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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease glioma
Comorbidity C0085113|neurofibromatosis
Sentences 11
PubMedID- 21822956 Therefore, the aim of our study was to find a clinical indicator for the presence of optic pathway gliomas in children with neurofibromatosis type 1 in order to facilitate early diagnosis and initiate further ophthalmological and neuroimaging investigations.
PubMedID- 23071069 In this study, the authors explored the hypothesis that hypotonia could be a clinical indicator of glioma in children with neurofibromatosis type 1.
PubMedID- 20451859 Optic pathway gliomas in patients with neurofibromatosis type 1: follow-up of 44 patients.
PubMedID- 22370674 Myopia associated with optic nerve gliomas in neurofibromatosis type 1.
PubMedID- 25381154 Identifying modifiers of glioma risk in patients with type i neurofibromatosis (nf1) could help support personalized tumor surveillance, advance understanding of gliomagenesis, and potentially identify novel therapeutic targets.
PubMedID- 21274014 Screening for symptomatic optic pathway glioma in children with neurofibromatosis type 1.
PubMedID- 26233602 The use of magnetic resonance imaging screening for optic pathway gliomas in children with neurofibromatosis type 1.
PubMedID- 21232732 Design: cross-sectional convenience sample, with prospective data collection, from a tertiary care children's hospital of patients with optic pathway gliomas associated with neurofibromatosis type 1, sporadic optic pathway gliomas, and neurofibromatosis type 1 without optic pathway gliomas.
PubMedID- 24488155 Purpose: to compare the optical coherence tomography (oct) findings of neurofibromatosis-1 (nf-1) patients with/without optic pathway glioma (opg) with those of healthy controls.
PubMedID- 24101736 Detection of tumor progression in optic pathway glioma with and without neurofibromatosis type 1.
PubMedID- 26294105 Risk of optic pathway glioma in children with neurofibromatosis type 1 and optic nerve tortuosity or nerve sheath thickening.

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