Neurofibromatosis type 1 (NF1), formerly known as von Recklinghausen disease is an autosomal dominant disease with multisystem involvement. In the peripheral nervous system, it leads to the development of benign tumors from the tissue of the spinal or cranial nerve sheaths, known as “neurofibromas.” We report the case of a 40-year-old patient with spinal cord compression syndrome in whom spinal MRI revealed cervical, dorsal and lumbosacral neurofibromas revealing neurofibromatosis type 1
Type I Neurofibromatosis (NF1) is an autosomal-dominant inheritable disorder, with an incidence of 1...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis fa...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
Spinal neurofibromas are rare benign lesions associated with neurofibromatosis Type 1. They can ofte...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Neurofibromatosis type 1 (NF1), referred to as von Recklinghausen’s disease, is a genetic disorder t...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Abstract Neurofibromatosis Type 1 (NF1) has been reported to be associated with a variety of spinal ...
Neurofibromatosis (NF) is a group of genetic disorders that primarily affect neural tissues. NF type...
Objective: Neurofibromatosis type 1 (NF1) is a common disorder in which affected individuals uncommo...
Rev. 2. ed.Available from British Library Document Supply Centre-DSC:3864.395(1) / BLDSC - British L...
Neurofibromatosis Type 1 (NF1) is a multisystemic disease, manifesting as abnormalities ofthe nervou...
Neurofibromatosis (NF) belongs to the group of phakomatoses characterized by benign tumors of periph...
Neurofibromatosis (von Recklinghausen disease) is a hereditary disease with varied manifestations6 ’...
Type I Neurofibromatosis (NF1) is an autosomal-dominant inheritable disorder, with an incidence of 1...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis fa...
Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of i...
Spinal neurofibromas are rare benign lesions associated with neurofibromatosis Type 1. They can ofte...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Neurofibromatosis type 1 (NF1), referred to as von Recklinghausen’s disease, is a genetic disorder t...
Neurofibromatosis (NF) is a term that has been applied to a variety of related syndromes, characteri...
Abstract Neurofibromatosis Type 1 (NF1) has been reported to be associated with a variety of spinal ...
Neurofibromatosis (NF) is a group of genetic disorders that primarily affect neural tissues. NF type...
Objective: Neurofibromatosis type 1 (NF1) is a common disorder in which affected individuals uncommo...
Rev. 2. ed.Available from British Library Document Supply Centre-DSC:3864.395(1) / BLDSC - British L...
Neurofibromatosis Type 1 (NF1) is a multisystemic disease, manifesting as abnormalities ofthe nervou...
Neurofibromatosis (NF) belongs to the group of phakomatoses characterized by benign tumors of periph...
Neurofibromatosis (von Recklinghausen disease) is a hereditary disease with varied manifestations6 ’...
Type I Neurofibromatosis (NF1) is an autosomal-dominant inheritable disorder, with an incidence of 1...
Neurofibromatosis type 1 (NF1) is a rare genetic disorder, characterized by the development of benig...
We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis fa...