نتایج جستجو برای: Retinoblastoma

تعداد نتایج: 7252  

Background and Aims: Retinoblastoma tumors are the most common intraocular malignancy in childhood, leading to death after two years. The Human Adenovirus (HAdV) infection could be critical in the retinoblastoma pathogenesis due to the virus and retinoblastoma 1 interactions. The objective of the current study was to investigate the possible presence of the HAdV genome in the retinoblastoma pat...

بشارتی, محمدرضا, خیراندیش, مریم, هاشمی, اعظم السادات,

Retinoblastoma is a retinal malignant tumor that occurs in early childhood. The annual incidence of retinoblastoma is approximately one per 14 000 live births. 250 to 300 new cases are reported in the United States each year. It develops due to inactivation of both alleles of the retinoblastoma susceptibility (RB1) gene. All hereditary cases (55%) are with bilateral and multifocal lesions, but ...

ژورنال: کومش 2019
Asadi Amoli , Fahimeh , Ghasemi , Fariba , Mokhtari-Dizaji , Manijhe , Moradi , Somayeh , Sheibani , Shahab ,

Introduction: Retinoblastoma is a malignant tumor in children. The goal of retinoblastoma treatment is to maintain vision and minimize side effects. In this study, the toxicity of the gold nanoparticle safety in vitro was investigated on an eye tumor of retinoblastoma under in vivo conditions. Materials and Methods: For the evaluation of the toxicity of gold nanoparticles using MTT test after 4...

Journal: :journal of current ophthalmology 0
فریبا قاسمی fariba ghassemi هرمز شمس hormoz chams سیامک صبور siamak sabour رضا کارخانه reza karkhaneh فرزاد فرزبد farzad farzbod مهدی خداپرست mahdi khodaparast پروانه وثوق

purpose : retinoblastoma (rb) is a relatively common childhood tumor. in this report we discuss the clinical characteristics, treatments and outcome of the treated rb patients from a referral center in iran in order to understand this medical problem in our society. methods : a retrospective study was carried out on rb cases treated in farabi eye hospital since 1979 to 2007. the variables analy...

Introduction: Retinoblastoma (RB) is a malignant retinal tumor, which affects infants and children. This cancer happens through a mutation in the retinoblastoma tumor suppressor genes (RB1). Inactivation of RB1 has been observed in more than 97% of all retinoblastoma patients with mutations. In recent years, RB treatment has developed significantly. RBchr('39')s treatment methods can be one or ...

Journal: :بینا 0
احمدعلی فردوسی aa ferdosi ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranدانشگاه علوم پزشکی شهید بهشتی آزاده دوزنده a doozandeh

purpose: to introduce a case of neglected advanced retinoblastoma. case report: a 6 year old girl presented with a large orbital mass enlarging over her cheek on the right side. she underwent exenteration and histopathologic evaluation. a diagnosis of retinoblastoma was made with free margins. this case presents a rare form of retinoblastoma with extensive local progression but no metastasis or...

Journal: :Advances in Bioscience and Biotechnology 2023

The Retinoblastoma 1 (RB1) gene, located on chromosome 13q14 and encodes the tumor-suppressor retinoblastoma protein, is cause of Retinoblastoma. mutational inactivation both gene alleles brings this cancer. (RB) high-risk histopathological characteristics indicate metastasis or local recurrence with rapid progresses following RB1 inactivation. There growing interest in regulatory activities un...

Journal: :acta medica iranica 0
f. asadi amoli n. piri h. shams

retinoblastoma is the most common primary intraocular malignancy in childhood. enucleation remains the treatment of choice in many children because the eye can not be salvaged with any other treatment modality. in some cases after enucleation etiologies other than retinoblastoma are detected in histopathologic review (pseudoretinoblastomas). this study aims to evaluate the prevalence and etiolo...

Journal: :Neuro-oncology 2022

Abstract Retinoblastoma, the most common intraocular tumor of childhood, was recently shown to comprise two major molecular subtypes. Subtype 1 includes heritable forms, with germline mutation RB1 and a cone-differentiated state. 2 is often non-hereditary, exhibits stemness features, increased expression MYCN its target genes, high risk metastasis. Relative subtype 1, tumors have worse prognosi...

Journal: :acta medica iranica 0
mojgan mirakholi department of pathology, faculty of medicine and health sciences, university putra malaysia, 43400 upm serdang, malaysia. touraj mahmoudi department of cancer, research center for gastroenterology and liver diseases (rcgld), shahid beheshti university of medical sciences, tehran, iran. mansour heidari department of medical genetics, faculty of medicine, tehran university of medical sciences, tehran, iran. and stem cell preparation unit, farabi eye hospital, tehran university of medical sciences, tehran, iran.

in the retinoblastoma research, it is of great interest to identify molecular markers associated with the genetics of tumorigenesis. micrornas (mirnas) are small non-coding rna molecules that play a regulatory role in many crucial cellular pathways such as differentiation, cell cycle progression, and apoptosis. a body of evidences showed dysregulation of mirnas in tumor biology and many disease...

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