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Neurofibromatoses

Known as: Neurofibromas, Multiple, Neurofibromata, Neurofibromatosis Syndrome 
An autosomal dominant hereditary neoplastic syndrome. Two distinct clinicopathological entities are recognized: neurofibromatosis type 1 and… Expand
National Institutes of Health

Papers overview

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Review
2019
Review
2019
BACKGROUND Paediatric low-grade glioma is the most common CNS tumour of childhood. Although overall survival is good, disease… Expand
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Review
2015
Review
2015
The mitogen-activated protein kinases (MAPKs) in mammals include c-Jun NH2-terminal kinase (JNK), p38 MAPK, and extracellular… Expand
  • figure 1
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Highly Cited
2013
Highly Cited
2013
Preparing the books to read every day is enjoyable for many people. However, there are still many people who also don't like… Expand
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Highly Cited
2011
Highly Cited
2011
s / Neuroscience Research 71S (2011) e108–e415 e127 P2-e02 Generation of neural crest progenitor cells from human induced… Expand
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Review
2009
Review
2009
Autism spectrum disorders (ASD) are diagnosed on the basis of three behavioral features namely deficits in social communication… Expand
  • figure 1
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Review
2006
Review
2006
Gastrointestinal (GI) stromal tumors (GISTs) are the most common mesenchymal tumors specific to the GI tract, generally defined… Expand
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Highly Cited
2002
Highly Cited
2002
Neurofibromatosis type 1 (NF1) is one of the most prevalent dominantly inherited genetic diseases of the nervous system. NF1… Expand
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Review
2001
Review
2001
Neurofibromatosis type 1 and type 2 both occur in mosaic forms. Mosaicism results from somatic mutations. Early somatic mutations… Expand
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Highly Cited
1994
Highly Cited
1994
Takayasu arteritis is a chronic, idiopathic, inflammatory disease that primarily affects large vessels, such as the aorta and its… Expand
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Highly Cited
1988
Highly Cited
1988
  • Archives of neurology
  • 1988
  • Corpus ID: 28502353
 
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