Neurofibromatosis type 1 (NF1) is a hereditary cancer syndrome, characterized by café-au-lait skin spots and multiple ne...
Neurofibromatosis Type 1 (NF1) is one of the most common inherited neurological disorders and predisposes patients to de...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders. It can cause plexiform neurof...
...NF1). Although these tumors are typically low-grade gliomas, the clinical course and natural history are highly variable...
Neurofibromatosis type I (NF1) has been only rarely reported in association with anti-phospholipid syndrome (APS). We re...
Neurofibromatosis type 1 (NF1) is an autosomal dominant condition with a worldwide incidence of approximately 1 per 2500...
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary disease of high penetrance and variable expression. E...
...Nf1(flox/mut)GFAP-Cre mice) in vivo using Manganese-Enhanced Magnetic Resonance Imaging (MEMRI). In a blinded study, 23 ...
...NF1) and extensive cranial defects associated with underlying dural ectasia. Cranioplasties were performed in both patie...
...NF1). Without a complete surgical excision, prognosis is guarded. We describe a 10-year-old male with NF1 with MPNST, wh...
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