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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibromatosis
Comorbidity C0206728|plexiform neurofibromas
Sentences 8
PubMedID- 22407214 The objective of this study was to investigate the predictive value of [18f]-fluorodeoxyglucose positron emission tomography (fdg-pet) in detecting malignant transformation of plexiform neurofibromas in children with neurofibromatosis type 1 (nf1).
PubMedID- 21415691 Resection of plexiform neurofibromas in children with neurofibromatosis type 1.
PubMedID- 23598713 Purpose: the aim of this study was to analyze growth rate and identify prognostic factors for progression of postoperative plexiform neurofibromas in patients with neurofibromatosis type 1.
PubMedID- 24681606 Malignant peripheral nerve sheath tumors (mpnsts) are soft tissue sarcomas that occur spontaneously, or from benign plexiform neurofibromas, in the context of the genetic disorder neurofibromatosis type 1 (nf1).
PubMedID- 20680410 plexiform neurofibromas commonly found in patients with neurofibromatosis type i (nf1) have a 5% risk of being transformed into malignant peripheral nerve sheath tumors (mpnst).
PubMedID- 23035791 Background: to examine the natural growth dynamics of internal plexiform neurofibromas (pns) in patients with neurofibromatosis 1 (nf1).
PubMedID- 23099009 Imatinib mesylate for plexiform neurofibromas in patients with neurofibromatosis type 1: a phase 2 trial.
PubMedID- 21621223 plexiform neurofibromas in children with neurofibromatosis type 1: frequency and associated clinical deficits.

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