Publications by authors named "F Baldan"

Article Synopsis
  • - Liquid biopsy is being researched as a method to improve the diagnosis and monitoring of head and neck squamous cell carcinoma (HNSCC), which has a high chance of recurrence after treatment.
  • - A study with 17 patients analyzed saliva samples for genetic mutations, finding that a significant portion contained pathogenic variants, with TP53 being the most commonly mutated gene.
  • - The findings suggest that analyzing salivary DNA could help in early detection of disease recurrence, paving the way for more personalized treatment options based on individual mutations.
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Chromoanagenesis events consist of complex chromosome rearrangements with multiple breakpoints in one or few chromosomes. Mechanisms of chromoanagenesis are split into three major groups: chromothripsis, chromoanasynthesis and chromoplexy. This study aims to delineate a chromoanagenesis event at the level of chromosome 22 in an individual showing obesity and borderline cognitive performance as major disturbances.

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In the last decade, an incredible improvement has been made in elucidating the genetic bases of cardiomyopathies. Here we report the impact of either the European Society of Cardiology (ESC) guidelines or the use of whole exome sequencing (WES) in terms of a number of variants of uncertain significance (VUS) and missed diagnoses in a series of 260 patients affected by inherited cardiac disorders. Samples were analyzed using a targeted gene panel of 128 cardiac-related genes and/or WES in a subset of patients, with a three-tier approach.

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Thyroid cancer is the most common endocrine carcinoma and, among its different subtypes, the papillary subtype (PTC) is the most frequent. Generally, PTCs are well differentiated, but a minor percentage of PTCs are characterized by a worse prognosis and more aggressive behavior. Phytochemicals, naturally found in plant products, represent a heterogeneous group of bioactive compounds that can interfere with cell proliferation and the regulation of the cell cycle, taking part in multiple signaling pathways that are often disrupted in tumor initiation, proliferation, and progression.

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Article Synopsis
  • The study focuses on congenital ocular diseases, particularly anterior segment dysgenesis (ASD), highlighting the complexities in diagnosing and classifying these conditions due to genetic variability.
  • Over 20 years, researchers analyzed 162 patients using various genomic techniques, finding that 66.7% had pathogenic variants in the PAX6 gene, crucial for ASD, and 20.3% exhibited deletions affecting the 11p13 locus.
  • Whole exome sequencing (WES) proved essential in identifying known ASD gene variants as well as rare phenotypes, enhancing diagnostic accuracy for ocular dysgenesis cases with overlapping symptoms.
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