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Nederlands Tijdschrift Voor Geneeskunde|February 1, 2002
[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation]C M A van Ravenswaaij-Arts, A M W van den Ouweland, A J M Hoogeboom, et al.
Journal of the Neurological Sciences|December 1, 1983
Hereditary neuralgic amyotrophy. Clinical, genetic, electrophysiological and histopathological studiesW F Arts, H F Busch, H J Van den Brand, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 28, 2017
Tubular discectomy versus conventional microdiscectomy for the treatment of lumbar disc herniation: long-term results of a randomised controlled trialGijsbert M Overdevest, Wilco C Peul, Ronald Brand, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|March 7, 2009
Efficacy of the long-acting repeatable formulation of the somatostatin analogue octreotide in postoperative dumpingJoris Arts, Philip Caenepeel, Raf Bisschops, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 17, 2012
Muscle ultrasonography: a diagnostic tool for amyotrophic lateral sclerosisIlse M P Arts, Sebastiaan Overeem, Sigrid Pillen, et al.
Journal of the International Society of Sports Nutrition|April 19, 2012
Adenosine 5'-triphosphate (ATP) supplements are not orally bioavailable: a randomized, placebo-controlled cross-over trial in healthy humansIlja Cw Arts, Erik Jcm Coolen, Martijn Jl Bours, et al.
The EMBO Journal|April 1, 1993
Implications of novel guide RNA features for the mechanism of RNA editing in Crithidia fasciculataG J Arts, H van der Spek, D Speijer, et al.
Environmental Research|July 22, 2014
Risk-benefit of consuming Lake Erie fishMargaret R Neff, Satyendra P Bhavsar, Felicity J Ni, et al.
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