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American Journal of Ophthalmology|February 1, 1996
Cobalt-60 treatment of choroidal hemangiomasL Zografos, L Bercher, L Chamot, et al.The Journal of Cardiovascular Surgery|September 6, 2006
Clinical results of autologous infrainguinal revascularization using grafts originating distal to the femoral bifurcation in patients with mild inflow diseaseH Probst, F Saucy, M Dusmet, et al.Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies]E Millá, E Héon, B Piguet, et al.Ophthalmology|November 1, 1992
Natural history of diffuse uveal melanocytic proliferation. Case reportF X Borruat, P Othenin-Girard, S Uffer, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|January 1, 1991
Neuron-associated class III beta-tubulin isotype, microtubule-associated protein 2, and synaptophysin in human retinoblastomas in situ. Further immunohistochemical observations on the Flexner-Wintersteiner rosettesC D Katsetos, M M Herman, A Frankfurter, et al.European Radiology|April 21, 2005
Posttraumatic pseudolipoma: MRI appearancesN Theumann, A Abdelmoumene, M Wintermark, et al.Ophthalmic Paediatrics and Genetics|June 1, 1989
Constitutional karyotype in retinoblastoma. Case report and review of literatureF Munier, G Pescia, M Jotterand-Bellomo, et al.Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.Klinische Monatsblatter Fur Augenheilkunde|March 24, 2005
[Optical coherence tomography in Malattia Leventinese]M-C Gaillard, T J Wolfensberger, S Uffer, et al.Pageof 12