Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

NEUROFIBROMATOSIS, FAMILIAL SPINAL

Known as: FSNF 
 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal dominant inheritanceLower limb muscle weaknessParaparesis

Broader (1)

Neurofibromatoses

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Spinal neurofibromatosis in a family with classical neurofibromatosis type 1 and a novel NF1 gene mutation
Familial spinal neurofibromatosis (FSNF) is a rare form of neurofibromatosis type 1 (NF1) characterized by multiple… Expand
Is this relevant?
Highly Cited
2009
Highly Cited
2009
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas
Neurofibromatosis type 1 (NF1) is a common inherited complex multi-system disorder associated with the growth of various benign… Expand
  • figure 1
  • figure 2
Is this relevant?
2007
2007
Familial spinal neurofibromatosis.
Familial spinal neurofibromatosis (FSNF) is a rare localized subtype of NF1 which shows neurological symptomatology during adult… Expand
  • table 1
  • figure 1
  • table 2
  • table 3
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE