Sfoglia per ???browse.type.metadata.typeResearch??? AREA06 - SCIENZE MEDICHE
Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions
2000 Askanas, Valerie; Engel, W. King; Alvarez, Renate; Mcferrin, Janis; Broccolini, Aldobrando
Novel insights in fibrotic pulmonary sarcoidosis
2022 Comes, Alessia; Sofia, Carmelo; Richeldi, Luca
Novel Insights Into the Interactions Between the Gut Microbiome, Inflammasomes, and Gasdermins During Colorectal Cancer
2022 Privitera, Giuseppe; Rana, N.; Scaldaferri, Franco; Armuzzi, Alessandro; Pizarro, T. T.
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease
2014 Ciotti, Paolo; Luigetti, Marco; Geroldi, A; Capponi, S; Pezzini, I; Gulli, R; Pazzaglia, Costanza; Padua, Luca; Massa, R; Mandich, P; Bellone, E.
A novel low-density lipoprotein receptor variant in a Ukrainian patient: a case report and overview of the disease-causing low-density lipoprotein receptor variants associated to familial hypercholesterolemia
2021 Moffa, Simona; Onori, Maria Elisabetta; De Paolis, Elisa; Ricciardi Tenore, Claudio; Perrucci, Alessia; Pontecorvi, Alfredo; Giaccari, Andrea; Urbani, Andrea; Minucci, Angelo
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
2020 Sims, Matthew C; Mayer, Louisa; Collins, Janine; Bariana, Tadbir; Megy, Karyn; Lavenu-Bombled, Cecile; Seyres, Denis; Kollipara, Laxmikanth; Burden, Frances; Greene, Daniel; Lee, Dave; Rodriguez-Romera, Antonio; Alessi, Marie-Christine; Astle, William John; Bahou, Wadie; Bury, Loredana; Chalmers, Elizabeth; Da Silva, Rachael; De Candia, Erica; Deevi, Sri V V; Farrow, Samantha; Gomez, Keith; Grassi, Luigi; Greinacher, Andreas; Gresele, Paolo; Hart, Daniel Patrick; Hurtaud, Marie-Françoise; Kelly, Anne; Kerr, Ron; Le Quellec, Sandra; Leblanc, Thierry M; Leinøe, Eva B; Mapeta, Rutendo P; Mckinney, Harriet; Michelson, Alan D; Morais, Sara; Nugent, Diane J; Papadia, Sofia; Park, Soo J; Pasi, John; Podda, Gian Marco; Poon, Man-Chiu; Reed, Rachel; Sekhar, Mallika; Shalev, Hanna; Sivapalaratnam, Suthesh; Steinberg-Shemer, Orna; Stephens, Jonathan C; Tait, Robert C; Turro, Ernest; Wu, John K; Zieger, Barbara Maria Hildegard; Bioresource, Nihr; Kuijpers, Taco W; Whetton, Anthony D; Sickmann, Albert; Freson, Kathleen; Downes, Kate; Erber, Wendy; Frontini, Mattia; Nurden, Paquita; Ouwehand, Willem Hendrik; Favier, Remi; Guerrero, Jose A
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family
2021 Brown, K. M.; Xu, M.; Sargen, M.; Jang, H.; Zhang, M.; Zhang, T.; Zhu, B.; Jones, K.; Kim, J.; Mendoza, L.; Hayward, N. K.; Tucker, M. A.; Goldstein, A. M.; Yang, X. R.; Stewart, D. R.; Hicks, B.; Consonni, D.; Pesatori, A. C.; Fargnoli, Maria Concetta; Peris, Ketty; Stratigos, A.; Menin, C.; Ghiorzo, P.; Puig, S.; Nagore, E.; Andresson, T.; Nussinov, R.; Calista, D.; Landi, M. T.
A novel MEN1 pathogenic variant in an Italian patient with multiple endocrine neoplasia type 1
2020 Corsello, Andrea; Bruno, Carmine; Rizza, Roberta; Concolino, Paola; Papi, Giampaolo; Pontecorvi, Alfredo; Rindi, Guido; Paragliola, Rosa Maria
A novel method for post-mortem interval estimation based on tissue nano-mechanics
2019 De Giorgio, Fabio; Nardini, Matteo; Foti, Federica; Minelli, Eleonora; Papi, Massimiliano; D'Aloja, Ernesto; Pascali, Vincenzo Lorenzo; De Spirito, Marco; Ciasca, Gabriele
A novel methodology for large-scale phylogeny partition
2011 Prosperi, Mcf; Ciccozzi, M; Fanti, Iuri; Saladini, F; Pecorari, Mauro; Borghi, Vando; Di Giambenedetto, Simona; Bruzzone, B; Capetti, A; Vivarelli, A; Rusconi, S; Re, Mc; Gismondo, Mr; Sighinolfi, L; Gray, Rr; Salemi, M; Zazzi, M; De Luca, Andrea
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer
2005 Lucci-Cordisco, E; Zollino, Marcella; Baglioni, S; Mancuso, I; Lecce, R; Gurrieri, Fiorella; Crucitti, Antonio; Papi, L; Neri, G; Genuardi, Maurizio
A Novel Mini-invasive Approach to the Treatment of Neuropathic Pain: The PENS Study
2016 Rossi, M; De Carolis, G; Liberatoscioli, G; Iemma, D; Nosella, P; Nardi, Lf
A novel mitochondrial DNA point mutation in the tRNAIIe gene is associated with progressive external ophtalmoplegia
1996 Silvestri, Gabriella; Servidei, Serenella; Rana, M.; Ricci, Enzo; Spinazzola, A.; Paris, E.; Tonali, P.
A Novel Monocyte Subset as a Unique Signature of Atherosclerotic Plaque Rupture
2021 Vinci, Ramona; Pedicino, Daniela; Bonanni, Alice; D'Aiello, A.; Severino, Anna; Pisano, Eugenia; Ponzo, Myriana; Canonico, Francesco; Ciampi, Pellegrino; Russo, Giovanni; Di Sario, Marianna; Montone, Rocco Antonio; Trani, Carlo; Conte, Caterina; Grimaldi, Maria Chiara; Cribari, Francesco; Massetti, Massimo; Crea, Filippo; Liuzzo, Giovanna
A novel multi-marker discovery approach identifies new serum biomarkers for Parkinson’s disease in older people: an EXosomes in PArkiNson Disease (EXPAND) ancillary study
2020 Calvani, R.; Picca, A.; Landi, G.; Marini, F.; Biancolillo, A.; Coelho-Junior, H. J.; Gervasoni, J.; Persichilli, S.; Primiano, A.; Arcidiacono, A.; Urbani, A.; Bossola, M.; Bentivoglio, A. R.; Cesari, M.; Bernabei, R.; Monaco, M. R. L.; Marzetti, E.
A novel mutation of the insulin receptor gene in a preterm infant with Donohue syndrome and heart failure
2012 Nobile, Stefano; K Semple, Robert; P Carnielli, Virgilio
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy
2006 Cardaioli, E.; Gallus, G. N.; Da Pozzo, P.; Rufa, A.; Franceschini, R.; Motolese, E.; Caporossi, Aldo; Dotti, M. T.; Federico, A.
Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa responsive parkinsonism
2011 Silvestri, Gabriella; Guidubaldi, Arianna; Tessa, A; Petracca, Martina; Bentivoglio, Anna Rita; Santorelli, Fm
Novel nicastrin mutation in hidradenitis suppurativa-Dowling Degos disease clinical phenotype: more than just clinical overlap?
2020 Garcovich, Simone; Tricarico, P M; Meddour, C N; Giovanardi, Giulia; Peris, Ketty; Crovella, S; Boniotto, M
A Novel Nomogram to Predict the Prognosis of Patients Undergoing Liver Resection for Neuroendocrine Liver Metastasis: an Analysis of the Italian Neuroendocrine Liver Metastasis Database
2017 Ruzzenente, Andrea; Bagante, Fabio; Bertuzzo, Francesca; Aldrighetti, Luca; Ercolani, Giorgio; Giuliante, Felice; Ferrero, Alessandro; Torzilli, Guido; Grazi, Gian Luca; Ratti, Francesca; Cucchetti, Alessandro; De Rose, Agostino Maria; Russolillo, Nadia; Cimino, Matteo; Perri, Pasquale; Cataldo, Ivana; Scarpa, Aldo; Guglielmi, Alfredo; Iacono, Calogero
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2000 | Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions | Askanas, Valerie; Engel, W. King; Alvarez, Renate; Mcferrin, Janis; Broccolini, Aldobrando | |
1-gen-2022 | Novel insights in fibrotic pulmonary sarcoidosis | Comes, Alessia; Sofia, Carmelo; Richeldi, Luca | |
1-gen-2022 | Novel Insights Into the Interactions Between the Gut Microbiome, Inflammasomes, and Gasdermins During Colorectal Cancer | Privitera, Giuseppe; Rana, N.; Scaldaferri, Franco; Armuzzi, Alessandro; Pizarro, T. T. | |
1-gen-2014 | A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease | Ciotti, Paolo; Luigetti, Marco; Geroldi, A; Capponi, S; Pezzini, I; Gulli, R; Pazzaglia, Costanza; Padua, Luca; Massa, R; Mandich, P; Bellone, E. | |
1-gen-2021 | A novel low-density lipoprotein receptor variant in a Ukrainian patient: a case report and overview of the disease-causing low-density lipoprotein receptor variants associated to familial hypercholesterolemia | Moffa, Simona; Onori, Maria Elisabetta; De Paolis, Elisa; Ricciardi Tenore, Claudio; Perrucci, Alessia; Pontecorvi, Alfredo; Giaccari, Andrea; Urbani, Andrea; Minucci, Angelo | |
1-gen-2020 | Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome | Sims, Matthew C; Mayer, Louisa; Collins, Janine; Bariana, Tadbir; Megy, Karyn; Lavenu-Bombled, Cecile; Seyres, Denis; Kollipara, Laxmikanth; Burden, Frances; Greene, Daniel; Lee, Dave; Rodriguez-Romera, Antonio; Alessi, Marie-Christine; Astle, William John; Bahou, Wadie; Bury, Loredana; Chalmers, Elizabeth; Da Silva, Rachael; De Candia, Erica; Deevi, Sri V V; Farrow, Samantha; Gomez, Keith; Grassi, Luigi; Greinacher, Andreas; Gresele, Paolo; Hart, Daniel Patrick; Hurtaud, Marie-Françoise; Kelly, Anne; Kerr, Ron; Le Quellec, Sandra; Leblanc, Thierry M; Leinøe, Eva B; Mapeta, Rutendo P; Mckinney, Harriet; Michelson, Alan D; Morais, Sara; Nugent, Diane J; Papadia, Sofia; Park, Soo J; Pasi, John; Podda, Gian Marco; Poon, Man-Chiu; Reed, Rachel; Sekhar, Mallika; Shalev, Hanna; Sivapalaratnam, Suthesh; Steinberg-Shemer, Orna; Stephens, Jonathan C; Tait, Robert C; Turro, Ernest; Wu, John K; Zieger, Barbara Maria Hildegard; Bioresource, Nihr; Kuijpers, Taco W; Whetton, Anthony D; Sickmann, Albert; Freson, Kathleen; Downes, Kate; Erber, Wendy; Frontini, Mattia; Nurden, Paquita; Ouwehand, Willem Hendrik; Favier, Remi; Guerrero, Jose A | |
1-gen-2021 | Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family | Brown, K. M.; Xu, M.; Sargen, M.; Jang, H.; Zhang, M.; Zhang, T.; Zhu, B.; Jones, K.; Kim, J.; Mendoza, L.; Hayward, N. K.; Tucker, M. A.; Goldstein, A. M.; Yang, X. R.; Stewart, D. R.; Hicks, B.; Consonni, D.; Pesatori, A. C.; Fargnoli, Maria Concetta; Peris, Ketty; Stratigos, A.; Menin, C.; Ghiorzo, P.; Puig, S.; Nagore, E.; Andresson, T.; Nussinov, R.; Calista, D.; Landi, M. T. | |
1-gen-2020 | A novel MEN1 pathogenic variant in an Italian patient with multiple endocrine neoplasia type 1 | Corsello, Andrea; Bruno, Carmine; Rizza, Roberta; Concolino, Paola; Papi, Giampaolo; Pontecorvi, Alfredo; Rindi, Guido; Paragliola, Rosa Maria | |
1-gen-2019 | A novel method for post-mortem interval estimation based on tissue nano-mechanics | De Giorgio, Fabio; Nardini, Matteo; Foti, Federica; Minelli, Eleonora; Papi, Massimiliano; D'Aloja, Ernesto; Pascali, Vincenzo Lorenzo; De Spirito, Marco; Ciasca, Gabriele | |
1-gen-2011 | A novel methodology for large-scale phylogeny partition | Prosperi, Mcf; Ciccozzi, M; Fanti, Iuri; Saladini, F; Pecorari, Mauro; Borghi, Vando; Di Giambenedetto, Simona; Bruzzone, B; Capetti, A; Vivarelli, A; Rusconi, S; Re, Mc; Gismondo, Mr; Sighinolfi, L; Gray, Rr; Salemi, M; Zazzi, M; De Luca, Andrea | |
1-gen-2005 | A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer | Lucci-Cordisco, E; Zollino, Marcella; Baglioni, S; Mancuso, I; Lecce, R; Gurrieri, Fiorella; Crucitti, Antonio; Papi, L; Neri, G; Genuardi, Maurizio | |
1-gen-2016 | A Novel Mini-invasive Approach to the Treatment of Neuropathic Pain: The PENS Study | Rossi, M; De Carolis, G; Liberatoscioli, G; Iemma, D; Nosella, P; Nardi, Lf | |
1-gen-1996 | A novel mitochondrial DNA point mutation in the tRNAIIe gene is associated with progressive external ophtalmoplegia | Silvestri, Gabriella; Servidei, Serenella; Rana, M.; Ricci, Enzo; Spinazzola, A.; Paris, E.; Tonali, P. | |
1-gen-2021 | A Novel Monocyte Subset as a Unique Signature of Atherosclerotic Plaque Rupture | Vinci, Ramona; Pedicino, Daniela; Bonanni, Alice; D'Aiello, A.; Severino, Anna; Pisano, Eugenia; Ponzo, Myriana; Canonico, Francesco; Ciampi, Pellegrino; Russo, Giovanni; Di Sario, Marianna; Montone, Rocco Antonio; Trani, Carlo; Conte, Caterina; Grimaldi, Maria Chiara; Cribari, Francesco; Massetti, Massimo; Crea, Filippo; Liuzzo, Giovanna | |
1-gen-2020 | A novel multi-marker discovery approach identifies new serum biomarkers for Parkinson’s disease in older people: an EXosomes in PArkiNson Disease (EXPAND) ancillary study | Calvani, R.; Picca, A.; Landi, G.; Marini, F.; Biancolillo, A.; Coelho-Junior, H. J.; Gervasoni, J.; Persichilli, S.; Primiano, A.; Arcidiacono, A.; Urbani, A.; Bossola, M.; Bentivoglio, A. R.; Cesari, M.; Bernabei, R.; Monaco, M. R. L.; Marzetti, E. | |
1-gen-2012 | A novel mutation of the insulin receptor gene in a preterm infant with Donohue syndrome and heart failure | Nobile, Stefano; K Semple, Robert; P Carnielli, Virgilio | |
1-gen-2006 | A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy | Cardaioli, E.; Gallus, G. N.; Da Pozzo, P.; Rufa, A.; Franceschini, R.; Motolese, E.; Caporossi, Aldo; Dotti, M. T.; Federico, A. | |
1-gen-2011 | Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa responsive parkinsonism | Silvestri, Gabriella; Guidubaldi, Arianna; Tessa, A; Petracca, Martina; Bentivoglio, Anna Rita; Santorelli, Fm | |
1-gen-2020 | Novel nicastrin mutation in hidradenitis suppurativa-Dowling Degos disease clinical phenotype: more than just clinical overlap? | Garcovich, Simone; Tricarico, P M; Meddour, C N; Giovanardi, Giulia; Peris, Ketty; Crovella, S; Boniotto, M | |
1-gen-2017 | A Novel Nomogram to Predict the Prognosis of Patients Undergoing Liver Resection for Neuroendocrine Liver Metastasis: an Analysis of the Italian Neuroendocrine Liver Metastasis Database | Ruzzenente, Andrea; Bagante, Fabio; Bertuzzo, Francesca; Aldrighetti, Luca; Ercolani, Giorgio; Giuliante, Felice; Ferrero, Alessandro; Torzilli, Guido; Grazi, Gian Luca; Ratti, Francesca; Cucchetti, Alessandro; De Rose, Agostino Maria; Russolillo, Nadia; Cimino, Matteo; Perri, Pasquale; Cataldo, Ivana; Scarpa, Aldo; Guglielmi, Alfredo; Iacono, Calogero |
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