[Coats Plus: Coats disease with systemic features].
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M. Labetoulle | A. Rousseau | C. Denier | G. Nasser | S. Cohen | S. Touhami | Y. Troumani | F. Ackermann
[1] Matthew W. Wilson,et al. Current management of Coats disease. , 2014, Survey of ophthalmology.
[2] A. Alexopoulou,et al. Bevacizumab in the treatment of hereditary hemorrhagic telangiectasia , 2013, Expert opinion on biological therapy.
[3] O. Mäkitie,et al. Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts. , 2012, American journal of human genetics.
[4] Jonathan E. Dickerson,et al. Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus , 2012, Nature Genetics.
[5] Y. Crow,et al. Treatment of Gastrointestinal Bleeding in a Probable Case of Cerebroretinal Microangiopathy with Calcifications and Cysts , 2010, Molecular Syndromology.
[6] E. Bertini,et al. Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) , 2008, American journal of medical genetics. Part A.
[7] A. Paetau,et al. Cerebroretinal microangiopathy with calcifications and cysts , 2006, Neurology.
[8] J. Tolmie,et al. Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument , 2004, Neuropediatrics.
[9] J. Tolmie,et al. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait. , 1988, Journal of medical genetics.