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European Journal of Human Genetics : EJHG|November 28, 2013
Structural genomic variation in childhood epilepsies with complex phenotypesIngo Helbig, Marielle E M Swinkels, Emmelien Aten, et al.
Research and Practice in Thrombosis and Haemostasis|February 4, 2021
Heavy menstrual bleeding on direct factor Xa inhibitors: Rationale and design of the MEDEA studyEva N Hamulyák, Hanke M G Wiegers, Luuk J J Scheres, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 2, 2024
Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhageJulie W Rutten, Minne N Cerfontaine, Kyra L Dijkstra, et al.
Journal of Cachexia, Sarcopenia and Muscle|November 6, 2025
Anabolic Effects of Salbutamol Are Lost Upon ImmobilizationJelle C B C de Jong, Tom S O Jameson, Rob C Andrews, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 21, 2023
Transition readiness among adolescents and young adults with haemophilia in the Netherlands: Nationwide questionnaire studyMartijn R Brands, Ebony A M Janssen, Marjon H Cnossen, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|November 21, 2020
Hospital variation in combined liver resection and thermal ablation for colorectal liver metastases and impact on short-term postoperative outcomes: a nationwide population-based studyArthur K E Elfrink, Sanne Nieuwenhuizen, M Petrousjka van den Tol, et al.
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