Publications by authors named "Dora Fabbro"

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The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases.
Catia Mio, Jessica Zucco, Dora Fabbro, Elisa Bregant, Federica Baldan

Clin Genet· October 2024

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Filamin C (FLNC) truncating mutation in a fatal arrhythmogenic left ventricular cardiomyopathy (ALVC).
Francesco Simonit, Ugo Da Broi, Angela Valentina D'Elia, Dora Fabbro, Catia Mio

Leg Med (Tokyo)· July 2024

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JAK2 V617F-mutated polycythemia vera developing in a patient with a 20-year-long chronic myeloid leukemia at the time of first molecular response.
Luca Tosoni, Dora Fabbro, Umberto Pizzano, Rikard Mullai, Gianluca Morelli

Ann Hematol· May 2023

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Rare spontaneous monochorionic dizygotic twins: a case report and a systematic review.
Giulia Trombetta, Dora Fabbro, Eliana Demori, Lorenza Driul, Giuseppe Damante

BMC Pregnancy Childbirth· July 2022

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A novel de novo NIPA1 missense mutation associated to hereditary spastic paraplegia.
Dora Fabbro, Catia Mio, Federico Fogolari, Giuseppe Damante

J Hum Genet· December 2021

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NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
Elena Cavaliere, Anna Jolanda Gortan, Nadia Passon, Dora Fabbro, Dario Marin

Clin Genet· July 2021

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Temperament and character influence on depression treatment outcome.
Martina Balestri, Stefano Porcelli, Daniel Souery, Siegfried Kasper, Dimitris Dikeos, Dora Fabbro

J Affect Disord· June 2019

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Temperament and Character Inventory in Bipolar Disorder versus Healthy Controls and Modulatory Effects of 3 Key Functional Gene Variants.
Stefano Porcelli, Agnese Marsano, Elisabetta Caletti, Michela Sala, Vera Abbiati, Dora Fabbro

Neuropsychobiology· July 2018

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Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect.
Pierguido Sala, Antonio Colatutto, Dora Fabbro, Laura Mariuzzi, Stefania Marzinotto

Eur J Med Genet· April 2016

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Association between low-activity allele of cathecolamine-O-methyl-transferase (COMT) and Borderline Personality Disorder in an Italian population.
Matteo Lazzaretti, Dora Fabbro, Michela Sala, Kether Del Toso, Giulia de Vidovich

Behav Med· December 2013

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BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patients.
Daniela Damiani, Mario Tiribelli, Alessandra Franzoni, Angela Michelutti, Dora Fabbro

Am J Hematol· October 2013

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Q141K polymorphism of ABCG2 protein is associated with poor prognosis in adult acute myeloid leukemia treated with idarubicin-based chemotherapy.
Mario Tiribelli, Dora Fabbro, Alessandra Franzoni, Renato Fanin, Giuseppe Damante

Haematologica· March 2013

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Expression of fetal hemoglobin in adult humans exposed to high altitude hypoxia.
Angela Risso, Dora Fabbro, Giuseppe Damante, Guglielmo Antonutto

Blood Cells Mol Dis· March 2012

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Histone post-translational modifications associated to BAALC expression in leukemic cells.
Alessandra Franzoni, Nadia Passon, Dora Fabbro, Mario Tiribelli, Daniela Damiani

Biochem Biophys Res Commun· January 2012

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Using the recognition code to swap homeodomain target specificity in cell culture.
Cinzia Puppin, Dora Fabbro, Lucia Pellizzari, Giuseppe Damante

Mol Biol Rep· November 2011

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Concomitant ABCG2 overexpression and FLT3-ITD mutation identify a subset of acute myeloid leukemia patients at high risk of relapse.
Mario Tiribelli, Antonella Geromin, Angela Michelutti, Margherita Cavallin, Annalisa Pianta, Dora Fabbro

Cancer· May 2011

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Plasminogen activator inhibitor-1 gene polymorphisms in pre-eclampsia.
Angela V D'Elia, Dora Fabbro, Lorenza Driul, Giovanni Barillari, Diego Marchesoni

Semin Thromb Hemost· March 2011

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Osteopontin expression correlates with nuclear factor-κB activation and apoptosis downregulation in clear cell renal cell carcinoma.
Koviljka Matušan-Ilijaš, Giuseppe Damante, Dora Fabbro, Gordana Dorđević, Ita Hadžisejdić

Pathol Res Pract· February 2011

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A novel de novo germ-line V292M mutation in the extracellular region of RET in a patient with phaeochromocytoma and medullary thyroid carcinoma: functional characterization.
Maria D Castellone, Antonella Verrienti, Deva Magendra Rao, Marialuisa Sponziello, Dora Fabbro

Clin Endocrinol (Oxf)· October 2010

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Two novel NPM1 mutations in a therapy-responder AML patient.
Annalisa Pianta, Dora Fabbro, Daniela Damiani, Mario Tiribelli, Renato Fanin

Hematol Oncol· September 2010

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Fludarabine-based induction therapy does not overcome the negative effect of ABCG2 (BCRP) over-expression in adult acute myeloid leukemia patients.
Daniela Damiani, Mario Tiribelli, Angela Michelutti, Antonella Geromin, Margherita Cavallin, Dora Fabbro

Leuk Res· July 2010

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Nucleophosmin is overexpressed in thyroid tumors.
Annalisa Pianta, Cinzia Puppin, Alessandra Franzoni, Dora Fabbro, Carla Di Loreto

Biochem Biophys Res Commun· July 2010

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Unexpected phenotype of a typical NPM1 mutant.
Annalisa Pianta, Dora Fabbro, Daniela Damiani, Mario Tiribelli, Renato Fanin

Br J Haematol· December 2009

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Prohibitin is overexpressed in papillary thyroid carcinomas bearing the BRAF(V600E) mutation.
Alessandra Franzoni, Mariavittoria Dima, Maria D'Agostino, Cinzia Puppin, Dora Fabbro

Thyroid· March 2009

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Relationship between vascular endothelial growth factor and nuclear factor-kappaB in renal cell tumors.
Gordana Djordjević, Koviljka Matusan-Ilijas, Emina Sinozić, Giuseppe Damante, Dora Fabbro

Croat Med J· October 2008

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