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Last Updated: 03/06/2025
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Found 115 publications
RADIATION RETINOPATHY AND BENIGN LYMPHOPROLIFERATIVE ORBITAL TUMOR PRESENTING 47 YEARS AFTER TREATMENT OF HEREDITARY RETINOBLASTOMA.
Journal: Retinal cases & brief reports
Published: December 06, 2023
Secondary leiomyosarcoma of the nasal cavity in a treated patient with possible hereditary retinoblastoma with germline reciprocal translocation of RB1 and DMXL1 and somatic TP53 mutation: A case report.
Journal: Molecular and clinical oncology
Published: February 15, 2023
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignancies.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 12, 2022
13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report.
Journal: Annals of medicine and surgery (2012)
Published: September 22, 2020
Orbital leiomyosarcoma post-irradiated hereditary retinoblastoma: A case study
Journal: Journal francais d'ophtalmologie
Published: March 16, 2020
Bone and Soft-Tissue Sarcoma Risk in Long-Term Survivors of Hereditary Retinoblastoma Treated With Radiation.
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: October 18, 2019
Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma with Myxoid Stroma in a Hereditary Retinoblastoma Survivor.
Journal: Ocular oncology and pathology
Published: June 05, 2019
Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapy.
Journal: European journal of medical genetics
Published: January 07, 2018
Prenatal ultrasonographic detection and prenatal (prior to birth) management of hereditary retinoblastoma.
Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
Published: September 04, 2017
Erratum to: "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
Journal: Clinical epigenetics
Published: February 02, 2017
A polymorphism in mir-34b/c as a potential biomarker for early onset of hereditary retinoblastoma.
Journal: Cancer biomarkers : section A of Disease markers
Published: January 21, 2017
Last Updated: 03/06/2025