To investigate a correlation between pathologic and radiologic findings with regard to the characteristic high-signal-intensity foci seen on long repetition time (TR) magnetic resonance (MR) images of the brain in patients with neurofibromatosis type 1 (NF-1). Three girls with NF-1 and abnormal ...
type I neurofibromatosis (diagnosis),neurofibromatosis type I (von Recklinghausen's disease),von Recklinghausen's disease,type I neurofibromatosis,Von Recklinghausen's disease (of nerve),NF1 (Neurofibromatosis 1),Neurofibromatosis Type 1,Neurofibromatosis, Type 1,Type 1 Neurofibromatosis,Type 1, ...
1. [Objective] To explore the molecular pathogenesis of neurofibromas in the patients with neurofibromatosis type 1 (NF1). 【目的】 探讨1型神经纤维瘤病(NF1)患者神经纤维瘤发生、发展的分子病理机制。 2. Methods: CT and MR images of 16 patients with a pathologically proven pelvic BPNST( includ...
Existing research has demonstrated elevated autistic behaviours in children with neurofibromatosis type 1 (NF1), but the autistic phenotype and its relationship to other neurodevelopmental manifestations of NF1 remains unclear. To address this gap, we performed detailed characterisation of autistic behaviours...
Menor F., Marti-Bonmati I. (1992) CT detection of basal ganglion lesions in neurofibromatosis type I: correlation with MRI. Neuroradiology 34:305–307 ArticleCASPubMedGoogle Scholar Mirowitz SA, Sartor K, Gado M (1989) High-intensity basal ganglia lesions on T1-weighted MR images in neurofibro...
Neurofibromatosis type 1 (NF1) is a genetic condition characterized by various somatic manifestations and cognitive impairments, but the latter are sparsely described in adults. This study aimed at characterizing potential impairments of neurocognitive functions using neuropsychological tests as well as a ...
Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with cutaneous, neurologic, and orthopedic as major manifestations which lead to significant morbidity or mortality. Indeed, NF1 ...
neurofibromatosis type 1scoliosis classificationPurpose: We developed a system that can automatically classify cases of scoliosis secondary to neurofibromatosis type 1 (NF1-S) using deep learning algorithms (DLAs) and improve the accuracy and effectiveness of classification, thereby assisting surgeons with ...
Disappearing enhancing brain lesion in a child with neurofibromatosis type I. Pediatr Radiol - PW, CM - 1997 () Citation Context ... T1-weighted images (Fig.). Typically, NBOs may remain stationary, or regress slowly, or even spontaneously disappear without any treatment. On the other hand,...
Neurofibromatosis type 1 is an autosomal dominant genetic disorder caused by mutation in the neurofibromin 1 (NF1) gene. Its hallmarks are cutaneous findings including neurofibromas, benign peripheral nerve sheath tumors. We analyzed the collagen and mat