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NPJ Parkinson'S Disease|February 17, 2025
Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s diseaseClara Krüger, Shen-Yang Lim, Alissa Buhrmann, et al.
Blood Cells, Molecules & Diseases|November 13, 2021
Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestryTimothy M Bahr, Archana M Agarwal, Jessica A Meznarich, et al.
British Journal of Sports Medicine|December 10, 2023
Injury and illness among Norwegian Olympic athletes during preparation for five consecutive Summer and Winter GamesBenjamin Clarsen, Hilde Moseby Berge, Fredrik Bendiksen, et al.
Zeitschrift Fur Kardiologie|July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Stem Cells Translational Medicine|June 24, 2020
Treatment of chronic GvHD with mesenchymal stromal cells induces durable responses: A phase II studyErik Boberg, Lena von Bahr, Gabriel Afram, et al.
Italian Heart Journal : Official Journal of the Italian Federation of Cardiology|June 1, 2000
Gene-specific differences in the circadian variation of ventricular repolarization in the long QT syndrome: a key to sudden death during sleep?M Stramba-Badiale, S G Priori, C Napolitano, et al.
European Journal of Human Genetics : EJHG|December 7, 2007
Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activityP Yang, T T Koopmann, A Pfeufer, et al.
Scandinavian Journal of Gastroenterology|December 5, 2009
Membranous Budd-Chiari syndrome in CaucasiansSandra Ciesek, Kinan Rifai, Matthias J Bahr, et al.
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