects only L-cones and M-cones. The rods and S-cones are normal. The estimated prevalence is 1 in 100,00 individuals.作者: STELL 時(shí)間: 2025-3-29 06:33
Autosomal Dominant Retinitis PigmentosaMore than 70 genes (over 3000 mutations) are known to cause non-syndromic retinitis pigmentosa (RP), including autosomal dominant (AD), autosomal recessive (AR), X-linked, and simplex forms (inheritance not known). The AD form accounts for approximately 15–25% of cases; AR, 5–20%; X-linked, 5–15%; and simplex, 40–50%.作者: FLAG 時(shí)間: 2025-3-29 07:21
Best Vitelliform Macular DystrophyBest vitelliform macular dystrophy (VMD or BVMD) is one of the most common macular dystrophies, affecting 1 in 10,000 individuals. The clinical presentation varies, depending on the stage of the disease at which the patient presents, usually one of these five stages:作者: Alcove 時(shí)間: 2025-3-29 13:49
https://doi.org/10.1007/978-3-319-95046-4inherited retinal disease; genetic eye disorder; molecular genetics; genome testing; exon sequencing; gen作者: Measured 時(shí)間: 2025-3-29 16:08 作者: 字謎游戲 時(shí)間: 2025-3-29 23:34
Atlas of Inherited Retinal Diseases978-3-319-95046-4Series ISSN 0065-2598 Series E-ISSN 2214-8019 作者: 壓艙物 時(shí)間: 2025-3-30 02:33
Bedarf an Frühen Hilfen: Epidemiologie the early 2000s. The introduction of spectral-domain OCT in the mid-2000s and the later introduction of swept-source OCT provided faster scanning strategies and high-resolution images of the retina and choroid.作者: 乞丐 時(shí)間: 2025-3-30 06:36 作者: 憎惡 時(shí)間: 2025-3-30 10:25
Bedarf an Frühen Hilfen: Epidemiologiehumans, with size varying from a few hundred DNA bases to more than 2 million bases. Most genes are the same in all people; less than 1% differ. Each person has two copies of each gene, one inherited from each parent. Each chromosome contains many genes.作者: carotenoids 時(shí)間: 2025-3-30 15:27 作者: essential-fats 時(shí)間: 2025-3-30 17:59
Carolin Demuth,Marina Root,Sarah Gerwingtients usually present with reduced vision, photophobia, nystagmus, and strabismus. Many patients have problem in perceiving depth (stereoscopic vision). The visual loss is permanent, but XLOA is a nonprogressive disorder and visual acuity remains stable throughout life.作者: foppish 時(shí)間: 2025-3-30 22:53
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