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Relevant bibliographies by topics / Retinoblastoma

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Academic literature on the topic 'Retinoblastoma'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Retinoblastoma"

1

Johnson, Dennis L., Roma Chandra, Wink S. Fisher, M. Kathryn Hammock, and Craig A. McKeown. "Trilateral retinoblastoma: ocular and pineal retinoblastomas." Journal of Neurosurgery 63, no. 3 (1985): 367–70. http://dx.doi.org/10.3171/jns.1985.63.3.0367.

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✓ 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 usually obtained. The retinal tumors are often quiescent at the time that the pineal tumor is discovered, and show no evidence of metastatic spread after enucleation of the globes. Pathologically, the pineal tumor is indistinguishable from the ocul

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Putri, Mutia Arnisa. "Molecular Genetics Mutations of Retinoblastoma." Sriwijaya Journal of Ophthalmology 4, no. 2 (2021): 85–89. http://dx.doi.org/10.37275/sjo.v4i2.50.

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Retinoblastoma is a cancer that arises because both copies of the RB1 gene that normally suppresses retinoblastoma are lost from a developing retinal cell in fetuses, babies, and young children. Retinoblastoma is the prototype genetic cancer in one or both eyes of young children, most retinoblastomas are initiated by biallelic mutation of the retinoblastoma tumor suppressor gene, RB1, in a developing retinal cell. All those with bilateral retinoblastoma have heritable cancer, although 95% have not inherited the RB1 mutation. Nonheritable retinoblastoma is always unilateral, with 98% caused

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Kitazawa, Koji, Kenji Nagata, Yukito Yamanaka, et al. "Diffuse Anterior Retinoblastoma with Sarcoidosis-Like Nodule." Case Reports in Ophthalmology 6, no. 3 (2015): 443–47. http://dx.doi.org/10.1159/000442744.

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Background: Retinoblastomas account for 4% of malignancies in children, 1-2% of which are diffuse infiltrating retinoblastomas. Diffuse anterior retinoblastoma is rare and does not involve the retina. Here, we report on a diffuse anterior retinoblastoma with large sarcoidosis-like nodules on the iris that were responsive to anti-inflammatory therapy. Case: We present a 6-year-old girl who had anterior uveitis with white nodules on the iris and posterior surface of the cornea in her right eye. The nodules initially responded well to anti-inflammatory treatment. However, anterior segment optical

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Laurie, Nikia, Adithi Mohan, Justina McEvoy, et al. "Changes in Retinoblastoma Cell Adhesion Associated with Optic Nerve Invasion." Molecular and Cellular Biology 29, no. 23 (2009): 6268–82. http://dx.doi.org/10.1128/mcb.00374-09.

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ABSTRACT In the 1970s, several human retinoblastoma cell lines were developed from cultures of primary tumors. As the human retinoblastoma cell lines were established in culture, growth properties and changes in cell adhesion were described. Those changes correlated with the ability of the human retinoblastoma cell lines to invade the optic nerve and metastasize in orthotopic xenograft studies. However, the mechanisms that underlie these changes were not determined. We used the recently developed knockout mouse models of retinoblastoma to begin to characterize the molecular, cellular, and gene

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Katayama, Yoichi, Takashi Tsubokawa, Takamitsu Yamamoto, and Norimichi Nemoto. "Ectopic Retinoblastoma within the 3rd Ventricle: Case Report." Neurosurgery 28, no. 1 (1991): 158–61. http://dx.doi.org/10.1227/00006123-199101000-00024.

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Abstract Ectopic intracranial retinoblastomas arc rare. These tumors usually occur in the pineal, parasellar. or suprasellar regions several years after the successful treatment of ocular retinoblastomas with no evidence of direct extension or distant metastasis. We report here a case of ectopic retinoblastoma occurring within the third ventricle. The tumor was surgically excised by the transventricular approach. Ectopic retinoblastomas exhibit greater differentiation than one would expect to observe in a metastatic lesion of this tumor. The distinction of ectopic retinoblastomas and metastasi

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Setiawan, Arif. "Classification of Retinoblastoma Eye Disease on Digital Fundus Images Using Geometric Features and Machine Learning." Jurnal RESTI (Rekayasa Sistem dan Teknologi Informasi) 9, no. 3 (2025): 227–36. https://doi.org/10.29207/resti.v9i3.6337.

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Medical image analysis is essential for detecting retinoblastoma tumors due to the ability of this method to assist doctors in examining the morphology, density, and distribution of blood vessels. The classification of normal and retinoblastoma-affected retinas is a preliminary step in treating retinoblastoma tumors. Therefore, this study aimed to propose a new method for classifying normal and retinoblastoma-affected retinas using geometric feature extraction and machine learning. The workflow consisted of (1) fundus image data collection for retinoblastomas, (2) image segmentation, (3) featu

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Giri, Winda W., Yuli Anandasari, Ni Nyoman Margiani, Dwija Putra Ayusta, Ketut Ariawati, and Sri Mahendra Dewi. "Retinoblastoma or Neuroblastoma: an imaging polemic issues." International Journal of Research in Medical Sciences 8, no. 2 (2020): 771. http://dx.doi.org/10.18203/2320-6012.ijrms20200273.

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Both retinoblastoma and neuroblastoma are common childhood malignancy, which classified as malignant round cell tumors, but have different diagnostic, therapeutic, prognostic criteria and metastases pattern. A case was evaluated with an imaging examination resembled neuroblastoma metastatic process but was diagnosed as retinoblastoma. A 2-years-old boy came with chief complaint swollen right eye. Prior history was itchy and increasingly swollen right eye, decreased vision and gradually increases pain. There was no sign of leukocoria. Histopathology result confirmed malignant round cell tumor.

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Lindahl, S. "Computed Tomography of Retinoblastoma." Acta Radiologica. Diagnosis 27, no. 5 (1986): 513–18. http://dx.doi.org/10.1177/028418518602700505.

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Retinoblastoma is the most common primary malignant intraocular tumor in children. The clinical features are leucocoria and/or strabismus. The ophthalmic diagnosis is straight forward in clear eye media with a white gray mass in the fundus. With opaque ocular media, other diagnostic procedures such as CT and ultrasonography are important. In the present study the results of CT examinations of 23 patients with histologically proven retinoblastomas are presented. The mean age of the patients was two years. The characteristic CT finding is a partly calcified intravitreous mass lesion mostly confi

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Fang, Xiaolian, Huanmin Wang, Xiaoli Ma, et al. "Clinical Features of Children with Retinoblastoma and Neuroblastoma." Journal of Ophthalmology 2020 (July 10, 2020): 1–8. http://dx.doi.org/10.1155/2020/9315784.

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Purpose. Retinoblastoma and neuroblastoma are the most common malignant extracranial solid tumors in children. This study aimed to summarize the clinical features, especially the delayed diagnosis in children with retinoblastoma and neuroblastoma. Methods. In a single hospital-based case-control study, a retrospective cohort of 175 children with retinoblastoma and neuroblastoma diagnosed from January 2016 to January 2018 were reviewed. The state of enucleation in retinoblastomas and pathological prognosis in neuroblastomas were outcome indicators. Hereby, the patients were divided into two gro

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Eagle Jr, Ralph C. "High-Risk Features and Tumor Differentiation in Retinoblastoma: A Retrospective Histopathologic Study." Archives of Pathology & Laboratory Medicine 133, no. 8 (2009): 1203–9. http://dx.doi.org/10.5858/133.8.1203.

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Abstract Context.—Certain histopathologic risk factors in enucleated eyes are important indicators for adjuvant chemotherapy in patients with retinoblastoma. Objectives.—To determine the frequency of histopathologic risk factors in a large series of retinoblastomas treated by enucleation on file in the pathology laboratory of a large American eye hospital, assess the relationship between tumor differentiation and age at enucleation, and investigate the frequency of photoreceptor differentiation and the role of retinoma/retinocytoma as retinoblastoma precursor. Design.—Retrospective histopathol

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Dissertations / Theses on the topic "Retinoblastoma"

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Ribeiro, Maria Cecilia Menks. "Aspectos citogeneticos do retinoblastoma." São Paulo (SP), 1988. https://repositorio.ufsc.br/handle/123456789/106296.

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Walther, Jan. "Efficient Photodynamic Therapy on Human Retinoblastoma Cell Lines." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-169627.

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Die Photodynamische Therapie (PDT) hat sich zunehmend als vielversprechende Methode zur Behandlung von verschiedenen malignen Neubildungen gezeigt. Die photodynamische Zerstörung der Tumore wird erreicht indem zunächst ein Photosensibilisator entweder lokal oder systemisch appliziert wird und im Anschluss an eine gewisse Inkubationszeit die Tumormasse mittels einer Lichtquelle mit einer spezifischen Wellenlänge durchleuchtet wird. Aufgrund der bevorzugten Anreicherung des Photosensibilisators in Tumorzellen, erlaubt diese Methode eine selektive Abtötung des malignen Tumors, während das umliege

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Walther, Jan, Stanislas Schastak, Sladjana Dukic-Stefanovic, Peter Wiedemann, Jochen Neuhaus, and Thomas Claudepierre. "Efficient photodynamic therapy on human retinoblastoma cell lines." Universitätsbibliothek Leipzig, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-148182.

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Photodynamic therapy (PDT) has shown to be a promising technique to treat various forms of malignant neoplasia. The photodynamic eradication of the tumor cells is achieved by applying a photosensitizer either locally or systemically and following local activation through irradiation of the tumor mass with light of a specific wavelength after a certain time of incubation. Due to preferential accumulation of the photosensitizer in tumor cells, this procedure allows a selective inactivation of the malignant tumor while sparing the surrounding tissue to the greatest extent. These features and requ

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Kleinerman, Ruth. "Second cancers following treatment for retinoblastoma." Thesis, City, University of London, 2016. http://openaccess.city.ac.uk/17330/.

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Improvements in treatment over the past century have greatly increased survival for retinoblastoma, a rare childhood tumour of the eye, caused by mutations of the RB1 tumour suppressor gene. However, as survival for retinoblastoma has improved, those with the hereditary form of the disease (RB1 germline mutation) have elevated risks of developing additional cancers, mostly bone and soft tissue sarcomas and melanoma. Despite advances in understanding of second cancer risks following treatment for retinoblastoma, key research questions remained including 1) risks of common adult onset cancers, s

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Lillington, Debra Mia. "The investigation of genomic imbalance in retinoblastoma." Thesis, Queen Mary, University of London, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499104.

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Chew, Yat Peng. "Regulation of the retinoblastoma protein by phosphorylation." Thesis, Institute of Cancer Research (University Of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391767.

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Sefta, Meriem. "Comprehensive Molecular and Clinical Characterization of Retinoblastoma." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS074/document.

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Le rétinoblastome est un cancer pédiatrique rare de la rétine en cours de développement. Si dans les pays développés, le taux de survie avoisine 100%, une énucléation de l’oeil atteint est cependant nécessaire dans plus de 70% des cas.En 1971, Knudson émit l’hypothèse des deux “hits”, qui permit de comprendre que le rétinoblastome s’initie généralement après une perte bi-allélique du gène RB1. Cependant, les autres mécanismes moléculaires qui régissent ce cancer restent depuis peu connus. Par exemple, peu d’études génomiques ont été conduites. Ainsi, la nature de la cellule d’origine, ainsi qu

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Côté, Richard Gaston. "Characterization of the retinoblastoma binding protein 2 (RBP2)." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33388.

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The retinoblastoma (RB) family of proteins plays a pivotal role in cell cycle regulation. Its members, p105/Rb, p107 and p130, interact with the E2F and DP family of transcription factors to regulate transcription of essential cell cycle and DNA synthesis genes. Several reports have mapped the regulation of E217 by RB family members to the "pocket" domain of these proteins. We demonstrate here that RBP2, a pocket-binding protein that encodes multiple DNA-binding and protein-protein interaction domains, is a transcriptional repressor. Overexpression of RBP2 inhibits E2F-dependent transcription

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Inche, Adam. "The post translational modification of the retinoblastoma protein." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491620.

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The retinoblastoma protein (pRb) is a central figure in the control of not only the cell cycle, but also other cellular functions such as differentiation. The regulation of pRb function is through a variety of post translational modifications, either on pRb itself, or by the controlling influence of pRb on the post translational modification of the histone proteins. Phosphorylation of pRb is a key mechanism in the regulation of the cell cycle. pRb is also involved in the recruitment of histone methyltransferase (HMT) and acetyltransferase (HAT) to the chromatin to modify histones. Previous wor

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Markham, Douglas James. "Acetylation control of the retinoblastoma tumour suppressor protein." Thesis, University of Glasgow, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433229.

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Books on the topic "Retinoblastoma"

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Rodriguez-Galindo, Carlos, and Matthew W. Wilson, eds. Retinoblastoma. Springer US, 2010. http://dx.doi.org/10.1007/978-0-387-89072-2.

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1917-, Blodi Frederick C., ed. Retinoblastoma. Churchill Livingstone, 1985.

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Rodríguez-Gallego, Carlos, and Matthew W. Wilson. Retinoblastoma. Springer, 2010.

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Santiago-Cardona, Pedro G., ed. The Retinoblastoma Protein. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7565-5.

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Francis, Jasmine H., and David H. Abramson, eds. Recent Advances in Retinoblastoma Treatment. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19467-7.

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Burcescu, Irina D. The role of the retinoblastoma protein in retinal development. National Library of Canada, 2001.

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Zhu, Xiaoping. Analysis of loss of heterozygosity for the retinoblastoma gene. National Library of Canada, 1991.

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Ehlers, Niels. Effects of ionizing radiation on retinoblastoma and on the normal ocular fundus in infants: A photographic and fluorescein angiographic study. Scriptor, 1987.

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9

N, Bornfeld, ed. Tumors of the eye: Proceedings of the international symposiums in Geneva, Switzerland, November 23-27, 1987, and Essen, FRG, September 21-23, 1989. Kugler Publications, 1991.

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Parker, James N., and Philip M. Parker. Retinoblastoma: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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Book chapters on the topic "Retinoblastoma"

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Dyer, Michael A. "Biology of Retinoblastoma." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_1.

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Hoehn, M. E. "Visual Rehabilitation." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_10.

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Chantada, G. L., S. Luna-Fineman, I. Qaddoumi, A. Furmanchuk, and J. Wilimas. "Retinoblastoma in Developing Countries." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_11.

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Orjuela, M. "Epidemiology." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_2.

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Chévez-Barrios, P., and D. S. Gombos. "Clinical Features, Diagnosis, Pathology." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_3.

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Dimaras, H., and B. L. Gallie. "Genetics of Retinoblastoma and Genetic Counseling." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_4.

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Merchant, T. E. "Radiation Therapy in the Management of Retinoblastoma." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_5.

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Rodriguez-Galindo, C. "Chemotherapy in the Management of Retinoblastoma." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_6.

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Wilson, M. W. "Treatment of Intraocular Retinoblastoma." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_7.

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Chantada, G. L., and I. J. Dunkel. "Treatment of Extraocular and Metastatic Retinoblastoma." In Retinoblastoma. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89072-2_8.

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Conference papers on the topic "Retinoblastoma"

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Park, Jun Hon, Sourabh Madhav Mehta, Ramasamy Paulmurugan, and Jeremy J. Dahl. "Ultrasound-assisted targeted delivery of drug-loaded nanoparticles for retinoblastoma treatment." In 2024 IEEE Ultrasonics, Ferroelectrics, and Frequency Control Joint Symposium (UFFC-JS). IEEE, 2024. https://doi.org/10.1109/uffc-js60046.2024.10793607.

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Alharbi, Shuaa. "Retinoblastoma Detection: Leveraging Deep Learning and Residual Connections for Enhanced Diagnostic Accuracy." In 12th International Conference on Bioimaging. SCITEPRESS - Science and Technology Publications, 2025. https://doi.org/10.5220/0013099000003911.

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Oliveira, Eduardo da Silva, Luana da Silva Fernandes, Juliana Maria de Oliveira Corrêa, and Mariana Pinto Ferreira. "RETINOBLASTOMA: UMA ANÁLISE SOBRE A IMPORTÂNCIA DO DIAGNÓSTICO PRECOCE E FORMAS DE TRATAMENTO." In IX Congresso Acadêmico-Científico do UNIFESO. Even3, 2024. https://doi.org/10.29327/1449322.9-84.

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SILVA, LARISSA FREITAS PEREIRA MARQUES DA. "Função Coclear em Crianças com Retinoblastoma." In Anais do XXIX Simpósio e XIV Jornada de Fonoaudiologia da UNIFESP. Even3, 2018. http://dx.doi.org/10.29327/18052.29-1.

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Souza, Thifisson Ribeiro de, CAROLINA RUSSO BORDIN, VICENTE FELIZARI JUNIOR, and RAFAEL MORAIS FERNANDEZ. "FATORES PREDISPONENTES À INCIDÊNCIA DE RETINOBLASTOMA." In V Congresso Brasileiro de Saúde On-line. Revista Multidisciplinar em Saúde, 2024. http://dx.doi.org/10.51161/conbrasau2024/35305.

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Matsumoto, Caroline Mary, Bruna Cristina Mattos de Pieri, Gabrielle Gonçalves, Kawanna Izabella Buzzo Feitosa, and Sophia Oliveira Basso. "O ESTUDO DA PATOGÊNESE E DA HISTOPATOLOGIA DO RETINOBLASTOMA NO CENÁRIO DE PESQUISA CIENTÍFICA BRASILEIRA: UMA REVISÃO DE LITERATURA." In I Congresso On-line Nacional de Histologia e Embriologia Humana. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/rems/3210.

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Introdução: O retinoblastoma (RB) é uma neoplasia maligna intraocular da infância, sendo o quarto câncer pediátrico mais frequente no Brasil. Quando analisados dados prognósticos, há distinção entre países desenvolvidos e subdesenvolvidos devido ao tempo do diagnóstico. Se identificado tardiamente, o RB conduz à cegueira, torna-se extraocular e até fatal se tiver alcance do sistema nervoso central. Objetivos: Realizar um estudo sobre a patogênese e a histopatologia do RB através do conteúdo existente no cenário de pesquisa acadêmica brasileira. Material e métodos: Houve a análise da literatura

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Vargas-Cuentas, Natalia I., Fiorella Flores Medina, Kevin Rodriguez Villarreal, and Avid Roman-Gonzalez. "System for the Early Detection of Retinoblastoma." In 2019 IEEE 39th Central America and Panama Convention (CONCAPAN XXXIX). IEEE, 2019. http://dx.doi.org/10.1109/concapanxxxix47272.2019.8977025.

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Ghanaati, Hossein, Kavous Firouznia, and Fariba Ghasemi. "Outcome of Retinoblastoma after Intra-Arterial Chemotherapy." In PAIRS Annual Meeting. Thieme Medical and Scientific Publishers Pvt. Ltd., 2019. http://dx.doi.org/10.1055/s-0041-1730524.

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Zhang, Michelle Garying, Dawn Owens, Stefan Kurtenbach, et al. "Abstract 3027: Role of BCOR in retinoblastoma." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-3027.

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Shokuhfar, T., R. Abdalla, S. Ansari, M. Hurley, B. Rahmani, and A. Shaibani. "O-030 Opthalmic artery chemotherapy in retinoblastoma." In SNIS 16TH ANNUAL MEETING. BMJ Publishing Group Ltd., 2019. http://dx.doi.org/10.1136/neurintsurg-2019-snis.30.

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Reports on the topic "Retinoblastoma"

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Watznauer, Brittany. Retinoblastoma: Symptoms, Pathology, Genetics, and Treatments. Iowa State University, 2019. http://dx.doi.org/10.31274/cc-20240624-1232.

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Rajabi, Hasan N. The Mechanism of Retinoblastoma Protein-Mediated Terminal Cell Cycle Arrest. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada421731.

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Churchill, M. E., M. A. Gemmell, and G. E. Woloschak. PCR detection of retinoblastoma gene deletions in radiation-induced mouse lung adenocarcinomas. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10149484.

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Churchill, M. E., M. A. Gemmell, and G. E. Woloschak. Polymerase chain reaction detection of retinoblastoma gene deletions in paraffin-embedded mouse lung adenocarcinomas. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/10173425.

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Langan, Thomas. Role of Changes in the Expression of Cyclins and Retinoblastoma Protein in the Development of Breast Cancer. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada368340.

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Langan, Thomas A. Role of Changes in the Expression of Cyclins and Retinoblastoma Protein in the Development of Breast Cancer. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada371210.

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Langan, Thomas A. Role of Changes in the Expression of Cyclins and Retinoblastoma Protein in the Development of Breast Cancer. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada303157.

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Langan, Thomas A. Role of Changes in the Expression of Cyclins and Retinoblastoma Protein in the Development of Breast Cancer. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada337790.

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Ely, Kathryn R. Tumor Suppressors and Breast Cancer: Molecular Interaction of Retinoblastoma Protein (Rb) with a New Rb-binding Protein (RIZ). Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada383081.

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Grafi, Gideon, and Brian Larkins. Endoreduplication in Maize Endosperm: An Approach for Increasing Crop Productivity. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7575285.bard.

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The focus of this research project is to investigate the role of endoreduplication in maize endosperm development and the extent to which this process contributes to high levels of starch and storage protein synthesis. Although endoreduplication has been widely observed in many cells and tissues, especially those with high levels of metabolic activity, the molecular mechanisms through which the cell cycle is altered to produce consecutive cycles of S-phase without an intervening M-phase are unknown. Our previous research has shown that changes in the expression of several cell cycle regulatory

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