A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 von GAMBARDELLA, A, ANNESI, G, ZAPPIA, M, BALLABIO, A, CASARI, G, QUATTRONE, A, DE FUSCO, M, PATRIGNANI, A, AGUGLIA, U, ANNESI, F, PASQUA, A. A, SPADAFORA, P, OLIVERI, R. L, VALENTINE, P

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Relaparoscopic approach for recurrence after laparoscopic incisional hernia repair - a video vignette von Capitano, S., del Pozo, A. C., Bartolotta, V., De Fusco, M., Chiodi, L., Boccoli, G.

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Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear von Aridon, Paolo, Marini, Carla, Di Resta, Chiara, Brilli, Elisa, De Fusco, Maurizio, Politi, Fausta, Parrini, Elena, Manfredi, Irene, Pisano, Tiziana, Pruna, Dario, Curia, Giulia, Cianchetti, Carlo, Pasqualetti, Massimo, Becchetti, Andrea, Guerrini, Renzo, Casari, Giorgio

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Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome von MASTROIANNI, N, BETTINELLI, A, BIANCHETTI, M, COLUSSI, G, DE FUSCO, M, SERENI, F, BALLABIO, A, CASARI, G

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Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry von Cetica, Valentina, PhD, Sieni, Elena, MD, Pende, Daniela, PhD, Danesino, Cesare, MD, De Fusco, Carmen, MD, Locatelli, Franco, MD, Micalizzi, Concetta, MD, Putti, Maria Caterina, MD, Biondi, Andrea, MD, Fagioli, Franca, MD, Moretta, Lorenzo, MD, Griffiths, Gillian M., PhD, Luzzatto, Lucio, MD, Aricò, Maurizio, MD

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Clinical pharmacology of chronic oral etoposide in patients with small cell and non-small cell lung cancer von ZUCCHETTI, M, PAGANI, O, CAVALLI, F, TORRI, V, SESSA, C, D'INCALCI, M, DE FUSCO, M, DE JONG, J, GENTILI, D, MARTINELLI, G, TINAZZI, A

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The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy von De Fusco, M, Becchetti, A, Patrignani, A, Annesi, G, Gambardella, A, Quattrone, A, Ballabio, A, Wanke, E, Casari, G

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Autosomal dominant hereditary spastic paraplegia: report of a large Italian family with R581X spastin mutation von Aridon, P, Ragonese, P, De Fusco, M, Lo Coco, D, Salemi, G, Casari, G, Savettieri, G

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Molecular Cloning, Expression Pattern, and Chromosomal Localization of the Human Na–Cl Thiazide-Sensitive Cotransporter (SLC12A3) von Mastroianni, Nadia, Fusco, Maurizio De, Zollo, Massimo, Arrigo, Giulia, Zuffardi, Orsetta, Bettinelli, Alberto, Ballabio, Andrea, Casari, Giorgio

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Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease von Casari, Giorgio, De Fusco, Maurizio, Ciarmatori, Sonia, Zeviani, Massimo, Mora, Marina, Fernandez, Patricio, De Michele, Giuseppe, Filla, Alessandro, Cocozza, Sergio, Marconi, Roberto, Dürr, Alexandre, Fontaine, Bertrand, Ballabio, Andrea

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Clinical and pharmacokinetic study of oral NK611, a new podophyllotoxin derivative von PAGANI, O, ZUCCHETTI, M, SESSA, C, DE JONG, J, D'INCALCI, M, DE FUSCO, M, KAESER-FRÖHLICH, A, HANAUSKE, A, CAVALLI, F

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Phase I clinical and pharmacokinetic study of oral etoposide phosphate von SESSA, C, ZUCCHETTI, M, SCHACTER, L, WINOGRAD, B, D'INCALCI, M, CERNY, T, PAGANI, O, CAVALLI, F, DE FUSCO, M, DE JONG, J, GENTILI, D, MCDANIEL, C, PRINS, C

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Comparative Efficacies of Quinupristin-Dalfopristin, Linezolid, Vancomycin, and Ciprofloxacin in Treatment, Using the Antibiotic-Lock Technique, of Experimental Catheter-Related In... von GIACOMETTI, Andrea, CIRIONI, Oscar, SCALISE, Giorgio, GHISELLI, Roberto, ORLANDO, Fiorenza, MOCCHEGIANI, Federico, SILVESTRI, Carmela, LICCI, Alberto, DE FUSCO, Matteo, PROVINCIALI, Mauro, SABA, Vittorio

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Integrated imaging of systemic Langerhans cell histiocytosis in an infant von Cariello, Valentina, Lombardo, Patrizia, Castelli, Luisa, Brillantino, Carmela, De Fusco, Carmela, Rossi, Antonio, Minelli, Rocco, Paviglianiti, Giuseppe, Grassi, Roberto, Rossi, Eugenio

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Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23 von Marconi, Roberto, De Fusco, Maurizio, Aridon, Paolo, Plewnia, Katrin, Rossi, Maja, Carapelli, Sadia, Ballabio, Andrea, Morgante, Letterio, Musolino, Rosa, Epifanio, Antonio, Micieli, Giuseppe, De Michele, Giuseppe, Casari, Giorgio

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Autosomal recessive Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2 von Guerrini, Renzo, Bonanni, Paolo, Nardocci, Nardo, Parmeggiani, Lucio, Piccirilli, Massimo, De Fusco, Maurizio, Aridon, Paolo, Ballabio, Andrea, Carrozzo, Romeo, Casari, Giorgio

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A recessive variant of the Romano-Ward long-QT syndrome? von PRIORI, S. G, SCHWARTZ, P. J, NAPOLITANO, C, BIANCHI, L, DENNIS, A, DE FUSCO, M, BROWN, A. M, CASARI, G

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Identification of a New Locus for Medullary Cystic Disease, on Chromosome 16p12 von Scolari, Francesco, Puzzer, Daniela, Amoroso, Antonio, Caridi, Gianluca, Ghiggeri, Gian Marco, Maiorca, Rosario, Aridon, Paolo, De Fusco, Maurizio, Ballabio, Andrea, Casari, Giorgio

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A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3 von De Michele, Giuseppe, De Fusco, Maurizio, Cavalcanti, Francesca, Filla, Alessandro, Marconi, Roberto, Volpe, Giampiero, Monticelli, Antonella, Ballabio, Andrea, Casari, Giorgio, Cocozza, Sergio

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The functional properties of the human ether-à-go-go-like (HELK2) K+ channel von Becchetti, Andrea, De Fusco, Maurizio, Crociani, Olivia, Cherubini, Alessia, Restano-Cassulini, Rita, Lecchi, Marzia, Masi, Alessio, Arcangeli, Annarosa, Casari, Giorgio, Wanke, Enzo

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