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Results: 1-17 |
Results: 17
ABCR UNITES WHAT OPHTHALMOLOGISTS DIVIDE(S)
Authors: VANDRIEL MA MAUGERI A KLEVERING BJ HOYNG CB CREMERS FPM
Citation: Ma. Vandriel et al., ABCR UNITES WHAT OPHTHALMOLOGISTS DIVIDE(S), Ophthalmic genetics, 19(3), 1998, pp. 117-122
AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR
Authors: DENHOLLANDER A VANDEPOL DJR VANDRIEL M VANHAREN FJJ KNOERS NVAM TIJMES N BERGEN AAB ROHRSCHNEIDER K BLANKENAGEL A PINCKERS AJLG DEUTMAN AF HOYNG CB CREMERS FPM
Citation: A. Denhollander et al., AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR, European journal of human genetics, 6, 1998, pp. 501-501
AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR
Authors: CREMERS FPM VANDEPOL DJR VANDRIEL M DENHOLLANDER AI VANHAREN FJJ KNOERS NVAM TIJMES N BERGEN AAB ROHRSCHNEIDER K BLANKENAGEL A PINCKERS AJLG DEUTMAN AF HOYNG CB
Citation: Fpm. Cremers et al., AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR, Human molecular genetics, 7(3), 1998, pp. 355-362
COMPLETE EXON-INTRON STRUCTURE OF THE RETINA-SPECIFIC ATP BINDING TRANSPORTER GENE (ABCR) ALLOWS THE IDENTIFICATION OF NOVEL MUTATIONS UNDERLYING STARGARDT-DISEASE
Authors: GERBER S ROZET JM VANDEPOL TJR HOYNG CB MUNNICH A BLANKENAGEL A KAPLAN J CREMERS FPM
Citation: S. Gerber et al., COMPLETE EXON-INTRON STRUCTURE OF THE RETINA-SPECIFIC ATP BINDING TRANSPORTER GENE (ABCR) ALLOWS THE IDENTIFICATION OF NOVEL MUTATIONS UNDERLYING STARGARDT-DISEASE, Genomics, 48(1), 1998, pp. 139-142
A RANDOMIZED CONTROLLED CLINICAL-TRIAL ON THE EFFICACY OF RADIATION-THERAPY IN THE CONTROL OF SUBFOVEAL CHOROIDAL NEOVASCULARIZATION IN AGE-RELATED MACULAR DEGENERATION - RADIATION VERSUS OBSERVATION
Authors: BERGINK GJ HOYNG CB VANDERMAAZEN RWM VINGERLING JR VANDAAL WAJ DEUTMAN AF
Citation: Gj. Bergink et al., A RANDOMIZED CONTROLLED CLINICAL-TRIAL ON THE EFFICACY OF RADIATION-THERAPY IN THE CONTROL OF SUBFOVEAL CHOROIDAL NEOVASCULARIZATION IN AGE-RELATED MACULAR DEGENERATION - RADIATION VERSUS OBSERVATION, Graefe's archive for clinical and experimental ophthalmology, 236(5), 1998, pp. 321-325
CYTOMEGALOVIRUS (CMV) STRAIN DIFFERENCES BETWEEN THE EYE AND BLOOD INAIDS PATIENTS WITH CMV RETINITIS
Authors: VERBRAAK FD BRUINENBERG M VANDENHORN GJ MEENKEN C VANDERLELIJ A HOYNG CB KIJLSTRA A PEEK R
Citation: Fd. Verbraak et al., CYTOMEGALOVIRUS (CMV) STRAIN DIFFERENCES BETWEEN THE EYE AND BLOOD INAIDS PATIENTS WITH CMV RETINITIS, AIDS, 12(7), 1998, pp. 713-718
INCREASED PRESENCE OF EPSTEIN-BARR-VIRUS DNA IN OCULAR FLUID SAMPLES FROM HIV-NEGATIVE IMMUNOCOMPROMISED PATIENTS WITH UVEITIS
Authors: ONGKOSUWITO JV VANDERLELIJ A BRUINENBERG M WIENESENVANDOORN M FERON EJC HOYNG CB DEKEIZER RJW KLOK AM KIJLSTRA A
Citation: Jv. Ongkosuwito et al., INCREASED PRESENCE OF EPSTEIN-BARR-VIRUS DNA IN OCULAR FLUID SAMPLES FROM HIV-NEGATIVE IMMUNOCOMPROMISED PATIENTS WITH UVEITIS, British journal of ophthalmology, 82(3), 1998, pp. 245-251
GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13
Authors: HOYNG CB DEUTMAN AF VANDEPOL D KNOERS N PINCKERS A CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3690-3690
CENTRAL AREOLAR CHOROIDAL DYSTROPHY AND SLOWLY PROGRESSIVE SENSORINEURAL HEARING-LOSS
Authors: HOYNG CB VANRIJN PM DEUTMAN AF
Citation: Cb. Hoyng et al., CENTRAL AREOLAR CHOROIDAL DYSTROPHY AND SLOWLY PROGRESSIVE SENSORINEURAL HEARING-LOSS, Acta ophthalmologica Scandinavica, 74(6), 1996, pp. 639-641
ECCENTRIC VIEWING SPECTACLES IN EVERYDAY LIFE, FOR THE OPTIMUM USE OFRESIDUAL FUNCTIONAL RETINAL AREAS, IN PATIENTS WITH AGE-RELATED MACULAR DEGENERATION
Authors: VEREZEN CA VOLKERDIEBEN HJ HOYNG CB
Citation: Ca. Verezen et al., ECCENTRIC VIEWING SPECTACLES IN EVERYDAY LIFE, FOR THE OPTIMUM USE OFRESIDUAL FUNCTIONAL RETINAL AREAS, IN PATIENTS WITH AGE-RELATED MACULAR DEGENERATION, Optometry and vision science, 73(6), 1996, pp. 413-417
THE DEVELOPMENT OF CENTRAL AREOLAR CHOROIDAL DYSTROPHY
Authors: HOYNG CB DEUTMAN AF
Citation: Cb. Hoyng et Af. Deutman, THE DEVELOPMENT OF CENTRAL AREOLAR CHOROIDAL DYSTROPHY, Graefe's archive for clinical and experimental ophthalmology, 234(2), 1996, pp. 87-93
GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE
Authors: HOYNG CB POPPELAARS F VANDEPOL TJR KREMER H PINCKERS AJLG DEUTMAN AF CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE, Human genetics, 98(4), 1996, pp. 500-504
GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE
Authors: HOYNG CB POPPELAARS F PINCKERS AJLG DEUTMAN AF CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE, Vision research, 36, 1996, pp. 3234-3234
VISUAL-ACUITY AND SCAR SIZE IN EYES WITH AGE-RELATED SUBFOVEAL CHOROIDAL NEOVASCULAR LESIONS, 30 MONTHS AFTER RADIATION-THERAPY
Authors: BERGINK GJ HOYNG CB VANDERMAAZEN RWM DEUTMAN AF VANDAAL WAJ
Citation: Gj. Bergink et al., VISUAL-ACUITY AND SCAR SIZE IN EYES WITH AGE-RELATED SUBFOVEAL CHOROIDAL NEOVASCULAR LESIONS, 30 MONTHS AFTER RADIATION-THERAPY, Documenta ophthalmologica, 92(1), 1996, pp. 61-75
AUTOSOMAL-DOMINANT CENTRAL AREOLAR CHOROIDAL DYSTROPHY CAUSED BY A MUTATION IN CODON-142 IN THE PERIPHERIN RDS GENE/
Authors: HOYNG CB HEUTINK P TESTERS L PINCKERS A DEUTMAN AF OOSTRA BA
Citation: Cb. Hoyng et al., AUTOSOMAL-DOMINANT CENTRAL AREOLAR CHOROIDAL DYSTROPHY CAUSED BY A MUTATION IN CODON-142 IN THE PERIPHERIN RDS GENE/, American journal of ophthalmology, 121(6), 1996, pp. 623-629
A MUTATION IN CODON-142 IN CENTRAL AREOLAR CHOROIDAL DYSTROPHY
Authors: HOYNG CB HEUTINK P DEUTMAN AF OOSTRA BA
Citation: Cb. Hoyng et al., A MUTATION IN CODON-142 IN CENTRAL AREOLAR CHOROIDAL DYSTROPHY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 825-825
PIGMENTARY IRREGULARITIES AND OPTIC DISC EDEMA AFTER HEART-TRANSPLANTATION
Authors: KLAVER CCW HOYNG CB DEJONG PTVM
Citation: Ccw. Klaver et al., PIGMENTARY IRREGULARITIES AND OPTIC DISC EDEMA AFTER HEART-TRANSPLANTATION, Archives of ophthalmology, 113(10), 1995, pp. 1281-1285
Risultati: 1-17 |