Sturge-Weber Syndrome With Congenital Glaucoma and Cytochrome P450 (CYP1B1) Gene Mutations-Reference-Cited by-同舟云学术

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Sturge-Weber Syndrome With Congenital Glaucoma and Cytochrome P450 (CYP1B1) Gene Mutations

Published:2010-08 Issue:6 Volume:19 Page:398-404
ISSN:1057-0829
Container-title:Journal of Glaucoma
language:en
Short-container-title:

Author:

Tanwar Mukesh,Sihota Ramanjit,Dada Tanuj,Gupta Vinay,Das Taposh K.,Yadav Usha,Dada Rima

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Reference38 articles.

1. Ein fall von teleangiektasie an account of telangiectasia. Graefes;Schirmer;Arch Ophthalmol,1860

2. A case of partial epilepsy apparently due to a lesion of one of the vasomotor centres of the brain;Sturge;Trans Clin Soc Land,1879

3. Sturge-Weber syndrome revisited: the role of neuroradiology;Griffiths;Neuropediatrics,1996

4. Hydrophthalmia or Congrnital glaucoma;Anderson,1939

5. The Sturge-Weber Syndrome;Alexander,1960

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ophthalmic genetics practice and research in India: Vision in 2020;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2020-08-31

2. Bilateral diffuse choroidal hemangioma in Sturge Weber syndrome: A case report highlighting the role of multimodal imaging and a brief review of the literature;Journal of Current Ophthalmology;2019-06

3. Glaucoma in Patients with Eyes Close to Areas Affected by Port-wine Stain has Lateral and Gender Predilection;Chinese Medical Journal;2017-12-20

4. Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis);Asia-Pacific Journal of Ophthalmology;2014

5. A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation inCYP1B1;Ophthalmic Genetics;2013-09-11

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