Introduction: Neurofibromatosis Type I (NF1), is often mentioned among the heritable neurocutaneous disorders associated with stenoses or aneurysmal arterial disease affecting predominantly the renal arteries and less often the abdominal aorta (middle aortic syndrome), and mesenteric and peripheral arteries, but the association with intracranial aneurysms, has not been firmly established. Here, we report a case of multiple intracranial arterial aneurisms occurring in a patient affected by NF1. Materials and methods: A 21-year-old man affected by NF1 was admitted to the hospital with a history of left painful ophthalmoplegia occurred 1 month before admission. A MR Imaging (MRI) of the brain with MR and CT Angiography, of ...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations i...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Introduction: Among the rare cerebrovascular abnormalities found in patients with NF1, the most co...
Introduction: Among the rare cerebrovascular abnormalities found in patients with NF1, the most co...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Relato de caso de neurofibromatose tipo I associada a doença oclusiva extensa do sistema carotídeo e...
Introduction: Neurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized by caf...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
An internal carotid artery (ICA) pseudoaneurysm associated with neurofibromatosis type 1 (NF-1) is r...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations i...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
SUMMARY: Although neurofibromatosis type 1 (NF-1) is commonly considered neurocutaneous, se-vere art...
Introduction: Among the rare cerebrovascular abnormalities found in patients with NF1, the most co...
Introduction: Among the rare cerebrovascular abnormalities found in patients with NF1, the most co...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Neurofibromatosis type 1 (NF1) is a relatively common single-gene disorder, and is caused by heteroz...
Relato de caso de neurofibromatose tipo I associada a doença oclusiva extensa do sistema carotídeo e...
Introduction: Neurofibromatosis type 1 (NF-1) is an autosomal dominant disorder characterized by caf...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
An internal carotid artery (ICA) pseudoaneurysm associated with neurofibromatosis type 1 (NF-1) is r...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Neurofibromatosis (NF) is a common autosomal dominant disease characterized by the development of ha...
Abstract Introduction Intrinsic lesions of the arterial wall are important manifestations of Neurofi...
Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations i...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...