DSpace at RU >

Browsing by Author Pinckers, A.J.L.G.

Full Text	Issue Date	Title	Author(s)
	1997	Pattern reversal visual evoked potentials in patients with epiretinal membrane	Bemelmans, N.A.M.; Tilanus, M.A.D.; Cuijpers, M.H.M.; Pinckers, A.J.L.G.
	1997	Localization of a novel X-linked progressive cone dystrophy gene to Xq27 : Evidence for genetic heterogeneity	Bergen, A.A.B.; Pinckers, A.J.L.G.
	1997	Cornea-anesthesie bij kinderen met multipele congenitale afwijkingen (vertebral, anal, cardiovascular, tracheo-esophageal, renal and limb defects of VACTERL-associatie)	Cruysberg, J.R.M.; Draaijer, R.W.; Pinckers, A.J.L.G.; Brunner, H.G.
	1997	Reticular dystrophy of the retinal pigment epithelium and choroidal neovascularization : a fluorescein and ICGV study	Marano, F.; Deutman, A.F.; Pinckers, A.J.L.G.; Aandekerk, A.L.; Rijneveld, W.J.
	1997	Pattern reversal evoked potentials in eyes with macular holes and their fellow eyes	Bemelmans, N.A.M.; Tilanus, M.A.D.; Cuypers, M.H.M.; Pinckers, A.J.L.G.
	1997	Localization of a novel X-linked progressive cone dystrophy gene to Xq27 : evidence for genetic heterogeneity	Bergen, A.A.B.; Pinckers, A.J.L.G.
	1997	Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia : Boucher-Neuhäuser syndrome	Rump, P.; Hamel, B.C.J.; Pinckers, A.J.L.G.; Dop, P.A. van
	1997	Pattern reversal visual evoked potential in eyes with macular holes and their fellow eyes	Bemelmans, N.A.M.; Tilanus, M.A.D.; Cuijpers, M.H.M.; Pinckers, A.J.L.G.
	1997	Prognostic value of pattern reversal visual evoked potentials in idiopatic epiretinal membrane.	Tilanus, M.A.D.; Cuijpers, M.H.M.; Bemelmans, N.A.M.; Pinckers, A.J.L.G.
	1997	Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) gene	Hurk, J.A.J.M. van den; Schwartz, M.; Bokhoven, H. van; Pol, T.J.R. van de; Bogerd, L., et al
	1996	Prognostic value of pattern reversal visual evoked potentials in idiopathic epiretinal membrane	Cuypers, M.H.M.; Tilanus, M.A.D.; Pinckers, A.J.L.G.; Bemelmans, M.A.; Deutman, A.F.
	1996	Stabiel en progressief gehoorverlies bij het Usher syndroom, type 2A.	Aarem, A. van; Huygen, P.L.M.; Pinckers, A.J.L.G.; Bleeker-Wagemakers, E.M.; Kimberling, W.J., et al
	1996	Genetic fine mapping of the gene for recessive Stargardt disease	Hoyng, C.B.; Poppelaars, F.; Pol, T.J.R. van de; Kremer, H.; Pinckers, A.J.L.G., et al
	1996	Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin-RDS gene	Hoyng, C.B.; Heutink, P.; Testers, L.; Pinckers, A.J.L.G.; Deutman, A.F., et al
	1996	Stable and progressive hearing loss in type 2A Usher's syndrome	Aarem, A. van; Huygen, P.L.M.; Pinckers, A.J.L.G.; Bleeker-Wagemakers, E.M.; Kimberling, W.J., et al
	1996	Gyrate atrophy and choroidal neovascularization	Marano, F.; Deutman, A.F.; Pinckers, A.J.L.G.; Aandekerk, A.L.
	1996	The EOG in Best's disease and dominant cystoid macular dystrohpy (DCMD)	Pinckers, A.J.L.G.; Cuijpers, M.H.M.; Aandekerk, A.L.
	1996	Positional cloning of the gene for X-linked retinitis pigmentosa : homology with the guanine-nucleotide-exchange factor RCC1	Roepman, R.; Duijnhoven, G. van; Rosenberg, T.; Pinckers, A.J.L.G.; Bleeker-Wagemakers, E.M., et al
	1996	Genetic fine mapping of the gene for recessive Stargardt disease	Hoyng, C.B.; Poppelaars, F.; Pinckers, A.J.L.G.; Deutman, A.F.; Cremers, F.P.M.
	1996	Positional cloning of the gene for x-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1	Roepman, R.; Duijnhoven, G.C.F. van; Rosenberg, T.; Pinckers, A.J.L.G.; Bleeker-Wagemakers, P.L.M., et al
	1996	Stable and progressive hearing loss in type 2A Ushers syndrome	Aarem, A. van; Huygen, P.L.M.; Pinckers, A.J.L.G.; Bleeker-Wagemakers, E.M.; Kimberling, W.J., et al
	1995	Leber-opticusatrofie; een mitochondriaal overervende ziekte	Cruysberg, J.R.M.; Pinckers, A.J.L.G.
	1995	Clinical findings in obligate carriers of type I Usher syndrome	Wagenaar, M.; Rahe, B. ter; Aarem, A. van; Huygen, P.L.M.; Admiraal, R.J.C., et al
	1995	Ocular and systemic manifestations of cerebrotendinous xanthomatosis	Cruysberg, J.R.M.; Wevers, R.A.; Engelen, B.G.M. van; Pinckers, A.J.L.G.; Spreeken, A.C.G.A. van, et al
	1995	Discriminative Power of Visual-Evoked Potential Characteristics in Multiple-Sclerosis	Cuypers, M.H.M.; Dickson, K.; Pinckers, A.J.L.G.; Thijssen, J.M.; Hommes, O.R.
	1995	Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)	Taschner, P.E.M.; Vos, N. de; Post, J.G.; Meijers-Heijboer, E.J.; Hofman, I., et al
	1995	Clinical findings in obligate carriers carriers of type I usher syndrome	Wagenaar, M.; Rahe, B. ter; Aarem, A. van; Huygen, P.L.M.; Admiraal, R.J.C., et al
	1995	Ectopia lentis et pupillae syndrome in three generations	Cruysberg, J.R.M.; Pinckers, A.J.L.G.
	1995	Ophthalmic findings in Usher syndrome type 2A	Aarem, A. van; Wagenaar, M.; Pinckers, A.J.L.G.; Huygen, P.L.M.; Bleeker-Wagemakers, E.M., et al
	1995	The Usher syndrome type 2A: clinical findings in obligate carriers	Aarem, A. van; Cremers, C.W.R.J.; Pinckers, A.J.L.G.; Huygen, P.L.M.; Hombergen, G.C.J., et al
	1995	The Usher syndrome type 2A. Clinical findings in obligate carriers	Aarem, A. van; Cremers, C.W.R.J.; Pinckers, A.J.L.G.; Huygen, P.L.M.; Hombergen, G.C.J., et al
	1995	Autosomal Recessive Melnick-Needles Syndrome or ter Haar Syndrome? : Report of a Patient and Reappraisal of an Earlier Report	Hamel, B.C.J.; Draaisma, J.M.T.; Pinckers, A.J.L.G.; Boetes, C.; Hoppe, R.L.E., et al
	1995	Pattern-Reversal Visual-Evoked Potentials - Influence of Age, Gender and Check Size in the Diagnosis of Multiple-Sclerosis	Bemelmans, N.A.M.; Cuypers, M.H.M.; Pinckers, A.J.L.G.; Hommes, O.R.
	1995	Effect of steady hypothermia and normothermia on multimodality evoked potentials in human poikilothermia	MacKenzie, M.A.; Vingerhoets, H.M.; Colon, E.J.; Pinckers, A.J.L.G.; Notermans, S.L.H.
	1995	Discriminative power of visual evoked potential characteristics in multiple sclerosis	Cuijpers, M.H.M.; Dickson, K.; Pinckers, A.J.L.G.; Thijssen, J.M.; Hommes, O.R.
	1995	Multipoint linkage analysis and soneogeneity tests in 15 Dutch X-linked retinitis pigmentosa families	Bergen, A.A.B.; Born, L.I. van den; Schuurman, E.J.M.; Pinckers, A.J.L.G.; Ommen, G.J.B. van, et al
	1995	Autosomal recessive Melnick-Needless Syndrome or ter Haar Syndrome? : Report of a patient and reappraisal of an earlier report	Hamel, B.C.J.; Draaisma, J.M.; Pinckers, A.J.L.G.; Boetes, C.; Hoppe, R.L.E., et al
	1995	Pattern reversal visual evoked potentials: influence of age, gender and check size in the diagnosis of multiple sclerosis	Bemelmans, N.A.M.; Cuijpers, M.H.M.; Pinckers, A.J.L.G.; Hommes, O.R.
	1995	Autosomal recessive Melnick-Needless syndrome or ter Haar syndrome?	Hamel, B.C.J.; Draaisma, J.M.; Pinckers, A.J.L.G.; Boetes, C.; Hoppe, R.L.E., et al
	1995	A spider hits the eye	Cruysberg, J.R.M.; Pinckers, A.J.L.G.; Castelijns, H.E.J.M.; Verbeek, A.M.; Deutman, A.F.
	1995	Visual evoked potentials: normative values and discriminative power of VEP characteristics in multiple sclerosis	Cuijpers, M.H.M.; Dickson, K.; Pinckers, A.J.L.G.; Thijssen, J.M.; Hommes, O.R.
	1995	Effect of steady hypothermia and normothermia on multimodality evoked potentials in human poikilothermia	MacKenzie, M.A.; Vingerhoets, D.M.; Colon, E.J.; Pinckers, A.J.L.G.; Notermans, S.L.H.