...NF1 were systematically reviewed and compared to data from the literature. All of our patients had clinical signs of NF1...
...NF1 to this region of the hsd17b7 promoter. Furthermore, knockdown of NF1 family members, NF1B, NF1A, and NF1X, complete...
Neurofibromatosis type 1 (NF1) or von Recklinghausen's disease is a genetic disease generally characterized by café-au-l...
...NF1. The detection of lesions might be independent of MRI appearance in NF1, i.e. although the brain is affected, MRI ap...
Neurofibromatosis type 1 (NF1) is a genetic disorder characterised by multiple neurofibromas, café-au-lait spots, and ir...
With increasing knowledge of the molecular pathways contributing to the progression of neurofibromatosis type 1 (NF1)-re...
Neurofibromatosis 1 (NF1) is a common autosomal dominant disorder with high penetrance but extreme variability of expres...
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder that affects multiple organ systems, most commonly the ...
Café-au-lait macules (CALMs) are often the earliest visible sign of neurofibromatosis type 1 (NF1), a genetic disorder w...
...NF1) in the Unified Health System (SUS). This was an observational and retrospective study using administrative data fro...
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