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Journal of Inherited Metabolic Disease|June 8, 2020
Effects of higher and more frequent dosing of alglucosidase alfa and immunomodulation on long-term clinical outcome of classic infantile Pompe patientsEsther Poelman, Jan J A van den Dorpel, Marianne Hoogeveen-Westerveld, et al.Trials|December 4, 2014
Expanding Paramedicine in the Community (EPIC): study protocol for a randomized controlled trialIan R Drennan, Katie N Dainty, Paul Hoogeveen, et al.Journal of the American Geriatrics Society|July 31, 2019
High-Sensitive Troponin T, Natriuretic Peptide, and Cognitive ChangeYashashwi Pokharel, Farah Mouhanna, Andrea L C Schneider, et al.Human Mutation|August 21, 2012
Functional assessment of TSC2 variants identified in individuals with tuberous sclerosis complexMarianne Hoogeveen-Westerveld, Rosemary Ekong, Sue Povey, et al.Experimental Cell Research|May 1, 2019
Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cellsJulianna Kobolák, Kinga Molnár, Eszter Varga, et al.Clinical Genetics|February 22, 2011
Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindredsM Wentink, M Nellist, M Hoogeveen-Westerveld, et al.JACC. Advances|February 21, 2025
Does Adiponectin Inform Cardiovascular Risk in Older Adults?: The ARIC StudyLayla A Abushamat, Xiaoming Jia, Lu Xu, et al.Circulation. Cardiovascular Genetics|December 19, 2012
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studiesBing Yu, Maja Barbalic, Ariel Brautbar, et al.Circulation. Heart Failure|May 17, 2012
Prediction of incident heart failure in general practice: the Atherosclerosis Risk in Communities (ARIC) StudySunil K Agarwal, Lloyd E Chambless, Christie M Ballantyne, et al.Journal of Inherited Metabolic Disease|April 24, 2016
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcomeChristiaan P Sentner, Irene J Hoogeveen, David A Weinstein, et al.Pageof 79