IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 40
Titolo Data di pubblicazione Autore(i) File
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor 1-gen-2000 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Scuccimarra, G; Cirillo, G; Bellini, Giulia; Pascotto, Antonio
A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia 1-gen-2001 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Bellini, Giulia; Cirillo, G; Scuccimarra, G; Pascotto, Antonio
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 1-gen-2003 Coppola, G; Castaldo, P; MIRAGLIA DEL GIUDICE, Emanuele; Bellini, Giulia; Galasso, F; Soldovieri, Mv; Anzalone, L; Sferro, C; Annunziato, L; Pascotto, Antonio; Taglialatela, M.
A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia 1-gen-2003 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Bellini, Giulia; Ledaal, P; Hertz, Jm; Pascotto, Antonio
EXCLUSION DE LINKAGE A 8Q24 DANS UNE FAMILLE AVEC ABSENCE DE L'ENFANCE A DEBUT PRECOCE ET TOLERANCE REDUITE AU VPA 1-gen-2004 Titomanlio, L; Romano, A; MIRAGLIA DEL GIUDICE, Emanuele; Iuliano, R; Bellini, Giulia; Coppola, G; Pascotto, Antonio; DEL GIUDICE, E.
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists 1-gen-2004 Castaldo, P; Stefanoni, P; Miceli, F; Coppola, G; MIRAGLIA DEL GIUDICE, Emanuele; Bellini, Giulia; Pascotto, Antonio; Trudell, Jr; Harrison, Nl; Annunziato, L; Taglialatela, M.
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy. 1-gen-2005 Bellini, Giulia; Bravaccio, C.; Calamoneri, F.; Cocuzza, D.; Fiorillo, P.; Gagliano, A.; Mazzone, D.; MIRAGLIA DEL GIUDICE, Emanuele; Scuccimarra, G.; Militerni, R.; Pascotto, Antonio
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions 1-gen-2006 Soldovieri, Mv; Castaldo, P; Iodice, L; Miceli, F; Barrese, V; Bellini, Giulia; MIRAGLIA DEL GIUDICE, Emanuele; Pascotto, Antonio; Bonatti, S; Annunziato, L; Taglialatela, M.
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy 1-gen-2006 Coppola, G; Veggiotti, P; MIRAGLIA DEL GIUDICE, Emanuele; Bellini, Giulia; Longaretti, F; Taglialatela, M; Pascotto, Antonio
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions 1-gen-2007 Soldovieri, Mv; Cilio, Mr; Miceli, F; Bellini, Giulia; MIRAGLIA DEL GIUDICE, Emanuele; Castaldo, P; Hernandez, Cc; Shapiro, Ms; Pascotto, Antonio; Annunziato, L; Taglialatela, M.
Hyperekplexia caused by dominant-negative suppression of glyra1 function 1-gen-2007 Bellini, Giulia; Miceli, F; Mangano, S; MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Barbagallo, A; Taglialatela, M; Pascotto, Antonio
Familial occurrence of early-onset childhood absence epilepsy 1-gen-2007 Titomanlio, L.; Romano, A.; Bellini, Giulia; Pascotto, Antonio; Iuliano, R.; MIRAGLIA DEL GIUDICE, Emanuele; Del Giudice, E.
Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures 1-gen-2009 Miceli, F; Soldovieri, Mv; Lugli, L; Bellini, Giulia; Ambrosino, P; Migliore, M; MIRAGLIA DEL GIUDICE, Emanuele; Ferrari, F; Pascotto, Antonio; Taglialatela, M.
The endovanilloid/endocannabinoid system in human osteoclasts: Possible involvement in bone formation and resorption 1-gen-2009 Rossi, F.; Siniscalco, D.; Luongo, L.; De Petrocellis, L.; Bellini, G.; Petrosino, S.; Torella, M.; Santoro, C.; Nobili, B.; Perrotta, S.; Di Marzo, V.; Maione, S.
Benign Familial Neonatal Seizures . In: editors. Seattle (WA): Apr 27 1-gen-2010 Bellini, Giulia; Miceli, F; Soldovieri, Mv; MIRAGLIA DEL GIUDICE, Emanuele; Pascotto, Antonio; Taglialatela, M.
Benign Familial Neonatal Seizures 1-gen-2010 Bellini, Giulia; Miceli, F; Soldovieri, M. V.; MIRAGLIA DEL GIUDICE, Emanuele; Pascotto, Antonio; Taglialatela, M.
The blockade of the transient receptor potential vanilloid type 1 and fatty acid amide hydrolase decreases symptoms and central sequelae in the medial prefrontal cortex of neuropathic rats. 1-gen-2011 DE NOVELLIS, Vito; Vita, D; Gatta, L; Luongo, Livio; Bellini, Giulia; De Chiaro, M; Marabese, Ida; Siniscalco, D; Boccella, S; Piscitelli, F; Di Marzo, V; Palazzo, Enza; Rossi, Francesco; Maione, Sabatino
Association of the cannabinoid receptor 2 (CB2) Gln63Arg polymorphism with indices of liver damage in obese children: An alternative way to highlight the CB2 hepatoprotective properties. 1-gen-2011 Rossi, Francesca; Bellini, Giulia; Nobili, Bruno; Maione, Sabatino; Perrone, Laura; MIRAGLIA DEL GIUDICE, Emanuele
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. 1-gen-2011 Rossi, Francesca; Mancusi, S; Bellini, Giulia; Roberti, D; Punzo, F; Vetrella, S; Matarese, Sm; Nobili, Bruno; Maione, Sabatino; Perrotta, Silverio
EP1 receptor within the ventrolateral periaqueductal grey controls thermonociception and rostral ventromedial medulla cell activity in healthy and neuropathic rat 1-gen-2011 Palazzo, Enza; Guida, Francesca; Gatta, L; Luongo, Livio; Boccella, S; Bellini, Giulia; Marabese, Ida; DE NOVELLIS, Vito; Rossi, Francesca; Maione, Sabatino
Mostrati risultati da 1 a 20 di 40
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile