Abstract
Retinoblastoma: How Advancements in Neurology and Neuroscience Can Help
Retinoblastoma is a significant cause of childhood eye cancer world-wide with prognosis dependent upon early diagnosis and treatment but also upon accurate classification of tumours. Unilateral incidence is normally non-hereditary compared with bilateral incidence. Survivorship is much better for unilateral compared with bilateral and trilateral retinoblastoma but the early signs are important to detect and photography can assist in identifying no return of “red-eye” during flash photography or a distinctive white or yellow appearance of the tumour.
Author(s):
Simon B N Thompson
Abstract | Full-Text | PDF
Share this
30+ Million Readerbase
Abstracted/Indexed in
- Google Scholar
- Open J Gate
- Genamics JournalSeek
- The Global Impact Factor (GIF)
- China National Knowledge Infrastructure (CNKI)
- Directory of Research Journal Indexing (DRJI)
- WorldCat
- Proquest Summons
- Scientific Journal Impact Factor
- Secret Search Engine Labs
- Euro Pub
Open Access Journals
- Aquaculture & Veterinary Science
- Chemistry & Chemical Sciences
- Clinical Sciences
- Engineering
- General Science
- Genetics & Molecular Biology
- Health Care & Nursing
- Immunology & Microbiology
- Materials Science
- Mathematics & Physics
- Medical Sciences
- Neurology & Psychiatry
- Oncology & Cancer Science
- Pharmaceutical Sciences