Sfoglia per Autore
Identification and characterization of the first dmt1 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of dmt1 gene
2012-01-01 De Falco, L; Bruno, Mariasole; Andolfo, I; David, Bp; Girelli, D; Noce, Fd; Camaschella, C; Iolascon, A.
Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene.
2012-01-01 De Falco, L; Bruno, Mariasole; Andolfo, I; David, Bp; Girelli, Domenico; Di Noce, F; Camaschella, C; Iolascon, A.
Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?
2013-01-01 Yilmaz Keskin, E; Sal, E; de Falco, L; Bruno, Mariasole; Iolascon, A; Koçak, U; Yenicesu, I.
Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP+ as Parkinson's disease cellular model
2013-01-01 Asci, R; Vallefuoco, F; Andolfo, I; Bruno, Mariasole; De Falco, L; Iolascon, A.
IAP/APA evidence-based guidelines for the management of acute pancreatitis
2013-01-01 Besselink, M; van Santvoort, H; Freeman, M; Gardner, T; Mayerle, J; Vege, Ss; Werner, J; Banks, P; Mckay, C; Fernandez del Castillo, C; French, J; Gooszen, H; Johnson, C; Sarr, M; Takada, T; Windsor, J; Saluja, A; Liddle, R; Papachristou, G; Singh, V; Rünzi, M; Mayerle, J; Wu, B; Singh, V; Windsor, J; Banks, P; Papachristou, G; Bollen, T; Morgan, D; Mortele, K; Mittal, A; Windsor, J; En qiang, M; Gardner, T; Mayerle, J; Mayerle, J; Johnson, C; de Waele, J; van Santvoort, H; Petrov, M; Dellinger, P; Besselink, M; Lerch, Mm; Gardner, T; Petrov, M; Anderson, R; Mcclave, S; Gardner, T; Hartwig, W; van Santvoort, H; Freeman, M; Bruno, Mariasole; Oria, A; Banks, P; Mayerle, J; Besselink, M; Gardner, T; Gooszen, H; Baron, T; Castillo, Cf; Werner, J; Fagenholz, P; Besselink, M; van Santvoort, H; Baron, T; Horvath, K; Bollen, T; Mortele, K; Werner, J; Freeman, M; van Baal, M; Nealon, W; Gardner, T; Mayerle, J; Andren Sandberg, A; Bakker, O; Bassi, Claudio; Buchler, M; Boermeester, M; Bradley, E; Chari, S; Charnley, R; Connor, S; Dervenis, C; Deviere, J; Dudeja, V; Fockens, P; Forsmark, C; Friess, H; Isaji, S; Isenmann, R; Klar, E; Lévy, P; Lillemoe, K; Liu, X; Löhr, Cm; Mayumi, T; Mossner, J; Neoptolemos, J; Nordback, I; Olah, Anett; Padbury, R; Parks, R; Radenkovic, D; Rau, B; Rebours, V; Seewald, S; Seifert, H; Shimosegawa, T; Siriwardena, A; Steinberg, W; Sutton, R; Tanaka, M; Takeda, K; Tse, F; van Goor, H; Warshaw, A; Wang, C; Whitcomb, D; Zhao, Y; Zyromski, N.
European experts consensus statement on cystic tumours of the pancreas
2013-01-01 Del Chiaro, M; Verbeke, C; Salvia, Roberto; Werner, J; Mckay, C; Friess, H; Manfredi, Riccardo; Van Cutsem, E; Löhr, M; Segersvärd, R; Abakken, L; Adham, M; Albin, N; Andren Sandberg, Å; Arnelo, U; Bruno, Mariasole; Cahen, D; Cappelli, C; Costamagna, G; Delle Fave, G; Esposito, Ilaria; Falconi, Massimo; Ghaneh, P; Gladhaug, Ip; Haas, S; Hauge, T; Izbicki, Jr; Klöppel, G; Lerch, M; Lundell, L; Lüttges, J; Mayerle, J; Oppong, K; Pukitis, Ap; Rangelova, E; Rosch, T; Schulick, R; Sufferlein, T; van der Merwe, Sw; Zamboni, Giulia
Functional and clinical impact of novel tmprss6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies.
2014-01-01 De Falco, L; Silvestri, L; Kannengiesser, C; Morán, E; Oudin, C; Rausa, M; Bruno, Mariasole; Aranda, J; Argiles, B; Yenicesu, I; Falcon Rodriguez, M; Yilmaz Keskin, E; Kocak, U; Beaumont, C; Camaschella, C; Iolascon, A; Grandchamp, B; Sanchez, M.
How I Diagnose Non-thalassemic Microcytic Anemias
2015-01-01 Bruno, Mariasole; De Falco, L; Iolascon, A.
Peroxiredoxin-2: A Novel Factor Involved in Iron Homeostasis
2015-01-01 Matte', Alessandro; Falco, Luigia De; Federti, Enrica; Levi, Sonia; Iolascon, Achille; Federico, Giorgia; Mohandas, Narla; Janin, Anne; Bruno, Mariasole; Leboeuf, Christophe; Choi, Soo Young; Kim, Dae Won; Dima, Francesco; Siciliano, Angela; DE FRANCESCHI, Lucia
The interplay between peroxiredoxin-2 and Nrf2 is important in limiting oxidative mediated dysfunction in b-thalassemic erythropoiesis
2015-01-01 Matte', Alessandro; De Falco, Luigia; Iolascon, Achille; Mohandas, Narla; An, Xiuli; Siciliano, Angela; Leboeuf, Christophe; Janin, Anne; Bruno, Mariasole; Choi, Soo Young; Kim, Dae Won; DE FRANCESCHI, Lucia
Pathogenesis of iron overload in congenital dyserythropoietic anemia type II (CDAII)
2016-01-01 Bruno, Mariasole
Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II
2016-01-01 Russo, R; Andolfo, I; Manna, F; De Rosa, G; De Falco, L; Gambale, A; Bruno, Mariasole; Matte', Alessandro; Ricchi, P; Girelli, Domenico; DE FRANCESCHI, Lucia; Iolascon, A.
The role of Matriptase-2 during the early postnatal development in humans
2016-01-01 De Falco, L; Bruno, Mariasole; Yilmaz Keskin, E; Sal, E; Büyükavci, M; Kaya, Z; Girelli, Domenico; Iolascon, A.
The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease
2018-01-01 De Falco, Luigia; Tortora, Raffaella; Imperatore, Nicola; Bruno, Mariasole; Capasso, Mario; Girelli, Domenico; Castagna, Annalisa; Caporaso, Nicola; Iolascon, Achille; Rispo, Antonio
PEROXIREDOXIN-2: A NOVEL REGULATOR OF IRON HOMEOSTASIS IN INEFFECTIVE ERYTHROPOIESIS
2018-01-01 Matte', Alessandro; De Falco, Luigia; Federti, Enrica; Cozzi, Anna; Iolascon, Achille; Levi, Sonia; Mohandas, Narla; Zamo', Alberto; Bruno, Mariasole; Leboeuf, Christophe; Janin, Anne; Siciliano, Angela; Ganz, Thomas; Federico, Giorgia; Carlomagno, Francesca; Mueller, Sebastian; Silva, Ines; Carbone, Carmine; Melisi, Davide; Kim, D. W; Choi, Soo Young; DE FRANCESCHI, Lucia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Identification and characterization of the first dmt1 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of dmt1 gene | 1-gen-2012 | De Falco, L; Bruno, Mariasole; Andolfo, I; David, Bp; Girelli, D; Noce, Fd; Camaschella, C; Iolascon, A. | |
| Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene. | 1-gen-2012 | De Falco, L; Bruno, Mariasole; Andolfo, I; David, Bp; Girelli, Domenico; Di Noce, F; Camaschella, C; Iolascon, A. | |
| Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations? | 1-gen-2013 | Yilmaz Keskin, E; Sal, E; de Falco, L; Bruno, Mariasole; Iolascon, A; Koçak, U; Yenicesu, I. | |
| Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP+ as Parkinson's disease cellular model | 1-gen-2013 | Asci, R; Vallefuoco, F; Andolfo, I; Bruno, Mariasole; De Falco, L; Iolascon, A. | |
| IAP/APA evidence-based guidelines for the management of acute pancreatitis | 1-gen-2013 | Besselink, M; van Santvoort, H; Freeman, M; Gardner, T; Mayerle, J; Vege, Ss; Werner, J; Banks, P; Mckay, C; Fernandez del Castillo, C; French, J; Gooszen, H; Johnson, C; Sarr, M; Takada, T; Windsor, J; Saluja, A; Liddle, R; Papachristou, G; Singh, V; Rünzi, M; Mayerle, J; Wu, B; Singh, V; Windsor, J; Banks, P; Papachristou, G; Bollen, T; Morgan, D; Mortele, K; Mittal, A; Windsor, J; En qiang, M; Gardner, T; Mayerle, J; Mayerle, J; Johnson, C; de Waele, J; van Santvoort, H; Petrov, M; Dellinger, P; Besselink, M; Lerch, Mm; Gardner, T; Petrov, M; Anderson, R; Mcclave, S; Gardner, T; Hartwig, W; van Santvoort, H; Freeman, M; Bruno, Mariasole; Oria, A; Banks, P; Mayerle, J; Besselink, M; Gardner, T; Gooszen, H; Baron, T; Castillo, Cf; Werner, J; Fagenholz, P; Besselink, M; van Santvoort, H; Baron, T; Horvath, K; Bollen, T; Mortele, K; Werner, J; Freeman, M; van Baal, M; Nealon, W; Gardner, T; Mayerle, J; Andren Sandberg, A; Bakker, O; Bassi, Claudio; Buchler, M; Boermeester, M; Bradley, E; Chari, S; Charnley, R; Connor, S; Dervenis, C; Deviere, J; Dudeja, V; Fockens, P; Forsmark, C; Friess, H; Isaji, S; Isenmann, R; Klar, E; Lévy, P; Lillemoe, K; Liu, X; Löhr, Cm; Mayumi, T; Mossner, J; Neoptolemos, J; Nordback, I; Olah, Anett; Padbury, R; Parks, R; Radenkovic, D; Rau, B; Rebours, V; Seewald, S; Seifert, H; Shimosegawa, T; Siriwardena, A; Steinberg, W; Sutton, R; Tanaka, M; Takeda, K; Tse, F; van Goor, H; Warshaw, A; Wang, C; Whitcomb, D; Zhao, Y; Zyromski, N. | |
| European experts consensus statement on cystic tumours of the pancreas | 1-gen-2013 | Del Chiaro, M; Verbeke, C; Salvia, Roberto; Werner, J; Mckay, C; Friess, H; Manfredi, Riccardo; Van Cutsem, E; Löhr, M; Segersvärd, R; Abakken, L; Adham, M; Albin, N; Andren Sandberg, Å; Arnelo, U; Bruno, Mariasole; Cahen, D; Cappelli, C; Costamagna, G; Delle Fave, G; Esposito, Ilaria; Falconi, Massimo; Ghaneh, P; Gladhaug, Ip; Haas, S; Hauge, T; Izbicki, Jr; Klöppel, G; Lerch, M; Lundell, L; Lüttges, J; Mayerle, J; Oppong, K; Pukitis, Ap; Rangelova, E; Rosch, T; Schulick, R; Sufferlein, T; van der Merwe, Sw; Zamboni, Giulia | |
| Functional and clinical impact of novel tmprss6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies. | 1-gen-2014 | De Falco, L; Silvestri, L; Kannengiesser, C; Morán, E; Oudin, C; Rausa, M; Bruno, Mariasole; Aranda, J; Argiles, B; Yenicesu, I; Falcon Rodriguez, M; Yilmaz Keskin, E; Kocak, U; Beaumont, C; Camaschella, C; Iolascon, A; Grandchamp, B; Sanchez, M. | |
| How I Diagnose Non-thalassemic Microcytic Anemias | 1-gen-2015 | Bruno, Mariasole; De Falco, L; Iolascon, A. | |
| Peroxiredoxin-2: A Novel Factor Involved in Iron Homeostasis | 1-gen-2015 | Matte', Alessandro; Falco, Luigia De; Federti, Enrica; Levi, Sonia; Iolascon, Achille; Federico, Giorgia; Mohandas, Narla; Janin, Anne; Bruno, Mariasole; Leboeuf, Christophe; Choi, Soo Young; Kim, Dae Won; Dima, Francesco; Siciliano, Angela; DE FRANCESCHI, Lucia | |
| The interplay between peroxiredoxin-2 and Nrf2 is important in limiting oxidative mediated dysfunction in b-thalassemic erythropoiesis | 1-gen-2015 | Matte', Alessandro; De Falco, Luigia; Iolascon, Achille; Mohandas, Narla; An, Xiuli; Siciliano, Angela; Leboeuf, Christophe; Janin, Anne; Bruno, Mariasole; Choi, Soo Young; Kim, Dae Won; DE FRANCESCHI, Lucia | |
| Pathogenesis of iron overload in congenital dyserythropoietic anemia type II (CDAII) | 1-gen-2016 | Bruno, Mariasole | |
| Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II | 1-gen-2016 | Russo, R; Andolfo, I; Manna, F; De Rosa, G; De Falco, L; Gambale, A; Bruno, Mariasole; Matte', Alessandro; Ricchi, P; Girelli, Domenico; DE FRANCESCHI, Lucia; Iolascon, A. | |
| The role of Matriptase-2 during the early postnatal development in humans | 1-gen-2016 | De Falco, L; Bruno, Mariasole; Yilmaz Keskin, E; Sal, E; Büyükavci, M; Kaya, Z; Girelli, Domenico; Iolascon, A. | |
| The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease | 1-gen-2018 | De Falco, Luigia; Tortora, Raffaella; Imperatore, Nicola; Bruno, Mariasole; Capasso, Mario; Girelli, Domenico; Castagna, Annalisa; Caporaso, Nicola; Iolascon, Achille; Rispo, Antonio | |
| PEROXIREDOXIN-2: A NOVEL REGULATOR OF IRON HOMEOSTASIS IN INEFFECTIVE ERYTHROPOIESIS | 1-gen-2018 | Matte', Alessandro; De Falco, Luigia; Federti, Enrica; Cozzi, Anna; Iolascon, Achille; Levi, Sonia; Mohandas, Narla; Zamo', Alberto; Bruno, Mariasole; Leboeuf, Christophe; Janin, Anne; Siciliano, Angela; Ganz, Thomas; Federico, Giorgia; Carlomagno, Francesca; Mueller, Sebastian; Silva, Ines; Carbone, Carmine; Melisi, Davide; Kim, D. W; Choi, Soo Young; DE FRANCESCHI, Lucia |
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