Torthaí cuardaigh - Christoph Sandmann

Cardiomyopathy and mitochondrial encephalomyopathy in a female child associated with a heterozygous X-linked AIFM1 variant de réir Christoph Sandmann, Swathi Gudapati, Johannes A. Mayr, Rami Abou Jamra, Alexander Kovacevic, Steffen Syrbe

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RMC-6272, a selective third-generation bi-steric mTORC1 inhibitor, improves cardiac function in pressure overload-induced cardiac hypertrophy de réir Mariam Rogge, Johannes Fischer, Tobias Jakobi, Zoe Loewenthal, Parul Gupta, Lonny Jürgensen, Norbert Frey, Christoph Sandmann, Mirko Völkers

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Yield on Reinterpretation of Genetic Variants in Pediatric Cardiomyopathy de réir Takanori Suzuki, Robert Lesurf, Rajadurai Akilen, Xiaoqiao Xu, Eva Maria Batke, Vinay J. Rao, Rebekah Jobling, Laura Zahavich, Natasha Henden, Jodie Ingles, Edgardo Alania Torres, Keiichi Hirono, Nathalie Roux‐buisson, Perundurai S. Dhandapany, Christoph Sandmann, Seema Mital

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