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Sporadic Retinoblastoma
Known as:
Retinoblastoma, Sporadic
, Retinoblastomas, Sporadic
, Sporadic Retinoblastomas
A retinoblastoma that occurs in a patient without a family history of the disease.
National Institutes of Health
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Related topics
Related topics
13 relations
Calcinosis
Chromosome 13q deletion
Eye
Familial Retinoblastoma
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Broader (1)
Retinoblastoma
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3)
R. Sparkes
,
M. Sparkes
,
R. E. Kalina
,
R. Pagon
,
D. Salk
,
C. Disteche
Human Genetics
2004
Corpus ID: 25187225
SummaryA chromosome 13 deletion in a patient with sporadic retinoblastoma appears to have separated the loci for retinoblastoma…
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1999
1999
Late presentation of a unilateral sporadic retinoblastoma in a 16-year-old girl.
J. Park
,
G. Gole
,
S. Finnigan
,
K. Vandeleur
Australian and New Zealand journal of…
1999
Corpus ID: 23571606
BACKGROUND Retinoblastoma is the commonest intraocular tumour of childhood with the majority of cases being diagnosed before 5…
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1996
1996
Identification of mutations in the Ki-ras gene in human retinoblastoma.
D. Bautista
,
J. Emanuel
,
C. Granville
,
R. Howard
,
J. Costa
Investigative Ophthalmology and Visual Science
1996
Corpus ID: 24818938
PURPOSE To investigate the mutational status of the Ki-ras gene in retinoblastoma and to evaluate a correlation of the genotype…
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1996
1996
Orbital rhabdomyosarcoma fifty-seven years after radiotherapy for retinoblastoma
Martin C. Wilson
,
J. Shields
,
C. Shields
,
L. Litzky
1996
Corpus ID: 72776641
A 58-year-old man developed a left orbital mass 57 years after bilateral enucleation and external beam radiotherapy for bilateral…
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1994
1994
Inactivation of oncoprotein binding by a single Cys706‐to‐Tyr substitution in the retinoblastoma protein
M. Saijo
,
M. Kato
,
M. Sasaki
,
K. Ishizaki
,
Y. Taya
FEBS Letters
1994
Corpus ID: 30253701
1994
1994
Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.
A. Naumova
,
M. Hansen
,
+7 authors
L. Donoso
American Journal of Human Genetics
1994
Corpus ID: 9607961
Two hypotheses are capable of explaining nonrandom loss of one parent's alleles at tumor suppressor loci in sporadic cases of…
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1990
1990
Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.
R. Leach
,
A. N. Magewu
,
+6 authors
P. Jones
Cell growth & differentiation : the molecular…
1990
Corpus ID: 8195499
The origins of the initial mutations in sporadic retinoblastoma were explored using polymorphic markers from chromosome 13q. The…
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Review
1990
Review
1990
The molecular genetics of retinoblastoma.
D. Goodrich
,
W. Lee
Cancer Surveys
1990
Corpus ID: 24775869
Retinoblastoma is a potentially hereditary cancer. Refinement of the genetic and epidemiological analysis of the disease has…
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Highly Cited
1978
Highly Cited
1978
X-ray sensitivity of diploid fibroblasts from patients with hereditary or sporadic retinoblastoma.
R. Weichselbaum
,
J. Nove
,
J. Little
Proceedings of the National Academy of Sciences…
1978
Corpus ID: 10103533
Fibroblasts derived from patients with hereditary retinoblastoma appear to be more sensitive to the lethal effects of x-rays than…
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1976
1976
Cea family syndrome—Abnormal carcino embryonic antigen (CEA) levels in asymptomatic retinoblastoma family members
N. Felberg
,
J. B. Michelson
,
J. Shields
Cancer
1976
Corpus ID: 21315224
Plasma carcinoembryonic antigen (CEA) levels were studied in all available members of 17 families in which a presumed sporadic…
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