Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maria Adele Sanna"'
Autor:
Giovanni Monni, D. Gasperini, C. Rosatelli, Maria Antonietta Melis, L Maccioni, Antonio Cao, Maria Adele Sanna, Renzo Galanello
Publikováno v:
Clinical Genetics. 38:327-331
This paper describes the first case of Hb Bart's hydrops fetalis syndrome in the Sardinian population. Despite the high frequency of a-thalassemia, fetal hydrops is extraordinarily rare in the Sardinian population because a-thalassemia is more usuall
Autor:
Guido Lucarelli, F Argiolu, Licinio Contu, Franco Locatelli, Maria Adele Sanna, Adriana Vacca, Piero De Stefano, Antonella Pizzati, M Arras, Antonio Ledda, Claudio Giardini, Giorgio La Nasa
Publikováno v:
Blood. 99:4350-4356
Allogeneic bone marrow transplantation (BMT) from a genotypically identical family donor is an accepted therapeutic option for homozygous beta-thalassemia. However, only a minority of patients have access to this curative procedure. The aim of this s
Autor:
Javid Gaziev, F Argiolu, Francesco Cucca, Maria Adele Sanna, Giorgio La Nasa, Antonio Cao, Maria Grazia Orofino, Daniela Contu, Adriana Vacca
Publikováno v:
Transplantation. 82(11)
The donor-recipient sex-related mismatch has been reported as a risk factor for acute graft-versus-host disease (GVHD). However, the results obtained in previous studies appear to be contradictory. Here we evaluate the impact of donor-recipient sex-r
Autor:
Maria Adele Sanna, F. Scintu, Manuela Badiali, F Argiolu, Rita Pillai, Maria Serafina Ristaldi, Valeria Sogos, Camilla Reali
Publikováno v:
BMC Neuroscience, Vol 7, Iss 1, p 14 (2006)
BMC Neuroscience
BMC Neuroscience
Background It has recently been demonstrated that the fate of adult cells is not restricted to their tissues of origin. In particular, it has been shown that bone marrow stem cells can give rise to cells of different tissues, including neural cells,
Autor:
F Argiolu, Maria Adele Sanna, F. Scintu, Stefano Cabras, Camilla Reali, Rita Pillai, Manuela Badiali, Valeria Sogos, Maria Serafina Ristaldi
Publikováno v:
Experimental neurology. 197(2)
It has recently been reported that adult hematopoietic stem cells can differentiate into neural cells, opening new frontiers in therapy for neurodegenerative diseases. In this study, adult human hematopoietic stem cells (HSCs) were isolated via magne
Autor:
Paola Cossu, Maria Adele Sanna, Maria Grazia Orofino, Antonio Cao, Manuela Badiali, Maria Eliana Lai, Maria Cristina Rosatelli, F Argiolu, Rosalba Puddu, M T Scalas, T Tuveri
Publikováno v:
Lancet (London, England). 362(9377)
Summary Stem-cell transplantation can cure β thalassaemia. We aimed to assess whether fetal HLA typing done early in the pregnancy of couples who were at risk of β thalassaemia could provide an alternative to pregnancy termination if the prospect o
Autor:
F Argiolu, Nicolina Giagu, Monica Broglia, Antonio Piroddi, Maria Rosa Scalas, Rocco Ferrara, Carmen Addari, Fabiana Rizzo, Maria Adele Sanna, Renzo Galanello, Maria Grazia Orofino, Fausto Cossu, Antonella Bartoli
Publikováno v:
Blood. 112:4338-4338
Until now few patients with renal failure on hemodialysis have undergone haematopoietic stem-cell transplantation (HSCT), and none with thalassaemia. Case report. Patient of 45 years, UPN 168, with β Thalassaemia major, genetic compound β0 39 C-->T
Autor:
Antonio Piroddi, Giuseppa Fabiana Rizzo, F Argiolu, Maria Adele Sanna, M C Addari, Renzo Galanello, Fausto Cossu, Maria Grazia Orofino, Manuela Badiali
Publikováno v:
Blood. 104:5175-5175
Stem cell transplantation is presently the best treatment for Fanconi Anaemia (FA) patients developing bone marrow failure. 70% of success is reported in patients with a HLA identical sibling whereas the outcome for HSCT in those transplanted from un
Autor:
E Dessi, Maria Addis, E Cacace, F Argiolu, Maria Adele Sanna, C. Rosatelli, Renzo Galanello, Maria Antonietta Melis, M. P. Turco, Nicolina Giagu
Publikováno v:
Blood. 74:823-827
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin gene polymorphisms in a group of patients with thalassemia intermedia of Sardinian descent. A group of patients (109) with thalassemia major of the sam