Neurofibromatosis 1 is an autosomal dominant disorder characterized by multiple café-au-
lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, and iris Lisch …

Neurofibromatosis type 1 (NF1) is an autosomal dominant, multisystem disorder affecting
approximately 1 in 3500 people. Significant advances in the understanding of the …

Purpose We conducted a prospective trial to evaluate late effects in pediatric patients with
low-grade glioma (LGG) treated with conformal radiation therapy (CRT). Patients and …

Aim This systematic review aimed to pull together the findings from research into
behavioural systems and attention in children with neurofibromatosis type 1 (NF1) and to …

Long-term morbidity for children with low-grade glioma (LGG) requires exposure-specific
characterization. Overall survival (OS) and progression-free survival (PFS) were estimated …

Background Neurofibromatosis of types 1 and 2 (NF1, NF2) and schwannomatosis are the
diseases that make up the neurofibromatosis spectrum. With respective incidences of 1 in …

Context Neurofibromatosis type 1 (NF1) is among the most common genetic disorders that
cause learning disabilities. Recently, it was shown that statin-mediated inhibition of 3 …

Aim The last systematic review of research on the behavior of children with
neurofibromatosis type 1 (NF1) was in 2012. Since then, several important findings have …

The aim of this study was to examine functional attention and executive deficits present in
everyday living in a large sample of children with neurofibromatosis type 1 (NF1). Data are …

Abstract Neurofibromatosis Type 1 (NF1) is a genetic disorder characterized by partial loss
of growth control that affects the central nervous system. NF1 has been consistently …