retinoblastoma造句1 Results All the 12 cases of retinoblastoma showed increased and inhomogeneous density of vitreous body.
2 Radiological feature is retinoblastoma involving in the optic nerve, and lesions within the eye encroach the optic nerve and chiasm violations in MRI.
3 The results were horrifying. Every link pointed towards retinoblastoma , a cancer of the retina.
4 Materials and Methods:15 cases of Retinoblastoma examined with CT and confirmed by operation and pathology.
5 Trilateral retinoblastoma is a rare malignancy of childhood with high mortality. We reported such a case with delayed treatment.
6 The extraocular extension account for about 20% of retinoblastoma of the same period.
7 Results The main ophthalmologic signs of retinoblastoma consisted of elevation of intraocular pressure, white-pupil sign, yellow-white mass in fundus and new blood vessels on the surface of the mass.
8 Retinoblastoma with massive tumor necrosis was proved by pathology after enucleation.
9 ObjectiveTo observe whether apoptosis is the primary type of cell death in retinoblastoma(RB)or not.
10 Mortality information is limited among long-term survivors who were irradiated for hereditary retinoblastoma.
11 Harmatoma of RPE are rare fundus lesions, but careful to identify them is important because they may be mistaken for choroid melanoma or retinoblastoma .
12 This article reports our experiences in the clinical treatment of these complicated retinoblastoma .
13 The most common origins are the orbit and the kidneys and the predominant tumors are retinoblastoma and nephroblastoma respectively. In contrast to those found in Shanghai and Shandong, the inciden...
14 The tumor is associated with mutations of a protein called Rb, or retinoblastoma protein.
15 The result suggests X-knife stereotactic radiotherapy is a safe and effective method for treatment of retinoblastoma.
16 Materials and Methods The clinic data and CT findings of 9 cases with retinoblastoma confirmed by operation and pathology or follow-up were retrospectively analyzed.
17 Objective In order to observe the growth and metastasis of the tumor directly, a new orthotopic retinoblastoma model was established with human RB cells expressing green fluorescent protein (GFP).
18 Cyclin D1 encodes the regulatory subunit of a holoenzyme that phosphorylates and inactivates the retinoblastoma protein and promotes progression through the G1-S phase of the cell cycle.
19 At 27 months after therapy, one patient was free of measurable retinoblastoma .
20 Background: Subsequent malignant neoplasms are a major cause of premature death in survivors of hereditary retinoblastoma.
21 Objective: To investigate the relationship between CT findings and pathologic diagnosis of retinoblastoma and their value in diagnosis and differentiation.
22 Because the risk is so much lower, Nunney argues, natural selection cannot drive the spread of new defenses against retinoblastoma.
23 Materials and Methods: The CT findings of 11 cases with retinoblastoma confirmed by operation and pathology were analyzed retrospectively.