Objective Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease that causes the dysregulated growth of Schwann cells. Most reported studies of brain morphology in NF1 patients have included only children, and clinical implications of the observed changes later in life remain unclear. In this study, we used MRI to characterize brain morphology in adults with NF1. Methods Planar (2D) MRI measurements of 29 intracranial structures were compared in 389 adults with NF1 and 112 age- and sex-matched unaffected control subjects. The 2D measurements were correlated with volumetric (3D) brain measurements in 99 of the adults with NF1 to help interpret the 2D f...
Neurofibromatosis type 1 (NF1) is associated with cognitive dysfunction and structural brain abnorma...
Neurofibromatosis type 1 (NF1) is one of the most common single gene disorders affecting the human n...
The relationship between cognitive impairment, fine motor deficits, and T2-weighted MRI intensities ...
Background Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease character...
BACKGROUND AND PURPOSE: After an early progression of signal intensity changes in T2-weighted MR ima...
brain volumes compared with age-matched controls and the CCs are disproportionately large. The purpo...
Neurofibromatosis (NF1) represents the most common single gene cause of learning disabilities. NF1 p...
Purpose To evaluate whether patients with neurofibromatosis type 1 (NF1)-a multisystem neurodevelopm...
Purpose: Alterations of the brain microstructure and metabolism have been identified in patients wit...
Contains fulltext : 154738.pdf (publisher's version ) (Open Access)Neurofibromatos...
Background: Neurofibromatosis type 1 (NF1) is a monogenic disorder associated with cognitive impairm...
Objective To provide the basis for early diagnosis of neurofibromatosis type 1 (NF1) through summari...
Neurofibromatosis type 1 (NF1) is a genetic disease with a wide range of neurological manifestations...
Introduction: Gliomas in the brain and the optic pathway affect up to 20% of all children with neuro...
Neurofibromatosis type 1 (NF1) is one of the most common single gene disorders affecting the human n...
Neurofibromatosis type 1 (NF1) is associated with cognitive dysfunction and structural brain abnorma...
Neurofibromatosis type 1 (NF1) is one of the most common single gene disorders affecting the human n...
The relationship between cognitive impairment, fine motor deficits, and T2-weighted MRI intensities ...
Background Neurofibromatosis 1 (NF1) is a rare autosomal dominant disease character...
BACKGROUND AND PURPOSE: After an early progression of signal intensity changes in T2-weighted MR ima...
brain volumes compared with age-matched controls and the CCs are disproportionately large. The purpo...
Neurofibromatosis (NF1) represents the most common single gene cause of learning disabilities. NF1 p...
Purpose To evaluate whether patients with neurofibromatosis type 1 (NF1)-a multisystem neurodevelopm...
Purpose: Alterations of the brain microstructure and metabolism have been identified in patients wit...
Contains fulltext : 154738.pdf (publisher's version ) (Open Access)Neurofibromatos...
Background: Neurofibromatosis type 1 (NF1) is a monogenic disorder associated with cognitive impairm...
Objective To provide the basis for early diagnosis of neurofibromatosis type 1 (NF1) through summari...
Neurofibromatosis type 1 (NF1) is a genetic disease with a wide range of neurological manifestations...
Introduction: Gliomas in the brain and the optic pathway affect up to 20% of all children with neuro...
Neurofibromatosis type 1 (NF1) is one of the most common single gene disorders affecting the human n...
Neurofibromatosis type 1 (NF1) is associated with cognitive dysfunction and structural brain abnorma...
Neurofibromatosis type 1 (NF1) is one of the most common single gene disorders affecting the human n...
The relationship between cognitive impairment, fine motor deficits, and T2-weighted MRI intensities ...