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IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control|March 23, 2007
PMN-PT single crystal, high-frequency ultrasonic needle transducers for pulsed-wave Doppler applicationQifa Zhou, Xiaochen Xu, Emanuel J Gottlieb, et al.Gene|April 23, 2013
Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patientsMaría Martín, Irene A Pichel, Juan P Flórez Muñoz, et al.IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control|December 31, 2009
Design and fabrication of PIN-PMN-PT single-crystal high-frequency ultrasound transducersPing Sun, Qifa Zhou, Benpeng Zhu, et al.JACC. Case Reports|February 16, 2024
Bileaflet Tethering With Preserved LV Geometry and Function: An Unusual Mechanism of Functional Mitral RegurgitationDario Donia, Kamil Stankowski, Stefano Figliozzi, et al.Scientific Reports|February 24, 2019
Vitamin D Receptor Polymorphism and DHCR7 Contribute to the Abnormal Interplay Between Vitamin D and Lipid Profile in Rheumatoid ArthritisJavier Rodríguez-Carrio, Mercedes Alperi-López, Manuel Naves-Díaz, et al.IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control|April 29, 2005
Fabrication and characterization of micromachined high-frequency tonpilz transducers derived by PZT thick filmsQifa Zhou, Jonathan M Cannata, Richard J Meyer, et al.European Journal of Pharmacology|June 11, 2008
Effects of phytoestrogen genistein on cytogenetic biomarkers in postmenopausal women: 1 year randomized, placebo-controlled studyMarco Atteritano, Francesco Pernice, Susanna Mazzaferro, et al.Hemoglobin|August 29, 2019
Double Heterozygosity for Hb Durham-N.C. (<i>HBB</i>: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (<i>HBB</i>: c.93-21G>A) Causing a Severe β-Thalassemia PhenotypeMonica Cannata, Filippo Cassarà, Margherita Vinciguerra, et al.Calcified Tissue International|November 15, 2020
Chronic Kidney Disease-Mineral and Bone Disorders: Pathogenesis and ManagementJorge B Cannata-Andía, Beatriz Martín-Carro, Julia Martín-Vírgala, et al.Molecular Biology Reports|June 22, 2012
New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathyCristina Alonso-Montes, Manuel Naves-Diaz, Jose Luis Fernandez-Martin, et al.Pageof 110