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Combined cilioretinal artery and hemi-retinal vein occlusion in Sturge Weber syndrome: Expanding the clinical spectrum

机译：Ciltimetinal动脉和半视网膜静脉闭塞在鲟鱼综合征：扩大临床光谱

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Sawsan S. Bakri; Deema Jomar; Sulaiman M. Alsulaiman; Marwan A. Abouammoh;
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1. Combined cilioretinal artery and hemi-retinal vein occlusion in Sturge Weber syndrome: Expanding the clinical spectrum [J] . Sawsan S. Bakri, Deema Jomar, Sulaiman M. Alsulaiman, Saudi Journal of OphthalmologybElectronic resource . 2018,第3期

机译：Sturge Weber综合征合并睫状体视网膜动脉和半视网膜静脉阻塞：扩大临床范围
2. Postoperative cilioretinal artery occlusion in Sturge Weber-associated glaucoma. [J] . Chang L, Mruthyunjaya P, Rodriguez Rosa RE, Journal of AAPOS: The official publication of the American Association for Pediatric Ophthalmology and Strabismus . 2010,第4期

机译：斯特奇·韦伯相关性青光眼的术后睫状体视网膜动脉闭塞。
3. Cardiovascular risk factors in patients with combined central retinal vein occlusion and cilioretinal artery occlusion: Case report [J] . Grzybowski Andrzej, Elikowski Waldemar, Gaca-Wysocka Magdalena Medicine. . 2018,第1期

机译：联合中央视网膜静脉闭塞患者心血管危险因素及菌闭塞症：案例报告
4. Detection of RASA1 mutations in patients with sporadic Sturge-Weber syndrome [C] . Qin Zhou, Jia-wei Zheng, Xiu-juan Yang, Academic Committee Conference of Shanghai key lab of stomatology . 2011

机译：散发性Sturge-Weber综合征患者中RASA1突变的检测
5. A survey of human genetic variation reveals a basis for Sturge-Weber syndrome and non-syndromic port-wine stain. [D] . Shirley, Matthew D. 2013

机译：对人类遗传变异的调查揭示了Sturge-Weber综合征和非综合征性波特酒色斑的基础。
6. Combined cilioretinal artery and hemi-retinal vein occlusion in Sturge Weber syndrome: Expanding the clinical spectrum [O] . Sawsan S. Bakri, Deema Jomar, Sulaiman M. Alsulaiman, 2018

机译：Sturge Weber综合征合并睫状体视网膜动脉和半视网膜静脉阻塞：扩大临床范围
7. Cardiovascular risk factors in patients with combined central retinal vein occlusion and cilioretinal artery occlusion [O] . Andrzej Grzybowski, Waldemar Elikowski, Magdalena Gaca-Wysocka 2018

机译：中枢性视网膜静脉闭塞和CilioRetinal动脉闭塞患者心血管危险因素

Combined cilioretinal artery and hemi-retinal vein occlusion in Sturge Weber syndrome: Expanding the clinical spectrum

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