Dora Fabbro
Udine, Italy
Last Updated: 09/26/2026
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Found 13 publications
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases.
Journal: Clinical genetics
Published: March 20, 2024
Filamin C (FLNC) truncating mutation in a fatal arrhythmogenic left ventricular cardiomyopathy (ALVC).
Journal: Legal medicine (Tokyo, Japan)
Published: November 11, 2023
JAK2 V617F-mutated polycythemia vera developing in a patient with a 20-year-long chronic myeloid leukemia at the time of first molecular response.
Journal: Annals of hematology
Published: March 06, 2023
Rare spontaneous monochorionic dizygotic twins: a case report and a systematic review.
Journal: BMC pregnancy and childbirth
Published: February 18, 2022
A novel de novo NIPA1 missense mutation associated to hereditary spastic paraplegia.
Journal: Journal of human genetics
Published: March 15, 2021
NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
Journal: Clinical genetics
Published: January 07, 2021
Temperament and character influence on depression treatment outcome.
Journal: Journal of affective disorders
Published: August 14, 2018
Temperament and Character Inventory in Bipolar Disorder versus Healthy Controls and Modulatory Effects of 3 Key Functional Gene Variants.
Journal: Neuropsychobiology
Published: April 20, 2018
Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect.
Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect.
Journal: European journal of medical genetics
Published: September 25, 2015
Association between low-activity allele of cathecolamine-O-methyl-transferase (COMT) and Borderline Personality Disorder in an Italian population.
Journal: Behavioral medicine (Washington, D.C.)
Published: May 15, 2013
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patients.
Journal: American journal of hematology
Published: March 04, 2013
Q141K polymorphism of ABCG2 protein is associated with poor prognosis in adult acute myeloid leukemia treated with idarubicin-based chemotherapy.
Journal: Haematologica
Published: October 16, 2012
Last Updated: 09/26/2026