Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1955 1
1958 1
1964 1
1967 1
1969 2
1970 1
1971 2
1972 1
1973 1
1974 2
1975 8
1976 5
1977 9
1978 11
1979 7
1980 6
1981 12
1982 20
1983 22
1984 29
1985 14
1986 26
1987 32
1988 21
1989 49
1990 28
1991 28
1992 27
1993 27
1994 30
1995 26
1996 31
1997 25
1998 37
1999 38
2000 27
2001 52
2002 46
2003 52
2004 53
2005 47
2006 48
2007 59
2008 54
2009 84
2010 66
2011 78
2012 117
2013 117
2014 117
2015 148
2016 133
2017 118
2018 136
2019 122
2020 139
2021 160
2022 149
2023 118
2024 58

Text availability

Article attribute

Article type

Publication date

Search Results

2,547 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Retina neoplasm"
Page 1
Retinoblastoma, the visible CNS tumor: A review.
Dimaras H, Corson TW. Dimaras H, et al. J Neurosci Res. 2019 Jan;97(1):29-44. doi: 10.1002/jnr.24213. Epub 2018 Jan 3. J Neurosci Res. 2019. PMID: 29314142 Free PMC article. Review.
The pediatric ocular cancer retinoblastoma is the only central nervous system (CNS) tumor readily observed without specialized equipment: it can be seen by, and in, the naked eye. ...
The pediatric ocular cancer retinoblastoma is the only central nervous system (CNS) tumor readily observed without specialized equipm …
Retinoblastoma: From genes to patient care.
Bouchoucha Y, Matet A, Berger A, Carcaboso AM, Gerrish A, Moll A, Jenkinson H, Ketteler P, Dorsman JC, Chantada G, Beck-Popovic M, Munier F, Aerts I, Doz F, Golmard L; European Retinoblastoma Group EuRbG. Bouchoucha Y, et al. Eur J Med Genet. 2023 Jan;66(1):104674. doi: 10.1016/j.ejmg.2022.104674. Epub 2022 Dec 5. Eur J Med Genet. 2023. PMID: 36470558 Review.
Retinoblastoma is the most common paediatric neoplasm of the retina, and one of the earliest model of cancer genetics since the identification of the master tumour suppressor gene RB1. ...This is expected to facilitate assessment of the constitutional status of RB1, …
Retinoblastoma is the most common paediatric neoplasm of the retina, and one of the earliest model of cancer genetics since th …
Liquid biopsy in Retinoblastoma: A review.
Ghose N, Kaliki S. Ghose N, et al. Semin Ophthalmol. 2022 Oct-Nov;37(7-8):813-819. doi: 10.1080/08820538.2022.2078165. Epub 2022 May 23. Semin Ophthalmol. 2022. PMID: 35604935 Review.
Currently, there is a search for surrogate markers to allow accurate diagnosis and for prognostication, to predict the chances of globe salvage in RB. Therefore, biofluids such as plasma or aqueous humor have been studied to detect circulating tumor DNA (ctDNA) or cell-fre …
Currently, there is a search for surrogate markers to allow accurate diagnosis and for prognostication, to predict the chances of glo …
Reconstruct Human Retinoblastoma In Vitro.
Zhang X, Jin ZB. Zhang X, et al. J Vis Exp. 2022 Oct 11;(188). doi: 10.3791/62629. J Vis Exp. 2022. PMID: 36314812
Herein, the protocol describes the generation of two gene-edited hESC lines with a biallelic RB1 point mutation (RB1(Mut/Mut)) and an RB1 knockout mutation (RB1(-/-)), respectively. During the process of retinal development, the formation of RB is observed. The RB c …
Herein, the protocol describes the generation of two gene-edited hESC lines with a biallelic RB1 point mutation (RB1(Mut/Mut)) and an RB1 kn …
Retinoblastoma.
Aerts I, Lumbroso-Le Rouic L, Gauthier-Villars M, Brisse H, Doz F, Desjardins L. Aerts I, et al. Orphanet J Rare Dis. 2006 Aug 25;1:31. doi: 10.1186/1750-1172-1-31. Orphanet J Rare Dis. 2006. PMID: 16934146 Free PMC article. Review.
Retinoblastoma is a rare eye tumor of childhood that arises in the retina. It is the most common intraocular malignancy of infancy and childhood; with an incidence of 1/15,000-20,000 live births. ...Iris rubeosis, hypopyon, hyphema, buphthalmia, orbital cellulites and exop …
Retinoblastoma is a rare eye tumor of childhood that arises in the retina. It is the most common intraocular malignancy of infancy an …
Cavitary retinoblastoma: clinical observations.
Rishi P, Sharma U, Sharma T. Rishi P, et al. Eye (Lond). 2020 Apr;34(4):704-710. doi: 10.1038/s41433-019-0581-1. Epub 2019 Sep 18. Eye (Lond). 2020. PMID: 31534184 Free PMC article.
Tumour recurrence was noted in 1(8%) eye. Cavity rupture with release of vitreous seeds was observed in one eye. Two (20%) eyes with vitreous seeds were treated with intravitreal chemotherapy. ...
Tumour recurrence was noted in 1(8%) eye. Cavity rupture with release of vitreous seeds was observed in one eye. Two (20%) eyes with …
von Hippel-Lindau disease.
Singh AD, Shields CL, Shields JA. Singh AD, et al. Surv Ophthalmol. 2001 Sep-Oct;46(2):117-42. doi: 10.1016/s0039-6257(01)00245-4. Surv Ophthalmol. 2001. PMID: 11578646 Review.
The inheritance of VHL disease is autosomal dominant with high penetrance. Depending on the clinical circumstances, retinal capillary hemangioma may be managed by observation, laser photocoagulation, cryotherapy, and plaque radiotherapy. ...We review herein the opht …
The inheritance of VHL disease is autosomal dominant with high penetrance. Depending on the clinical circumstances, retinal capillary …
Genetics in ophthalmology: molecular blueprints of retinoblastoma.
Marković L, Bukovac A, Varošanec AM, Šlaus N, Pećina-Šlaus N. Marković L, et al. Hum Genomics. 2023 Sep 1;17(1):82. doi: 10.1186/s40246-023-00529-w. Hum Genomics. 2023. PMID: 37658463 Free PMC article. Review.
Retinoblastoma is an intraocular tumor with hereditary and sporadic forms. 8,000 new cases of this ocular malignancy of the developing retina are diagnosed each year worldwide. The major gene responsible for retinoblastoma is RB1, and it harbors a large spectrum of pathoge …
Retinoblastoma is an intraocular tumor with hereditary and sporadic forms. 8,000 new cases of this ocular malignancy of the developing re …
Presentation, Diagnostic Testing and Initial Treatment of Vitreoretinal Lymphoma.
International Vitreoretinal B-Cell Lymphoma Registry Investigator Group. International Vitreoretinal B-Cell Lymphoma Registry Investigator Group. Ophthalmol Retina. 2024 Jan;8(1):72-80. doi: 10.1016/j.oret.2023.08.012. Epub 2023 Aug 28. Ophthalmol Retina. 2024. PMID: 37648063 Free article.
This work describes presentation, diagnostic testing, and first treatment approaches in a recently diagnosed and treated patient cohort. DESIGN: Clinical registry-based observational study. SUBJECTS: Forty-eight women and 32 men (age range, 32-91 years; median age, 64 year …
This work describes presentation, diagnostic testing, and first treatment approaches in a recently diagnosed and treated patient cohort. DES …
Retinoblastoma in Taiwan: survival and clinical characteristics.
Chen PY, Kao LY, Chao AN, Wu WC, Sun MH, Su WW, Liu CH. Chen PY, et al. Jpn J Ophthalmol. 2021 Jul;65(4):546-553. doi: 10.1007/s10384-021-00836-6. Epub 2021 May 4. Jpn J Ophthalmol. 2021. PMID: 33948759
CONCLUSIONS: Improvement of survival and globe salvage rate was observed over time periods. National health insurance program has made medical care easily accessible to the public, leading to earlier diagnosis and treatment. ...
CONCLUSIONS: Improvement of survival and globe salvage rate was observed over time periods. National health insurance program has mad …
2,547 results