Background/Rationale for the Study: Neurofibromatosis-1 (NF1) is a common neurodevelopment genetic disorder affecting 1 in 3,000 individuals. Children with NF1 are at elevated risk of social, emotional, executive functioning, and attention difficulties. The current study examined psychosocial difficulties in young children with NF1 on the Behavior Assessment System for Children – Second Edition (BASC-II) content scales that were not on the previous edition of this measure and have rich clinical information.Methods: Participants were 62 children with NF1 (37 boys, 25 girls), ages 3 to 8 years (M = 4.95, SD = 1.62). The Behavior Assessment System for Children – Second Edition and the Conners Parent Rating Scale – Revised were completed by par...
textabstractObjective: To evaluate the appropriateness of cognitive and behavioral outcome measures ...
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Neurofibromatosis type one (NF1) is a disorder caused by a mutation of the NF1 gene on chromosome 17...
Longitudinal Study of Problem Behavior in Children with Neurofibromatosis-1 Geethika Pillai, Kristin...
AIM: We examined key features of two outcome measures for social dysfunction and autism spectrum dis...
INTRODUCTION: Children with the single-gene disorder neurofibromatosis type 1 (NF1) appear to be at ...
OBJECTIVE: Children with neurofibromatosis type 1 (NF1) often show cognitive and behavioral problems...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic condition. While considerable work h...
Objective: Neurofibromatosis Type I (NF1) is a single gene disorder associated with cognitive and be...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
In the present study the neuropsychological, academic and social-emotional profiles were examined in...
To assess emotional and behavioral problems in children and adolescents with neurofibromatosis type ...
Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people, and...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
International audienceBACKGROUND: To examine the impact of executive function disorders on health-re...
textabstractObjective: To evaluate the appropriateness of cognitive and behavioral outcome measures ...
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Neurofibromatosis type one (NF1) is a disorder caused by a mutation of the NF1 gene on chromosome 17...
Longitudinal Study of Problem Behavior in Children with Neurofibromatosis-1 Geethika Pillai, Kristin...
AIM: We examined key features of two outcome measures for social dysfunction and autism spectrum dis...
INTRODUCTION: Children with the single-gene disorder neurofibromatosis type 1 (NF1) appear to be at ...
OBJECTIVE: Children with neurofibromatosis type 1 (NF1) often show cognitive and behavioral problems...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic condition. While considerable work h...
Objective: Neurofibromatosis Type I (NF1) is a single gene disorder associated with cognitive and be...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
In the present study the neuropsychological, academic and social-emotional profiles were examined in...
To assess emotional and behavioral problems in children and adolescents with neurofibromatosis type ...
Neurofibromatosis 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people, and...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
International audienceBACKGROUND: To examine the impact of executive function disorders on health-re...
textabstractObjective: To evaluate the appropriateness of cognitive and behavioral outcome measures ...
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Neurofibromatosis type one (NF1) is a disorder caused by a mutation of the NF1 gene on chromosome 17...