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schwannomasDisease
NF2 is much less common than NF1, affecting 1:35,000 to 1:50,000 persons. CNS tumors are the major feature in NF2. Meningiomas, gliomas, and schwannomas are common, but bilateral vestibular schwannomas are nearly always present. In general, there are two categories of patients with NF2: those with an early-onset, rapid course associated with multiple other tumors in addition to bilateral vestibular schwannomas, and those with a late-onset, more benign course and only bilateral vestibular schwannomas
Neurofibromatosis type 2 (NF2) is an autosomal dominant disease with the hallmark of bilateral vesti...
Introduction Neurofibromatosis type 2 (NF2) and schwannomatosis are entities that may, due to the si...
The clinical features, age at onset of symptoms and survival of 150 patients with type 2 neurofibrom...
NF2 is much less common than NF1, affecting 1:35,000 to 1:50,000 persons. CNS tumors are the major f...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Neurofibromatosis type 2 (NF2) is an inherited disease which is mainly characterized by the developm...
Neurofibromatosis 2 (NF2) is a rare genetic disease that affects approximately 1 in 40000 people, s...
Background: Neurofibromatosis Type 2 (NF2) is a dominantly inherited tumour syndrome with a phenotyp...
Copyright © 2012 Kiran Gangadhar et al. This is an open access article distributed under the Creativ...
A 5-year-old girl presented with multiple tumours of the central nervous system. As on the first MRI...
associated with neurofibromatosis type 2. Although laryn-geal neurofibromas have previously been rep...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Clinical and genetic studies had for some time suggested two forms of neurofibromatosis. In 1988, a ...
Neurofibromatosis 2 (NF2) is an autosomal dominant disease that is characterized by tumors on the ve...
The radiological findings in six patients fulfilling the criteria of neurofibromatosis type 2 (NF2) ...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disease with the hallmark of bilateral vesti...
Introduction Neurofibromatosis type 2 (NF2) and schwannomatosis are entities that may, due to the si...
The clinical features, age at onset of symptoms and survival of 150 patients with type 2 neurofibrom...
NF2 is much less common than NF1, affecting 1:35,000 to 1:50,000 persons. CNS tumors are the major f...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Neurofibromatosis type 2 (NF2) is an inherited disease which is mainly characterized by the developm...
Neurofibromatosis 2 (NF2) is a rare genetic disease that affects approximately 1 in 40000 people, s...
Background: Neurofibromatosis Type 2 (NF2) is a dominantly inherited tumour syndrome with a phenotyp...
Copyright © 2012 Kiran Gangadhar et al. This is an open access article distributed under the Creativ...
A 5-year-old girl presented with multiple tumours of the central nervous system. As on the first MRI...
associated with neurofibromatosis type 2. Although laryn-geal neurofibromas have previously been rep...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
Clinical and genetic studies had for some time suggested two forms of neurofibromatosis. In 1988, a ...
Neurofibromatosis 2 (NF2) is an autosomal dominant disease that is characterized by tumors on the ve...
The radiological findings in six patients fulfilling the criteria of neurofibromatosis type 2 (NF2) ...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disease with the hallmark of bilateral vesti...
Introduction Neurofibromatosis type 2 (NF2) and schwannomatosis are entities that may, due to the si...
The clinical features, age at onset of symptoms and survival of 150 patients with type 2 neurofibrom...
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