Publications

Found 4 results

Filters: First Letter Of Last Name is N  [Clear All Filters]
2015
Early and effective treatment of KCNQ2 encephalopathy., Pisano, Tiziana, Numis Adam L., Heavin Sinéad B., Weckhuysen Sarah, Angriman Marco, Suls Arvid, Podesta Barbara, Thibert Ronald L., Shapiro Kevin A., Guerrini Renzo, et al. , Epilepsia, 2015 May, Volume 56, Issue 5, p.685-91, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/25880994?dopt=Abstract

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency., Tan, Chuan, Shard Chloe, Ranieri Enzo, Hynes Kim, Pham Duyen H., Leach Damian, Buchanan Grant, Corbett Mark, Shoubridge Cheryl, Kumar Raman, et al. , Human molecular genetics, 2015 Jun 29, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/26123493?dopt=Abstract

2014
Periventricular nodular heterotopia in Smith-Magenis syndrome., Capra, Valeria, Biancheri Roberta, Morana Giovanni, Striano Pasquale, Novara Francesca, Ferrero Giovanni Battista, Boeri Luca, Celle Maria Elena, Mancardi Maria Margherita, Zuffardi Orsetta, et al. , American journal of medical genetics. Part A, 2014 Dec, Volume 164A, Issue 12, p.3142-7, (2014) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/25257626?dopt=Abstract

1994
Band heterotopia: correlation of outcome with magnetic resonance imaging parameters., Barkovich, A. J., Guerrini R., Battaglia G., Kalifa G., N'Guyen T., Parmeggiani A., Santucci M., Giovanardi-Rossi P., Granata T., and D'Incerti L. , Annals of neurology, 1994 Oct, Volume 36, Issue 4, p.609-17, (1994) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/7524438?dopt=Abstract