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Gastroenterologia Y Hepatologia|June 10, 2022
Novel therapeutic avenues for the study of chronic liver disease and regeneration: The foundation of the Iberoamerican Consortium for the study of liver CirrhosisCarlos Sanz-Garcia, Yulia A Nevzorova, Eduardo Martínez-Naves, et al.
Clinical and Translational Gastroenterology|May 1, 2020
Altered Microbiota Diversity and Bile Acid Signaling in Cirrhotic and Noncirrhotic NASH-HCCSvenja Sydor, Jan Best, Insa Messerschmidt, et al.
Echocardiography (Mount Kisco, N.Y.)|January 26, 2016
Two-Dimensional Speckle Tracking Echocardiography in Heart Transplant Patients: Two-Year Follow-Up of Right and Left Ventricular FunctionVanessa Moñivas Palomero, Susana Mingo Santos, Josebe Goirigolzarri Artaza, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
The European Respiratory Journal|June 6, 2024
Poor cardiac output reserve in pulmonary arterial hypertension is associated with right ventricular stiffness and impaired interventricular dependenceIlton M Cubero Salazar, Andrew C Lancaster, Vivek P Jani, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 22, 2024
Donor-derived cell-free DNA as a new biomarker for cardiac allograft rejection: A prospective study (FreeDNA-CAR)Marta Jiménez-Blanco, Maria Generosa Crespo-Leiro, Maria Dolores García-Cosío Carmena, et al.
Clinical and Experimental Rheumatology|April 22, 2021
Tocilizumab in Behçet's disease with refractory ocular and/or neurological involvement: response according to different clinical phenotypesBelén Atienza-Mateo, Emma Beltrán, Marisa Hernández-Garfella, et al.
Lung Cancer (Amsterdam, Netherlands)|March 15, 2016
Aberrant gene methylation and bronchial dysplasia in high risk lung cancer patientsA Rosell, N Rodríguez, E Monsó, et al.
Neurology|November 2, 2018
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)David Genis, Sara Ortega-Cubero, Hector San Nicolás, et al.
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