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Titolo Data di pubblicazione Autore(i) File
P-Selectin Sustains Extramedullary Hematopoiesis in the Gata1 low Model of Myelofibrosis 1-gen-2016 J Spangrude, Gerald; Lewandowski, Daniel; Martelli, Fabrizio; Marra, Manuela; Zingariello, Maria; Sancillo, Laura; Rana, ROSA ALBA; FRANCO MIGLIACCIO, ANNA RITA
P13.4 Peripheral neural electrodes for natural biofeedback: a comparative analysis 1-gen-2011 Benvenuto, A.; Rossini, L.; Di Pino, G; Raspopovic, S.; Micera, S.; Guglielmelli, E.; Rossini, P. M.
P14 - percutaneous closure of acquired and congenital ventricular septal defect in adult population: institutional experience 1-gen-2006 Ussia, G; Caruso, E; Galassi, Ar; Mulè, M; Scandurra, S; Felis, S; La Manna, A; Licciardello, G
P15 - usefulness of the amplatzer multi-fenestrated septal occluder - "cribriform" for patent foramen ovale and multifenestrated atrial septal aneurism: institutional experience 1-gen-2006 Ussia, G; Calaciura, R; Privitera, A; Mangiafico, S; Mulè, M; Caruso, E; Barbanti, M; Galassi, Ar; Tamburino, C
P15INK4b/CDKN2B promoter region methylation in sporadic colorecatl cancer 1-gen-1999 Angeletti, S; Garcia-Foncillas, J; Okroujnov, I; Martinez, Mj; Jimenez, E; Dicuonzo, G; Brugarolas, A
P16-Severy pulmonary arterial hypertension associated to patent ductus arteriosus successfully treated with oral endothelin receptor antagonist therapy and percutaneous closure with amplatzer duct occluder 1-gen-2006 Ussia, G; Mulè, M; Caruso, E; Aiello, R; Calaciura, R; Montana, G; Scarabelli, M; Barbanti, M; Galassi, Ar; Tamburino, C
P17-Utilizzo di protesi ASD Amplatzer di diametro maggiore 38 MM in pazienti con DIA di grandi dimensioni 1-gen-2006 Ussia, G; Calaciura, R; Privitera, A; Mangiafico, S; Mulè, M; Caruso, E; De Luca, F; Galassi, Ar; Tamburino, C
P189: Does an intraneural interface short-term implant for robotic hand control modulate sensorimotor cortical integration? An EEG-TMS co-registration study on a human amputee 1-gen-2014 Guerra, A; Ferreri, F; Ponzo, D; Vollero, L; Di Pino, G; Petrichella, S; Benvenuto, A; Tombini, M; Rossini, L; Denaro, L; Micera, S; Iannello, G; Guglielmelli, E; Denaro, V; Rossini, P M
P2X7 receptor antagonism: Implications in diabetic retinopathy 1-gen-2017 Platania, Cbm; Giurdanella, G; Di Paola, L; Leggio, Gm; Drago, F; Salomone, S; Bucolo, C
P2X7R mutation disrupts the NLRP3-mediated Th program and predicts poor cardiac allograft outcomes 1-gen-2018 D'Addio, F; Vergani, A; Potena, L; Maestroni, A; Usuelli, V; Ben Nasr, M; Bassi, R; Tezza, S; Dellepiane, S; El Essawy, B; Iascone, M; Iacovoni, A; Borgese, L; Liu, K; Visner, G; Dhe-Paganon, S; Corradi, D; Abdi, R; Starling, Rc; Folli, F; Zuccotti, Gv; Sayegh, Mh; Heeger, Ps; Chandraker, A; Grigioni, F; Fiorina,
P37-Is atrial wall erosion a real issue of percutaneous closure of patent foramen ovale with Amplatzer septal occluder? 1-gen-2007 Ussia, G; Mulè, M; Caruso, E; Scarabelli, M; Calaciura, R; Magnifico, S; Moncada, R; Privitera, A; Aiello, R; Stimoli, F; Tamburino, C
P38-Assessment and management of cardiac perforation occurred during the percutaneous closure of left atrial appendage with the Plaato System 1-gen-2007 Ussia, G; Mulè, M; Mangiafico, S; Caruso, E; Scarabelli, M; Barbanti, M; Stimoli, F; Tamburino, C
P4-113 Interaction between the STH and APOE gene polymorphisms modifies risk for Alzheimer's disease 1-gen-2004 Davide, Seripa; Gloria Dal, Forno; Maria, G Matera; Rocco, P D'Andrea; Carolina, Gravina; Carlo, Masullo; Antonio, Daniele; Piero, Antuono; David, R Wekstein; Fazio, V. M.
P5 Cpg island promoter hypermethylation in breast cancer development and progression 1-gen-2005 P, Parrella; M, Scintu; M, Prencipe; Ap, Gallo; I, Carosi; Fazio, V. M.; Vm, Valori
p53 and telomerase control rat myocardial tissue response to hypoxia and ageing 1-gen-2009 Cataldi, A; Zara, S; Rapino, M; Zingariello, M; di Giacomo, V; Antonucci, A
p53 interference and growth inhibition in p53-mutant and overexpressing endometrial cancer cell lines 1-gen-1997 Janicek, Mf; Angioli, R; Unal, Ad; Sevin, Bu; Madrigal, M; Estape, R; Averette, He
P56: Human brain cortical effective connectivity and excitability in Alzheimer’s disease: a combined EEG-TMS study 1-gen-2014 Guerra, A; Ferreri, F; Vecchio, F; Pasqualetti, P; Vollero, L; Petrichella, S; Maeaettae, S; Ponzo, S; Mervaala, E; Scrascia, F; Ursini, F; Bernardini, S; Bressi, F; Iannello, G; Rossini, P M
p63 gene mutations in EEC syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation 1-gen-2001 van Bokhoven, H; Hamel, Bcj; Bamshad, M; Sangiorgi, E; Gurrieri, F; Duijf, Phg; Vanmolkot, Krj; van Beusekom, E; van Beersum, Sec; Celli, J; Merkx, Gfm; Tenconi, R; Fryns, Jp; Verloes, A; Newbury-Ecob, Ra; Raas-Rotschild, A; Majewski, F; Beemer, Fa; Janecke, A; Chitayat, D; Crisponi, G; Kayserili, H; Yates, Jrw; Neri, G; Brunner, Hg
p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation RID D-5697-2011 1-gen-2000 Brunner, H; Mcgrath, Ja; Celli, J; Duijf, P; Gurrieri, F; Mckeon, F; Propping, P; Bamshad, M; van Bokhoven, H; Hamel, B; Neri, G; Doetsch, V; de Waal, R; Yang, A; Vanmolkot, K
P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation. RID D-5697-2011 1-gen-2000 Van Bokhoven, H; Mcgrath, Ja; Duljf, P; Celli, J; Hamel, Bcj; de Waal, R; Yang, A; Mckeon, F; Doetsch, V; Vanmolkot, K; Propping, P; Gurrieri, F; Neri, G; Bamshad, M; Brunner, Hg
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