...NF1) who have symptomatic plexiform neurofibromas (PN) not amenable to complete resection. This article summarizes the m...
...NF1). Cherix et al. and Colby and Saul suggested that Jaffe-Campanacci syndrome (JCS) might be a distinct form of NF1. I...
...NF1) highlights the overlap between CMMRD and NF1, as their overlapping genetic pathologies can yield similar clinical m...
...NF1） is an autosomal dominant hereditary neurological disorder. One of the typical manifestations of NF1 is neurofibroma...
Almost all individuals with neurofibromatosis type 1 (NF1) develop peripheral nerve sheath tumors (PNSTs), mainly benign...
Neurofibromatosis 1 (NF1) is autosomally inherited disorder, characterized by café au lait spots and multiple neurofibro...
...NF1), contributes to the majority (∼90%) of Ras inactivation in dendritic spines of pyramidal neurons in the CA1 region ...
...NF1) are multiple and commonly involve the small intestine. This is a rare case of GISTs in NF1 involving the stomach an...
...NF1)-associated optic glioma, we now demonstrate that stromal microglia express the CX3CR1 chemokine receptor, such that...
...nf1a and nf1b, orthologues of NF1, and show neural crest and cardiovascular defects resulting from morpholino knockdown,...
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