Inconvénients des matériaux pour lentilles de contact en siloxanyl-alkyl-méthacrylate et en fluoro-silico-acrylates = Problems with SAHC and fluorosilicone acrylate contact lens materialsEGGINK, F. A. G. J; PINCKERS, A. J. L. G.Contactologia (Ed.française). 1988, Vol 10, Num 4, pp 169-171, issn 0171-9602Article

Localization of a novel X-linked progressive cone dystrophy gene to Xq27 : Evidence for genetic heterogeneityBERGEN, A. A. B; PINCKERS, A. J. L. G.American journal of human genetics. 1997, Vol 60, Num 6, pp 1468-1473, issn 0002-9297Article

Anomaloscope examination in macular gliosis, macular holes and central serous choroidopathyTILANUS, M. A. D; PINCKERS, A. J. L. G; AANDEKERK, A. L et al.Graefe's archive for clinical and experimental ophthalmology. 1998, Vol 236, Num 5, pp 326-332, issn 0721-832XArticle

Etude comparative de deux lentilles souples multifocales = Two soft concentric varifocal contact lenses = Two soft concentric Varifocal Contact LensesEGGINK, F. A. G. J; PINCKERS, A. J. L. G; DE GRAAF, R et al.Contactologia (Ed.française). 1993, Vol 15, Num 1, pp 26-29, issn 0171-9602Article

Opacités sous-épithéliales au cours du port journalier de lentilles de contact souples = Subepithelial opacities in daily wear high water content Soft contact LensesEGGINK, F. A. G. J; PINCKERS, A. J. L. G; AANDEKERK, A. L et al.Contactologia (Ed.française). 1991, Vol 13, Num 4, pp 173-176, issn 0171-9602Article

Tests de la vision des couleurs et potentiels évoqués visuels dans la sclérose en plaques = Color vision tests and visual evoked potentials in multiple sclerosisPINCKERS, A. J. L. G; VERRIEST, G; CRUYSBERG, J. R. M et al.Ophtalmologie. 1987, Vol 1, Num 1, pp 45-48Conference Paper

Evolution of benign concentric annular macular dystrophyVAN DEN BIESEN, P. R; DEUTMAN, A. F; PINCKERS, A. J. L. G et al.American journal of ophthalmology. 1985, Vol 100, pp 73-78, issn 0002-9394Article

The electro-oculogram in uveal melanoma : a prospective studyBRINK, H. M. A; PINCKERS, A. J. L. G; VERBEEK, A. M et al.Documenta ophthalmologica. 1990, Vol 75, Num 3-4, pp 329-334, issn 0012-4486, 6 p.Conference Paper

Prognostic value of pattern reversal visual-evoked potentials in idiopathic epiretinal membraneTILANUS, M. A. D; CUYPERS, M. H; BEMELMANS, N. A. M et al.Graefe's archive for clinical and experimental ophthalmology. 1997, Vol 235, Num 8, pp 474-479, issn 0721-832XArticle

Discriminative power of visual evoked potential characteristics in multiple sclerosisCUYPERS, M. H. M; DICKSON, K; PINCKERS, A. J. L. G et al.Documenta ophthalmologica. 1995, Vol 90, Num 3, pp 247-257, issn 0012-4486Article

Myotonic dystrophy : predictive value of normal results on clinical examinationBRUNNER, H. G; SMEETS, H. J. M; ROPERS, H.-H et al.Brain. 1991, Vol 114, pp 2303-2311, issn 0006-8950, 5Article

Visual acuity, spectacle blur and slit-lamp biomicroscopy on asymptomatic contact-lens-wearing recruitsROUWEN, A.-J.P; PINCKERS, A. J. L. G; PAD VOS BOSCH, A. A. I. V. P et al.Graefe's archive for clinical and experimental ophthalmology. 1983, Vol 221, Num 2, pp 73-77, issn 0721-832XArticle

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRCREMERS, F. P. M; VAN DE POL, D. J. R; PINCKERS, A. J. L. G et al.Human molecular genetics (Print). 1998, Vol 7, Num 3, pp 355-362, issn 0964-6906Article

Stable and progressive hearing loss in type 2A Usher's syndromeVAN AAREM, A; HUYGEN, P. L. M; PINCKERS, A. J. L. G et al.The Annals of otology, rhinology & laryngology. 1996, Vol 105, Num 12, pp 962-967, issn 0003-4894Article

Immune responsiveness to retinal S-antigen and opsin in serpiginous choroiditis and other retinal diseasesBROEKHUYSE, R. M; VAN HERCK, M; PINCKERS, A. J. L. G et al.Documenta ophthalmologica. 1988, Vol 69, Num 1, pp 83-93, issn 0012-4486Article

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneKLEVERING, B. J; VAN DRIEL, M; DE POL, D. J. R. V et al.British journal of ophthalmology. 1999, Vol 83, Num 8, pp 914-918, issn 0007-1161Article

The 2588G→C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseMAUGERI, A; VAN DRIEL, M. A; DAHL, N et al.American journal of human genetics. 1999, Vol 64, Num 4, pp 1024-1035, issn 0002-9297Article

The Usher syndrome type 2A : clinical findings in obligate carriersVAN AAREM, A; CREMERS, C. W. R. J; PINCKERS, A. J. L. G et al.International journal of pediatric otorhinolaryngology. 1995, Vol 31, Num 2-3, pp 159-174, issn 0165-5876Article

Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)TASCHNER, P. E. M; DE VOS, N; POST, J. G et al.American journal of medical genetics. 1995, Vol 57, Num 2, pp 333-337, issn 0148-7299Conference Paper

Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingVAN DEN HURK, J. A. J. M; VAN DE POL, T. J. R; ROPERS, H.-H et al.American journal of human genetics. 1992, Vol 50, Num 6, pp 1195-1202, issn 0002-9297Article

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabasesCREMERS, F. P. M; SANKILA, E.-M; DE LA CHAPELLE, A et al.American journal of human genetics. 1990, Vol 47, Num 4, pp 622-628, issn 0002-9297, 7 p.Article

Predictive value of pattern VEP, pattern ERG and hole size in macular hole surgeryTILANUS, M. A. D; CUYPERS, M. H. M; BEMELMANS, N. A. M et al.Graefe's archive for clinical and experimental ophthalmology. 1999, Vol 237, Num 8, pp 629-635, issn 0721-832XArticle

Positional cloning of the gene for X-linked retinitis pigmentosa 2SCHWAHN, U; LENZNER, S; PINCKERS, A. J. L. G et al.Nature genetics. 1998, Vol 19, Num 4, pp 327-332, issn 1061-4036Article

Genetic fine mapping of the gene for recessive Stargardt diseaseHOYNG, C. B; POPPELAARS, F; VAN DE POL, T. J. R et al.Human genetics. 1996, Vol 98, Num 4, pp 500-504, issn 0340-6717Article

Positional cloning of the gene for X-linked retinitis pigmentosa 3 : homology with the guanine-nucleotide-exchange factor RCC1ROEPMAN, R; VAN DUIJNHOVEN, G; CREMERS, F. P. M et al.Human molecular genetics (Print). 1996, Vol 5, Num 7, pp 1035-1042, issn 0964-6906, 7 p.Article