Elisa Brigonzi
Milan, Italy
Last Updated: 09/26/2026
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Found 9 publications
Incidence of amplification failure in DMPK allele due to allelic dropout event in a diagnostic laboratory.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 26, 2018
SCN4A as modifier gene in patients with myotonic dystrophy type 2.
Journal: Scientific reports
Published: April 24, 2018
Neuropsychological and Psychological Functioning Aspects in Myotonic Dystrophy Type 1 Patients in Italy.
Journal: Frontiers in neurology
Published: March 19, 2018
Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature.
Journal: Frontiers in neurology
Published: February 12, 2018
Development and Validation of a New Molecular Diagnostic Assay for Detection of Myotonic Dystrophy Type 2.
Journal: Genetic testing and molecular biomarkers
Published: October 28, 2015
Identification and characterization of DM1 patients by a new diagnostic certified assay: neuromuscular and cardiac assessments.
Journal: BioMed research international
Published: October 26, 2012
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomes.
Journal: International journal of cardiology
Published: September 21, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026