Sfoglia per Autore  DI RESTA, CHIARA

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Mostrati risultati da 1 a 20 di 76
Titolo Data di pubblicazione Autore(i) File
Human neuronal nicotinic receptors and epilepsy during sleep 1-gen-2005 Politi, F; DI RESTA, Chiara; Consonni, S; Amadeo, A; Becchetti, A.
Alpha2-I279N human nicotinic acetylcholine receptors, linked to a form of nocturnal epilepsy, present higher sensitivity to agonists 1-gen-2006 DI RESTA, Chiara; Taiana, M; Aridon, P; Casari, GIORGIO NEVIO; Becchetti, A.
Increased sensitivity of the neuronal nicotinic receptor alpha2 subunit causes familial epilepsy with nocturnal wandering and ictal fear 1-gen-2006 Marini, C; Aridon, P; DI RESTA, Chiara; Brilli, E; DE FUSCO, M; Politi, F; Parrini, E; Manfredi, I; Pisano, T; Pruna, D; Curia, G; Ciachetti, C; Pasqualetti, M; Becchetti, A; Guerrini, R; Casari, GIORGIO NEVIO
Increased sensitivity of the alpha-2 neuronal nicotinic receptor causes familial epilepsy with nocturnal wandering and ictal fear 1-gen-2006 Marini, C; Aridon, P; DI RESTA, Chiara; Brilli, E; De Fusco, M; Politi, F; Parrini, E; Manfredi, I; Pisano, T; Pruna, D; Curia, G; Cianchetti, C; Pasqualetti, M; Becchetti, A; Guerrini, R; Casari, GIORGIO NEVIO
Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear 1-gen-2006 Aridon, P; Marini, C; DI RESTA, Chiara; Brilli, E; De Fusco, M; Politi, F; Parrini, E; Manfredi, I; Pisano, T; Pruna, D; Curia, G; Cianchetti, C; Pasqualetti, M; Becchetti, A; Guerrini, R; Casari, GIORGIO NEVIO
Electrophysiological properties of mutant alpha2beta4 nAChR linked to a form of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) 1-gen-2007 DI RESTA, Chiara; Ambrosi, P; Morini, R; Becchetti, A.
Effect of carbamazepine and oxcarbazepine on wild-type and mutant neuronal nicotinic acetylcholine receptors linked to nocturnal frontal lobe epilepsy 1-gen-2010 DI RESTA, Chiara; Ambrosi, P; Curia, G; Becchetti, A.
Introduction to ion channels 1-gen-2010 DI RESTA, Chiara; Becchetti, A.
A Brugada Syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization 1-gen-2011 Marangoni, S; DI RESTA, Chiara; Rocchetti, M; Barile, L; Rizzetto, R; Summa, A; Severi, S; Sommariva, E; Pappone, C; Ferrari, Maurizio; Benedetti, S; Zaza, A.
Analytical Ancestry: Evolution of the Array in Analysis 1-gen-2012 Ferrari, Maurizio; DI RESTA, Chiara
Effect of Carbamazepine and Related Compounds on Ligand-Gated Channels: Possible Implications for Synaptic Transmission and Side Effects. 1-gen-2013 DI RESTA, Chiara; Becchetti, A.
Translating genes into health. 1-gen-2013 Kricka, L; DI RESTA, Chiara
Genetics can contribute to the prognosis of the Brugada syndrome: a pilot model for risk stratification. 1-gen-2013 Sommariva, E; Pappone, C; Martinelli Boneschi, F; DI RESTA, Chiara; Carbone, Mr; Salvi, E; Vergara, P; Sala, S; Cusi, D; Ferrari, Maurizio; Benedetti, S.
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratories 1-gen-2014 DI RESTA, Chiara; Manzoni, M; Berisso Zoni Berisso, M; Siciliano, G; Benedetti, S; Ferrari, Maurizio
Cardiac magneti resonance and arrhythmic risk stratification of cardiomyopathy associated with lamin A/C mutations: results from a 5 years study 1-gen-2015 Giovanni, Peretto; Sara, Benedetti; DI RESTA, Chiara; Simone, Sala; Ferrari, Maurizio; Paolo Della, Bella
Genetic factors predisposing to bronchopulmonary dysplasia. A pilot study by exome sequencing and pathways analysis 1-gen-2015 Somaschini, M; DI RESTA, Chiara; Volonteri, C; Castiglioni, E; Bonfiglios, ; Lazarevic, D; Cittaro, D; Stupka, E; Ferrari, Maurizio; Carrera, P; Bpd, ; Genetics Study, Group
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study 1-gen-2015 Carrera, P; Di Resta, C; Volonteri, C; Castiglioni, E; Bonfiglio, S; Lazarevic, D; Cittaro, D; Stupka, E; Ferrari, M; Somaschini, M; fort he BPD and Genetics Study, Group
Is laboratory medicine ready for the era of personalized medicine? A survey addressed to laboratory directors of hospitals/academic schools of medicine in Europe 1-gen-2015 Malentacchi, F; Mancini, I; Brandslund, I; Vermeersch, P; Schwab, M; Marc, J; van Schaik, Rh; Siest, G; Theodorsson, E; Pazzagli, M; Di Resta, C
Is laboratory medicine ready for the era of personalized medicine? A survey addressed to laboratory directors of hospitals/academic schools of medicine in Europe. 1-gen-2015 Malentacchi, F; Mancini, I; Brandslund, I; Vermeersch, P; Schwab, M; Marc, J; van Schaik, Rh; Siest, G; Theodorsson, E; Pazzagli, M; Di Resta, C; European Federation of Clinical Chemistry and Laboratory Medicine, (EFLM); European Society of Pharmacogenomics and Personalised Therapy (ESPT) Joint Working Group on Personalized Laboratory Medicine, (WG-PLM)
High-throughput genetic characterization of a cohort of Brugada syndrome patients. 1-gen-2015 DI RESTA, Chiara; Pietrelli, A; Sala, S; Della Bella, P; De Bellis, G; Ferrari, Maurizio; Bordoni, R; Benedetti, S.
Mostrati risultati da 1 a 20 di 76
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