Background Children and adolescents with neurofibromatosis type 1 (NF1) experience significant difficulties with social adjustment (SA), adversely impacting quality of life across the lifespan. SA refers to the quality of the child’s social relationships and their attainment of developmentally appropriate goals. Youth with NF1 also experience clinically significant impairments across a variety of neuropsychological domains including global intelligence, attention, and executive function. Despite evidence that neurocognitive weaknesses and family-systems factors contribute to worse SA in other pediatric neurological populations, few studies have examined these associations in children with NF1. A greater understanding of processes underlying...
Examined child and parent report measures of psychosocial, behavioral, and educational functioning i...
Abstract Background To examine the impact of executive function disorders on health-related quality ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
Neurofibromatosis type one (NF1) is a disorder caused by a mutation of the NF1 gene on chromosome 17...
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...
Research that has included children and adolescents with neurofibromatosis type 1 (NF1) suggests an ...
La neurofibromatose de type 1 (NF1) est une pathologie génétique pouvant entrainer des difficultés d...
Neurofibromatosis type 1 (NF1) is a rare neurological disorder that is estimated to affect about 1 i...
Children with neurofibromatosis type 1 (NF1) often experience executive dysfunction, attention defic...
AIM: We examined key features of two outcome measures for social dysfunction and autism spectrum dis...
Objective: Neurofibromatosis Type I (NF1) is a single gene disorder associated with cognitive and be...
Background/Rationale for the Study: Neurofibromatosis-1 (NF1) is a common neurodevelopment genetic d...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
OBJECTIVE: Children with neurofibromatosis type 1 (NF1) often show cognitive and behavioral problems...
Examined child and parent report measures of psychosocial, behavioral, and educational functioning i...
Abstract Background To examine the impact of executive function disorders on health-related quality ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
Neurofibromatosis type one (NF1) is a disorder caused by a mutation of the NF1 gene on chromosome 17...
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...
Research that has included children and adolescents with neurofibromatosis type 1 (NF1) suggests an ...
La neurofibromatose de type 1 (NF1) est une pathologie génétique pouvant entrainer des difficultés d...
Neurofibromatosis type 1 (NF1) is a rare neurological disorder that is estimated to affect about 1 i...
Children with neurofibromatosis type 1 (NF1) often experience executive dysfunction, attention defic...
AIM: We examined key features of two outcome measures for social dysfunction and autism spectrum dis...
Objective: Neurofibromatosis Type I (NF1) is a single gene disorder associated with cognitive and be...
Background/Rationale for the Study: Neurofibromatosis-1 (NF1) is a common neurodevelopment genetic d...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
OBJECTIVE: Children with neurofibromatosis type 1 (NF1) often show cognitive and behavioral problems...
Examined child and parent report measures of psychosocial, behavioral, and educational functioning i...
Abstract Background To examine the impact of executive function disorders on health-related quality ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...