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Browsing by Author Grottesi, Alessandro
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Showing results 5 to 8 of 8
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Issue Date
Title
Author(s)
2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy
Sicca, Federico
;
Ambrosini, Elena
;
Marchese, Maria
;
Sforna, Luigi
;
Servettini, Ilenio
;
Valvo, Giulia
;
Brignone, Maria Stefania
;
Lanciotti, Angela
;
Moro, Francesca
;
Grottesi, Alessandro
;
Catacuzzeno, Luigi
;
Baldini, Sara
;
Hasan, Sonia M.
;
D'Adamo, Maria Cristina
;
Franciolini, Fabio
;
Molinari, Paola
;
Santorelli, Filippo Maria
;
Pessia, Mauro
2014
Genetically induced dysfunctions of Kir2.1 channels : implications for short QT3 syndrome and autism-epilepsy phenotype
Ambrosini, Elena
;
Sicca, Federico
;
Brignone, Maria Stefania
;
D'Adamo, Maria Cristina
;
Napolitano, Carlo
;
Servettini, Ilenio
;
Moro, Francesca
;
Ruan, Yanfei
;
Guglielmi, Luca
;
Pieroni, Stefania
;
Servillo, Giuseppe
;
Lanciotti, Angela
;
Valvo, Giulia
;
Catacuzzeno, Luigi
;
Franciolini, Fabio
;
Molinari, Paola
;
Marchese, Maria
;
Grottesi, Alessandro
;
Guerrini, Renzo
;
Santorelli, Filippo Maria
;
Priori, Silvia Giuliana
;
Pessia, Mauro
2017
Lethal digenic mutations in the K+ 1 channels Kir4.1 (KCNJ10) and SLACK 2 (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay
Hasan, Sonia M.
;
Balobaid, Ameera
;
Grottesi, Alessandro
;
Dabbagh, Omar
;
Cenciarini, Marta
;
Rawashdeh, Rifaat
;
Al-Sagheir, Afaf
;
Bove, Cecilia
;
Macchioni, Lara
;
Pessia, Mauro
;
Al-Owain, Mohammed A.
;
D'Adamo, Maria Cristina
2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene
D'Adamo, Maria Cristina
;
Gallenmuller, Constanze
;
Servettini, Ilenio
;
Hartl, Elisabeth
;
Tucker, Stephen J.
;
Arning, Larissa
;
Biskup, Saskia
;
Grottesi, Alessandro
;
Guglielmi, Luca
;
Imbrici, Paola
;
Bernasconi, Pia
;
Di Giovanni, Giuseppe
;
Franciolini, Fabio
;
Catacuzzeno, Luigi
;
Pessia, Mauro
;
Klopstock, Thomas