Publications by authors named "Elisa Brigonzi"

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Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies.
Laura Valentina Renna, Francesca Bosè, Elisa Brigonzi, Barbara Fossati, Giovanni Meola

PLoS One· December 2019

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Incidence of amplification failure in DMPK allele due to allelic dropout event in a diagnostic laboratory.
Claudia De Siena, Rosanna Cardani, Elisa Brigonzi, Francesca Bosè, Barbara Fossati

Clin Chim Acta· September 2018

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Neuropsychological and Psychological Functioning Aspects in Myotonic Dystrophy Type 1 Patients in Italy.
Edward Callus, Enrico G Bertoldo, Maria Beretta, Sara Boveri, Rosanna Cardani, Elisa Brigonzi

Front Neurol· September 2018

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SCN4A as modifier gene in patients with myotonic dystrophy type 2.
Anna Binda, Laura V Renna, Francesca Bosè, Elisa Brigonzi, Annalisa Botta

Sci Rep· July 2018

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Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature.
Michele Cavalli, Barbara Fossati, Raffaele Vitale, Elisa Brigonzi, Vito A G Ricigliano

Front Neurol· May 2018

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Cardiac involvement in myotonic dystrophy: The role of troponins and N-terminal pro B-type natriuretic peptide.
Rea Valaperta, Claudia De Siena, Rosanna Cardani, Fortunata Lombardia, Edina Cenko, Elisa Brigonzi

Atherosclerosis· December 2017

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Development and Validation of a New Molecular Diagnostic Assay for Detection of Myotonic Dystrophy Type 2.
Rea Valaperta, Fortunata Lombardi, Rosanna Cardani, Barbara Fossati, Elisa Brigonzi

Genet Test Mol Biomarkers· December 2015

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Identification and characterization of DM1 patients by a new diagnostic certified assay: neuromuscular and cardiac assessments.
Rea Valaperta, Valeria Sansone, Fortunata Lombardi, Chiara Verdelli, Alessio Colombo, Elisa Brigonzi

Biomed Res Int· December 2013

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