Advanced coats-like retinopathy as the initial presentation of Familial Retinal Arterial Macroaneurysms
暂无分享,去创建一个
[1] F. He,et al. Familial , 2019, Definitions.
[2] E. Abboud,et al. Intravitreal triamcinolone in Coats' disease. , 2012, Ophthalmology.
[3] F. Alkuraya,et al. Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysms. , 2011, American journal of human genetics.
[4] M. Tsuji,et al. Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: A case study , 2009, Neuromuscular Disorders.
[5] C. Shields,et al. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child. , 2007, Archives of ophthalmology.
[6] E. Abboud,et al. FAMILIAL RETINAL ARTERIAL MACROANEURYSMS , 2002, Retina.
[7] C. Shields,et al. Classification and management of Coats disease: the 2000 Proctor Lecture. , 2001, American journal of ophthalmology.
[8] W. Stevenson,et al. Facioscapulohumeral muscular dystrophy: evidence for selective, genetic electrophysiologic cardiac involvement. , 1990, Journal of the American College of Cardiology.
[9] A. Bird,et al. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications. , 1987, Brain : a journal of neurology.
[10] M. Brooke,et al. Facioscapulohumeral dystrophy associated with hearing loss and coats syndrome , 1982, Annals of neurology.