Objective: To determine the rate of growth in vestibular schwannomas and the rate of hearing decline in neurofibromatosis type 2 (NF2) patients not undergoing active treatment Study Design: Prospective study. Setting: Data were collected at 10 NF2 centers, including hospital-based, academic, and tertiary care centers. Patients: 120 NF2 patients with 200 vestibular schwannomas. Outcome Measures: Hearing decline, defined as a decrease in word recognition score outside the 95% critical difference compared with baseline, and radiographic progression, defined as a 20% or greater increase in tumor volume compared with baseline. Results: During a total of 313.4 patient-years of follow-up, the rate of hearing decline was 5% at 1 year, 13% at 2...
ObjectiveTo understand the differences in characteristics of neurofibromatosis type 2 (NF2) and spor...
Number: 11 PMID: 33388984PURPOSES: The first aim is to describe the epidemiological, clinical, and r...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Objective: Early studies suggest that bevacizumab treatment can result in tumor shrinkage and hearin...
Objective: Describe the changes in hearing ability and pro-gression of disease over time in subjects...
Objective: The purpose of this study was to identify factors predicting growth and audiologic deteri...
Neurofibromatosis type 2 (NF2) is a tumor suppressor gene syndrome characterized by multiple schwann...
Four longitudinal studies of vestibular schwannoma (VS) growth rates in neurofibromatosis 2 (NF2) ha...
Objective: To determine the long-term, spontaneous growth arrest rates in a large cohort of Vestibul...
Objectives: Vestibular schwannomas are the hallmark of neurofibromatosis 2 (NF2), occurring in >95% ...
Contains fulltext : 81894timmer.pdf (publisher's version ) (Closed access)Manageme...
OBJECTIVES: To develop a prediction model to predict vestibular schwannoma (VS) growth for patients ...
Objectives Although vestibular schwannomas (VS) are known to cause cranial nerve deficits, cerebell...
Background: NF2 patients develop multiple nervous system tumors including bilateral vestibular schwa...
Item does not contain fulltextBACKGROUND: Intracanalicular vestibular schwannomas have a range of tr...
ObjectiveTo understand the differences in characteristics of neurofibromatosis type 2 (NF2) and spor...
Number: 11 PMID: 33388984PURPOSES: The first aim is to describe the epidemiological, clinical, and r...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Objective: Early studies suggest that bevacizumab treatment can result in tumor shrinkage and hearin...
Objective: Describe the changes in hearing ability and pro-gression of disease over time in subjects...
Objective: The purpose of this study was to identify factors predicting growth and audiologic deteri...
Neurofibromatosis type 2 (NF2) is a tumor suppressor gene syndrome characterized by multiple schwann...
Four longitudinal studies of vestibular schwannoma (VS) growth rates in neurofibromatosis 2 (NF2) ha...
Objective: To determine the long-term, spontaneous growth arrest rates in a large cohort of Vestibul...
Objectives: Vestibular schwannomas are the hallmark of neurofibromatosis 2 (NF2), occurring in >95% ...
Contains fulltext : 81894timmer.pdf (publisher's version ) (Closed access)Manageme...
OBJECTIVES: To develop a prediction model to predict vestibular schwannoma (VS) growth for patients ...
Objectives Although vestibular schwannomas (VS) are known to cause cranial nerve deficits, cerebell...
Background: NF2 patients develop multiple nervous system tumors including bilateral vestibular schwa...
Item does not contain fulltextBACKGROUND: Intracanalicular vestibular schwannomas have a range of tr...
ObjectiveTo understand the differences in characteristics of neurofibromatosis type 2 (NF2) and spor...
Number: 11 PMID: 33388984PURPOSES: The first aim is to describe the epidemiological, clinical, and r...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...