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Congenital Heart Disease|January 15, 2014
Variants in the NOTCH1 gene in patients with aortic coarctationOlga Freylikhman, Tatyana Tatarinova, Natalia Smolina, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2024
The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish PatientDilşad Türkdoğan, Natalia Smolina, Şeyma Tekgül, et al.
Molecular Genetics and Metabolism|May 19, 2015
Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific mannerAnna Malashicheva, Maria Bogdanova, Arsenii Zabirnyk, et al.
Genes|January 16, 2021
RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal HeartYuriy Vakhrushev, Alexandra Kozyreva, Andrey Semenov, et al.
Journal of Hypertension|July 3, 2015
Seventy years after the siege of Leningrad: does early life famine still affect cardiovascular risk and aging?Oxana Rotar, Ekaterina Moguchaia, Maria Boyarinova, et al.
Frontiers in Genetics|January 23, 2019
Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular HypertrophyAnastasia Knyazeva, Alexander Krutikov, Alexey Golovkin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 2024
Sacsin levels in PBMCs: A diagnostic assay for SACS variants in peripheral blood cells - A PROSPAX studyCeren Tunca, Eylül Ece İşlek Camadan, Natalia Smolina, et al.
Frontiers in Cardiovascular Medicine|May 24, 2021
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in ChildrenTatiana Kovalchuk, Elena Yakovleva, Svetlana Fetisova, et al.
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