Larysa N. Sivitskaya
MI 220072, Belarus
Last Updated: 09/26/2026
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Found 10 publications
Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland.
Journal: Biomedicines
Published: April 30, 2024
Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases.
Journal: Journal of clinical medicine
Published: June 22, 2021
New deletion in LAMP2 causing familial Danon disease. Effect of the X-chromosome inactivation.
Journal: Folia medica
Published: March 22, 2021
Splicing mutation in TAZ gene leading to exon skipping and Barth syndrome.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: January 08, 2021
AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients.
Journal: The pharmacogenomics journal
Published: October 14, 2020
Novel desmoplakin mutations in familial Carvajal syndrome.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: April 05, 2019
Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: May 18, 2018
Dilatation of the Chambers of the Heart Caused by a Mutation of Lamin Gene (LMNA)
Journal: Kardiologiia
Published: March 16, 2017
LMNA-related dilated cardiomyopathy.
Journal: Oxford medical case reports
Published: February 12, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026