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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease meningioma
Comorbidity C0085113|neurofibromatosis
Sentences 6
PubMedID- 24599662 Angiosarcoma arising in schwannoma of cerebellopontine angle and later associating with meningioma in a patient with neurofibromatosis type 2.
PubMedID- 26365467 Effect of bevacizumab on intracranial meningiomas in patients with neurofibromatosis type 2 - a retrospective case series.
PubMedID- 25751482 Intractable yawning caused by foramen magnum meningioma in a patient with neurofibromatosis type 2.
PubMedID- 25857641 A significant increase in risk of meningiomas is associated with neurofibromatosis type 2 (nf2) disease through mutation of the nf2 gene.
PubMedID- 25555193 Gamma knife radiosurgery for meningiomas in patients with neurofibromatosis type 2.
PubMedID- 24171707 Because of this and the development of meningiomas in patients with neurofibromatosis carrying mutations of the nf2 gene coded at chromosome 22q12.2, nf2 has long been considered as the most relevant gene targeted by chromosome 22 losses in meningiomas [7,32].

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