It has been suggested that executive dysfunction is a core deficit in children with NF1. Early identification of executive dysfunctions represents a public health issue. Despite this, they are largely underestimated in preschool-aged children with NF1. The aim of this thesis is to improve knowledge about children’s executive function (EF) impairment in this disease context. It is also a matter of providing reflection about EF’s assessment and support of these children. Thirty-three NF1 children aged 3 to 5 years old were matched to healthy children. Seven classic experimental tasks and daily life questionnaires completed by parents or teachers were submitted. The results support a specific and an early executive dysfunction in NF1 children....
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Abstract Background Children with the neurogenetic disorder neurofibromatosis type 1 (NF1) often hav...
Neurofibromatosis type 1 (NF1) is a neurogenetic disorder affecting approximately one in 2,500 birth...
Les troubles des fonctions exécutives (FE) seraient au cœur du phénotype cognitif de la neurofibro...
Neuropsychological troubles are among the current complications commonly associated with Neurofibrom...
International audienceAbstract Objectives: Neurofibromatosis type 1 (NF1) is a genetic disorder in w...
Abstract Background To examine the impact of executive function disorders on health-related quality ...
Few studies have examined the cognitive profile of young children with NF1. In this study, 26 childr...
Our study investigated spontaneous versus reactive cognitive flexibility in children with neurofibro...
Objective: It was hypothesized that neuropsychological impairments in children with neurofibromatosi...
Cognitive and behavioral difficulties are common in children with Neurofibromatosis type 1 (NF1), ho...
International audienceExecutive function in children: epistemological approach and clinical semiolog...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
Reading difficulties are reported in the majority of children with neurofibromatosis type 1 (NF1) an...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Abstract Background Children with the neurogenetic disorder neurofibromatosis type 1 (NF1) often hav...
Neurofibromatosis type 1 (NF1) is a neurogenetic disorder affecting approximately one in 2,500 birth...
Les troubles des fonctions exécutives (FE) seraient au cœur du phénotype cognitif de la neurofibro...
Neuropsychological troubles are among the current complications commonly associated with Neurofibrom...
International audienceAbstract Objectives: Neurofibromatosis type 1 (NF1) is a genetic disorder in w...
Abstract Background To examine the impact of executive function disorders on health-related quality ...
Few studies have examined the cognitive profile of young children with NF1. In this study, 26 childr...
Our study investigated spontaneous versus reactive cognitive flexibility in children with neurofibro...
Objective: It was hypothesized that neuropsychological impairments in children with neurofibromatosi...
Cognitive and behavioral difficulties are common in children with Neurofibromatosis type 1 (NF1), ho...
International audienceExecutive function in children: epistemological approach and clinical semiolog...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 people...
Reading difficulties are reported in the majority of children with neurofibromatosis type 1 (NF1) an...
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting 1 in 3,000 births...
Objective: To assess the frequency and severity of specific cognitive deficits in children with neur...
Abstract Background Children with the neurogenetic disorder neurofibromatosis type 1 (NF1) often hav...
Neurofibromatosis type 1 (NF1) is a neurogenetic disorder affecting approximately one in 2,500 birth...