Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irene Bova"'
Autor:
Massimo Martino, Angela Violi, Stefania Ciolli, Corrado Mammì, Bruno Martino, Irene Bova, Antonio Scopelliti, Jolanda Donatella Vincelli, Maria Grazia D'Errigo, B Oliva, Cristina Garreffa
Publikováno v:
Blood. 138:4735-4735
Until recently, MM was defined using strict clinical pathological criteria that required evidence of specific end-organ damage (CRAB) attributable to the underlying clonal plasma cell disorder. In the case of absence of end-organ damage, patients wit
Autor:
Al Sayyad Said, Maria Grazia D'Errigo, Massimo Martino, Iolanda Vincelli, Stefania Ciolli, Corrado Mammì, Giuseppina Caruso, Patrizia Cufari, B Oliva, Bruno Martino, Cristina Garreffa, Mauro Campello, Carmelo Toscano, Irene Bova
Publikováno v:
Blood. 136:37-37
Chronic lymphocytic leukemia (CLL) is an indolent lymphoproliferative disorder and is manifested by progressive accumulation of B cells in the blood, bone marrow and lymphatic tissues. Chronic Myeloid Leukemia (CML) is a clonal myeloproliferative dis
Autor:
Aspasia Stamatoullas, Maria Grazia D'Errigo, Anna Marina Liberati, Stefano Mancini, Monica Bocchia, Irene Santacaterina, Prassede Salutari, Esther N. Oliva, Patrizia Cufari, Enrico Balleari, Valeria Santini, Grazia Sanpaolo, Stefana Impera, Pierre Fenaux, Maria Antonietta Aloe Spiriti, Paola Carluccio, Gina Zini, Maria Teresa Voso, Irene Bova, Paolo Avanzini, Flavia Salvi, Austin G. Kulasekararaj, Pasquale Niscola, Giuseppe A. Palumbo, Agostino Cortelezzi, Antonella Poloni, Caterina Alati, Fortunato Morabito, Alfredo Molteni, Roberto Latagliata, Francesco Buccisano, Ulrich Germing
Publikováno v:
The Lancet. Haematology. 4(3)
Summary Background In myelodysplastic syndromes, thrombocytopenia is associated with mortality, but treatments in this setting are scarce. We tested whether eltrombopag, a thrombopoietin receptor agonist, might be effective in improving thrombocytope
Autor:
Manuela Priolo, Giovanna Campolo, Orsetta Zuffardi, Carmelo Laganà, Roberto Ciccone, Irene Bova
Publikováno v:
European journal of medical genetics. 50(2)
We report on a patient with mental and growth retardation, bilateral cleft lip and palate, hypertelorism, ptosis, hearing loss and mild epispadias, suggestive of Malpuech syndrome. High-resolution karyotype and microarray-CGH using an oligonucleotide