Dejerine-Sottas Disease (disorder)

Known as: dejerines diseases sottas, Dejerine Sottas Disease, DEJERINE-SOTTAS SYNDROME 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Cytosine DNA methylation protects eukaryotic genomes by silencing transposons and harmful DNAs, but also regulates gene… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2006
2006
This paper records parts of Dejerine and Sottas’s description of the syndrome that bears their names. It outlines biographical… (More)
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Methylation of cytosine residues in eukaryotic genomes is often associated with repeated sequences including transposons and… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
Is this relevant?
Highly Cited
2001
Highly Cited
2001
The periaxin gene (PRX) encodes two PDZ-domain proteins, L- and S-periaxin, that are required for maintenance of peripheral nerve… (More)
Is this relevant?
Highly Cited
1999
Highly Cited
1999
BACKGROUND Mutations in the early growth response 2 (EGR2) gene have recently been found in patients with congenital… (More)
Is this relevant?
Highly Cited
1997
Highly Cited
1997
Intermittently occurring field events, dentate spikes (DS), and sharp waves (SPW) in the hippocampus reflect population synchrony… (More)
Is this relevant?
Highly Cited
1997
Highly Cited
1997
Although cache-coherent shared-memory multiprocessors are often used to run commercial workloads, little work has been done to… (More)
Is this relevant?
Highly Cited
1997
Highly Cited
1997
Charcot-Marie-Tooth disease (CMT) and hereditary neuropathy with liability to pressure palsies (HNPP) are two inherited… (More)
  • table 1
  • table 2
  • figure 1
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Dejerine–Sottas syndrome is a hypertrophic, demyelinating neuropathy which appears to demonstrate autosomal recessive inheritance… (More)
Is this relevant?
1978
1978
1. A clinical, genetic, electrophysiological and nerve biopsy study of 49 index cases with peroneal muscular atrophy is reported… (More)
Is this relevant?