Ophthalmic Paediatrics and Genetics

Titel Veröffentlichungsdatum Sprache Zitate
Ophthalmic midline dysgenesis in Kallmann syndrome1987/01/01English13
Patterned dystrophies of the retinal pigment epithelium: A review1988/01/01English13
A histopathologic study of retinitis pigmentosa1982/01/01English13
Visual developmental delay1981/01/01English13
Mucolipidosis type IV Presentation of a mild variant1992/01/01English13
A retrospective study of registered retinitis pigmentosa patients in The Netherlands1992/01/01English12
Optic Atrophy in Marinesco-Sjögren Syndrome: An Additional Ocular Feature: Report of three Cases in two Families1993/01/01English12
Familial lecithin: Cholesterol acyltransferase (LCAT) deficiency: An updated review Spring 19881988/01/01English11
Retinoblastoma cell lines Y79, RB355 and WERI-Rb27 are genetically related1991/01/01English11
Ocular abnormalities in Patau syndrome (chromosome 13 trisomy syndrome)1990/01/01English11
Dominant exudative vitreoretinopathy1985/01/01English11
Bilateral congenital ocular cysts1991/01/01English11
Histopathological evaluation for the prognosis of retinoblastoma1989/01/01English11
Cumulative Incidence of Retinoblastoma in Riyadh, Saudi Arabia1992/01/01English11
Familial simple ectopia lentis a probable autosomal recessive form1986/01/01English11
Image size correction of the unilateral aphakic infant1983/01/01English10
Orbital computed tomography. Does it help in diagnosing the infiltration of choroid, sclera and/or optic nerve in retinoblastoma?1987/01/01English10
Unilateral lens dislocation and axial elongation in Marfan syndrome1988/01/01English10
Waardenburg syndrome: A variant with neurological involvement1987/01/01English10
Ocular pathology in disialotransferrin developmental deficiency syndrome1990/01/01English10
Retinoblastoma in the first year of life1992/01/01English10
Probable autosomal dominant optic atrophy with hearing loss1985/01/01English9
Partial trisomy 6q and bilateral retinal detachment1986/01/01English9
Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)1989/01/01English9
Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome1990/01/01English9
The pars plana approach in two cases of persistent hyperplastic primary vitreous (PHPV)1984/01/01English9
Evaluation of hairbulb incubation test and tyrosinase assay in the classification of albinism1982/01/01English9
Glucose-6-phosphate dehydrogenase deficiency and incidence of cataract in Sicily1985/01/01English9
Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis1990/01/01English9
Experimental models of anterior segment dysgenesis1989/01/01English9