NF-1

(redirected from Neurofibromatosis Type 1)
AcronymDefinition
NF-1Neurofibromatosis Type 1
References in periodicals archive ?
The potential benefit of the product in neurofibromatosis type 1 is being explored in the US National Cancer Institute-sponsored Phase I/II SPRINT trial in paediatric patients with symptomatic neurofibromatosis type 1 -related Plexiform neurofibromas.
TABLE Differential diagnosis for dermatomally distributed nodules (4) Neoplasms Benign Syringocystadenoma papilliferum, trichoepithelioma, cutaneous schwannoma Malignant Basal cell carcinoma, cutaneous metastases, lymphoma, plasmacytoma, squamous cell carcinoma Other mucocutaneous Granuloma annulare, neurofibromatosis type 1, conditions pseudolymphoma, rheumatoid nodules, sarcoidosis, xanthomas Adapted with permission from: Hager CM, Cohen PR, Tschen JA.
The Neurofibromatosis Type 1 Tumor Suppressor Controls Cell Growth by Regulating Signal Transducer and Activator of Transcription-3 Activity In vitro and In vivo.
Mum-of-four Sharon Phillips has a condition called neurofibromatosis type 1 which causes tumours to form all over her body.
A male child was diagnosed with neurofibromatosis type 1 and an optic pathway glioma, with onset at the age of 14 months.
Neurofibromatosis type 1 (NF1) involves the peripheral nerves with an incidence of 1:2500-3300; however, the involvement of the brachial plexus (BP) is rare (1).
Selumetinib is being explored as a treatment option in registration-enabling studies in patients with differentiated thyroid cancer where the treatment received Orphan Drug Designation, and patients with neurofibromatosis type 1, a genetic disorder that causes tumours to grow along nerve tissue.
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with high penetrance and variable expressivity.
We report a 10-year-old boy with neurofibromatosis type 1 demonstrating a single large cystic lesion in right parietal lobe of the brain with ring enhancement on CT scan with contrast.
Neurofibromatosis type 1 (NF1), also known as von Recklinghausen's disease, is a single gene hamartomatous disease inherited by the autosomal dominant trait [1, 2].
Kapucuoglu, "Neurofibroma of the mandible in a child with Neurofibromatosis Type 1," Archives of Oral Sciences & Research, vol.