Publications by authors named "Filomena Daraio"

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Droplet Digital PCR for Monitoring in Diagnostic Routine: Ready to Start?
Maria Teresa Bochicchio, Jessica Petiti, Paola Berchialla, Barbara Izzo, Emilia Giugliano, Filomena Daraio

Cancers (Basel)· October 2021

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Alignment of Qx100/Qx200 Droplet Digital (Bio-Rad) and QuantStudio 3D (Thermofisher) Digital PCR for Quantification of BCR-ABL1 in Ph+ Chronic Myeloid Leukemia.
Carmen Fava, Simona Bernardi, Enrico Marco Gottardi, Roberta Lorenzatti, Laura Galeotti, Filomena Daraio

Diseases· May 2021

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Treatment-Free Remission in Chronic Myeloid Leukemia Harboring Atypical BCR-ABL1 Transcripts.
Matteo Dragani, Jessica Petiti, Giovanna Rege-Cambrin, Enrico Gottardi, Filomena Daraio

Mediterr J Hematol Infect Dis· September 2020

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Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches.
Barbara Izzo, Enrico Marco Gottardi, Santa Errichiello, Filomena Daraio, Claudia Baratè

Front Oncol· September 2019

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Philadelphia-positive lymphoblastic lymphoma: a case report and review of the literature.
Matteo Dragani, Giacomo Andreani, Carmen Fava, Filomena Daraio, Enrico Gottardi

Stem Cell Investig· July 2019

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CALR-positive myeloproliferative disorder in a patient with Ph-positive chronic myeloid leukemia in durable treatment-free remission: a case report.
Irene Dogliotti, Carmen Fava, Anna Serra, Enrico Gottardi, Filomena Daraio

Stem Cell Investig· June 2017

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Early BCR-ABL1 Reduction Is Predictive of Better Event-free Survival in Patients With Newly Diagnosed Chronic Myeloid Leukemia Treated With Any Tyrosine Kinase Inhibitor.
Carmen Fava, Giovanna Rege-Cambrin, Irene Dogliotti, Enrico Gottardi, Paola Berchialla, Filomena Daraio

Clin Lymphoma Myeloma Leuk· August 2016

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Sensitive Replicate Real-Time Quantitative PCR of BCR-ABL Shows Deep Molecular Responses in Long-Term Post-Allogeneic Stem Cell Transplantation Chronic Myeloid Leukemia Patients.
Maya Koren-Michowitz, Avichai Shimoni, Filomena Daraio, Francesca Crasto, Roberta Lorenzatti

Biol Blood Marrow Transplant· October 2015

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Second-generation tyrosine kinase inhibitors can induce complete molecular response in Ph-positive acute lymphoblastic leukemia after allogeneic stem cell transplant.
Carmen Fava, Giovanna Rege-Cambrin, Alessandro Busca, Enrico Gottardi, Filomena Daraio

Clin Lymphoma Myeloma Leuk· September 2013

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Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia.
Lucia De Franceschi, Filomena Daraio, Alida Filippini, Sonia Carturan, Eva Maria Muchitsch

Haematologica· October 2006

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Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism.
Francesca Ferrari, Barbara Foglieni, Paolo Arosio, Clara Camaschella, Filomena Daraio

Hum Mutat· February 2006

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Genetic and clinical heterogeneity of ferroportin disease.
L Cremonesi, Gian Luca Forni, Nadia Soriani, Martina Lamagna, Isabella Fermo, Filomena Daraio

Br J Haematol· December 2005

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A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron.
Graça Porto, Antonella Roetto, Filomena Daraio, Jorge Pereira Pinto, Susana Almeida

Blood· October 2005

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Hepatic expression of hemochromatosis genes in two mouse strains after phlebotomy and iron overload.
Alessandro Bondi, Paola Valentino, Filomena Daraio, Paolo Porporato, Enrico Gramaglia

Haematologica· September 2005

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Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.
Giorgio Biasiotto, Antonella Roetto, Filomena Daraio, Anna Polotti, Gian Mario Gerardi

Blood Cells Mol Dis· April 2005

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Juvenile hemochromatosis HJV-related revealed by cardiogenic shock.
Mounir Filali, Claire Le Jeunne, Eric Durand, Jean-Michel Grinda, Antonella Roetto, Filomena Daraio

Blood Cells Mol Dis· February 2005

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Growth hormone (GH)-induced reconstitution of CD8+ CD28+ T lymphocytes in a rare case of severe lymphopenia associated with Juvenile Haemochromatosis and Turner's syndrome.
Graça Porto, Eugénia Cruz, Helena Pessegueiro Miranda, Beatriz Porto, José Carlos Vasconcelos, Filomena Daraio

Clin Endocrinol (Oxf)· October 2004

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Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.
Carmela Lanzara, Antonella Roetto, Filomena Daraio, Silvain Rivard, Romina Ficarella

Blood· June 2004

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Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R).
Antonella Roetto, Filomena Daraio, Paolo Porporato, Roberta Caruso, Timothy M Cox

Blood· March 2004

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Homozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.
Alberto Piperno, Antonella Roetto, Raffaella Mariani, Sara Pelucchi, Chiara Corengia, Filomena Daraio

Haematologica· March 2004

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Hemochromatosis due to mutations in transferrin receptor 2.
Antonella Roetto, Filomena Daraio, Federica Alberti, Paolo Porporato, Angelita Calì

Blood Cells Mol Dis· November 2003

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Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
Marco De Gobbi, Filomena Daraio, Christian Oberkanins, Anne Moritz, Fritz Kury

Haematologica· April 2003

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A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.
Antonella Roetto, Alison T Merryweather-Clarke, Filomena Daraio, Karen Livesey, Jennifer J Pointon

Blood· July 2002

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Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene.
Domenico Girelli, Claudia Bozzini, Antonella Roetto, Federica Alberti, Filomena Daraio

Gastroenterology· May 2002

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