Variations and natural history of primary intraparenchymal lesions associated with neurofibromatosis type 2
Author:
Funder
JSPS KAKENHI
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Neurology (clinical),Radiology, Nuclear Medicine and imaging
Link
https://link.springer.com/content/pdf/10.1007/s00234-021-02809-5.pdf
Reference10 articles.
1. Asthagiri AR, Parry DM, Butman JA et al (2009) Neurofibromatosis type 2. Lancet 373(9679):1974–1986
2. Vargas WS, Heier LA, Rodriguez F, Bergner A, Yohay K (2014) Incidental parenchymal magnetic resonance imaging findings in the brains of patients with neurofibromatosis type 2. Neuroimage Clin 4:258–265
3. Kanda Y (2013) Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics. Bone Marrow Transplant 48(3):452–458
4. Anand G, Vasallo G, Spanou M et al (2018) Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population. Arch Dis Child 103(5):463–469
5. Muir KE, Sargent M, Boelman C (2018) A surprising cause of epilepsy: whole exome sequencing in a child with focal cortical dysplasia identifies neurofibromatosis type 2. Pediatr Neurol 85:79–81
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