(Q50866521)

English

Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA?

scientific article published in July 2013

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scholarly article

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA? (English)

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

Mowat-Wilson syndrome

1 reference

based on heuristic

inferred from title

Duccio M. Cordelli

1

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

author name string

Alessandro Pellicciari

2

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

Demetrio Kiriazopulos

3

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

Emilio Franzoni

4

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

Livia Garavelli

5

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

publication date

1 July 2013

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

54

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

7

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

1331-1332

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

What is GABAergic inhibition? How is it modified in epilepsy?

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Mowat-Wilson syndrome: an underdiagnosed syndrome?

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Dlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneurons

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Mowat-Wilson syndrome

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Directed migration of cortical interneurons depends on the cell-autonomous action of Sip1.

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies

1 reference

https://api.crossref.org/works/10.1111%2FEPI.12204

21 January 2018

Identifiers

10.1111/EPI.12204

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

1 reference

Europe PubMed Central

24 March 2018

http://europepmc.org/abstract/MED/23815573

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