Ophthalmic Paediatrics and Genetics

Title Publication Date Language Citations
Pigmented Paravenous Retinochoroidal Atrophy (PPRCA) with Optic Disc Drusen1993/01/01English9
Cervico-Oculo-Acoustic Syndrome1985/01/01English9
Hereditary cases of congenital microcoria and goniodysgenesis1986/01/01English9
Inheritance and the pigmentary dispersion syndrome1985/01/01English9
Retinal adaptation in infants and children with retinal degenerations1983/01/01English8
Retinoblastoma: The Saudi Arabian experience1988/01/01English8
Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye1990/01/01English8
Failing accommodation in cases of Down's syndrome: A preliminary report1983/01/01English8
The ‘morning glory’ syndrome1985/01/01English8
Cellular and humoral immune parameters among patients with retinitis pigmentosa and other retinal disorders1984/01/01English8
Ocular ultrastructural studies of two cases of the Hurler syndrome (systemic mucopolysaccharidosis I-H)1983/01/01English8
Autosomal dominantly inherited optic nerve coloboma1988/01/01English8
Normal values of visual acuity in children up to 13 years as assessed by the acuity card procedure1992/01/01English8
Recurrent and new tumours during conservative treatment of bilateral retinoblastoma1991/01/01English8
Pars planitis in father and son1990/01/01English8
Hypomelanosis of Ito (incontinentia pigmenti achromians)1990/01/01English8
Trisomy 4q with morning glory disc anomaly1990/01/01English8
An ultrastructural study on retinal neural and pigment epithelial cells in ovine neuronal ceroid-lipofuscinosis1990/01/01English8
The Lenz microphthalmia syndrome: A case report1983/01/01English8
‘Leopard spot’ retinopathy in Warburg syndrome1986/01/01English8
Rieger's and Williams Syndrome: A Rare Clinical Case1985/01/01English8
High Symmetric Anisometropia in Monozygotic Twins1993/01/01English8
Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn)1989/01/01English8
Comparison of Cyclophosphamide and Diaziquone in a Retinoblastoma Xenograft Model1989/01/01English8
Porphyrin photodynamic therapy in an experimental retinoblastoma model1987/01/01English7
Hermansky-Pudlak oculocutaneous albinism: Clinical and genetic observations of six patients1983/01/01English7
Absence of hepatic molybdenum cofactor an inborn error of metabolism associated with lens dislocation1985/01/01English7
Hereditary cataract Perspective for prenatal screening1986/01/01English7
Leber's hereditary optic atrophy1989/01/01English7
Retinoblastoma, chromosome abnormalities and oncogene expression1987/01/01English7