Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease characterized by susceptibility to tumor formation, changes in skin pigmentation, skeletal abnormalities, and neuropsychological deficits. Clinical studies have shown impaired health-related quality of life (HQoL) in adults with NF1. However, little is known about HQoL in non-clinical NF1 samples. We conducted a cross-sectional self-report survey of 142 persons with NF1 (M age = 50.3 years, SD = 12.0, range 32 to 80; 62.0% females) recruited from non-clinical settings. Several HQoL domains, including life satisfaction, mental health, sleep, pain, gastrointestinal problems, oral health, and social support, were compared between the NF1 sample and 46,...
Background: Neurofibromatosis Type 1 (NF1) is a common autosomal disorder; the criteria for the diag...
Neurofibromatosis Type 1 (NF1) is a progressive genetic disorder characterized mainly by café-au-lai...
Objective: To explore the impact of plexiform neurofibromas on the lives of adults with neurofibroma...
Neurofibromatosis type 1 (NF1) is a common genetic disorder characterised by skin stigmata, benign a...
Abstract Background There is limited data regarding g...
Background Neurofibromatosis 1 (NF1) is an inherited, multi-system, tumour suppressor disorder with ...
The aim of this study was to review the literature on quality of life among adult patients with neur...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Background and purpose: Neurofibromatosis type 1 (NF1) is a dominant genetic disorder of the skin an...
Objective. Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, which oc...
Abstract Background Neurofibromatosis Type 1 (NF1) is a common genetic neurocutaneous disease, with ...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
Patients with neurofibromatosis 1 (NF1), NF2, and schwannomatosis share a predisposition to develop ...
Background: Neurofibromatosis type 1 (NF1) is a common tumor predisposition syndrome with varying ma...
Abstract Background Plexiform neurofibromas (PN) are complex, benign nerve-sheath tumours that occur...
Background: Neurofibromatosis Type 1 (NF1) is a common autosomal disorder; the criteria for the diag...
Neurofibromatosis Type 1 (NF1) is a progressive genetic disorder characterized mainly by café-au-lai...
Objective: To explore the impact of plexiform neurofibromas on the lives of adults with neurofibroma...
Neurofibromatosis type 1 (NF1) is a common genetic disorder characterised by skin stigmata, benign a...
Abstract Background There is limited data regarding g...
Background Neurofibromatosis 1 (NF1) is an inherited, multi-system, tumour suppressor disorder with ...
The aim of this study was to review the literature on quality of life among adult patients with neur...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Background and purpose: Neurofibromatosis type 1 (NF1) is a dominant genetic disorder of the skin an...
Objective. Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, which oc...
Abstract Background Neurofibromatosis Type 1 (NF1) is a common genetic neurocutaneous disease, with ...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
Patients with neurofibromatosis 1 (NF1), NF2, and schwannomatosis share a predisposition to develop ...
Background: Neurofibromatosis type 1 (NF1) is a common tumor predisposition syndrome with varying ma...
Abstract Background Plexiform neurofibromas (PN) are complex, benign nerve-sheath tumours that occur...
Background: Neurofibromatosis Type 1 (NF1) is a common autosomal disorder; the criteria for the diag...
Neurofibromatosis Type 1 (NF1) is a progressive genetic disorder characterized mainly by café-au-lai...
Objective: To explore the impact of plexiform neurofibromas on the lives of adults with neurofibroma...