Copyright © 2012 Molly M. Garwood et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Objective. To examine physical, cognitive, and social-emotional predictors of quality of life (HRQOL) and functional disability (FD) in adolescents diagnosed with Neurofibromatosis-1. Methods. Participants were twenty-seven adolescents with a diagnosis of NF-1 who were recruited through an NF-1 specialty clinic at a large Midwestern children’s hospital. Measurements of the adolescents ’ cognitive functioning, pain, FD, HRQOL, and social and emotional functioning were obtained with correspo...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Background Children and adolescents with neurofibromatosis type 1 (NF1) experience significant diffi...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
Objective This descriptive cross-sectional study aimed to determine how cognitive, disease, and envi...
Objective This descriptive cross-sectional study aimed to determine how cognitive, disease, and envi...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
Examined child and parent report measures of psychosocial, behavioral, and educational functioning i...
International audienceBACKGROUND: To examine the impact of executive function disorders on health-re...
The physical manifestations of neurofibromatosis type 1 (NF1) can cause chronic pain. This study inv...
Neurofibromatosis type 1 (NF1) is a rare neurological disorder that is estimated to affect about 1 i...
Background/Rationale for the Study: Neurofibromatosis-1 (NF1) is a common neurodevelopment genetic d...
To assess emotional and behavioral problems in children and adolescents with neurofibromatosis type ...
The objective was to investigate the serial mediating effects of speech difficulties, patient health...
From PubMed via Jisc Publications RouterHistory: received 2021-02-22, revised 2021-05-17, accepted 2...
Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease charact...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Background Children and adolescents with neurofibromatosis type 1 (NF1) experience significant diffi...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
Objective This descriptive cross-sectional study aimed to determine how cognitive, disease, and envi...
Objective This descriptive cross-sectional study aimed to determine how cognitive, disease, and envi...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
Examined child and parent report measures of psychosocial, behavioral, and educational functioning i...
International audienceBACKGROUND: To examine the impact of executive function disorders on health-re...
The physical manifestations of neurofibromatosis type 1 (NF1) can cause chronic pain. This study inv...
Neurofibromatosis type 1 (NF1) is a rare neurological disorder that is estimated to affect about 1 i...
Background/Rationale for the Study: Neurofibromatosis-1 (NF1) is a common neurodevelopment genetic d...
To assess emotional and behavioral problems in children and adolescents with neurofibromatosis type ...
The objective was to investigate the serial mediating effects of speech difficulties, patient health...
From PubMed via Jisc Publications RouterHistory: received 2021-02-22, revised 2021-05-17, accepted 2...
Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease charact...
Objective: To explore health-related quality of life (HRQoL) reported by individuals with neurofibro...
Background Children and adolescents with neurofibromatosis type 1 (NF1) experience significant diffi...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...