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ALTAMURA, CONCETTA

ALTAMURA, CONCETTA  

DIPARTIMENTO DI MEDICINA DI PRECISIONE E RIGENERATIVA E AREA JONICA DiMePRe-J  

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Titolo Data di pubblicazione Autore(i) File
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 1-gen-2017 Imbrici, Paola; Altamura, Concetta; Gualandi, Francesca; Mangiatordi, Giuseppe Felice; Neri, Marcella; De Maria, Giovanni; Ferlini, Alessandra; Padovani, Alessandro; D'Adamo, Maria Cristina; Nicolotti, Orazio; Pessia, Mauro; Conte, Diana; Filosto, Massimiliano; Desaphy, Jean-Francois
Bioisosteric Modification of To042: Synthesis and Evaluation of Promising Use-Dependent Inhibitors of Voltage-Gated Sodium Channels 1-gen-2021 Milani, G.; Cavalluzzi, M. M.; Altamura, C.; Santoro, A.; Perrone, M.; Muraglia, M.; Colabufo, N. A.; Corbo, F.; Casalino, E.; Franchini, C.; Pisano, I.; Desaphy, Jf; Carrieri, A.; Carocci, A.; Lentini, G.
Buprenorphine may be effective for treatment of paramyotonia congenita 1-gen-2021 Ravaglia, S.; Maggi, L.; Zito, Antonio; Arceri, S.; Gallotti, P.; Altamura, Concetta; Desaphy, Jf.; Bernasconi, P.; Alfonsi, E.
Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita 1-gen-2022 Altamura, Concetta; Conte, Elena; Campanale, Carmen; Laghetti, Paola; Saltarella, Ilaria; Camerino, Giulia Maria; Imbrici, Paola; Desaphy, Jean-Francois
ClC-1 chloride channels: state-of-the-art research and future challenges 1-gen-2015 Imbrici, Paola; Altamura, C; Pessia, M; Mantegazza, R; Desaphy, Jean Francois; Conte, Diana
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation 1-gen-2015 Imbrici, P; Maggi, L; Mangiatordi, G F; Dinardo, M M; Altamura, Concetta; Brugnoni, R; Alberga, D; Pinter, G L; Ricci, G; Siciliano, G; Micheli, R; Annicchiarico, G; Lattanzi, G; Nicolotti, O; Morandi, L; Bernasconi, P; Desaphy, J-F; Mantegazza, R; Camerino, D C
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita 1-gen-2015 Portaro, Simona; Altamura, Concetta; Licata, Norma; Camerino, GIULIA MARIA; Imbrici, Paola; Musumeci, Olimpia; Rodolico, Carmelo; Conte, Diana; Toscano, Antonio; Desaphy, Jean Francois
Coexistence of CLCN1 and SCN4A mutations in one family suffering from myotonia 1-gen-2017 Maggi, Lorenzo; Ravaglia, Sabrina; Farinato, Alessandro; Brugnoni, Raffaella; Altamura, Concetta; Imbrici, Paola; Conte, Diana; Padovani, Alessandro; Mantegazza, Renato; Bernasconi, Pia; Desaphy, Jean-François; Filosto, Massimiliano
Drug repurposing in skeletal muscle ion channelopathies 1-gen-2022 Altamura, Concetta; Saltarella, Ilaria; Campanale, Carmen; Laghetti, Paola; Desaphy, Jean-Francois
Effects of Benzothiazolamines on Voltage-Gated Sodium Channels 1-gen-2018 Farinato, Alessandro; Altamura, Concetta; Desaphy, Jean-François
Emerging roles for ion channels in ovarian cancer: Pathomechanisms and pharmacological treatment 1-gen-2021 Altamura, C.; Greco, M. R.; Carratu, M. R.; Cardone, R. A.; Desaphy, Jf.
Immersive and Non-Immersive Virtual Reality for Pain and Anxiety Management in Pediatric Patients with Hematological or Solid Cancer: A Systematic Review 1-gen-2023 Comparcini, Dania; Simonetti, Valentina; Galli, Francesco; Saltarella, Ilaria; Altamura, Concetta; Tomietto, Marco; Desaphy, Jean-François; Cicolini, Giancarlo
Increased sarcolemma chloride conductance as one of the mechanisms of action of carbonic anhydrase inhibitors in muscle excitability disorders 1-gen-2021 Altamura, Concetta; Fonzino, A.; Tarantino, N.; Conte, Elena; Liantonio, A.; Imbrici, P.; Carratu, Mr; Pierno, S.; Desaphy, Jf
Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy 1-gen-2021 Maggi, Lorenzo; Bonanno, Silvia; Altamura, Concetta; Desaphy, Jean Francois
Ion Channel Involvement in Tumor Drug Resistance 1-gen-2022 Altamura, Concetta; Gavazzo, P.; Pusch, M.; Desaphy, Jf.
Ion channels gene expression analysis in myotonia congenita patients carrying ClC-1 chloride channel mutations 1-gen-2015 Altamura, C.; Camerino, GIULIA MARIA; Imbrici, Paola; Portaro, S.; Musumeci, O.; Toscano, A.; Desaphy, Jean Francois; Conte Camerino, D.
Ion Channels in Multiple Myeloma: Pathogenic Role and Therapeutic Perspectives 1-gen-2022 Saltarella, Ilaria; Altamura, Concetta; Lamanuzzi, Aurelia; Apollonio, Benedetta; Vacca, Angelo; Frassanito, Maria Antonia; Desaphy, Jean-François
Mapping ligand binding pockets in ClC-1 channels through an integrated in silico and experimental approach using anthracene-9-carboxylic acid and niflumic acid 1-gen-2018 Altamura, C; Mangiatordi, G F; Nicolotti, O; Sahbani, D; Farinato, A; Leonetti, F; Carratù, M; Conte, D; Desaphy, J; Imbrici, P
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies 1-gen-2016 Imbrici, Paola; Altamura, Concetta; Camerino, GIULIA MARIA; Mangiatordi, Giuseppe Felice; Conte, Elena; Maggi, Lorenzo; Brugnoni, Raffaella; Musaraj, Kejla; Caloiero, Roberta; Alberga, Domenico; Marsano, RENE' MASSIMILIANO; Ricci, Giulia; Siciliano, Gabriele; Nicolotti, Orazio; Mora, Marina; Bernasconi, Pia; Desaphy, Jean Francois; Mantegazza, Renato; Conte, Diana
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel 1-gen-2021 Imbrici, Paola; Accogli, Andrea; Blunck, Rikard; Altamura, Concetta; Iacomino, Michele; D’Adamo, Maria Cristina; Allegri, Anna; Pedemonte, Marina; Brolatti, Noemi; Vari, Stella; Cataldi, Matteo; Capra, Valeria; Gustincich, Stefano; Zara, Federico; Desaphy, Jean-Francois; Fiorillo, Chiara