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The Annals of Otology, Rhinology, and Laryngology|November 24, 2025
Risk Factors for the Initial Misdiagnosis of Spontaneous Cerebrospinal Fluid RhinorrheaMatthew Y Liu, Erin M Lopez, Erik K Weitzel, et al.Der Nervenarzt|October 5, 2021
[E-Mental Health and healthcare apps in Germany]Elena Caroline Weitzel, Janine Quittschalle, Franziska Dinah Welzel, et al.European Journal of Nuclear Medicine and Molecular Imaging|August 4, 2010
PET/CT-guided biopsies of metabolically active bone lesions: applications and clinical impactBernd Klaeser, Jakub Wiskirchen, Jan Wartenberg, et al.Journal of Molecular Modeling|May 1, 2010
Interaction between alkaline earth cations and oxo-ligands. DFT study of the affinity of the Ca2+ cation for carbonyl ligandsLeonardo Moreira da Costa, José Walkimar de Mesquita Carneiro, Gilberto Alves Romeiro, et al.Physical Chemistry Chemical Physics : PCCP|March 8, 2017
Charge attachment induced transport - bulk and grain boundary diffusion of potassium in PrMnO3Johannes Martin, Melanie Gräf, Thilo Kramer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 18, 2005
Outcomes from intensive training in genetic cancer risk counseling for cliniciansKathleen R Blazer, Deborah J MacDonald, Charite Ricker, et al.Journal of Molecular Endocrinology|June 20, 2008
The role of thyroid hormone receptor DNA binding in negative thyroid hormone-mediated gene transcriptionAnne Wulf, Marianne G Wetzel, Maxim Kebenko, et al.Plos Genetics|November 7, 2015
Connecting Replication and Repair: YoaA, a Helicase-Related Protein, Promotes Azidothymidine Tolerance through Association with Chi, an Accessory Clamp Loader ProteinLaura T Brown, Vincent A Sutera, Shen Zhou, et al.Revista Chilena De Infectologia : Organo Oficial De La Sociedad Chilena De Infectologia|June 13, 2012
[Salmonellosis outbreaks and the size and role of the Chilean State]Alberto Fica, Gerardo Acosta, Jeannette Dabanch, et al.International Journal of Clinical Medicine|December 20, 2013
Hereditary leukemia due to rare RUNX1c splice variant (L472X) presents with eczematous phenotypeA Sorrell, C Espenschied, W Wang, et al.Pageof 131