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Vitréo-rétinopathie familiale exsudative de Criswick et Schepens : à propos de deux cas = Criswich and Schepens familial exsudative vitreoretinopathy: about two casesDELLAC, M; CASTIER, P; RYCKEWAERT, M et al.Bulletin des sociétés d'ophtalmologie de France. 1991, Vol 91, Num 1, pp 107-109, issn 0081-1270, 3 p.Article

The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533LI, Y; MÜLLER, B; FUHRMANN, C et al.American journal of human genetics. 1992, Vol 51, Num 4, pp 749-754, issn 0002-9297Article

Clinical Presentation of Familial Exudative VitreoretinopathyRANCHOD, Tushar M; HO, Lawrence Y; DRENSER, Kimberly A et al.Ophthalmology (Rochester, MN). 2011, Vol 118, Num 10, pp 2070-2075, issn 0161-6420, 6 p.Article

Le syndrome de Criswick-Schepens. Aspects cliniques et problèmes thérapeutiques = Criswick-Schepens syndrome. Clinical aspects and therapeutic considerationsCHACHIA, N; HARRABI, S; MIKATI, R et al.Ophtalmologie (Paris). 1994, Vol 8, Num 5, pp 470-474, issn 0989-3105Article

Signs, complications, and platelet aggregation in familial exudative vitreoretinopathyERIK VAN NOUHUYS, C.American journal of ophthalmology. 1991, Vol 111, Num 1, pp 34-41, issn 0002-9394, 8 p.Article

Clinical and Molecular Evaluation of Probands and Family Members with Familial Exudative VitreoretinopathyBOONSTRA, F. Nienke; VAN NOUHUYS, C. Erik; HOEFSLOOT, Lies H et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 9, pp 4379-4385, issn 0146-0404, 7 p.Article

Familial exudative vitreoretinopathy : surgical intervention and visual acuity outcomesSHUBERT, A; TASMAN, W.Graefe's archive for clinical and experimental ophthalmology. 1997, Vol 235, Num 8, pp 490-493, issn 0721-832XConference Paper

Novel Frizzled-4 Gene Mutations in Chinese Patients With Familial Exudative VitreoretinopathyJIA, Li-Yun; LI, Xiao-Xin; YU, Wen-Zhen et al.Archives of ophthalmology (1960). 2010, Vol 128, Num 10, pp 1341-1349, issn 0003-9950, 9 p.Article

Vitrectomy for rhegmatogenous or tractional retinal detachment with familial exudative vitreoretinopathyIKEDA, T; FUJIKADO, T; TANO, Y et al.Ophthalmology (Rochester, MN). 1999, Vol 106, Num 6, pp 1081-1085, issn 0161-6420Article

Electrophysiological findings in familial exudative vitreoretinopathyOHKUBO, H; TANINO, T.Documenta ophthalmologica. 1987, Vol 65, Num 4, pp 461-469, issn 0012-4486Article

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative VitreoretinopathyPOULTER, James A; ALI, Manir; PIERCE, Eric A et al.American journal of human genetics. 2010, Vol 86, Num 2, pp 248-253, issn 0002-9297, 6 p.Article

Improved surgical treatment of familial exudative vitreoretinopathy in childrenGLAZER, L. C; MAGUIRE, A; BLUMENKRANZ, M. S et al.American journal of ophthalmology. 1995, Vol 120, Num 4, pp 471-479, issn 0002-9394Article

The gene for autosomal dominant familial exudavie vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11YUN LI; FUHRMANN, C; SCHWINGER, E et al.American journal of ophthalmology. 1992, Vol 113, Num 6, pp 712-713, issn 0002-9394Article

Mutations in the TSPAN12 Gene in Japanese Patients with Familial Exudative VitreoretinopathyKONDO, Hiroyuki; KUSAKA, Shunji; YOSHINAGA, Aki et al.American journal of ophthalmology. 2011, Vol 151, Num 6, pp 1095-1100, issn 0002-9394, 6 p.Article

Juvenile retinal detachment as a complication of familial exudative vitreoretinopathyVAN NOUHUYS, C. E.Fortschritte der Ophthalmologie. 1989, Vol 86, Num 3, pp 221-223, issn 0723-8045Conference Paper

A model for familial exudative vitreoretinopathy caused by LPR5 mutationsXIA, Chun-Hong; HAIQUAN LIU; CHEUNG, Debra et al.Human molecular genetics (Print). 2008, Vol 17, Num 11, pp 1605-1612, issn 0964-6906, 8 p.Article

Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigreeBAMASHMUS, M. A; DOWNEY, L. M; INGLEHEARN, C. F et al.British journal of ophthalmology. 2000, Vol 84, Num 4, pp 358-363, issn 0007-1161Article

Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four familiesMÜLLER, B; ORTH, U; VAN NOUHUYS, C. E et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 2, pp 317-319, issn 0888-7543Article

Mapping studies of an X-linked familial exudative vitreoretinopathySHASTRY, B. S; TRESE, M. T.Biochemical and biophysical research communications (Print). 1993, Vol 193, Num 2, pp 599-603, issn 0006-291XArticle

Familial Exudative Vitreoretinopathy and DiGeorge Syndrome: A New Locus for Familial Exudative Vitreoretinopathy on Chromosome 22q11.2?GILMOUR, David F; DOWNEY, Louise M; SHERIDAN, Eamonn et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 8, pp 1522-1524, issn 0161-6420, 3 p.Article

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathyMINGHUI QIN; KONDO, Hiroyuki; TAHIRA, Tomoko et al.Human genetics. 2008, Vol 122, Num 6, pp 615-623, issn 0340-6717, 9 p.Article

Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigreeTOOMES, C; DOWNEY, L. M; BOTTOMLEY, H. M et al.British journal of ophthalmology. 2005, Vol 89, Num 2, pp 194-197, issn 0007-1161, 4 p.Article

Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivityKONDO, H; HAYASHI, H; OSHIMA, K et al.British journal of ophthalmology. 2003, Vol 87, Num 10, pp 1291-1295, issn 0007-1161, 5 p.Article

A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathyCHAMNEY, S; MCLOONE, E; WILLOUGHBY, C. E et al.Eye (London. 1987). 2011, Vol 25, Num 12, issn 0950-222X, p. 1658Article