4 Einträge gefunden

1. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular non-compaction phenotype

   1. Kolokotronis, Konstantinos
   2. Kühnisch, Jirko
   3. Klopocki, Eva
   4. Dartsch, Josephine
   5. Rost, Simone
   6. Huculak, Cathleen
   7. Mearini, Giulia

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
2. Gene therapy strategies in the treatment of hypertrophic cardiomyopathy

   1. Prondzynski, Maksymilian
   2. Mearini, Giulia
   3. Carrier, Lucie

   2019 - Forschungsinformationssystem des UKE
3. Analysis of Contractile Function of Permeabilized Human Hypertrophic Cardiomyopathy Multicellular Heart Tissue

   1. Kresin, Nico
   2. Stücker, Sabrina
   3. Krämer, Elisabeth
   4. Flenner, Frederik
   5. Mearini, Giulia
   6. Münch, Julia
   7. Patten, Monica

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
4. Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3

   1. Kühnisch, Jirko
   2. Herbst, Christopher
   3. Al-Wakeel-Marquard, Nadya
   4. Dartsch, Josephine
   5. Holtgrewe, Manuel
   6. Baban, Anwar
   7. Mearini, Giulia

   2019 - Forschungsinformationssystem des UKE