Results 201 to 210 of about 66,792 (243)
Guidelines for imaging retinoblastoma: imaging principles and MRI standardization [PDF]
Pediatric Radiology, 2011 Retinoblastoma is the most common intraocular tumor in children. The diagnosis is usually established by the ophthalmologist on the basis of fundoscopy and US.
Pim De Graaf +2 more
exaly +3 more sources
European Journal of Cancer, 1998 BackgroundRetinoblastoma is the most common intraocular malignancy of infants and children. With early diagnosis and treatment, survival is greater than 90%; however, patients with a germline retinoblastoma mutation have a substantial risk of having a ...
J M, Zucker, L, Desjardins, F, Doz
openaire +3 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Current Opinion in Ophthalmology, 2013
Retinoblastoma is the most common malignant intraocular tumor of childhood. Treatment and diagnostic modalities associated to this condition are changing rapidly as our understanding of this condition crystallizes. The purpose of this review is to provide an update of the current understanding of retinoblastoma.Knowledge on tumorigenesis and genomic ...
Victor M, Villegas +4 more
openaire +4 more sources
Retinoblastoma is the most common malignant intraocular tumor of childhood. Treatment and diagnostic modalities associated to this condition are changing rapidly as our understanding of this condition crystallizes. The purpose of this review is to provide an update of the current understanding of retinoblastoma.Knowledge on tumorigenesis and genomic ...
Victor M, Villegas +4 more
openaire +4 more sources
Cancer Nursing, 1991
Retinoblastoma, although a rare childhood cancer, is the most common primary malignant intraocular tumor of infancy and early childhood. In 75% of the cases, retinoblastoma is unilateral, and in 25% of the cases, retinoblastoma is bilateral. Presenting signs and symptoms of retinoblastoma, genetics, diagnostic tests, and their implications are reviewed
C A, Servodidio +2 more
openaire +2 more sources
Retinoblastoma, although a rare childhood cancer, is the most common primary malignant intraocular tumor of infancy and early childhood. In 75% of the cases, retinoblastoma is unilateral, and in 25% of the cases, retinoblastoma is bilateral. Presenting signs and symptoms of retinoblastoma, genetics, diagnostic tests, and their implications are reviewed
C A, Servodidio +2 more
openaire +2 more sources
Journal of Pediatric Ophthalmology & Strabismus, 1987
ABSTRACT Retinoblastoma was diagnosed in 74 patients between July 1967 and February 1987. Thirty cases (40%) were bilateral; 39 were female and 35 were male. Treatment in bilateral cases consisted of enucleation of the more involved eye and a combined approach of supervoltage irradiation, cryocoagulation, and photocoagulation to the remaining
E M, Helveston, K R, Knuth, F D, Ellis
openaire +2 more sources
ABSTRACT Retinoblastoma was diagnosed in 74 patients between July 1967 and February 1987. Thirty cases (40%) were bilateral; 39 were female and 35 were male. Treatment in bilateral cases consisted of enucleation of the more involved eye and a combined approach of supervoltage irradiation, cryocoagulation, and photocoagulation to the remaining
E M, Helveston, K R, Knuth, F D, Ellis
openaire +2 more sources
Clinics in Perinatology, 2021
Retinoblastoma is the most common ocular malignancy of childhood. With an estimated 300 cases annually in the United States, retinoblastoma is nevertheless considered a rare tumor. Although retinoblastoma primarily affects younger children, diagnosis during the neonatal age range is less common. However, an understanding of patients at risk is critical
Frank Y, Lin, Murali M, Chintagumpala
openaire +2 more sources
Retinoblastoma is the most common ocular malignancy of childhood. With an estimated 300 cases annually in the United States, retinoblastoma is nevertheless considered a rare tumor. Although retinoblastoma primarily affects younger children, diagnosis during the neonatal age range is less common. However, an understanding of patients at risk is critical
Frank Y, Lin, Murali M, Chintagumpala
openaire +2 more sources
2004
Retinoblastoma (Rb) is a malignant tumor that originates from developing retina. Diagnosis based on clinical signs and symptoms and is usually made in children under the age of five years. Mutations in both alleles of the RB1 gene are a prerequisite for this tumor to develop.
openaire +2 more sources
Retinoblastoma (Rb) is a malignant tumor that originates from developing retina. Diagnosis based on clinical signs and symptoms and is usually made in children under the age of five years. Mutations in both alleles of the RB1 gene are a prerequisite for this tumor to develop.
openaire +2 more sources
Bilateral retinoblastoma with ectopic intracranial retinoblastoma: Trilateral retinoblastoma
Cancer Genetics and Cytogenetics, 1982In 11 patients, bilateral retinoblastoma presented at a mean age of 6 months and pineoblastoma at 4 years. We suggest that the hereditary multicentric retinoblastoma arose in vestigeal photoreceptors in the pineal as well as in the hypothetical retinoblasts of the retina.
J L, Bader +6 more
openaire +2 more sources
Der Ophthalmologe, 2006
Retinoblastomas are the most frequent intraocular tumors in childhood. Untreated, the tumor is almost always fatal. Using a multidisciplinary approach combining the efforts of ophthalmologists, radiation oncologists, pediatric oncologists and geneticists a survival rate of more than 95% can be achieved.
Bornfeld, Norbert +6 more
openaire +3 more sources
Retinoblastomas are the most frequent intraocular tumors in childhood. Untreated, the tumor is almost always fatal. Using a multidisciplinary approach combining the efforts of ophthalmologists, radiation oncologists, pediatric oncologists and geneticists a survival rate of more than 95% can be achieved.
Bornfeld, Norbert +6 more
openaire +3 more sources
Trilateral retinoblastoma: ocular and pineal retinoblastomas
Journal of Neurosurgery, 1985✓ Trilateral retinoblastomas, the syndrome of bilateral retinoblastoma associated with ectopic retinoblastoma in the pineal gland, is rare but well recognized. In contrast to bilateral retinoblastomas alone, the ocular retinoblastomas in trilateral retinoblastoma develop before the age of 6 months, and a family history positive for retinoblastoma is ...
D L, Johnson +4 more
openaire +2 more sources