Retinoblastoma is a rare type of cancer of the eye, often developing in early childhood, that
affects the retina, the light sensitive tissue at the back of the eye that detects light and colour …

Purpose To review the progress made in understanding the genetic basis, molecular
pathology, and treatment of retinoblastoma since the previous Jackson lecture on the topic …

Background Retinoblastoma is a highly malignant tumor of the eye that manifests most often
in the first 3 years of life. Methods Published articles were reviewed to evaluate the clinical …

Retinoblastoma is the commonest primary ocular malignancy of childhood. There are two
forms—heritable and non heritable. Heritable retinoblastoma is a cancer susceptibility …

Progressive advances in the understanding of retinoblastoma pathogenesis continue to lead
treatment strategies. Improvements in the diagnosis and management of retinoblastoma are …

Retinoblastoma is the most common intraocular cancer of childhood (Shields and Shields
2015; JA and CL 1992; Kivela 2009; Ramasubramanian and Shields 2012a). This …

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Retinoblastoma (Rb) is the most common primary intraocular malignancy of childhood, but
an uncommon paediatric cancer, with a constant incidence worldwide of 1: 15,000–1 …

Retinoblastoma is the most common ocular malignancy in children, and is initiated by
mutation of the RB1 gene. The tumor may be unilateral or bilateral and can be inherited …

Retinoblastoma is the most common intraocular malignancy in children and one of the very
few life-threatening ophthalmic conditions. Genetically, the disease may be heritable or non …