skip to main content
Show Results with:
Refined by: collection: MEDLINE/PubMed (NLM) remove subject: Child remove author: Baulac, Stéphanie remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to My workspace

Mutations of DEPDC5 cause autosomal dominant focal epilepsies

Nature Genetics, 2013, Vol.45(5), p.552 [Peer Reviewed Journal]

No full-text

View all versions
2
Material Type:
Article
Add to My workspace

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy

Neurology, 2014, Vol.82(23), pp.2101-2106 [Peer Reviewed Journal]

No full-text

View all versions
3
Material Type:
Article
Add to My workspace

Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia.

Epilepsia, June 2016, Vol.57(6), pp.994-1003 [Peer Reviewed Journal]

No full-text

View all versions
4
Material Type:
Article
Add to My workspace

A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33

The American Journal of Human Genetics, 1999, Vol.65(4), pp.1078-1085 [Peer Reviewed Journal]

No full-text

View all versions
5
Material Type:
Article
Add to My workspace

Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

Epilepsy Research, 2007, Vol.76(1), pp.41-48 [Peer Reviewed Journal]

No full-text

View all versions

Refine Search Results

Try a new search

Ignore my search and look for everything

by this Author/Contributor:

  1. Picard, Fabienne
  2. Leguern, Eric
  3. Baulac, Michel
  4. Baulac, Stéphanie
  5. An-Gourfinkel, Isabelle

Searching Remote Databases, Please Wait