Showing results (561-570 of 718) with videos related to
Sort By:
Pageof 72
Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|December 8, 2009
Apoptotic pathways in degenerative disk lesions in the wristFrank Unglaub, Susanne B Thomas, Markus W Kroeber, et al.Archives of Orthopaedic and Trauma Surgery|May 6, 2009
Cartilage cell proliferation in degenerative TFCC wrist lesionsFrank Unglaub, Susanne B Thomas, Maya B Wolf, et al.Biomedica Biochimica Acta|January 1, 1983
[Uric acid determination in dilute serum with an enzyme electrochemical and enzyme-free sensor]M Jänchen, G Walzel, B Neef, et al.Biosensors & Bioelectronics|April 5, 2001
Non-invasive measurement of cell membrane associated proton gradients by ion-sensitive field effect transistor arrays for microphysiological and bioelectronical applicationsM Lehmann, W Baumann, M Brischwein, et al.The American Review of Respiratory Disease|April 1, 1989
Dyscoordinate expression of tumor necrosis factor-alpha by human blood monocytes and alveolar macrophagesE A Rich, J R Panuska, R S Wallis, et al.European Journal of Clinical Pharmacology|January 1, 1984
Assessment of adverse drug reactions in psychiatric hospitalsR Grohmann, H Hippius, B Müller-Oerlinghausen, et al.Human Molecular Genetics|May 1, 1997
Profound biotinidase deficiency caused by a point mutation that creates a downstream cryptic 3' splice acceptor site within an exon of the human biotinidase geneR J Pomponio, T R Reynolds, H Mandel, et al.Alzheimer'S Research & Therapy|September 4, 2013
Apolipoprotein E as a β-amyloid-independent factor in Alzheimer's diseaseAndrew B Wolf, Jon Valla, Guojun Bu, et al.Pediatric Research|December 13, 1997
Mutations in the human biotinidase gene that cause profound biotinidase deficiency in symptomatic children: molecular, biochemical, and clinical analysisR J Pomponio, J Hymes, T R Reynolds, et al.Multiple Sclerosis and Related Disorders|September 23, 2019
Rituximab-induced serum sickness in multiple sclerosis patientsAndrew B Wolf, Lana Zhovtis Ryerson, Krupa Pandey, et al.Pageof 72