PECCI, ALESSANDRO
PECCI, ALESSANDRO
DIPARTIMENTO DI MEDICINA INTERNA E TERAPIA MEDICA
3D silk bone marrow model: a promising tool to test efficacy of new biomimetic drugs on platelet production
2015-01-01 DI BUDUO, CHRISTIAN ANDREA; Pecci, A; Balduini, Cl; Kaplan, Dl; Balduini, A
5′UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia
2017-01-01 Marconi, Caterina; Canobbio, Ilaria; Bozzi, Valeria; Pippucci, Tommaso; Simonetti, Giorgia; Melazzini, Federica; Angori, Silvia; Martinelli, Giovanni; Saglio, Giuseppe; Torti, Mauro; Pastan, Ira; Seri, Marco; Pecci, Alessandro
A A386G biallelic GPIb alpha gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis.
2011-01-01 Vettore, S.; Tezza, F.; Malara, Alessandro; Vianello, F.; Pecci, Alessandro; Scandellari, R.; Floris, M.; Balduini, Alessandra; Fabris, F.
A case of metastatic malignant melanoma with bone marrow involvement.
2001-01-01 Invernizzi, Rosangela; Pecci, Alessandro
A case of phagocytic multiple myeloma
2000-01-01 Invernizzi, Rosangela; Pecci, Alessandro
A combination regimen of idarubicin and cytosine arabinoside for patients with high-risk myelodysplastic syndromes
1996-01-01 Invernizzi, Rosangela; Pecci, Alessandro; Iannone, A. M.; Dalessio, A.; Giusto, M.; Rossi, G.; Dezza, L.; Ascari, Edoardo
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect.
2010-01-01 Vettore, S.; De Rocco, D.; Gerber, B.; Scandellari, R.; Bianco, A. M.; Balduini, Carlo; Pecci, Alessandro; Fabris, F.; Savoia, A.
A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT)
2017-01-01 Noris, P; Marconi, C; De Rocco, D; Melazzini, F; Pippucci, T; Loffredo, G; Giangregorio, T; Cigalini, E; Pecci, A; Seri, M; Savoia, A
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene
2018-01-01 Noris, Patrizia; Marconi, Caterina; De Rocco, Daniela; Melazzini, Federica; Pippucci, Tommaso; Loffredo, Giuseppe; Giangregorio, Tania; Pecci, Alessandro; Seri, Marco; Savoia, Anna
A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibβ in the pathophysiology of bernard‐soulier syndrome and gpib‐ix complex assembly
2021-01-01 Barozzi, S.; Bozzi, V.; De Rocco, D.; Giangregorio, T.; Noris, P.; Savoia, A.; Pecci, A.
A qualitative and quantitative cytochemical assay of dihydrofolate reductase in megakariocytes of patients with 5q-syndrome.
2001-01-01 Nano, Rosanna; Invernizzi, Rosangela; Pecci, Alessandro; Facoetti, Angelica; Gerzeli, Giuseppe
A therapy-related myelodysplastic syndrome with unusual features in a patient treated for acute promyelocytic leukemia.
2001-01-01 Pecci, Alessandro; Invernizzi, Rosangela
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia
2018-01-01 Faleschini, Michela; Melazzini, Federica; Marconi, Caterina; Giangregorio, Tania; Pippucci, Tommaso; Cigalini, Elena; Pecci, Alessandro; Bottega, Roberta; Ramenghi, Ugo; Siitonen, Timo; Seri, Marco; Pastore, Annalisa; Savoia, Anna; Noris, Patrizia
ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype
2024-01-01 Eva Zanchetta, Melania; Barozzi, Serena; Isidori, Federica; Marconi, Caterina; Farinasso, Loredana; Bottega, Roberta; Savoia, Anna; Pecci, Alessandro; Faleschini, Michela
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.
2015-01-01 R., Bottega; C., Marconi; M., Faleschini; G., Baj; C., Cagioni; Pecci, Alessandro; T., Pippucci; U., Ramenghi; S., Pardini; L., Ngu; C., Baronci; S., Kunishima; Balduini, Carlo; M., Seri; A., Savoia; Noris, Patrizia
Adhesive receptors, extracellular proteins and myosin IIA orchestrate proplatelet formation by human megakaryocytes.
2008-01-01 Balduini, Alessandra; Pallotta, Isabella; Malara, Alessandro; Lova, P; Pecci, Alessandro; Viarengo, G; Balduini, Carlo; Torti, Mauro
Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome.
2012-01-01 Pecci, Alessandro; Biino, G.; Fierro, T.; Bozzi, V.; Mezzasoma, A.; Noris, Patrizia; Ramenghi, U.; Loffredo, G.; Fabris, F.; Momi, S.; Magrini, Umberto; Pirastu, M.; Savoia, A.; Balduini, Carlo; Gresele, P.
Altered cytoskeleton organization in platelets from patients with MYH9-related disease.
2005-01-01 Canobbio, Ilaria; Noris, Patrizia; Pecci, Alessandro; Balduini, Alessandra; Balduini, Carlo; Torti, Mauro
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia
2014-01-01 Noris, Patrizia; Schlegel, N; Klersy, C; Heller, Pg; Civaschi, E; Pujol Moix, N; Fabris, F; Favier, R; Gresele, P; Latger Cannard, V; Cuker, A; Nurden, P; Greinacher, A; Cattaneo, M; De Candia, E; Pecci, Alessandro; Hurtaud Roux, Mf; Glembotsky, Ac; Muñiz Diaz, E; Randi, Ml; Trillot, N; Bury, L; Lecompte, T; Marconi, C; Savoia, A; Balduini, Carlo; Bayart, S; Bauters, A; Benabdallah Guedira, S; Boehlen, F; Borg, Jy; Bottega, R; Bussel, J; De Rocco, D; De Maistre, E; Faleschini, M; Falcinelli, E; Ferrari, S; Ferster, A; Fierro, T; Fleury, D; Fontana, P; James, C; Lanza, F; Le Cam Duchez, V; Loffredo, G; Magini, P; Martin Coignard, D; Menard, F; Mercier, S; Mezzasoma, A; Minuz, P; Nichele, I; Notarangelo, Ld; Pippucci, T; Podda, Gm; Pouymayou, C; Rigouzzo, A; Royer, B; Sie, P; Siguret, V; Trichet, C; Tucci, A; Saposnik, B; Veneri, D.
Anemia in patients with Covid-19: pathogenesis and clinical significance
2021-01-01 Bergamaschi, G.; de Andreis, F. B.; Aronico, N.; Lenti, M. V.; Barteselli, C.; Merli, S.; Pellegrino, I.; Coppola, L.; Cremonte, E. M.; Croce, G.; Morda, F.; Lapia, F.; Ferrari, S.; Ballesio, A.; Parodi, A.; Calabretta, F.; Ferrari, M. G.; Fumoso, F.; Gentile, A.; Melazzini, F.; Di Sabatino, A.; Bertolino, G.; Codega, S.; Costanzo, F.; Cresci, R.; Derosa, G.; Di Stefano, M.; Falaschi, F.; Iadarola, C.; Lovati, E.; Lucotti, P. C.; Martignoni, A.; Mengoli, C.; Miceli, E.; Mugellini, A.; Muggia, C.; Noris, P.; Pagani, E.; Palumbo, I.; Pecci, A.; Perrone, T.; Pieresca, C.; Preti, P. S.; Russo, M. C.; Sgarlata, C.; Siciliani, L.; Staniscia, A.; Vjera, F. T.; Achilli, G.; Agostinelli, A.; Antoci, V.; Banfi, F.; Benedetti, I.; Brattoli, M.; Cambie, G.; Canta, R.; Cococcia, S.; Conca, F.; Delliponti, M.; Del Rio, V.; Di Terlizzi, F.; Fiengo, A.; Forni, T.; Freddi, G.; Frigerio, C.; Fusco, A.; Gabba, M.; Garolfi, M.; Gori, G.; Grandi, G.; Grimaldi, P.; Lampugnani, A.; Lepore, F.; Lettieri, G.; Mambella, J.; Mercanti, C.; Nardone, A.; Pace, L.; Padovini, L.; Pitotti, L.; Reduzzi, M.; Rigano, G.; Rotola, G.; Sabatini, U.; Salvi, L.; Santacroce, G.; Savioli, J.; Soriano, S.; Spataro, C.; Stefani, D.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 3D silk bone marrow model: a promising tool to test efficacy of new biomimetic drugs on platelet production | 1-gen-2015 | DI BUDUO, CHRISTIAN ANDREA; Pecci, A; Balduini, Cl; Kaplan, Dl; Balduini, A | |
| 5′UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia | 1-gen-2017 | Marconi, Caterina; Canobbio, Ilaria; Bozzi, Valeria; Pippucci, Tommaso; Simonetti, Giorgia; Melazzini, Federica; Angori, Silvia; Martinelli, Giovanni; Saglio, Giuseppe; Torti, Mauro; Pastan, Ira; Seri, Marco; Pecci, Alessandro | |
| A A386G biallelic GPIb alpha gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis. | 1-gen-2011 | Vettore, S.; Tezza, F.; Malara, Alessandro; Vianello, F.; Pecci, Alessandro; Scandellari, R.; Floris, M.; Balduini, Alessandra; Fabris, F. | |
| A case of metastatic malignant melanoma with bone marrow involvement. | 1-gen-2001 | Invernizzi, Rosangela; Pecci, Alessandro | |
| A case of phagocytic multiple myeloma | 1-gen-2000 | Invernizzi, Rosangela; Pecci, Alessandro | |
| A combination regimen of idarubicin and cytosine arabinoside for patients with high-risk myelodysplastic syndromes | 1-gen-1996 | Invernizzi, Rosangela; Pecci, Alessandro; Iannone, A. M.; Dalessio, A.; Giusto, M.; Rossi, G.; Dezza, L.; Ascari, Edoardo | |
| A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect. | 1-gen-2010 | Vettore, S.; De Rocco, D.; Gerber, B.; Scandellari, R.; Bianco, A. M.; Balduini, Carlo; Pecci, Alessandro; Fabris, F.; Savoia, A. | |
| A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT) | 1-gen-2017 | Noris, P; Marconi, C; De Rocco, D; Melazzini, F; Pippucci, T; Loffredo, G; Giangregorio, T; Cigalini, E; Pecci, A; Seri, M; Savoia, A | |
| A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene | 1-gen-2018 | Noris, Patrizia; Marconi, Caterina; De Rocco, Daniela; Melazzini, Federica; Pippucci, Tommaso; Loffredo, Giuseppe; Giangregorio, Tania; Pecci, Alessandro; Seri, Marco; Savoia, Anna | |
| A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibβ in the pathophysiology of bernard‐soulier syndrome and gpib‐ix complex assembly | 1-gen-2021 | Barozzi, S.; Bozzi, V.; De Rocco, D.; Giangregorio, T.; Noris, P.; Savoia, A.; Pecci, A. | |
| A qualitative and quantitative cytochemical assay of dihydrofolate reductase in megakariocytes of patients with 5q-syndrome. | 1-gen-2001 | Nano, Rosanna; Invernizzi, Rosangela; Pecci, Alessandro; Facoetti, Angelica; Gerzeli, Giuseppe | |
| A therapy-related myelodysplastic syndrome with unusual features in a patient treated for acute promyelocytic leukemia. | 1-gen-2001 | Pecci, Alessandro; Invernizzi, Rosangela | |
| ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia | 1-gen-2018 | Faleschini, Michela; Melazzini, Federica; Marconi, Caterina; Giangregorio, Tania; Pippucci, Tommaso; Cigalini, Elena; Pecci, Alessandro; Bottega, Roberta; Ramenghi, Ugo; Siitonen, Timo; Seri, Marco; Pastore, Annalisa; Savoia, Anna; Noris, Patrizia | |
| ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype | 1-gen-2024 | Eva Zanchetta, Melania; Barozzi, Serena; Isidori, Federica; Marconi, Caterina; Farinasso, Loredana; Bottega, Roberta; Savoia, Anna; Pecci, Alessandro; Faleschini, Michela | |
| ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. | 1-gen-2015 | R., Bottega; C., Marconi; M., Faleschini; G., Baj; C., Cagioni; Pecci, Alessandro; T., Pippucci; U., Ramenghi; S., Pardini; L., Ngu; C., Baronci; S., Kunishima; Balduini, Carlo; M., Seri; A., Savoia; Noris, Patrizia | |
| Adhesive receptors, extracellular proteins and myosin IIA orchestrate proplatelet formation by human megakaryocytes. | 1-gen-2008 | Balduini, Alessandra; Pallotta, Isabella; Malara, Alessandro; Lova, P; Pecci, Alessandro; Viarengo, G; Balduini, Carlo; Torti, Mauro | |
| Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome. | 1-gen-2012 | Pecci, Alessandro; Biino, G.; Fierro, T.; Bozzi, V.; Mezzasoma, A.; Noris, Patrizia; Ramenghi, U.; Loffredo, G.; Fabris, F.; Momi, S.; Magrini, Umberto; Pirastu, M.; Savoia, A.; Balduini, Carlo; Gresele, P. | |
| Altered cytoskeleton organization in platelets from patients with MYH9-related disease. | 1-gen-2005 | Canobbio, Ilaria; Noris, Patrizia; Pecci, Alessandro; Balduini, Alessandra; Balduini, Carlo; Torti, Mauro | |
| Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia | 1-gen-2014 | Noris, Patrizia; Schlegel, N; Klersy, C; Heller, Pg; Civaschi, E; Pujol Moix, N; Fabris, F; Favier, R; Gresele, P; Latger Cannard, V; Cuker, A; Nurden, P; Greinacher, A; Cattaneo, M; De Candia, E; Pecci, Alessandro; Hurtaud Roux, Mf; Glembotsky, Ac; Muñiz Diaz, E; Randi, Ml; Trillot, N; Bury, L; Lecompte, T; Marconi, C; Savoia, A; Balduini, Carlo; Bayart, S; Bauters, A; Benabdallah Guedira, S; Boehlen, F; Borg, Jy; Bottega, R; Bussel, J; De Rocco, D; De Maistre, E; Faleschini, M; Falcinelli, E; Ferrari, S; Ferster, A; Fierro, T; Fleury, D; Fontana, P; James, C; Lanza, F; Le Cam Duchez, V; Loffredo, G; Magini, P; Martin Coignard, D; Menard, F; Mercier, S; Mezzasoma, A; Minuz, P; Nichele, I; Notarangelo, Ld; Pippucci, T; Podda, Gm; Pouymayou, C; Rigouzzo, A; Royer, B; Sie, P; Siguret, V; Trichet, C; Tucci, A; Saposnik, B; Veneri, D. | |
| Anemia in patients with Covid-19: pathogenesis and clinical significance | 1-gen-2021 | Bergamaschi, G.; de Andreis, F. B.; Aronico, N.; Lenti, M. V.; Barteselli, C.; Merli, S.; Pellegrino, I.; Coppola, L.; Cremonte, E. M.; Croce, G.; Morda, F.; Lapia, F.; Ferrari, S.; Ballesio, A.; Parodi, A.; Calabretta, F.; Ferrari, M. G.; Fumoso, F.; Gentile, A.; Melazzini, F.; Di Sabatino, A.; Bertolino, G.; Codega, S.; Costanzo, F.; Cresci, R.; Derosa, G.; Di Stefano, M.; Falaschi, F.; Iadarola, C.; Lovati, E.; Lucotti, P. C.; Martignoni, A.; Mengoli, C.; Miceli, E.; Mugellini, A.; Muggia, C.; Noris, P.; Pagani, E.; Palumbo, I.; Pecci, A.; Perrone, T.; Pieresca, C.; Preti, P. S.; Russo, M. C.; Sgarlata, C.; Siciliani, L.; Staniscia, A.; Vjera, F. T.; Achilli, G.; Agostinelli, A.; Antoci, V.; Banfi, F.; Benedetti, I.; Brattoli, M.; Cambie, G.; Canta, R.; Cococcia, S.; Conca, F.; Delliponti, M.; Del Rio, V.; Di Terlizzi, F.; Fiengo, A.; Forni, T.; Freddi, G.; Frigerio, C.; Fusco, A.; Gabba, M.; Garolfi, M.; Gori, G.; Grandi, G.; Grimaldi, P.; Lampugnani, A.; Lepore, F.; Lettieri, G.; Mambella, J.; Mercanti, C.; Nardone, A.; Pace, L.; Padovini, L.; Pitotti, L.; Reduzzi, M.; Rigano, G.; Rotola, G.; Sabatini, U.; Salvi, L.; Santacroce, G.; Savioli, J.; Soriano, S.; Spataro, C.; Stefani, D. |