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Chemotherapy for Retinoblastoma
Ophthalmic Paediatrics and Genetics, 1989Fourteen patients with retinoblastoma treated with chemotherapy in our hospital were surveyed to study the effects of chemotherapy on retinoblastoma. These patients were compared with those registered in 1980 and 1981 in Japan. In unilateral retinoblastoma limited to the eyeball, there was no significant difference in outcome between the chemotherapy ...
K, Akiyama +3 more
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Human Genetics, 1979
The genetic basis of retinoblastoma is reviewed and the following conclusions are drawn: 1) The mode of inheritance of the hereditary variety of retinoblastoma (R) is autosomal dominant with about 90% penetrance. 2) About 68% of inherited cases are bilateral, and about 32%, unilateral.
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The genetic basis of retinoblastoma is reviewed and the following conclusions are drawn: 1) The mode of inheritance of the hereditary variety of retinoblastoma (R) is autosomal dominant with about 90% penetrance. 2) About 68% of inherited cases are bilateral, and about 32%, unilateral.
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Cryotherapy for Retinoblastoma
Archives of Ophthalmology, 1982Cryotherapy was applied to 138 intraocular retinoblastoma tumors from 113 patients who were followed up for a mean of 40 months (four to 144 months). Overall, 70% of tumors were cured with cryotherapy and 93% of patients treated with cryotherapy survived.
D H, Abramson +2 more
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Archives of Ophthalmology, 1949
IT HAS been well established that there is a strong hereditary tendency in retinoblastoma. Although the exact way in which the disease is transmitted has not been agreed on, evidence largely points to its being a dominant trait irregular in type. Some cases have been reported of collateral involvement in siblings whose parents were apparently normal ...
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IT HAS been well established that there is a strong hereditary tendency in retinoblastoma. Although the exact way in which the disease is transmitted has not been agreed on, evidence largely points to its being a dominant trait irregular in type. Some cases have been reported of collateral involvement in siblings whose parents were apparently normal ...
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Archives of Ophthalmology, 1948
Retinoblastoma is an intriguing subject because of the difficulty of early diagnosis, the fearful penalty for delay in treatment, the question of hereditary transmission and the implications of birth control in the affected families. For these and other reasons, the subject of retinoblastoma is presented in the clinical form of 6 case histories, with a
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Retinoblastoma is an intriguing subject because of the difficulty of early diagnosis, the fearful penalty for delay in treatment, the question of hereditary transmission and the implications of birth control in the affected families. For these and other reasons, the subject of retinoblastoma is presented in the clinical form of 6 case histories, with a
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Tropical Doctor, 1990
Etude retrospective de 64000 dossiers montrant 73 cas de retinoblastome avec un fort taux de mortalite du essentiellement au retard ...
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Etude retrospective de 64000 dossiers montrant 73 cas de retinoblastome avec un fort taux de mortalite du essentiellement au retard ...
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Retinoblastoma [Il retinoblastoma]
2013Retinoblastoma is the most frequently diagnosed intraocular malignancy in infants. Recently, there have been significant advances in the management of this disease. New therapeutic strategies, such as superselective intra-arterial chemotherapy and periocular/intravitreal chemotherapy, have been added to conservative treatments with a long consolidated ...
D'Ambrosio, Alfonso +10 more
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