Ophthalmic Paediatrics and Genetics

Titel Veröffentlichungsdatum Sprache Zitate
Second malignant neoplasms in retinoblastoma: Fact and fiction1988/01/01English7
Congenital and developmental cataracts and multimalformation syndromes1989/01/01English7
Retinoblastoma in Lebanon1986/01/01English7
Prognosis and treatment of retinoblastoma: 105 cases treated at Institut Curie1989/01/01English7
Retrobulbar cysts in Aicardi's syndrome1991/01/01English7
Ocular findings in partial trisomy 3q: A case report and review of the literature1988/01/01English7
Autosomal Dominant Congenital Miosis with Megalocornea1992/01/01English7
Nettleship-Falls X-linked ocular albinism with Axenfeld's anomaly a case report1986/01/01English7
Variable Phenotypic Expressivity of Best's Vitelliform Dystrophy1993/01/01English7
Cataracts in Morquio syndrome1993/01/01English7
The reliability of the VEP in infancy1983/01/01English7
Diagnosis of dominant infantile optic atrophy in early childhood1988/01/01English6
Ocular anomalies in Coffin-Siris syndrome1985/01/01English6
A family with iridoschisis, narrow anterior chamber angle, and presenile cataract1986/01/01English6
Treatment of bilateral retinoblastoma stage V at the Curie Foundation: 33 cases1987/01/01English6
Optic pit, microphthalmos and orbital cyst1988/01/01English6
Etiology of congenital glaucoma Genetic and extragenetic factors1985/01/01English6
Autosomal recessive juvenile cataract in Hutterites1987/01/01English6
Congenital alacrima without associated manifestations (AD) An affected father and son1991/01/01English6
Usher's syndrome1990/01/01English6
Ocular manifestations in Kniest syndrome, Smith-Lemli-Opitz syndrome, Hallermann-Streiff-François syndrome, Rubinstein-Taybi syndrome and median cleft face syndrome1985/01/01English6
Foveal and parafoveal cone electroretinograms in juvenile macular degeneration1983/01/01English6
Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosome1988/01/01English6
Congenital glaucoma in a child with partial lq duplication and 9p deletion1992/01/01English6
Association of epibulbar choristomas with linear cutaneous nevi Review of the literature1984/01/01English6
Assessment and educational implications of albinism1990/01/01English6
Transthyretin-Related TTR Hereditary Amyloidosis of the Vitreous Body: Clinical and Molecular Characterization in two Italian Families1993/01/01English6
One Hundred Years of Retinoblastoma Research: From the Clinic to the Gene and Back Again1989/01/01English6
Chemotherapy in Retinoblastoma Management1989/01/01English6
Cosmetic Possibilities and Problems in Eyelid Neurofibromas1993/01/01English6