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Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.Academic Article Why?
Parkin, PatriciaPerson Why?
A mouse model for the learning and memory deficits associated with neurofibromatosis type I.Academic Article Why?
Absence of the greater sphenoid wing in neurofibromatosis type I: congenital or acquired: case report.Academic Article Why?
An intracranial leiomyosarcoma in a child with neurofibromatosis type 1.Academic Article Why?
Brain structure and function in neurofibromatosis type 1: current concepts and future directions.Academic Article Why?
Cerebral arteriopathy in children with neurofibromatosis type 1.Academic Article Why?
Extensive central nervous system involvement in optic pathway gliomas in neurofibromatosis type 1.Academic Article Why?
Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation.Academic Article Why?
Gender as a disease modifier in neurofibromatosis type 1 optic pathway glioma.Academic Article Why?
Generalized metabolic bone disease in Neurofibromatosis type I.Academic Article Why?
Genotype-phenotype data from a case series of patients with mosaic neurofibromatosis type 1.Academic Article Why?
High-grade primary diffuse leptomeningeal gliomatosis in a child with neurofibromatosis Type 1.Academic Article Why?
Is a plexiform neurofibroma pathognomonic of neurofibromatosis type I?Academic Article Why?
Long-term visual outcomes of optic pathway gliomas in pediatric patients without neurofibromatosis type 1.Academic Article Why?
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