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You searched for: Author/Creator Villard, Eric

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2. A kpc-scale-resolved study of unobscured and obscured star formation activity in normal galaxies at z  = 1.5 and 2.2 from ALMA and HiZELS. Issue 4 (2nd October 2020)

3. A novel genetic variant in the transcription factor Islet‐1 exerts gain of function on myocyte enhancer factor 2C promoter activity. (March 2013)

4. A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk). (15th September 2021)

5. Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stress. Issue 2 (17th December 2019)

6. FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations. Issue 4 (18th July 2019)

7. Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects. (March 2018)

8. Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23. (3rd March 2021)

9. Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients. (15th June 2015)

10. Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients. (15th June 2015)