Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Mirella, Pasino"'
Autor:
Anna Rita Gigliotti, Stefano Parodi, Raffaella Defferrari, Cristina Rosanda, Mirella Pasino, Stefania Sorrentino, Gian Paolo Tonini, Bruno De Bernardi
Publikováno v:
Journal of Pediatric Hematology/Oncology. 34:154-158
We studied the prevalence and degree of tumor cell infiltration (TCI) in bone marrow (BM) aspirates of 89 infants with stage 4/4 S neuroblastoma and correlated them with MYCN gene status and patient outcome. TCI was scored 0, +, ++, and +++, the last
Autor:
M. Acquila, Mirella Pasino, F. Bottini, Tiziana Lanza, Maria Patrizia Bicocchi, Cristina Santoro, Angelo Claudio Molinari
Publikováno v:
Haemophilia. 9:717-720
Summary. Factor VIII gene inversion of intron 1 has recently been reported to be the mutation responsible for haemophilia A in about 5% of severe cases. In our series of patients, which is made up of 77 Italian cases negative for intron 22 inversion,
Autor:
Maria Patrizia Bicocchi, Pier G. Mori, F. Bottini, Angelo Claudio Molinari, Maura Acquila, Camillo Rosano, Elio Boeri, Mirella Pasino, Tiziana Lanza
Publikováno v:
British Journal of Haematology. 122:810-817
Summary. We describe 18 novel mutations, unreported in the Haemophilia A mutation Databases, that have been identified in a cohort of unrelated, Italian patients affected with haemophilia A (HA). Screening of the factor VIII gene (FVIII) was performe
Autor:
Anna Corcione, L Scarso, P G Mori, Stefano Amato, P De Biasio, Vito Pistoia, Mirella Pasino, Fernando Marotta, Tiziana Lanza
Publikováno v:
British Journal of Haematology. 108:793-800
AC133+ cells may represent an alternative source of transplantable haemopoietic progenitor cells to CD34+ cells. Here, we have addressed the characterization of umbilical cord blood (UCB) AC133+ cells and compared their immunophenotypic and functiona
Autor:
Mirella Pasino, Angelo Claudio Molinari, M. Acquila, M. Di Duca, F. Bottini, Maria Patrizia Bicocchi
Publikováno v:
Haemophilia. 14:625-627
Autor:
M. Acquila, Caprino D, Mirella Pasino, F. Bottini, Angelo Claudio Molinari, Maria Patrizia Bicocchi, Tiziana Lanza
Publikováno v:
Haemophilia. 10:744-746
Publikováno v:
Haemophilia. 8:730-732
Autor:
Maura, Acquila, Mirella, Pasino, Tiziana, Lanza, Angelo Claudio, Molinari, Camillo, Rosano, Maria Patrizia, Bicocchi
Publikováno v:
Haematologica. 90(7)
Ectopic mRNA was analyzed by reverse transcriptase polymerase chain reaction (RT-PCR) in patients with duplication of F8 gene exon 13, a mutation which has been demonstrated to be a cause of mild hemophilia A in 32% of Northern Italian subjects. Two
Autor:
Fabio Corsolini, Cristina Morerio, Barbara R. Migeon, Angelo Claudio Molinari, Elio Boeri, Mirella Pasino, F. Bottini, Maura Acquila, Tiziana Lanza, Maria Patrizia Bicocchi
Publikováno v:
European journal of human genetics : EJHG. 13(5)
A basic tenet of the Lyon hypothesis is that X inactivation occurs randomly with respect to parental origin of the X chromosome. Yet, nonrandom patterns of X inactivation are common - often ascertained in women who manifest recessive X-linked disorde
Autor:
Maura, Acquila, Mirella, Pasino, Tiziana, Lanza, Federico, Bottini, Angelo Claudio, Molinari, Maria Patrizia, Bicocchi
Publikováno v:
Haematologica. 89(6)
A rearrangement of exon 13 in the factor VIII gene has been identified as the causative mutation in 32% of Northern Italian patients with mild hemophilia A. We have demonstrated that all share a common haplotype, thus suggesting that the mutation lik