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Annals of the Rheumatic Diseases|January 6, 2019
Effect of a treat-to-target intervention of cardiovascular risk factors on subclinical and clinical atherosclerosis in rheumatoid arthritis: a randomised clinical trialBenjamin Burggraaf, Deborah F van Breukelen-van der Stoep, Marijke A de Vries, et al.
British Journal of Haematology|February 23, 2018
Time trend analysis of long term outcome of patients with haematological malignancies admitted at dutch intensive care unitsVera A de Vries, Marcella C A Müller, M Sesmu Arbous, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 3, 2025
Retinal optical coherence tomography angiography imaging in population studies for study of microvascular dysfunction in Alzheimer's disease and related dementiasAmir H Kashani, Tos T J M Berendschot, Sophie Bonnin, et al.
Gastroenterology|February 12, 2009
Improved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acidEdith M M Kuiper, Bettina E Hansen, Richard A de Vries, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstructionMarja W Wessels, Ingrid M B H van de Laar, Jolien Roos-Hesselink, et al.
Human Genetics|April 26, 2007
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomaliesL E L M Vissers, P Stankiewicz, S A Yatsenko, et al.
Human Mutation|January 12, 2017
Quantification of Phenotype Information Aids the Identification of Novel Disease GenesAnneke T Vulto-van Silfhout, Christian Gilissen, Jelle J Goeman, et al.
European Journal of Clinical Investigation|February 2, 2017
Erythrocyte-bound apolipoprotein B in atherosclerosis and mortalityMarijke A de Vries, Selvetta S van Santen, Boudewijn Klop, et al.
Molecular Psychiatry|February 22, 2025
YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programsMarlene F Pereira, Veronica Finazzi, Ludovico Rizzuti, et al.
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