Add to ORKGBackground: Retinoblastoma is an eye tumour of childhood that occurs in heritable and non-heritable forms. In the heritable form, there is a predisposition to the development of non-ocular subsequent primary tumours (SPTs)
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Background: Retinoblastoma occurs in both a heritable and a non-heritable form. In the heritable for...
BACKGROUND: Retinoblastoma occurs in both a heritable and a non-heritable form. In the heritable for...
PURPOSE: The principal objectives of this study were to estimate the incidence of second tumors amon...
In 1973, Strong and Knudson ( 1) predicted that second cancers would occur at an increased rate in s...
AIM: This paper describes the epidemiology and family history status of 1601 children with retinobla...
Aim: This paper describes the epidemiology and family history status of 1601 children with retinobla...
364 eyes from 230 patients with retinoblastoma diagnosed and treated at the Lausanne University Eye ...
Item does not contain fulltextSurvivors of hereditary retinoblastoma have a high risk of second prim...
Retinoblastoma is the most common primary, intraocular neoplasm of childhood. Histologically, retin...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Retinoblastoma represents the prototypic model for inherited cancers. The RB1 gene was the first tum...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Background: Retinoblastoma occurs in both a heritable and a non-heritable form. In the heritable for...
BACKGROUND: Retinoblastoma occurs in both a heritable and a non-heritable form. In the heritable for...
PURPOSE: The principal objectives of this study were to estimate the incidence of second tumors amon...
In 1973, Strong and Knudson ( 1) predicted that second cancers would occur at an increased rate in s...
AIM: This paper describes the epidemiology and family history status of 1601 children with retinobla...
Aim: This paper describes the epidemiology and family history status of 1601 children with retinobla...
364 eyes from 230 patients with retinoblastoma diagnosed and treated at the Lausanne University Eye ...
Item does not contain fulltextSurvivors of hereditary retinoblastoma have a high risk of second prim...
Retinoblastoma is the most common primary, intraocular neoplasm of childhood. Histologically, retin...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
Retinoblastoma represents the prototypic model for inherited cancers. The RB1 gene was the first tum...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
The new concept of retinoma, or retinocytoma, brings up the rare 'spontaneous regressions' long-repo...
Survivors of hereditary retinoblastoma have a high risk of second primary malignancies, but it has n...