15 results on '"Heliö Tiina"'
Search Results
2. Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations
3. Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients
4. Prognostic significance of incidental suspected transthyretin amyloidosis on routine bone scintigraphy
5. Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
6. DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy
7. CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutation
8. Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
9. Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2
10. Cardiovascular magnetic resonance of mitral valve length in hypertrophic cardiomyopathy
11. Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations
12. Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy
13. Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging
14. 2069 Assessment of genetic dilated cardiomyopathy in LMNA-mutation carriers by cardiac MRI
15. Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
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