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Molecular Genetics and Metabolism|February 5, 2013
Pitfalls in phenylalanine loading test in the diagnosis of dopa-responsive dystoniaThomas Opladen, Georg F Hoffmann, Andrea A Kühn, et al.
The American Journal of Physiology|May 1, 1995
Disturbances in renal microcirculation induced by myoglobin and hemorrhagic hypotension in anesthetized ratF Vetterlein, F Hoffmann, J Pedina, et al.
Zeitschrift Fur Rheumatologie|November 28, 2018
[Non-drug treatment of rheumatoid arthritis : An analysis of claims data and a survey of insured persons (Project PROCLAIR)]H Jacobs, J Callhoff, F Hoffmann, et al.
Integrative Biology : Quantitative Biosciences From Nano to Macro|June 14, 2018
Enhancing fluorescent protein photostability through robot-assisted photobleachingM D Wiens, F Hoffmann, Y Chen, et al.
Clinical Neurology and Neurosurgery|January 1, 1993
Ultrastructural study on avulsion effects of the cat cervical moto-axonal pathways in the spinal cordC F Hoffmann, H Choufoer, E Marani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2015
Ultra-orphan diseases: a quantitative analysis of the natural history of molybdenum cofactor deficiencyKonstantin Mechler, William K Mountford, Georg F Hoffmann, et al.
The Journal of Emergency Medicine|December 16, 2022
Bacteremia Prediction With Prognostic Scores and a Causal Probabilistic Network - A Cohort Study of Emergency Department PatientsKlaus N Jeppesen, Michael L Dalsgaard, Stig H Ovesen, et al.
European Journal of Emergency Medicine : Official Journal of the European Society for Emergency Medicine|August 30, 2019
The 7-day mortality associated with an early warning score varies between age groups in a cohort of adult Danish emergency department patientsJacob Dynesen, Maj J Skov, Julie Mackenhauer, et al.
Acta Anaesthesiologica Scandinavica|March 11, 2026
Bicarbonate and Other Buffer Therapies in Acute Metabolic Acidosis: A Systematic Review and Meta-AnalysisPeter C Lind, Frederik G Hansen, Mathias J Holmberg, et al.
Molecular Genetics and Metabolism|February 22, 2011
Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic)Bradley S Miller, Hudson H Freeze, Georg F Hoffmann, et al.
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