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UNIVERSITÀ DEGLI STUDI
DEL SANNIO   Benevento

Pubblicazioni di ateneo

Found 7 results
Author Titolo [ Tipo(Desc)] Anno
Filters: Author is De Maria, Michela  [Clear All Filters]
Journal Article
Soldovieri, M. Virginia, P. Ambrosino, I. Mosca, M. De Maria, E. Moretto, F. Miceli, A. Alaimo, N. Iraci, L. Manocchio, A. Medoro, et al., "Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate", SCIENTIFIC REPORTS, vol. 6, 2016.
Miceli, F., M. Virginia Soldovieri, P. Ambrosino, M. De Maria, M. Migliore, R. Migliore, and M. Taglialatela, "Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits", THE JOURNAL OF NEUROSCIENCE, vol. 35, pp. 3782–3793, 2015.
Ambrosino, P., A. Alaimo, S. Bartollino, L. Manocchio, M. De Maria, I. Mosca, C. Gomis-Perez, A. Alberdi, G. Scambia, G. Lesca, et al., "Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulin", BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE, vol. 1852, pp. 1856–1866, 2015.
Ambrosino, P., M. Virginia Soldovieri, M. De Maria, C. Russo, and M. Taglialatela, "Functional and biochemical interaction between PPARα receptors and TRPV1 channels: Potential role in PPARα agonists-mediated analgesia", PHARMACOLOGICAL RESEARCH, vol. 87, pp. 113–122, 2014.
Millichap, J. J., F. Miceli, M. De Maria, C. Keator, N. Joshi, B. Tran, M. Virginia Soldovieri, P. Ambrosino, V. Shashi, M. A. Mikati, et al., "Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant", EPILEPSIA, vol. 58, pp. e10–e15, 2017.
Miceli, F., M. Virginia Soldovieri, P. Ambrosino, M. De Maria, L. Manocchio, A. Medoro, and M. Taglialatela, "Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels", FRONTIERS IN CELLULAR NEUROSCIENCE, vol. 9, 2015.
Soldovieri, M. Virginia, N. Boutry-Kryza, M. Milh, D. Doummar, B. Heron, E. Bourel, P. Ambrosino, F. Miceli, M. De Maria, N. Dorison, et al., "Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: First evidence for an altered channel regulation by syntaxin-1A", HUMAN MUTATION, vol. 35, pp. 356–367, 2014.