R Listernick, J Charrow, M Greenwald, M Mets - The Journal of pediatrics, 1994 - Elsevier The natural history of OPT in children with NF-1 is unclear. Although the tumors
are benign, composed histologically of glial cells and a mucinous substance with
only rare mitotic figures, their rate of growth varies widely. Some ... Cited by 214 - Related articles - BL Direct - All 8 versions
AJ Janss, R Grundy, A Cnaan, PJ Savino, RJ … - CA A Cancer Journal for Clinicians - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 113 - Related articles - BL Direct - All 3 versions
R Listernick, C Darling, M Greenwald, L … - The Journal of pediatrics, 1995 - Elsevier The clinical manifestations and natural history of OPT that are not associated
with NF-1 are less well known. Some reports have demonstrated longer survival in
children with OPT and NF-1, 4 and 5 but conflicting results have been ... Cited by 79 - Related articles - BL Direct - All 5 versions
R Listernick, J Charrow, DH Gutmann - American journal of medical genetics, 1999 - interscience.wiley.com Dr. Listernick is an associate professor of pediatrics at Northwestern
University Medical School. He is co-director of the Neurofibromatosis Clinic and
director of the Diagnostic and Consultation Service of the Children's ... Cited by 64 - Related articles - BL Direct - All 4 versions
J Debus… - International Journal of Radiation Oncology* Biology* …, 1999 - Elsevier Results: All patients treated by definitive radiotherapy remained free from
local tumor progression during the follow-up period (range 12–72 months)
except the 1 patient treated for recurrence after previous radiotherapy. A ... Cited by 44 - Related articles - BL Direct - All 7 versions
R Delfini, P Missori, R Tarantino, P Ciappetta … - Surgical neurology, 1996 - Elsevier “En bloc” removal in patients with optic nerve glioma led to complete visual
deficit but ensures excellent long-term prognosis. Because optic nerve
meningiomas are typically circumferential to the optic nerve and adhere ... Cited by 27 - Related articles - BL Direct - All 5 versions
K North, C Cochineas, E Tang, E Fagan - Pediatric neurology, 1994 - Elsevier Optic gliomas occur in 15% of patients with neurofibromatosis type 1 (NF 1) and
are a significant cause of morbidity. Of these tumors, 20–30% become
symptomatic, usually before age 10 years. Previous studies have suggested ... Cited by 23 - Related articles - All 7 versions
J Charrow, R Listernick, MJ Greenwald, L … - Pediatric Blood & Cancer - interscience.wiley.com Optic pathway tumors are common in children with neurofibromatosis-1 (NF-1). The
optimal management of these tumors is unknown, particularly when the optic
chiasm and other brain structures are involved. We report the dramatic ... Cited by 12 - Related articles - BL Direct - All 3 versions
