Publications by authors named "Maura Acquila"

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Pediatric SARS-CoV-2-Related Diplopia and Mesencephalic Abnormalities.
Sara Signa, Noemi Brolatti, Chiara Trincianti, Domenico Tortora, Carolina Saffioti, Maura Acquila

Neurol Clin Pract· October 2022

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Antibodies against Receptor Binding Domain of SARS-CoV-2 spike protein induced by BNT162b2 vaccine: results from a pragmatic, real-life study.
Marcello Mariani, Maura Acquila, Gino Tripodi, Raffaele Spiazzi, Elio Castagnola

J Infect Public Health· October 2021

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Unusual presentation of haemophilia in two paediatric patients.
Maia De Luca, Francesca I Calò Carducci, Valeria Pansini, Valentina Coletti, Filippo M Tucci, Maura Acquila

Blood Coagul Fibrinolysis· September 2013

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Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation.
Maria Patrizia Bicocchi, Camillo Rosano, Maura Acquila

Eur J Haematol· April 2013

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Diagnostic potential of hepcidin testing in pediatrics.
Giuliana Cangemi, Angela Pistorio, Maurizio Miano, Marco Gattorno, Maura Acquila

Eur J Haematol· April 2013

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MicroRNA-125b-1 and BLID upregulation resulting from a novel IGH translocation in childhood B-Cell precursor acute lymphoblastic leukemia.
Elisa Tassano, Maura Acquila, Elisa Tavella, Concetta Micalizzi, Claudio Panarello

Genes Chromosomes Cancer· August 2010

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Inversion (11)(p15q22) with NUP98-DDX10 fusion gene in pediatric acute myeloid leukemia.
Cristina Morerio, Maura Acquila, Annamaria Rapella, Elisa Tassano, Cristina Rosanda

Cancer Genet Cytogenet· December 2006

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Exon skipping partially restores factor VIII coagulant activity in patients with mild hemophilia A with exon 13 duplication.
Maura Acquila, Mirella Pasino, Tiziana Lanza, Angelo Claudio Molinari, Camillo Rosano

Haematologica· July 2005

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Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A.
Maria Patrizia Bicocchi, Barbara R Migeon, Mirella Pasino, Tiziana Lanza, Federico Bottini, Maura Acquila

Eur J Hum Genet· May 2005

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t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.
Cristina Morerio, Maura Acquila, Cristina Rosanda, Annamaria Rapella, Elisa Tassano

Leuk Res· April 2005

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Small FVIII gene rearrangements in 18 hemophilia A patients: five novel mutations.
Maria Patrizia Bicocchi, Mirella Pasino, Tiziana Lanza, Federico Bottini, Angelo Claudio Molinari, Maura Acquila

Am J Hematol· February 2005

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Ectopic mRNA analysis and molecular modelling substantiate severe haemophilia in a patient with a FVIII gene splice mutation.
Maria Patrizia Bicocchi, Mirella Pasino, Tiziana Lanza, Federico Bottini, Angelo Claudio Molinari, Maura Acquila

Thromb Haemost· February 2005

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Duplication of exon 13 causes one third of the cases of mild hemophilia A in northern Italy.
Maura Acquila, Mirella Pasino, Tiziana Lanza, Federico Bottini, Angelo Claudio Molinari

Haematologica· June 2004

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HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2).
Cristina Morerio, Maura Acquila, Cristina Rosanda, Annamaria Rapella, Carlo Dufour

Cancer Res· April 2004

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Analysis of 18 novel mutations in the factor VIII gene.
Maria P Bicocchi, Mirella Pasino, Tiziana Lanza, Federico Bottini, Elio Boeri, Maura Acquila

Br J Haematol· September 2003

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Mutation analysis impact on the genetic counseling of sporadic hemophilia B families.
Maria Patrizia Bicocchi, Mirella Pasino, Federico Bottini, Tiziana Lanza, Pier Giorgio Mori, Maura Acquila

Am J Med Genet A· May 2003

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Frequency of factor VIII intron 1 inversion in a cohort of severe hemophilia A Italian patients.
Maura Acquila, Mirella Pasino, Tiziana Lanza, Federico Bottini, Elio Boeri

Haematologica· May 2003

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