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Results: 1-17 |
Results: 17
Fundus-controlled function testing of the macula using scanning laser ophthalmoscopy
Authors: Rohrschneider, K Bultmann, S
Citation: K. Rohrschneider et S. Bultmann, Fundus-controlled function testing of the macula using scanning laser ophthalmoscopy, OPHTHALMOLO, 98(1), 2001, pp. 3-9
Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene
Authors: den Hollander, AI Heckenlively, JR van den Born, LI de Kok, YJM van der Velde-Visser, SD Kellner, U Jurklies, B van Schooneveld, MJ Blankenagel, A Rohrschneider, K Wissinger, B Cruysberg, JRM Deutman, AF Brunner, HG Apfeldstedt-Sylla, E Hoyng, CB Cremers, FPM
Citation: Ai. Den Hollander et al., Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene, AM J HU GEN, 69(1), 2001, pp. 198-203
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
Authors: Kramer, F White, K Pauleikhoff, D Gehrig, A Passmore, L Rivera, A Rudolph, G Kellner, U Andrassi, M Lorenz, B Rohrschneider, K Blankenagel, A Jurklies, B Schilling, H Schutt, F Holz, FG Weber, BHF
Citation: F. Kramer et al., Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration, EUR J HUM G, 8(4), 2000, pp. 286-292
Ab interno trabeculotomy using a Nd : YLF picosecond laser
Authors: Rohrschneider, K Kruse, FE Kessler, R Golz, S Bille, JF Volcker, HE
Citation: K. Rohrschneider et al., Ab interno trabeculotomy using a Nd : YLF picosecond laser, OPHTHALMOLO, 97(11), 2000, pp. 748-752
Cryopreserved human amniotic membrane for ocular surface reconstruction
Authors: Kruse, FE Joussen, AM Rohrschneider, K You, LT Sinn, B Baumann, J Volcker, HE
Citation: Fe. Kruse et al., Cryopreserved human amniotic membrane for ocular surface reconstruction, GR ARCH CL, 238(1), 2000, pp. 68-75
Stereotactic radiation therapy for malignant choroidal tumors - Preliminary, short-term results
Authors: Bellmann, C Fuss, M Holz, FG Debus, J Rohrschneider, K Volcker, HE Wannenmacher, M
Citation: C. Bellmann et al., Stereotactic radiation therapy for malignant choroidal tumors - Preliminary, short-term results, OPHTHALMOL, 107(2), 2000, pp. 358-365
Use of a new night vision enhancement device (DAVIS)
Authors: Rohrschneider, K Spandau, U Wechsler, S Blankenagel, A
Citation: K. Rohrschneider et al., Use of a new night vision enhancement device (DAVIS), KLIN MONATS, 217(2), 2000, pp. 88-93
Orbital cysticercosis. Case report, clinical and histological findings andreview of the literature
Authors: Wabbels, B Kruse, F Helmke, B Rohrschneider, K Voicker, HE
Citation: B. Wabbels et al., Orbital cysticercosis. Case report, clinical and histological findings andreview of the literature, KLIN MONATS, 217(2), 2000, pp. 109-113
Ophtalmological emergencies
Authors: Kruse, FE Rohrschneider, K Volcker, HE
Citation: Fe. Kruse et al., Ophtalmological emergencies, INTERNIST, 41(8), 2000, pp. 733-735
Treatment of corneal neovascularization with dietary isoflavonoids and flavonoids
Authors: Joussen, AM Rohrschneider, K Reichling, J Kirchhof, B Kruse, FE
Citation: Am. Joussen et al., Treatment of corneal neovascularization with dietary isoflavonoids and flavonoids, EXP EYE RES, 71(5), 2000, pp. 483-487
Scanning laser ophthalmoscope fundus perimetry before and after laser photocoagulation for clinically significant diabetic macular edema
Authors: Rohrschneider, K Bultmann, S Gluck, R Kruse, FE Fendrich, T Volcker, HE
Citation: K. Rohrschneider et al., Scanning laser ophthalmoscope fundus perimetry before and after laser photocoagulation for clinically significant diabetic macular edema, AM J OPHTH, 129(1), 2000, pp. 27-32
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy
Authors: Maugeri, A Klevering, BJ Rohrschneider, K Blankenagel, A Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM
Citation: A. Maugeri et al., Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy, AM J HU GEN, 67(4), 2000, pp. 960-966
Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg
Authors: Rohrschneider, K Bruder, I Blankenagel, A
Citation: K. Rohrschneider et al., Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg, OPHTHALMOLO, 96(9), 1999, pp. 611-616
Experimental external irradiation of corneal neovascularization
Authors: Joussen, AM Kruse, FE Otzel, D Holz, FG Debus, J Rohrschneider, K Volcker, HE
Citation: Am. Joussen et al., Experimental external irradiation of corneal neovascularization, OPHTHALMOLO, 96(4), 1999, pp. 234-239
Techniques for reconstruction of the corneal surface by transplantation ofpreserved human amniotic membrane
Authors: Kruse, FE Rohrschneider, K Volcker, HE
Citation: Fe. Kruse et al., Techniques for reconstruction of the corneal surface by transplantation ofpreserved human amniotic membrane, OPHTHALMOLO, 96(10), 1999, pp. 673-678
Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers
Authors: Kruse, FE Rohrschneider, K Volcker, HE
Citation: Fe. Kruse et al., Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers, OPHTHALMOL, 106(8), 1999, pp. 1504-1510
The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease
Authors: Maugeri, A van Driel, MA van de Pol, DJR Klevering, BJ van Haren, FJJ Tijmes, N Bergen, AAB Rohrschneider, K Blankenagel, A Pinckers, AJLG Dahl, N Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM
Citation: A. Maugeri et al., The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease, AM J HU GEN, 64(4), 1999, pp. 1024-1035
Risultati: 1-17 |