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Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations

โœ Scribed by Michelucci, Roberto; Pasini, Elena; Malacrida, Sandro; Striano, Pasquale; Bonaventura, Carlo Di; Pulitano, Patrizia; Bisulli, Francesca; Egeo, Gabriella; Santulli, Lia; Sofia, Vito; Gambardella, Antonio; Elia, Maurizio; de Falco, Arturo; Neve, Angela la; Banfi, Paola; Coppola, Giangennaro; Avoni, Patrizia; Binelli, Simona; Boniver, Clementina; Pisano, Tiziana; Marchini, Marco; Dazzo, Emanuela; Fanciulli, Manuela; Bartolini, Yerma; Riguzzi, Patrizia; Volpi, Lilia; de Falco, Fabrizio A.; Giallonardo, Anna Teresa; Mecarelli, Oriano; Striano, Salvatore; Tinuper, Paolo; Nobile, Carlo


Book ID
120312091
Publisher
Wiley (Blackwell Publishing)
Year
2013
Tongue
English
Weight
258 KB
Volume
54
Category
Article
ISSN
0013-9580

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LGI1 mutations in autosomal dominant and
โœ Carlo Nobile; Roberto Michelucci; Simonetta Andreazza; Elena Pasini; Silvio C.E. ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 275 KB

Autosomal dominant lateral temporal epilepsy (ADLTE) or autosomal dominant partial epilepsy with auditory features (ADPEAF) is an inherited epileptic syndrome with onset in childhood/adolescence and benign evolution. The hallmark of the syndrome consists of typical auditory auras or ictal aphasia in